Townson, Reid W
2013-01-01
Due to the increasing complexity of radiotherapy delivery, accurate dose verification has become an essential part of the clinical treatment process. The purpose of this work was to develop an electronic portal image (EPI) based pre-treatment verification technique capable of quickly reconstructing 3D dose distributions from both coplanar and non-coplanar treatments. The dose reconstruction is performed in a spherical water phantom by modulating, based on EPID measurements, pre-calculated Monte Carlo (MC) doselets defined on a spherical coordinate system. This is called the spherical doselet modulation (SDM) method. This technique essentially eliminates the statistical uncertainty of the MC dose calculations by exploiting both azimuthal symmetry in a patient-independent phase-space and symmetry of a virtual spherical water phantom. The symmetry also allows the number of doselets necessary for dose reconstruction to be reduced by a factor of about 250. In this work, 51 doselets were used. The SDM method mitiga...
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To evaluate the dosimetric differences between Superposition/Convolution (SC) and Monte Carlo (MC) calculated dose distributions for simultaneous integrated boost (SIB) prostate cancer intensity modulated radiotherapy (IMRT) compared to experimental (film) measurements and the implications for clinical treatments. Twenty-two prostate patients treated with an in-house SIB-IMRT protocol were selected. SC-based plans used for treatment were re-evaluated with EGS4-based MC calculations for treatment verification. Accuracy was evaluated with-respect-to film-based dosimetry. Comparisons used gamma (γ)-index, distance-to-agreement (DTA), and superimposed dose distributions. The treatment plans were also compared based on dose-volume indices and 3-D γ index for targets and critical structures. Flat-phantom comparisons demonstrated that the MC algorithm predicted measurements better than the SC algorithm. The average PTVprostate D98 agreement between SC and MC was 1.2% ± 1.1. For rectum, the average differences in SC and MC calculated D50 ranged from -3.6% to 3.4%. For small bowel, there were up to 30.2% ± 40.7 (range: 0.2%, 115%) differences between SC and MC calculated average D50 index. For femurs, the differences in average D50 reached up to 8.6% ± 3.6 (range: 1.2%, 14.5%). For PTVprostate and PTVnodes, the average gamma scores were >95.0%. MC agrees better with film measurements than SC. Although, on average, SC-calculated doses agreed with MC calculations within the targets within 2%, there were deviations up to 5% for some patient's treatment plans. For some patients, the magnitude of such deviations might decrease the intended target dose levels that are required for the treatment protocol, placing the patients in different dose levels that do not satisfy the protocol dose requirements
Application of a Monte Carlo linac model in routine verifications of dose calculations
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The analysis of some parameters of interest in Radiotherapy Medical Physics based on an experimentally validated Monte Carlo model of an Elekta Precise lineal accelerator, was performed for 6 and 15 Mv photon beams. The simulations were performed using the EGSnrc code. As reference for simulations, the optimal beam parameters values (energy and FWHM) previously obtained were used. Deposited dose calculations in water phantoms were done, on typical complex geometries commonly are used in acceptance and quality control tests, such as irregular and asymmetric fields. Parameters such as MLC scatter, maximum opening or closing position, and the separation between them were analyzed from calculations in water. Similarly simulations were performed on phantoms obtained from CT studies of real patients, making comparisons of the dose distribution calculated with EGSnrc and the dose distribution obtained from the computerized treatment planning systems (TPS) used in routine clinical plans. All the results showed a great agreement with measurements, finding all of them within tolerance limits. These results allowed the possibility of using the developed model as a robust verification tool for validating calculations in very complex situation, where the accuracy of the available TPS could be questionable. (Author)
Ma, C.-M.; Pawlicki, T.; Jiang, S. B.; Li, J. S.; Deng, J.; Mok, E.; Kapur, A.; Xing, L.; Ma, L.; Boyer, A. L.
2000-09-01
The purpose of this work was to use Monte Carlo simulations to verify the accuracy of the dose distributions from a commercial treatment planning optimization system (Corvus, Nomos Corp., Sewickley, PA) for intensity-modulated radiotherapy (IMRT). A Monte Carlo treatment planning system has been implemented clinically to improve and verify the accuracy of radiotherapy dose calculations. Further modifications to the system were made to compute the dose in a patient for multiple fixed-gantry IMRT fields. The dose distributions in the experimental phantoms and in the patients were calculated and used to verify the optimized treatment plans generated by the Corvus system. The Monte Carlo calculated IMRT dose distributions agreed with the measurements to within 2% of the maximum dose for all the beam energies and field sizes for both the homogeneous and heterogeneous phantoms. The dose distributions predicted by the Corvus system, which employs a finite-size pencil beam (FSPB) algorithm, agreed with the Monte Carlo simulations and measurements to within 4% in a cylindrical water phantom with various hypothetical target shapes. Discrepancies of more than 5% (relative to the prescribed target dose) in the target region and over 20% in the critical structures were found in some IMRT patient calculations. The FSPB algorithm as implemented in the Corvus system is adequate for homogeneous phantoms (such as prostate) but may result in significant under- or over-estimation of the dose in some cases involving heterogeneities such as the air-tissue, lung-tissue and tissue-bone interfaces.
Petoukhova, A. L.; van Wingerden, K.; Wiggenraad, R. G. J.; van de Vaart, P. J. M.; van Egmond, J.; Franken, E. M.; van Santvoort, J. P. C.
2010-08-01
This study presents data for verification of the iPlan RT Monte Carlo (MC) dose algorithm (BrainLAB, Feldkirchen, Germany). MC calculations were compared with pencil beam (PB) calculations and verification measurements in phantoms with lung-equivalent material, air cavities or bone-equivalent material to mimic head and neck and thorax and in an Alderson anthropomorphic phantom. Dosimetric accuracy of MC for the micro-multileaf collimator (MLC) simulation was tested in a homogeneous phantom. All measurements were performed using an ionization chamber and Kodak EDR2 films with Novalis 6 MV photon beams. Dose distributions measured with film and calculated with MC in the homogeneous phantom are in excellent agreement for oval, C and squiggle-shaped fields and for a clinical IMRT plan. For a field with completely closed MLC, MC is much closer to the experimental result than the PB calculations. For fields larger than the dimensions of the inhomogeneities the MC calculations show excellent agreement (within 3%/1 mm) with the experimental data. MC calculations in the anthropomorphic phantom show good agreement with measurements for conformal beam plans and reasonable agreement for dynamic conformal arc and IMRT plans. For 6 head and neck and 15 lung patients a comparison of the MC plan with the PB plan was performed. Our results demonstrate that MC is able to accurately predict the dose in the presence of inhomogeneities typical for head and neck and thorax regions with reasonable calculation times (5-20 min). Lateral electron transport was well reproduced in MC calculations. We are planning to implement MC calculations for head and neck and lung cancer patients.
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Proton beam radiotherapy is an effective and non-invasive treatment for uveal melanoma. Recent research efforts have focused on improving the dosimetric accuracy of treatment planning and overcoming the present limitation of relative analytical dose calculations. Monte Carlo algorithms have been shown to accurately predict dose per monitor unit (D/MU) values, but this has yet to be shown for analytical algorithms dedicated to ocular proton therapy, which are typically less computationally expensive than Monte Carlo algorithms. The objective of this study was to determine if an analytical method could predict absolute dose distributions and D/MU values for a variety of treatment fields like those used in ocular proton therapy. To accomplish this objective, we used a previously validated Monte Carlo model of an ocular nozzle to develop an analytical algorithm to predict three-dimensional distributions of D/MU values from pristine Bragg peaks and therapeutically useful spread-out Bragg peaks (SOBPs). Results demonstrated generally good agreement between the analytical and Monte Carlo absolute dose calculations. While agreement in the proximal region decreased for beams with less penetrating Bragg peaks compared with the open-beam condition, the difference was shown to be largely attributable to edge-scattered protons. A method for including this effect in any future analytical algorithm was proposed. Comparisons of D/MU values showed typical agreement to within 0.5%. We conclude that analytical algorithms can be employed to accurately predict absolute proton dose distributions delivered by an ocular nozzle.
Tyagi, N.; Curran, B. H.; Roberson, P. L.; Moran, J. M.; Acosta, E.; Fraass, B. A.
2008-02-01
IMRT often requires delivering small fields which may suffer from electronic disequilibrium effects. The presence of heterogeneities, particularly low-density tissues in patients, complicates such situations. In this study, we report on verification of the DPM MC code for IMRT treatment planning in heterogeneous media, using a previously developed model of the Varian 120-leaf MLC. The purpose of this study is twofold: (a) design a comprehensive list of experiments in heterogeneous media for verification of any dose calculation algorithm and (b) verify our MLC model in these heterogeneous type geometries that mimic an actual patient geometry for IMRT treatment. The measurements have been done using an IMRT head and neck phantom (CIRS phantom) and slab phantom geometries. Verification of the MLC model has been carried out using point doses measured with an A14 slim line (SL) ion chamber inside a tissue-equivalent and a bone-equivalent material using the CIRS phantom. Planar doses using lung and bone equivalent slabs have been measured and compared using EDR films (Kodak, Rochester, NY).
Künzler, Thomas; Fotina, Irina; Stock, Markus; Georg, Dietmar
2009-12-01
The dosimetric performance of a Monte Carlo algorithm as implemented in a commercial treatment planning system (iPlan, BrainLAB) was investigated. After commissioning and basic beam data tests in homogenous phantoms, a variety of single regular beams and clinical field arrangements were tested in heterogeneous conditions (conformal therapy, arc therapy and intensity-modulated radiotherapy including simultaneous integrated boosts). More specifically, a cork phantom containing a concave-shaped target was designed to challenge the Monte Carlo algorithm in more complex treatment cases. All test irradiations were performed on an Elekta linac providing 6, 10 and 18 MV photon beams. Absolute and relative dose measurements were performed with ion chambers and near tissue equivalent radiochromic films which were placed within a transverse plane of the cork phantom. For simple fields, a 1D gamma (γ) procedure with a 2% dose difference and a 2 mm distance to agreement (DTA) was applied to depth dose curves, as well as to inplane and crossplane profiles. The average gamma value was 0.21 for all energies of simple test cases. For depth dose curves in asymmetric beams similar gamma results as for symmetric beams were obtained. Simple regular fields showed excellent absolute dosimetric agreement to measurement values with a dose difference of 0.1% ± 0.9% (1 standard deviation) at the dose prescription point. A more detailed analysis at tissue interfaces revealed dose discrepancies of 2.9% for an 18 MV energy 10 × 10 cm2 field at the first density interface from tissue to lung equivalent material. Small fields (2 × 2 cm2) have their largest discrepancy in the re-build-up at the second interface (from lung to tissue equivalent material), with a local dose difference of about 9% and a DTA of 1.1 mm for 18 MV. Conformal field arrangements, arc therapy, as well as IMRT beams and simultaneous integrated boosts were in good agreement with absolute dose measurements in the
Fragoso, Margarida; Wen, Ning; Kumar, Sanath; Liu, Dezhi; Ryu, Samuel; Movsas, Benjamin; Munther, Ajlouni; Chetty, Indrin J.
2010-08-01
Modern cancer treatment techniques, such as intensity-modulated radiation therapy (IMRT) and stereotactic body radiation therapy (SBRT), have greatly increased the demand for more accurate treatment planning (structure definition, dose calculation, etc) and dose delivery. The ability to use fast and accurate Monte Carlo (MC)-based dose calculations within a commercial treatment planning system (TPS) in the clinical setting is now becoming more of a reality. This study describes the dosimetric verification and initial clinical evaluation of a new commercial MC-based photon beam dose calculation algorithm, within the iPlan v.4.1 TPS (BrainLAB AG, Feldkirchen, Germany). Experimental verification of the MC photon beam model was performed with film and ionization chambers in water phantoms and in heterogeneous solid-water slabs containing bone and lung-equivalent materials for a 6 MV photon beam from a Novalis (BrainLAB) linear accelerator (linac) with a micro-multileaf collimator (m3 MLC). The agreement between calculated and measured dose distributions in the water phantom verification tests was, on average, within 2%/1 mm (high dose/high gradient) and was within ±4%/2 mm in the heterogeneous slab geometries. Example treatment plans in the lung show significant differences between the MC and one-dimensional pencil beam (PB) algorithms within iPlan, especially for small lesions in the lung, where electronic disequilibrium effects are emphasized. Other user-specific features in the iPlan system, such as options to select dose to water or dose to medium, and the mean variance level, have been investigated. Timing results for typical lung treatment plans show the total computation time (including that for processing and I/O) to be less than 10 min for 1-2% mean variance (running on a single PC with 8 Intel Xeon X5355 CPUs, 2.66 GHz). Overall, the iPlan MC algorithm is demonstrated to be an accurate and efficient dose algorithm, incorporating robust tools for MC
Yuan, Jiankui; Lo, Simon S; Zheng, Yiran; Sohn, Jason W; Sloan, Andrew E; Ellis, Rodney; Machtay, Mitchell; Wessels, Barry
2016-01-01
Detailed Monte Carlo (MC) modeling of the Leksell Gamma Knife (GK) Perfexion (PFX) collimator system is the only accurate ab initio approach appearing in the literature. As a different approach, in this work, we present a MC model based on film measurement. By adjusting the model parameters and fine-tuning the derived fluence map for each individual source to match the manufacturer's ring output factors, we created a reasonable virtual source model for MC simulations to verify treatment planning dose for the GK PFX radiosurgery system. The MC simulation model was commissioned by simple single shots. Dose profiles and both ring and collimator output factors were compared with the treatment planning system (TPS). Good agreement was achieved for dose profiles especially for the region of plateau (< 2%), while larger difference (< 5%) came from the penumbra region. The maximum difference of the calculated output factor was within 0.7%. The model was further validated by a clinical test case. Good agreement was obtained. The DVHs for brainstem and the skull were almost identical and, for the target, the volume covered by the prescription (12.5 Gy to 50% isodose line) was 95.6% from MC calculation versus 100% from the TPS. PMID:27455497
Simple dose verification system for radiotherapy radiation
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The aim of this paper is to investigate an accurate and convenient quality assurance programme that should be included in the dosimetry system of the radiotherapy level radiation. We designed a mailed solid phantom and used TLD-100 chips and a Rexon UL320 reader for the purpose of dosimetry quality assurance in Taiwanese radiotherapy centers. After being assembled, the solid polystyrene phantom weighted only 375 g which was suitable for mailing. The Monte Carlo BEAMnrc code was applied in calculations of the dose conversion factor of water and polystyrene phantom: the dose conversion factor measurements were obtained by switching the TLDs at the same calibration depth of water and the solid phantom to measure the absorbed dose and verify the accuracy of the theoretical calculation results. The experimental results showed that the dose conversion factors from TLD measurements and the calculation values from the BEAMnrc were in good agreement with a difference within 0.5%. Ten radiotherapy centers were instructed to deliver to the TLDs on central beam axis absorbed dose of 2 Gy. The measured doses were compared with the planned ones. A total of 21 beams were checked. The dose verification differences under reference conditions for 60Co, high energy X-rays of 6, 10 and 15 MV were truly within 4% and that proved the feasibility of applying the method suggested in this work in radiotherapy dose verification
SU-E-T-29: A Web Application for GPU-Based Monte Carlo IMRT/VMAT QA with Delivered Dose Verification
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Folkerts, M [The University of Texas Southwestern Medical Ctr, Dallas, TX (United States); University of California, San Diego, La Jolla, CA (United States); Graves, Y [University of California, San Diego, La Jolla, CA (United States); Tian, Z; Gu, X; Jia, X; Jiang, S [The University of Texas Southwestern Medical Ctr, Dallas, TX (United States)
2014-06-01
Purpose: To enable an existing web application for GPU-based Monte Carlo (MC) 3D dosimetry quality assurance (QA) to compute “delivered dose” from linac logfile data. Methods: We added significant features to an IMRT/VMAT QA web application which is based on existing technologies (HTML5, Python, and Django). This tool interfaces with python, c-code libraries, and command line-based GPU applications to perform a MC-based IMRT/VMAT QA. The web app automates many complicated aspects of interfacing clinical DICOM and logfile data with cutting-edge GPU software to run a MC dose calculation. The resultant web app is powerful, easy to use, and is able to re-compute both plan dose (from DICOM data) and delivered dose (from logfile data). Both dynalog and trajectorylog file formats are supported. Users upload zipped DICOM RP, CT, and RD data and set the expected statistic uncertainty for the MC dose calculation. A 3D gamma index map, 3D dose distribution, gamma histogram, dosimetric statistics, and DVH curves are displayed to the user. Additional the user may upload the delivery logfile data from the linac to compute a 'delivered dose' calculation and corresponding gamma tests. A comprehensive PDF QA report summarizing the results can also be downloaded. Results: We successfully improved a web app for a GPU-based QA tool that consists of logfile parcing, fluence map generation, CT image processing, GPU based MC dose calculation, gamma index calculation, and DVH calculation. The result is an IMRT and VMAT QA tool that conducts an independent dose calculation for a given treatment plan and delivery log file. The system takes both DICOM data and logfile data to compute plan dose and delivered dose respectively. Conclusion: We sucessfully improved a GPU-based MC QA tool to allow for logfile dose calculation. The high efficiency and accessibility will greatly facilitate IMRT and VMAT QA.
SU-E-T-29: A Web Application for GPU-Based Monte Carlo IMRT/VMAT QA with Delivered Dose Verification
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Purpose: To enable an existing web application for GPU-based Monte Carlo (MC) 3D dosimetry quality assurance (QA) to compute “delivered dose” from linac logfile data. Methods: We added significant features to an IMRT/VMAT QA web application which is based on existing technologies (HTML5, Python, and Django). This tool interfaces with python, c-code libraries, and command line-based GPU applications to perform a MC-based IMRT/VMAT QA. The web app automates many complicated aspects of interfacing clinical DICOM and logfile data with cutting-edge GPU software to run a MC dose calculation. The resultant web app is powerful, easy to use, and is able to re-compute both plan dose (from DICOM data) and delivered dose (from logfile data). Both dynalog and trajectorylog file formats are supported. Users upload zipped DICOM RP, CT, and RD data and set the expected statistic uncertainty for the MC dose calculation. A 3D gamma index map, 3D dose distribution, gamma histogram, dosimetric statistics, and DVH curves are displayed to the user. Additional the user may upload the delivery logfile data from the linac to compute a 'delivered dose' calculation and corresponding gamma tests. A comprehensive PDF QA report summarizing the results can also be downloaded. Results: We successfully improved a web app for a GPU-based QA tool that consists of logfile parcing, fluence map generation, CT image processing, GPU based MC dose calculation, gamma index calculation, and DVH calculation. The result is an IMRT and VMAT QA tool that conducts an independent dose calculation for a given treatment plan and delivery log file. The system takes both DICOM data and logfile data to compute plan dose and delivered dose respectively. Conclusion: We sucessfully improved a GPU-based MC QA tool to allow for logfile dose calculation. The high efficiency and accessibility will greatly facilitate IMRT and VMAT QA
Directory of Open Access Journals (Sweden)
Grządziel Małgorzata
2014-07-01
Full Text Available Verification of calculations of the depth-dose distributions in water, using GEANT4 (version of 4.9.3 and MCNPX (version of 2.7.0 Monte Carlo codes, was performed for the scatterer-phantom system used in the dosimetry measurements in the proton therapy of eye tumours. The simulated primary proton beam had the energy spectra distributed according to the Gauss distribution with the cut at energy greater than that related to the maximum of the spectrum. The energy spectra of the primary protons were chosen to get the possibly best agreement between the measured relative depth-dose distributions along the central-axis of the proton beam in a water phantom and that derived from the Monte Carlo calculations separately for the both tested codes. The local depth-dose differences between results from the calculations and the measurements were mostly less than 5% (the mean value of 2.1% and 3.6% for the MCNPX and GEANT4 calculations. In the case of the MCNPX calculations, the best fit to the experimental data was obtained for the spectrum with maximum at 60.8 MeV (more probable energy, FWHM of the spectrum of 0.4 MeV and the energy cut at 60.85 MeV whereas in the GEANT4 calculations more probable energy was 60.5 MeV, FWHM of 0.5 MeV, the energy cut at 60.7 MeV. Thus, one can say that the results obtained by means of the both considered Monte Carlo codes are similar but they are not the same. Therefore the agreement between the calculations and the measurements has to be verified before each application of the MCNPX and GEANT4 codes for the determination of the depth-dose curves for the therapeutic protons.
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Garnica-Garza, H M [Centro de Investigacion y de Estudios Avanzados del Instituto Politecnico Nacional Unidad Monterrey, VIa del Conocimiento 201 Parque de Investigacion e Innovacion Tecnologica, Apodaca NL C.P. 66600 (Mexico)], E-mail: hgarnica@cinvestav.mx
2009-03-21
Monte Carlo simulation was employed to calculate the response of TLD-100 chips under irradiation conditions such as those found during accelerated partial breast irradiation with the MammoSite radiation therapy system. The absorbed dose versus radius in the last 0.5 cm of the treated volume was also calculated, employing a resolution of 20 {mu}m, and a function that fits the observed data was determined. Several clinically relevant irradiation conditions were simulated for different combinations of balloon size, balloon-to-surface distance and contents of the contrast solution used to fill the balloon. The thermoluminescent dosemeter (TLD) cross-calibration factors were derived assuming that the calibration of the dosemeters was carried out using a Cobalt 60 beam, and in such a way that they provide a set of parameters that reproduce the function that describes the behavior of the absorbed dose versus radius curve. Such factors may also prove to be useful for those standardized laboratories that provide postal dosimetry services.
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Monte Carlo simulation was employed to calculate the response of TLD-100 chips under irradiation conditions such as those found during accelerated partial breast irradiation with the MammoSite radiation therapy system. The absorbed dose versus radius in the last 0.5 cm of the treated volume was also calculated, employing a resolution of 20 μm, and a function that fits the observed data was determined. Several clinically relevant irradiation conditions were simulated for different combinations of balloon size, balloon-to-surface distance and contents of the contrast solution used to fill the balloon. The thermoluminescent dosemeter (TLD) cross-calibration factors were derived assuming that the calibration of the dosemeters was carried out using a Cobalt 60 beam, and in such a way that they provide a set of parameters that reproduce the function that describes the behavior of the absorbed dose versus radius curve. Such factors may also prove to be useful for those standardized laboratories that provide postal dosimetry services.
A quality assurance phantom for IMRT dose verification
Ma, C.-M.; Jiang, S. B.; Pawlicki, T.; Chen, Y.; Li, J. S.; Deng, J.; Boyer, A. L.
2003-03-01
This paper investigates a quality assurance (QA) phantom specially designed to verify the accuracy of dose distributions and monitor units (MU) calculated by clinical treatment planning optimization systems and by the Monte Carlo method for intensity-modulated radiotherapy (IMRT). The QA phantom is a PMMA cylinder of 30 cm diameter and 40 cm length with various bone and lung inserts. A procedure (and formalism) has been developed to measure the absolute dose to water in the PMMA phantom. Another cylindrical phantom of the same dimensions, but made of water, was used to confirm the results obtained with the PMMA phantom. The PMMA phantom was irradiated by 4, 6 and 15 MV photon beams and the dose was measured using an ionization chamber and compared to the results calculated by a commercial inverse planning system (CORVUS, NOMOS, Sewickley, PA) and by the Monte Carlo method. The results show that the dose distributions calculated by both CORVUS and Monte Carlo agreed to within 2% of dose maximum with measured results in the uniform PMMA phantom for both open and intensity-modulated fields. Similar agreement was obtained between Monte Carlo calculations and measured results with the bone and lung heterogeneity inside the PMMA phantom while the CORVUS results were 4% different. The QA phantom has been integrated as a routine QA procedure for the patient's IMRT dose verification at Stanford since 1999.
Monte Carlo Calculations Supporting Patient Plan Verification in Proton Therapy.
Lima, Thiago V M; Dosanjh, Manjit; Ferrari, Alfredo; Molineli, Silvia; Ciocca, Mario; Mairani, Andrea
2016-01-01
Patient's treatment plan verification covers substantial amount of the quality assurance (QA) resources; this is especially true for Intensity-Modulated Proton Therapy (IMPT). The use of Monte Carlo (MC) simulations in supporting QA has been widely discussed, and several methods have been proposed. In this paper, we studied an alternative approach from the one being currently applied clinically at Centro Nazionale di Adroterapia Oncologica (CNAO). We reanalyzed the previously published data (Molinelli et al. (1)), where 9 patient plans were investigated in which the warning QA threshold of 3% mean dose deviation was crossed. The possibility that these differences between measurement and calculated dose were related to dose modeling (Treatment Planning Systems (TPS) vs. MC), limitations on dose delivery system, or detectors mispositioning was originally explored, but other factors, such as the geometric description of the detectors, were not ruled out. For the purpose of this work, we compared ionization chambers' measurements with different MC simulation results. It was also studied that some physical effects were introduced by this new approach, for example, inter-detector interference and the delta ray thresholds. The simulations accounting for a detailed geometry typically are superior (statistical difference - p-value around 0.01) to most of the MC simulations used at CNAO (only inferior to the shift approach used). No real improvement was observed in reducing the current delta ray threshold used (100 keV), and no significant interference between ion chambers in the phantom were detected (p-value 0.81). In conclusion, it was observed that the detailed geometrical description improves the agreement between measurement and MC calculations in some cases. But in other cases, position uncertainty represents the dominant uncertainty. The inter-chamber disturbance was not detected for the therapeutic protons energies, and the results from the current delta threshold
Monte Carlo calculations supporting patient plan verification in proton therapy
Directory of Open Access Journals (Sweden)
Thiago Viana Miranda Lima
2016-03-01
Full Text Available Patient’s treatment plan verification covers substantial amount of the quality assurance (QA resources, this is especially true for Intensity Modulated Proton Therapy (IMPT. The use of Monte Carlo (MC simulations in supporting QA has been widely discussed and several methods have been proposed. In this paper we studied an alternative approach from the one being currently applied clinically at Centro Nazionale di Adroterapia Oncologica (CNAO. We reanalysed the previously published data (Molinelli et al. 2013, where 9 patient plans were investigated in which the warning QA threshold of 3% mean dose deviation was crossed. The possibility that these differences between measurement and calculated dose were related to dose modelling (Treatment Planning Systems (TPS vs MC, limitations on dose delivery system or detectors mispositioning was originally explored but other factors such as the geometric description of the detectors were not ruled out. For the purpose of this work we compared ionisation-chambers measurements with different MC simulations results. It was also studied some physical effects introduced by this new approach for example inter detector interference and the delta ray thresholds. The simulations accounting for a detailed geometry typically are superior (statistical difference - p-value around 0.01 to most of the MC simulations used at CNAO (only inferior to the shift approach used. No real improvement were observed in reducing the current delta-ray threshold used (100 keV and no significant interference between ion chambers in the phantom were detected (p-value 0.81. In conclusion, it was observed that the detailed geometrical description improves the agreement between measurement and MC calculations in some cases. But in other cases position uncertainty represents the dominant uncertainty. The inter chamber disturbance was not detected for the therapeutic protons energies and the results from the current delta threshold are
Monte Carlo Calculations Supporting Patient Plan Verification in Proton Therapy
Lima, Thiago V. M.; Dosanjh, Manjit; Ferrari, Alfredo; Molineli, Silvia; Ciocca, Mario; Mairani, Andrea
2016-01-01
Patient’s treatment plan verification covers substantial amount of the quality assurance (QA) resources; this is especially true for Intensity-Modulated Proton Therapy (IMPT). The use of Monte Carlo (MC) simulations in supporting QA has been widely discussed, and several methods have been proposed. In this paper, we studied an alternative approach from the one being currently applied clinically at Centro Nazionale di Adroterapia Oncologica (CNAO). We reanalyzed the previously published data (Molinelli et al. (1)), where 9 patient plans were investigated in which the warning QA threshold of 3% mean dose deviation was crossed. The possibility that these differences between measurement and calculated dose were related to dose modeling (Treatment Planning Systems (TPS) vs. MC), limitations on dose delivery system, or detectors mispositioning was originally explored, but other factors, such as the geometric description of the detectors, were not ruled out. For the purpose of this work, we compared ionization chambers’ measurements with different MC simulation results. It was also studied that some physical effects were introduced by this new approach, for example, inter-detector interference and the delta ray thresholds. The simulations accounting for a detailed geometry typically are superior (statistical difference – p-value around 0.01) to most of the MC simulations used at CNAO (only inferior to the shift approach used). No real improvement was observed in reducing the current delta ray threshold used (100 keV), and no significant interference between ion chambers in the phantom were detected (p-value 0.81). In conclusion, it was observed that the detailed geometrical description improves the agreement between measurement and MC calculations in some cases. But in other cases, position uncertainty represents the dominant uncertainty. The inter-chamber disturbance was not detected for the therapeutic protons energies, and the results from the current delta
Monte Carlo dose computation for IMRT optimization*
Laub, W.; Alber, M.; Birkner, M.; Nüsslin, F.
2000-07-01
A method which combines the accuracy of Monte Carlo dose calculation with a finite size pencil-beam based intensity modulation optimization is presented. The pencil-beam algorithm is employed to compute the fluence element updates for a converging sequence of Monte Carlo dose distributions. The combination is shown to improve results over the pencil-beam based optimization in a lung tumour case and a head and neck case. Inhomogeneity effects like a broader penumbra and dose build-up regions can be compensated for by intensity modulation.
Monte Carlo dose mapping on deforming anatomy
Zhong, Hualiang; Siebers, Jeffrey V.
2009-10-01
This paper proposes a Monte Carlo-based energy and mass congruent mapping (EMCM) method to calculate the dose on deforming anatomy. Different from dose interpolation methods, EMCM separately maps each voxel's deposited energy and mass from a source image to a reference image with a displacement vector field (DVF) generated by deformable image registration (DIR). EMCM was compared with other dose mapping methods: energy-based dose interpolation (EBDI) and trilinear dose interpolation (TDI). These methods were implemented in EGSnrc/DOSXYZnrc, validated using a numerical deformable phantom and compared for clinical CT images. On the numerical phantom with an analytically invertible deformation map, EMCM mapped the dose exactly the same as its analytic solution, while EBDI and TDI had average dose errors of 2.5% and 6.0%. For a lung patient's IMRT treatment plan, EBDI and TDI differed from EMCM by 1.96% and 7.3% in the lung patient's entire dose region, respectively. As a 4D Monte Carlo dose calculation technique, EMCM is accurate and its speed is comparable to 3D Monte Carlo simulation. This method may serve as a valuable tool for accurate dose accumulation as well as for 4D dosimetry QA.
Monte Carlo dose distributions for radiosurgery
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The precision of Radiosurgery Treatment planning systems is limited by the approximations of their algorithms and by their dosimetrical input data. This fact is especially important in small fields. However, the Monte Carlo methods is an accurate alternative as it considers every aspect of particle transport. In this work an acoustic neurinoma is studied by comparing the dose distribution of both a planning system and Monte Carlo. Relative shifts have been measured and furthermore, Dose-Volume Histograms have been calculated for target and adjacent organs at risk. (orig.)
Verification of Monte Carlo transport codes FLUKA, Mars and Shield
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The present study is a continuation of the project 'Verification of Monte Carlo Transport Codes' which is running at GSI as a part of activation studies of FAIR relevant materials. It includes two parts: verification of stopping modules of FLUKA, MARS and SHIELD-A (with ATIMA stopping module) and verification of their isotope production modules. The first part is based on the measurements of energy deposition function of uranium ions in copper and stainless steel. The irradiation was done at 500 MeV/u and 950 MeV/u, the experiment was held at GSI from September 2004 until May 2005. The second part is based on gamma-activation studies of an aluminium target irradiated with an argon beam of 500 MeV/u in August 2009. Experimental depth profiling of the residual activity of the target is compared with the simulations. (authors)
International Nuclear Information System (INIS)
Intensity Modulated Radiation Therapy (IMRT) treatments are some of the most complex being delivered by modern megavoltage radiotherapy accelerators. Therefore verification of the dose, or the presecribed Monitor Units (MU), predicted by the planning system is a key element to ensuring that patients should receive an accurate radiation dose plan during IMRT. One inherently accurate method is by comparison with absolute calibrated Monte Carlo simulations of the IMRT delivery by the linac head and corresponding delivery of the plan to a patient based phantom. In this work this approach has been taken using BEAMnrc for simulation of the treatment head, and both DOSXYZnrc and Geant4 for the phantom dose calculation. The two Monte Carlo codes agreed to within 1% of each other, and these matched very well to our planning system for IMRT plans to the brain, nasopharynx, and head and neck.
Development and verification of Monte Carlo burnup calculation system
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Monte Carlo burnup calculation code system has been developed to evaluate accurate various quantities required in the backend field. From the Actinide Research in a Nuclear Element (ARIANE) program, by using, the measured nuclide compositions of fuel rods in the fuel assemblies irradiated in the commercial Netherlands BWR, the analyses have been performed for the code system verification. The code system developed in this paper has been verified through analysis for MOX and UO2 fuel rods. This system enables to reduce large margin assumed in the present criticality analysis for LWR spent fuels. (J.P.N.)
Dose verification exercise at Agrosurg irradiators (India)
International Nuclear Information System (INIS)
Accurate dose measurements traceable to recognized national standards are essential components of industrial radiation processing. M/s Agrosurg, Vasai, India designed for source strength of 37 PBq (1000 kCi) of Cobalt-60, is a fully automatic and continuous gamma irradiation facility for sterilization of medical or surgical products and disinfestations of Agro products. Dose verification exercise for processing of poha was carried out using Ceric-cerous (3 mM) dosimeter and Alanine EPR pellet dosimeter by Agrosurg and RP and AD respectively. The Dmin and Dmax values specified for poha for insect disinfestations are 0.2 kGy and 1 kGy respectively. The overall uncertainty in dose delivered to food product, during routine food irradiation, shall not exceed ± 10 % (1σ). Dmin and Dmax values for both the boxes agree very well. The maximum difference observed between individual Agrosurg and RP and AD dose value was within 10%. The Over Dose Ratio of 1.42 measured by Agrosurg agree well with the ODR value 1.45 measured by RP and AD. As overall average dose delivered to the food product agrees within ±10 % (1σ), the Gamma Irradiation Facility viz., Agrosurg was issued license for food irradiation by the competent authority
Development and validation of MCNPX-based Monte Carlo treatment plan verification system
Directory of Open Access Journals (Sweden)
Iraj Jabbari
2015-01-01
Full Text Available A Monte Carlo treatment plan verification (MCTPV system was developed for clinical treatment plan verification (TPV, especially for the conformal and intensity-modulated radiotherapy (IMRT plans. In the MCTPV, the MCNPX code was used for particle transport through the accelerator head and the patient body. MCTPV has an interface with TiGRT planning system and reads the information which is needed for Monte Carlo calculation transferred in digital image communications in medicine-radiation therapy (DICOM-RT format. In MCTPV several methods were applied in order to reduce the simulation time. The relative dose distribution of a clinical prostate conformal plan calculated by the MCTPV was compared with that of TiGRT planning system. The results showed well implementation of the beams configuration and patient information in this system. For quantitative evaluation of MCTPV a two-dimensional (2D diode array (MapCHECK2 and gamma index analysis were used. The gamma passing rate (3%/3 mm of an IMRT plan was found to be 98.5% for total beams. Also, comparison of the measured and Monte Carlo calculated doses at several points inside an inhomogeneous phantom for 6- and 18-MV photon beams showed a good agreement (within 1.5%. The accuracy and timing results of MCTPV showed that MCTPV could be used very efficiently for additional assessment of complicated plans such as IMRT plan.
Verification of Monte Carlo transport codes by activation experiments
International Nuclear Information System (INIS)
With the increasing energies and intensities of heavy-ion accelerator facilities, the problem of an excessive activation of the accelerator components caused by beam losses becomes more and more important. Numerical experiments using Monte Carlo transport codes are performed in order to assess the levels of activation. The heavy-ion versions of the codes were released approximately a decade ago, therefore the verification is needed to be sure that they give reasonable results. Present work is focused on obtaining the experimental data on activation of the targets by heavy-ion beams. Several experiments were performed at GSI Helmholtzzentrum fuer Schwerionenforschung. The interaction of nitrogen, argon and uranium beams with aluminum targets, as well as interaction of nitrogen and argon beams with copper targets was studied. After the irradiation of the targets by different ion beams from the SIS18 synchrotron at GSI, the γ-spectroscopy analysis was done: the γ-spectra of the residual activity were measured, the radioactive nuclides were identified, their amount and depth distribution were detected. The obtained experimental results were compared with the results of the Monte Carlo simulations using FLUKA, MARS and SHIELD. The discrepancies and agreements between experiment and simulations are pointed out. The origin of discrepancies is discussed. Obtained results allow for a better verification of the Monte Carlo transport codes, and also provide information for their further development. The necessity of the activation studies for accelerator applications is discussed. The limits of applicability of the heavy-ion beam-loss criteria were studied using the FLUKA code. FLUKA-simulations were done to determine the most preferable from the radiation protection point of view materials for use in accelerator components.
MCDE: a new Monte Carlo dose engine for IMRT.
Reynaert, N; De Smedt, B; Coghe, M; Paelinck, L; Van Duyse, B; De Gersem, W; De Wagter, C; De Neve, W; Thierens, H
2004-07-21
A new accurate Monte Carlo code for IMRT dose computations, MCDE (Monte Carlo dose engine), is introduced. MCDE is based on BEAMnrc/DOSXYZnrc and consequently the accurate EGSnrc electron transport. DOSXYZnrc is reprogrammed as a component module for BEAMnrc. In this way both codes are interconnected elegantly, while maintaining the BEAM structure and only minimal changes to BEAMnrc.mortran are necessary. The treatment head of the Elekta SLiplus linear accelerator is modelled in detail. CT grids consisting of up to 200 slices of 512 x 512 voxels can be introduced and up to 100 beams can be handled simultaneously. The beams and CT data are imported from the treatment planning system GRATIS via a DICOM interface. To enable the handling of up to 50 x 10(6) voxels the system was programmed in Fortran95 to enable dynamic memory management. All region-dependent arrays (dose, statistics, transport arrays) were redefined. A scoring grid was introduced and superimposed on the geometry grid, to be able to limit the number of scoring voxels. The whole system uses approximately 200 MB of RAM and runs on a PC cluster consisting of 38 1.0 GHz processors. A set of in-house made scripts handle the parallellization and the centralization of the Monte Carlo calculations on a server. As an illustration of MCDE, a clinical example is discussed and compared with collapsed cone convolution calculations. At present, the system is still rather slow and is intended to be a tool for reliable verification of IMRT treatment planning in the case of the presence of tissue inhomogeneities such as air cavities. PMID:15357203
MCDE: a new Monte Carlo dose engine for IMRT
International Nuclear Information System (INIS)
A new accurate Monte Carlo code for IMRT dose computations, MCDE (Monte Carlo dose engine), is introduced. MCDE is based on BEAMnrc/DOSXYZnrc and consequently the accurate EGSnrc electron transport. DOSXYZnrc is reprogrammed as a component module for BEAMnrc. In this way both codes are interconnected elegantly, while maintaining the BEAM structure and only minimal changes to BEAMnrc.mortran are necessary. The treatment head of the Elekta SLiplus linear accelerator is modelled in detail. CT grids consisting of up to 200 slices of 512 x 512 voxels can be introduced and up to 100 beams can be handled simultaneously. The beams and CT data are imported from the treatment planning system GRATIS via a DICOM interface. To enable the handling of up to 50 x 106 voxels the system was programmed in Fortran95 to enable dynamic memory management. All region-dependent arrays (dose, statistics, transport arrays) were redefined. A scoring grid was introduced and superimposed on the geometry grid, to be able to limit the number of scoring voxels. The whole system uses approximately 200 MB of RAM and runs on a PC cluster consisting of 38 1.0 GHz processors. A set of in-house made scripts handle the parallellization and the centralization of the Monte Carlo calculations on a server. As an illustration of MCDE, a clinical example is discussed and compared with collapsed cone convolution calculations. At present, the system is still rather slow and is intended to be a tool for reliable verification of IMRT treatment planning in the case of the presence of tissue inhomogeneities such as air cavities. (note)
SU-E-T-578: MCEBRT, A Monte Carlo Code for External Beam Treatment Plan Verifications
Energy Technology Data Exchange (ETDEWEB)
Chibani, O; Ma, C [Fox Chase Cancer Center, Philadelphia, PA (United States); Eldib, A [Fox Chase Cancer Center, Philadelphia, PA (United States); Al-Azhar University, Cairo (Egypt)
2014-06-01
Purpose: Present a new Monte Carlo code (MCEBRT) for patient-specific dose calculations in external beam radiotherapy. The code MLC model is benchmarked and real patient plans are re-calculated using MCEBRT and compared with commercial TPS. Methods: MCEBRT is based on the GEPTS system (Med. Phys. 29 (2002) 835–846). Phase space data generated for Varian linac photon beams (6 – 15 MV) are used as source term. MCEBRT uses a realistic MLC model (tongue and groove, rounded ends). Patient CT and DICOM RT files are used to generate a 3D patient phantom and simulate the treatment configuration (gantry, collimator and couch angles; jaw positions; MLC sequences; MUs). MCEBRT dose distributions and DVHs are compared with those from TPS in absolute way (Gy). Results: Calculations based on the developed MLC model closely matches transmission measurements (pin-point ionization chamber at selected positions and film for lateral dose profile). See Fig.1. Dose calculations for two clinical cases (whole brain irradiation with opposed beams and lung case with eight fields) are carried out and outcomes are compared with the Eclipse AAA algorithm. Good agreement is observed for the brain case (Figs 2-3) except at the surface where MCEBRT dose can be higher by 20%. This is due to better modeling of electron contamination by MCEBRT. For the lung case an overall good agreement (91% gamma index passing rate with 3%/3mm DTA criterion) is observed (Fig.4) but dose in lung can be over-estimated by up to 10% by AAA (Fig.5). CTV and PTV DVHs from TPS and MCEBRT are nevertheless close (Fig.6). Conclusion: A new Monte Carlo code is developed for plan verification. Contrary to phantombased QA measurements, MCEBRT simulate the exact patient geometry and tissue composition. MCEBRT can be used as extra verification layer for plans where surface dose and tissue heterogeneity are an issue.
An integrated Monte Carlo dosimetric verification system for radiotherapy treatment planning
Yamamoto, T.; Mizowaki, T.; Miyabe, Y.; Takegawa, H.; Narita, Y.; Yano, S.; Nagata, Y.; Teshima, T.; Hiraoka, M.
2007-04-01
An integrated Monte Carlo (MC) dose calculation system, MCRTV (Monte Carlo for radiotherapy treatment plan verification), has been developed for clinical treatment plan verification, especially for routine quality assurance (QA) of intensity-modulated radiotherapy (IMRT) plans. The MCRTV system consists of the EGS4/PRESTA MC codes originally written for particle transport through the accelerator, the multileaf collimator (MLC), and the patient/phantom, which run on a 28-CPU Linux cluster, and the associated software developed for the clinical implementation. MCRTV has an interface with a commercial treatment planning system (TPS) (Eclipse, Varian Medical Systems, Palo Alto, CA, USA) and reads the information needed for MC computation transferred in DICOM-RT format. The key features of MCRTV have been presented in detail in this paper. The phase-space data of our 15 MV photon beam from a Varian Clinac 2300C/D have been developed and several benchmarks have been performed under homogeneous and several inhomogeneous conditions (including water, aluminium, lung and bone media). The MC results agreed with the ionization chamber measurements to within 1% and 2% for homogeneous and inhomogeneous conditions, respectively. The MC calculation for a clinical prostate IMRT treatment plan validated the implementation of the beams and the patient/phantom configuration in MCRTV.
Source localisation and dose verification for a novel brachytherapy unit
Metaxas, Marinos G.
A recent development in the field of radiotherapy has been the introduction of the PRS Intrabeam system (Carl Zeiss Surgical GmbH, Oberkochen, Germany). This is essentially a portable, miniaturised, electron-driven photon generator that allows high intensity, soft-energy x-rays (50 kVp) to be delivered directly to the tumour site in a single fraction. The system has been used for the interstitial radiation treatment of both brain and breast tumours. At present, a standardised in-vivo dose verification technique is not available for the PRS treatments. The isotropical distribution of photons about the tip of the PRS probe inserted in the tissue can effectively be viewed as a point source of radiation buried in the body. This work has looked into ways of localising the PRS source utilising its own radiation field. Moreover, the response of monoenergetic sources, mimicking realistic brachytherapy sources, has also been investigated. The purpose of this project was to attempt to localise the source as well as derive important dosimetric information from the resulting image. A detection system comprised of a well-collimated Germanium detector (HPGe) has been devised in a rotate-translate Emission Computed Tomography (ECT) modality. The superior energy resolving ability of the detection system allowed for energy selective reconstruction to be carried out in the case of the monoenergetic source (241Am). Results showed that the monoenergetic source can be localised to within 1 mm and the continuous PRS x-ray source to within 3mm. For the PRS dose map derivation, Monte Carlo studies have been employed in order to extract information on the dosimetric aspect of the resulting image. The final goal of this work was therefore to formulate a direct mathematical relation (Transform Map) between the image created by the escaping photons and the dose map as predicted by the theoretical model. The formation therefore of the in-vivo PRS image could allow for a real-time monitoring
Monte Carlo dose calculations for dynamic IMRT treatments
International Nuclear Information System (INIS)
Dose calculations for intensity modulated radiation therapy (IMRT) face new challenges due to the complex leaf geometry and time dependent nature of the delivery. A fast method of particle transport through a dynamic multileaf collimator (MLC) geometry that accounts for photon attenuation and first-scattered Compton photon production has been incorporated into an existing Monte Carlo code used for patient dose calculations. Dosimetric agreement between calculation and measurement for two photon energies and MLC types is within experimental error for the sliding window tests. For a patient IMRT field, the Monte Carlo calculations are closer to measured dose than similar superposition or pencil beam calculations. (author)
Dosimetry investigation of MOSFET for clinical IMRT dose verification.
Deshpande, Sudesh; Kumar, Rajesh; Ghadi, Yogesh; Neharu, R M; Kannan, V
2013-06-01
In IMRT, patient-specific dose verification is followed regularly at each centre. Simple and efficient dosimetry techniques play a very important role in routine clinical dosimetry QA. The MOSFET dosimeter offers several advantages over the conventional dosimeters such as its small detector size, immediate readout, immediate reuse, multiple point dose measurements. To use the MOSFET as routine clinical dosimetry system for pre-treatment dose verification in IMRT, a comprehensive set of experiments has been conducted, to investigate its linearity, reproducibility, dose rate effect and angular dependence for 6 MV x-ray beam. The MOSFETs shows a linear response with linearity coefficient of 0.992 for a dose range of 35 cGy to 427 cGy. The reproducibility of the MOSFET was measured by irradiating the MOSFET for ten consecutive irradiations in the dose range of 35 cGy to 427 cGy. The measured reproducibility of MOSFET was found to be within 4% up to 70 cGy and within 1.4% above 70 cGy. The dose rate effect on the MOSFET was investigated in the dose rate range 100 MU/min to 600 MU/min. The response of the MOSFET varies from -1.7% to 2.1%. The angular responses of the MOSFETs were measured at 10 degrees intervals from 90 to 270 degrees in an anticlockwise direction and normalized at gantry angle zero and it was found to be in the range of 0.98 ± 0.014 to 1.01 ± 0.014. The MOSFETs were calibrated in a phantom which was later used for IMRT verification. The measured calibration coefficients were found to be 1 mV/cGy and 2.995 mV/cGy in standard and high sensitivity mode respectively. The MOSFETs were used for pre-treatment dose verification in IMRT. Nine dosimeters were used for each patient to measure the dose in different plane. The average variation between calculated and measured dose at any location was within 3%. Dose verification using MOSFET and IMRT phantom was found to quick and efficient and well suited for a busy radiotherapy
Inverse treatment planning for radiation therapy based on fast Monte Carlo dose calculation
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An inverse treatment planning system based on fast Monte Carlo (MC) dose calculation is presented. It allows optimisation of intensity modulated dose distributions in 15 to 60 minutes on present day personal computers. If a multi-processor machine is available, parallel simulation of particle histories is also possible, leading to further calculation time reductions. The optimisation process is divided into two stages. The first stage results influence profiles based on pencil beam (PB) dose calculation. The second stage starts with MC verification and post-optimisation of the PB dose and fluence distributions. Because of the potential to accurately model beam modifiers, MC based inverse planning systems are able to optimise compensator thicknesses and leaf trajectories instead of intensity profiles only. The corresponding techniques, whose implementation is the subject for future work, are also presented here. (orig.)
International Nuclear Information System (INIS)
In some postmastectomy breast radiotherapy, patients are often irradiated with a temporary tissue expander. Most tissue expanders present a high density metallic disk inside which produce severe streaking artifacts in CT images and, as a consequence, is expected to affect the dose calculations . With the implementation of complex technique such as the IMRT technique, more rigorous verification is required in order to ensure the accurate determination of the absorbed dose before the treatment delivery. Monte Carlo (MC) algorithms have shown to be a reliable tool to provide improved dose accuracy in such situations. The aim of this work is to assess the accuracy of the dose calculation performed with a commercial TPS for breast IMRT radiotherapy in presence of metallic expanders (model McGhan Style 150). A MC method is used as gold standard for this evaluation. (Author)
Energy Technology Data Exchange (ETDEWEB)
Zarza-Moreno, M.; Calvo Ortega, J. F.; Jesus, A. P.; Casals Farran, J.
2013-07-01
In some postmastectomy breast radiotherapy, patients are often irradiated with a temporary tissue expander. Most tissue expanders present a high density metallic disk inside which produce severe streaking artifacts in CT images and, as a consequence, is expected to affect the dose calculations . With the implementation of complex technique such as the IMRT technique, more rigorous verification is required in order to ensure the accurate determination of the absorbed dose before the treatment delivery. Monte Carlo (MC) algorithms have shown to be a reliable tool to provide improved dose accuracy in such situations. The aim of this work is to assess the accuracy of the dose calculation performed with a commercial TPS for breast IMRT radiotherapy in presence of metallic expanders (model McGhan Style 150). A MC method is used as gold standard for this evaluation. (Author)
Dose verification by OSLDs in the irradiation of cell cultures
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The determination of value of irradiation dose presents difficulties when targets are irradiated located in regions where electronic equilibrium of charged particle is not reached, as in the case of irradiation -in vitro- of cell lines monolayer-cultured, in culture dishes or flasks covered with culture medium. The present study aimed to implement a methodology for dose verification in irradiation of cells in culture media by optically stimulated luminescence dosimetry (OSLD). For the determination of the absorbed dose in terms of cell proliferation OSL dosimeters of aluminum oxide doped with carbon (Al2O3:C) were used, which were calibrated to the irradiation conditions of culture medium and at doses that ranged from 0.1 to 15 Gy obtained with a linear accelerator of 6 MV photons. Intercomparison measurements were performed with an ionization chamber of 6 cm3. Different geometries were evaluated by varying the thicknesses of solid water, air and cell culture medium. The results showed deviations below 2.2% when compared with the obtained doses of OSLDs and planning system used. Also deviations were observed below 3.4% by eccentric points of the irradiation plane, finding homogeneous dose distribution. Uncertainty in the readings was less than 2%. The proposed methodology contributes a contribution in the dose verification in this type of irradiations, eliminating from the calculation uncertainties, potential errors in settling irradiation or possible equipment failure with which is radiating. It also provides certainty about the survival curves to be plotted with the experimental data. (Author)
International Nuclear Information System (INIS)
Even with state of the art treatment planning systems the photon dose calculation can be erroneous under certain circumstances. In these cases Monte Carlo methods promise a higher accuracy. We have used the photon transport code CHILD of the GSF-Forschungszentrum, which was developed to calculate dose in diagnostic radiation protection matters. The code was refined for application in radiotherapy for high energy photon irradiation and should serve for dose verification in individual cases. The irradiation phantom can be entered as any desired 3D matrix or be generated automatically from an individual CT database. The particle transport takes into account pair production, photo, and Compton effect with certain approximations. Efficiency is increased by the method of 'fractional photons'. The generated secondary electrons are followed by the unscattered continuous-slowing-down-approximation (CSDA). The developed Monte Carlo code Monaco Matrix was tested with simple homogeneous and heterogeneous phantoms through comparisons with simulations of the well known but slower EGS4 code. The use of a point source with a direction independent energy spectrum as simplest model of the radiation field from the accelerator head is shown to be sufficient for simulation of actual accelerator depth dose curves. Good agreement (<2%) was found for depth dose curves in water and in bone. With complex test phantoms and comparisons with EGS4 calculated dose profiles some drawbacks in the code were found. Thus, the implementation of the electron multiple-scattering should lead us to step by step improvement of the algorithm. (orig.)
METHODS AND HARDWARE OF DOSE OUTPUT VERIFICATION FOR DYNAMIC RADIOTHERAPY
Y. V. Tsitovich; A. I. Hmyrak; A. I. Tarutin; M. G. Kiselev
2013-01-01
The design of special verification phantom for dynamic radiotherapy checking is described. This phantom permits to insert the dose distribution cross-calibration before every days patients irradiation on Linac with RapidArc. Cross-calibration factor is defined by approximation of large number correction factors measured in phantom at different angles of gantry rotation and middle quantity calculation. The long range stability of all correction factors have been evaluated during checking of se...
Inclusion type radiochromic gel dosimeter for threedimensional dose verification
International Nuclear Information System (INIS)
For the verification of 3D dose distributions in modern radiation therapy, a new inclusion type radiochromic gel detector has been developed. In this gel, a hydrophobic leuco dye (leucomalachite green: LMG) was dissolved in water as an inclusion complex with highly branched cyclic dextrin. The radiation induced radical oxidation property of the LMG gel with various sensitizers was investigated. As a result, the optical dose responses were enhanced by the addition of bromoacetic acid and manganese (II) chloride. Unfavorable auto-oxidation of the gel was reduced when it was stored at 4°C
Monte Carlo simulation of PET images for injection dose optimization
Czech Academy of Sciences Publication Activity Database
Boldyš, Jiří; Dvořák, Jiří; Bělohlávek, O.; Skopalová, M.
London : Taylor and Francis, 2011 - (Manuel, J.; Tavares, R.; Jorge, N.), s. 1-6 ISBN 978-0-415-68395-1. [VipIMAGE 2011 - third ECCOMAS thematic conference on computational vision and medical image processing. Olhao, Algarve (PT), 12.10.2011-14.10.2011] R&D Projects: GA MŠk(CZ) 1M0572 Institutional research plan: CEZ:AV0Z10750506 Keywords : positron emission tomography * Monte Carlo simulation * biological system modeling * image quality Subject RIV: BD - Theory of Information http://library.utia.cas.cz/separaty/2012/ZOI/boldys-monte carlo simulation of pet images for injection dose optimization.pdf
Independent verification of the delivered dose in High-Dose Rate (HDR) brachytherapy
International Nuclear Information System (INIS)
An important aspect of a Quality Assurance program in Clinical Dosimetry is an independent verification of the dosimetric calculation done by the Treatment Planning System for each radiation treatment. The present paper is aimed at creating a spreadsheet for the verification of the dose recorded at a point of an implant with radioactive sources and HDR in gynecological injuries. An 192Ir source automatic differed loading equipment, GammaMedplus model, Varian Medical System with HDR installed at the Angel H. Roffo Oncology Institute has been used. The planning system implemented for getting the dose distribution is the BraquiVision. The sources coordinates as well as those of the calculation point (Rectum) are entered into the Excel-devised verification program by assuming the existence of a point source in each one of the applicators' positions. Such calculation point has been selected as the rectum is an organ at risk, therefore determining the treatment planning. The dose verification is performed at points standing at a sources distance having at least twice the active length of such sources, so they may be regarded as point sources. Most of the sources used in HDR brachytherapy with 192Ir have a 5 mm active length for all equipment brands. Consequently, the dose verification distance must be at least of 10 mm. (author)
SU-E-T-278: Realization of Dose Verification Tool for IMRT Plan Based On DPM
Energy Technology Data Exchange (ETDEWEB)
Cai, Jinfeng; Cao, Ruifen; Dai, Yumei; Pei, Xi; Hu, Liqin [Institute of Nuclear Energy Safety Technology, Chinese Academy of Sciences, Hefei, Anhui (China); LIN, Hui [Institute of Nuclear Energy Safety Technology, Chinese Academy of Sciences, Hefei, Anhui (China); School of Electronic Science and Application Physics, Hefei University of Technology, Hefei, Anhui (China); Zhang, Jun [University of Science and Technology of China, Hefei, Anhui (China)
2014-06-01
Purpose: To build a Monte Carlo dose verification tool for IMRT Plan by implementing a irradiation source model into DPM code. Extend the ability of DPM to calculate any incident angles and irregular-inhomogeneous fields. Methods: With the virtual source and the energy spectrum which unfolded from the accelerator measurement data,combined with optimized intensity maps to calculate the dose distribution of the irradiation irregular-inhomogeneous field. The irradiation source model of accelerator was substituted by a grid-based surface source. The contour and the intensity distribution of the surface source were optimized by ARTS (Accurate/Advanced Radiotherapy System) optimization module based on the tumor configuration. The weight of the emitter was decided by the grid intensity. The direction of the emitter was decided by the combination of the virtual source and the emitter emitting position. The photon energy spectrum unfolded from the accelerator measurement data was adjusted by compensating the contaminated electron source. For verification, measured data and realistic clinical IMRT plan were compared with DPM dose calculation. Results: The regular field was verified by comparing with the measured data. It was illustrated that the differences were acceptable (<2% inside the field, 2–3mm in the penumbra). The dose calculation of irregular field by DPM simulation was also compared with that of FSPB (Finite Size Pencil Beam) and the passing rate of gamma analysis was 95.1% for peripheral lung cancer. The regular field and the irregular rotational field were all within the range of permitting error. The computing time of regular fields were less than 2h, and the test of peripheral lung cancer was 160min. Through parallel processing, the adapted DPM could complete the calculation of IMRT plan within half an hour. Conclusion: The adapted parallelized DPM code with irradiation source model is faster than classic Monte Carlo codes. Its computational accuracy and
Monte Carlo dose calculation in dental amalgam phantom
Mohd Zahri Abdul Aziz; Yusoff, A. L.; N D Osman; R. Abdullah; Rabaie, N. A.; M S Salikin
2015-01-01
It has become a great challenge in the modern radiation treatment to ensure the accuracy of treatment delivery in electron beam therapy. Tissue inhomogeneity has become one of the factors for accurate dose calculation, and this requires complex algorithm calculation like Monte Carlo (MC). On the other hand, computed tomography (CT) images used in treatment planning system need to be trustful as they are the input in radiotherapy treatment. However, with the presence of metal amalgam in treatm...
Nanodosimetric verification in proton therapy: Monte Carlo Codes Comparison
International Nuclear Information System (INIS)
Full text: Nanodosimetry strives to develop a novel dosimetry concept suitable for advanced modalities of cancer radiotherapy, such as proton therapy. This project aims to evaluate the plausibility of the physical models implemented in the Geant4 Very Low Energy (Geant4-DNA) extensions by comparing nanodosimetric quantities calculated with Geant4-DNA and the PTB Monte Carlo track structure code. Nanodosimetric track structure parameters were calculated for cylindrical targets representing DNA and nucleosome segments and converted into the probability of producing a DSB using the model proposed by Garty et al. [1]. Monoenergetic protons and electrons of energies typical for 6-electron spectra were considered as primary particles. Good agreement was found between the two codes for electrons of energies above 200 eV. Below this energy Geant4-DNA produced slightly higher numbers of ionisations in the sensitive volumes and higher probabilities for DSB formation. For protons, Geant4-DNA also gave higher numbers of ionisations and DSB probabilities, particularly in the low energy range, while a satisfactory agreement was found for energies higher than I MeV. Comparing two codes can be useful as any observed divergence in results between the two codes provides valuable information as to where further consideration of the underlying physical models used in each code may be required. Consistently it was seen that the largest difference between the codes was in the low energy ranges for each particle type. (author)
Adjoint Monte Carlo techniques and codes for organ dose calculations
International Nuclear Information System (INIS)
Adjoint Monte Carlo simulations can be effectively used for the estimation of doses in small targets when the sources are extended in large volumes or surfaces. The main features of two computer codes for calculating doses at free points or in organs of an anthropomorphic phantom are described. In the first program (REBEL-3) natural gamma-emitting sources are contained in the walls of a dwelling room; in the second one (POKER-CAMP) the user can specify arbitrary gamma sources with different spatial distributions in the environment: in (or on the surface of) the ground and in the air. 3 figures
Directory of Open Access Journals (Sweden)
Sunil D Sharma
2012-01-01
Conclusion: The measured dose values were found in good agreement with the dose values calculated using the TPS. The MOSFET dosimeter can be a suitable choice for routine dose verification in the Gamma Knife radiosurgery.
International Nuclear Information System (INIS)
Monte Carlo (MC) methods provide the most accurate to-date dose calculations in heterogeneous media and complex geometries, and this spawns increasing interest in incorporating MC calculations into treatment planning quality assurance process. This involves MC dose calculations for clinically produced treatment plans. To perform these calculations, a number of treatment plan parameters specifying radiation beam
Verification of Monte Carlo transport codes: FLUKA, MARS and SHIELD-A
International Nuclear Information System (INIS)
Monte Carlo transport codes like FLUKA, MARS and SHIELD are widely used for the estimation of radiation hazards in accelerator facilities. Accurate simulations are especially important with increasing energies and intensities of the machines. As the physical models implied in the codes are being constantly further developed, the verification is needed to make sure that the simulations give reasonable results. We report on the verification of electronic stopping modules and the verification of nuclide production modules of the codes. The verification of electronic stopping modules is based on the results of irradiation of stainless steel, copper and aluminum by 500 MeV/u and 950 MeV/u uranium ions. The stopping ranges achieved experimentally are compared with the simulated ones. The verification of isotope production modules is done via comparing the experimental depth profiles of residual activity (aluminum targets were irradiated by 500 MeV/u and 950 MeV/u uranium ions) with the results of simulations. Correspondences and discrepancies between the experiment and the simulations are discussed.
Verification of Monte Carlo transport codes: FLUKA, MARS and SHIELD-A
Energy Technology Data Exchange (ETDEWEB)
Chetvertkova, Vera [IAP, J. W. Goethe-University, Frankfurt am Main (Germany); GSI Helmholtzzentrum fuer Schwerionenforschung, Darmstadt (Germany); Mustafin, Edil; Strasik, Ivan [GSI Helmholtzzentrum fuer Schwerionenforschung, Darmstadt (Germany); Ratzinger, Ulrich [IAP, J. W. Goethe-University, Frankfurt am Main (Germany); Latysheva, Ludmila; Sobolevskiy, Nikolai [Institute for Nuclear Research RAS, Moscow (Russian Federation)
2011-07-01
Monte Carlo transport codes like FLUKA, MARS and SHIELD are widely used for the estimation of radiation hazards in accelerator facilities. Accurate simulations are especially important with increasing energies and intensities of the machines. As the physical models implied in the codes are being constantly further developed, the verification is needed to make sure that the simulations give reasonable results. We report on the verification of electronic stopping modules and the verification of nuclide production modules of the codes. The verification of electronic stopping modules is based on the results of irradiation of stainless steel, copper and aluminum by 500 MeV/u and 950 MeV/u uranium ions. The stopping ranges achieved experimentally are compared with the simulated ones. The verification of isotope production modules is done via comparing the experimental depth profiles of residual activity (aluminum targets were irradiated by 500 MeV/u and 950 MeV/u uranium ions) with the results of simulations. Correspondences and discrepancies between the experiment and the simulations are discussed.
A Monte Carlo dose calculation algorithm for proton therapy
International Nuclear Information System (INIS)
A Monte Carlo (MC) code (VMCpro) for treatment planning in proton beam therapy of cancer is introduced. It is based on ideas of the Voxel Monte Carlo algorithm for photons and electrons and is applicable to human tissue for clinical proton energies. In the present paper the implementation of electromagnetic and nuclear interactions is described. They are modeled by a Class II condensed history algorithm with continuous energy loss, ionization, multiple scattering, range straggling, δ-electron transport, nuclear elastic proton nucleus scattering and inelastic proton nucleus reactions. VMCpro is faster than the general purpose MC codes FLUKA by a factor of 13 and GEANT4 by a factor of 35 for simulations in a phantom with inhomogeneities. For dose calculations in patients the speed improvement is larger, because VMCpro has only a weak dependency on the heterogeneity of the calculation grid. Dose distributions produced with VMCpro are in agreement with GEANT4 results. Integrated or broad beam depth dose curves show maximum deviations not larger than 1% or 0.5 mm in regions with large dose gradients for the examples presented here
Approach to 3D dose verification by utilizing autoactivation
Energy Technology Data Exchange (ETDEWEB)
Nakajima, Yasunori, E-mail: yasunori.nkjm@gmail.com [Tokyo Institute of Technology, Yokohama-shi (Japan); Kohno, Toshiyuki [Tokyo Institute of Technology, Yokohama-shi (Japan); Inaniwa, Taku; Sato, Shinji; Yoshida, Eiji; Yamaya, Taiga [National Institute of Radiological Sciences, Chiba-shi (Japan); Tsuruta, Yuki [Tokyo Institute of Technology, Yokohama-shi (Japan); Sihver, Lembit [Chalmers University of Technology, Gothenburg (Sweden)
2011-08-21
To evaluate the deposited dose distribution in a target, we have proposed to utilize the annihilation gamma-rays emitted from the positron emitters distributed in the target irradiated with stable heavy-ion beams. Verification of the one dimensional (1-D) dose distributions along and perpendicular to a beam axis was achieved through our previous works. The purpose of this work is to verify 3-D dose distributions. As the first attempt uniform PMMA targets were irradiated in simple rectangular parallelepiped shapes, and the annihilation gamma-rays were detected with a PET scanner. By comparing the detected annihilation gamma-ray distributions with the calculated ones the dose distributions were estimated. As a result the estimated positions of the distal edges of the dose distributions were in agreement with the measured ones within 1 mm. However, the estimated positions of the proximal edges were different from the measured ones by 5-9 mm depending on the thickness of the irradiation filed.
A software tool for 3D dose verification and analysis
Sa'd, M. Al; Graham, J.; Liney, G. P.
2013-06-01
The main recent developments in radiotherapy have focused on improved treatment techniques in order to generate further significant improvements in patient prognosis. There is now an internationally recognised need to improve 3D verification of highly conformal radiotherapy treatments. This is because of the very high dose gradients used in modern treatment techniques, which can result in a small error in the spatial dose distribution leading to a serious complication. In order to gain the full benefits of using 3D dosimetric technologies (such as gel dosimetry), it is vital to use 3D evaluation methods and algorithms. We present in this paper a software solution that provides a comprehensive 3D dose evaluation and analysis. The software is applied to gel dosimetry, which is based on magnetic resonance imaging (MRI) as a read-out method. The software can also be used to compare any two dose distributions, such as two distributions planned using different methods of treatment planning systems, or different dose calculation algorithms.
A software tool for 3D dose verification and analysis
International Nuclear Information System (INIS)
The main recent developments in radiotherapy have focused on improved treatment techniques in order to generate further significant improvements in patient prognosis. There is now an internationally recognised need to improve 3D verification of highly conformal radiotherapy treatments. This is because of the very high dose gradients used in modern treatment techniques, which can result in a small error in the spatial dose distribution leading to a serious complication. In order to gain the full benefits of using 3D dosimetric technologies (such as gel dosimetry), it is vital to use 3D evaluation methods and algorithms. We present in this paper a software solution that provides a comprehensive 3D dose evaluation and analysis. The software is applied to gel dosimetry, which is based on magnetic resonance imaging (MRI) as a read-out method. The software can also be used to compare any two dose distributions, such as two distributions planned using different methods of treatment planning systems, or different dose calculation algorithms.
Dose verification using a pelvic phantom in high dose rate (HDR) brachytherapy
International Nuclear Information System (INIS)
High dose rate (HDR) brachytherapy for treating a cervix carcinoma has become popular, because it eliminates many of the problems associated with conventional brachytherapy. In order to improve the clinical effectiveness with HDR brachytherapy, a dose calculation algorithm, optimization procedures, and image registrations need to be verified by comparing the dose distributions from a planning computer and those from a humanoid phantom. In this study, the humanoid phantom was fabricated in order to verify the absolute doses and the relative dose distributions. The measured doses from the humanoid phantom were then compared with the treatment planning system for the dose verification. The humanoid phantom needs to be designed such that the dose distributions can be quantitatively evaluated thermoluminescent dosimeter (TLD) chips with a dimension of 1/8 and film dosimetry with a spatial resolution of <1 mm used to measure the radiation dosages in the phantom. The humanoid phantom called a pelvic phantom was made from water and the tissue-equivalent acrylic plates. In order to firmly hold the HDR applicators in the water phantom, the applicators were inserted into the grooves of the applicator holder. The dose distributions around the applicators, such as Point A and B, were measured by placing a series of TLD chips (TLD-tp-TLD distance: 5mm) in the three TLD holders, and placing three verification films in the orthogonal planes. This study used a Nucletron Plato treatment planning system and a Microselectron Ir-192 source unit. The results showed good agreement between the treatment plan and measurement. The comparisons of the absolute dose showed agreement within 1.48 %-2.95 % of the dose at point A and B, and 2.07 %-3.74 % of the dose at the bladder and rectum point. In addition, the relative dose distributions by film dosimetry and those calculated by the planning computer show good agreement. This pelvic phantom could be a useful to verify the dose calculation
Dose calculation of 6 MV Truebeam using Monte Carlo method
International Nuclear Information System (INIS)
The purpose of this work is to simulate 6 MV Varian Truebeam linac dosimeter characteristics using Monte Carlo method and to investigate the availability of phase space file and the accuracy of the simulation. With the phase space file at linac window supplied by Varian to be a source, the patient-dependent part was simulated. Dose distributions in a water phantom with a 10 cm × 10 cm field were calculated and compared with measured data for validation. Evident time reduction was obtained from 4-5 h which a whole simulation cost on the same computer to around 48 minutes. Good agreement between simulations and measurements in water was observed. Dose differences are less than 3% for depth doses in build-up region and also for dose profiles inside the 80% field size, and the effect in penumbra is good. It demonstrate that the simulation using existing phase space file as the EGSnrc source is efficient. Dose differences between calculated data and measured data could meet the requirements for dose calculation. (authors)
A Monte Carlo dose calculation tool for radiotherapy treatment planning
Ma, C.-M.; Li, J. S.; Pawlicki, T.; Jiang, S. B.; Deng, J.; Lee, M. C.; Koumrian, T.; Luxton, M.; Brain, S.
2002-05-01
A Monte Carlo user code, MCDOSE, has been developed for radiotherapy treatment planning (RTP) dose calculations. MCDOSE is designed as a dose calculation module suitable for adaptation to host RTP systems. MCDOSE can be used for both conventional photon/electron beam calculation and intensity modulated radiotherapy (IMRT) treatment planning. MCDOSE uses a multiple-source model to reconstruct the treatment beam phase space. Based on Monte Carlo simulated or measured beam data acquired during commissioning, source-model parameters are adjusted through an automated procedure. Beam modifiers such as jaws, physical and dynamic wedges, compensators, blocks, electron cut-outs and bolus are simulated by MCDOSE together with a 3D rectilinear patient geometry model built from CT data. Dose distributions calculated using MCDOSE agreed well with those calculated by the EGS4/DOSXYZ code using different beam set-ups and beam modifiers. Heterogeneity correction factors for layered-lung or layered-bone phantoms as calculated by both codes were consistent with measured data to within 1%. The effect of energy cut-offs for particle transport was investigated. Variance reduction techniques were implemented in MCDOSE to achieve a speedup factor of 10-30 compared to DOSXYZ.
Uncertainties in Monte Carlo-based absorbed dose calculations for an experimental benchmark
International Nuclear Information System (INIS)
There is a need to verify the accuracy of general purpose Monte Carlo codes like EGSnrc, which are commonly employed for investigations of dosimetric problems in radiation therapy. A number of experimental benchmarks have been published to compare calculated values of absorbed dose to experimentally determined values. However, there is a lack of absolute benchmarks, i.e. benchmarks without involved normalization which may cause some quantities to be cancelled. Therefore, at the Physikalisch-Technische Bundesanstalt a benchmark experiment was performed, which aimed at the absolute verification of radiation transport calculations for dosimetry in radiation therapy. A thimble-type ionization chamber in a solid phantom was irradiated by high-energy bremsstrahlung and the mean absorbed dose in the sensitive volume was measured per incident electron of the target. The characteristics of the accelerator and experimental setup were precisely determined and the results of a corresponding Monte Carlo simulation with EGSnrc are presented within this study. For a meaningful comparison, an analysis of the uncertainty of the Monte Carlo simulation is necessary. In this study uncertainties with regard to the simulation geometry, the radiation source, transport options of the Monte Carlo code and specific interaction cross sections are investigated, applying the general methodology of the Guide to the expression of uncertainty in measurement. Besides studying the general influence of changes in transport options of the EGSnrc code, uncertainties are analyzed by estimating the sensitivity coefficients of various input quantities in a first step. Secondly, standard uncertainties are assigned to each quantity which are known from the experiment, e.g. uncertainties for geometric dimensions. Data for more fundamental quantities such as photon cross sections and the I-value of electron stopping powers are taken from literature. The significant uncertainty contributions are identified as
Uncertainties in Monte Carlo-based absorbed dose calculations for an experimental benchmark
Renner, F.; Wulff, J.; Kapsch, R.-P.; Zink, K.
2015-10-01
There is a need to verify the accuracy of general purpose Monte Carlo codes like EGSnrc, which are commonly employed for investigations of dosimetric problems in radiation therapy. A number of experimental benchmarks have been published to compare calculated values of absorbed dose to experimentally determined values. However, there is a lack of absolute benchmarks, i.e. benchmarks without involved normalization which may cause some quantities to be cancelled. Therefore, at the Physikalisch-Technische Bundesanstalt a benchmark experiment was performed, which aimed at the absolute verification of radiation transport calculations for dosimetry in radiation therapy. A thimble-type ionization chamber in a solid phantom was irradiated by high-energy bremsstrahlung and the mean absorbed dose in the sensitive volume was measured per incident electron of the target. The characteristics of the accelerator and experimental setup were precisely determined and the results of a corresponding Monte Carlo simulation with EGSnrc are presented within this study. For a meaningful comparison, an analysis of the uncertainty of the Monte Carlo simulation is necessary. In this study uncertainties with regard to the simulation geometry, the radiation source, transport options of the Monte Carlo code and specific interaction cross sections are investigated, applying the general methodology of the Guide to the expression of uncertainty in measurement. Besides studying the general influence of changes in transport options of the EGSnrc code, uncertainties are analyzed by estimating the sensitivity coefficients of various input quantities in a first step. Secondly, standard uncertainties are assigned to each quantity which are known from the experiment, e.g. uncertainties for geometric dimensions. Data for more fundamental quantities such as photon cross sections and the I-value of electron stopping powers are taken from literature. The significant uncertainty contributions are identified as
Augustine, Kurt E.; Walsh, Timothy J.; Beltran, Chris J.; Stoker, Joshua B.; Mundy, Daniel W.; Parry, Mark D.; Bues, Martin; Fatyga, Mirek
2016-04-01
The use of radiation therapy for the treatment of cancer has been carried out clinically since the late 1800's. Early on however, it was discovered that a radiation dose sufficient to destroy cancer cells can also cause severe injury to surrounding healthy tissue. Radiation oncologists continually strive to find the perfect balance between a dose high enough to destroy the cancer and one that avoids damage to healthy organs. Spot scanning or "pencil beam" proton radiotherapy offers another option to improve on this. Unlike traditional photon therapy, proton beams stop in the target tissue, thus better sparing all organs beyond the targeted tumor. In addition, the beams are far narrower and thus can be more precisely "painted" onto the tumor, avoiding exposure to surrounding healthy tissue. To safely treat patients with proton beam radiotherapy, dose verification should be carried out for each plan prior to treatment. Proton dose verification systems are not currently commercially available so the Department of Radiation Oncology at the Mayo Clinic developed its own, called DOSeCHECK, which offers two distinct dose simulation methods: GPU-based Monte Carlo and CPU-based analytical. The three major components of the system include the web-based user interface, the Linux-based dose verification simulation engines, and the supporting services and components. The architecture integrates multiple applications, libraries, platforms, programming languages, and communication protocols and was successfully deployed in time for Mayo Clinic's first proton beam therapy patient. Having a simple, efficient application for dose verification greatly reduces staff workload and provides additional quality assurance, ultimately improving patient safety.
An improved Monte Carlo (MC) dose simulation for charged particle cancer therapy
Energy Technology Data Exchange (ETDEWEB)
Ying, C. K. [Advanced Medical and Dental Institute, AMDI, Universiti Sains Malaysia, Penang, Malaysia and School of Medical Sciences, Universiti Sains Malaysia, Kota Bharu (Malaysia); Kamil, W. A. [Advanced Medical and Dental Institute, AMDI, Universiti Sains Malaysia, Penang, Malaysia and Radiology Department, Hospital USM, Kota Bharu (Malaysia); Shuaib, I. L. [Advanced Medical and Dental Institute, AMDI, Universiti Sains Malaysia, Penang (Malaysia); Matsufuji, Naruhiro [Research Centre of Charged Particle Therapy, National Institute of Radiological Sciences, NIRS, Chiba (Japan)
2014-02-12
Heavy-particle therapy such as carbon ion therapy are more popular nowadays because of the nature characteristics of charged particle and almost no side effect to patients. An effective treatment is achieved with high precision of dose calculation, in this research work, Geant4 based Monte Carlo simulation method has been used to calculate the radiation transport and dose distribution. The simulation have the same setting with the treatment room in Heavy Ion Medical Accelerator, HIMAC. The carbon ion beam at the isocentric gantry nozzle for the therapeutic energy of 290 MeV/u was simulated, experimental work was carried out in National Institute of Radiological Sciences, NIRS, Chiba, Japan by using the HIMAC to confirm the accuracy and qualities dose distribution by MC methods. The Geant4 based simulated dose distribution were verified with measurements for Bragg peak and spread out Bragg peak (SOBP) respectively. The verification of results shows that the Bragg peak depth-dose and SOBP distributions in simulation has good agreement with measurements. In overall, the study showed that Geant4 based can be fully applied in the heavy-ion therapy field for simulation, further works need to be carry on to refine and improve the Geant4 MC simulations.
An improved Monte Carlo (MC) dose simulation for charged particle cancer therapy
Ying, C. K.; Kamil, W. A.; Shuaib, I. L.; Matsufuji, Naruhiro
2014-02-01
Heavy-particle therapy such as carbon ion therapy are more popular nowadays because of the nature characteristics of charged particle and almost no side effect to patients. An effective treatment is achieved with high precision of dose calculation, in this research work, Geant4 based Monte Carlo simulation method has been used to calculate the radiation transport and dose distribution. The simulation have the same setting with the treatment room in Heavy Ion Medical Accelerator, HIMAC. The carbon ion beam at the isocentric gantry nozzle for the therapeutic energy of 290 MeV/u was simulated, experimental work was carried out in National Institute of Radiological Sciences, NIRS, Chiba, Japan by using the HIMAC to confirm the accuracy and qualities dose distribution by MC methods. The Geant4 based simulated dose distribution were verified with measurements for Bragg peak and spread out Bragg peak (SOBP) respectively. The verification of results shows that the Bragg peak depth-dose and SOBP distributions in simulation has good agreement with measurements. In overall, the study showed that Geant4 based can be fully applied in the heavy-ion therapy field for simulation, further works need to be carry on to refine and improve the Geant4 MC simulations.
An analytical solution to a simplified EDXRF model for Monte Carlo code verification
International Nuclear Information System (INIS)
The objective of this study is to obtain an analytical solution to the scalar photon transport equation that can be used to obtain benchmark results for the verification of energy dispersive X-Ray fluorescence (EDXRF) Monte Carlo simulation codes. The multi-collided flux method (multiple scattering method) is implemented to obtain analytical expressions for the space-, energy-, and angle-dependent scalar photon flux for a one dimensional EDXRF model problem. In order to obtain benchmark results, higher-order multiple scattering terms are included in the multi-collided flux method. The details of the analytical solution and of the proposed EDXRF model problem are presented. Analytical expressions obtained are then used to calculate the energy-dependent current. The analytically-calculated energy-dependent current is compared with Monte Carlo code results. The findings of this study show that analytical solutions to the scalar photon transport equation with the proposed model problem can be used as a verification tool in EDXRF Monte Carlo code development.
Monte Carlo dosimetric study of the medium dose rate CSM40 source
International Nuclear Information System (INIS)
The 137Cs medium dose rate (MDR) CSM40 source model (Eckert and Ziegler BEBIG, Germany) is in clinical use but no dosimetric dataset has been published. This study aims to obtain dosimetric data for the CSM40 source for its use in clinical practice as required by the American Association of Physicists in Medicine (AAPM) and the European Society for Radiotherapy and Oncology (ESTRO). Penelope2008 and Geant4 Monte Carlo codes were used to characterize this source dosimetrically. It was located in an unbounded water phantom with composition and mass density as recommended by AAPM and ESTRO. Due to the low photon energies of 137Cs, absorbed dose was approximated by collisional kerma. Additional simulations were performed to obtain the air-kerma strength, sK. Mass–energy absorption coefficients in water and air were consistently derived and used to calculate collisional kerma. Results performed with both radiation transport codes showed agreement typically within 0.05%. Dose rate constant, radial dose function and anisotropy function are provided for the CSM40 and compared with published data for other commercially available 137Cs sources. An uncertainty analysis has been performed. The data provided by this study can be used as input data and verification in the treatment planning systems. - Highlights: • A dosimetric dataset is obtained for the 137Cs medium dose rate CSM40 source model. • Along-away table and TG-43 formalism parameters and functions are derived as recommended by AAPM-ESTRO. • This can be used as input data and verification in the treatment planning systems used in clinical practice
Assessment of patient dose in mammography using Monte Carlo simulation
International Nuclear Information System (INIS)
Breast doses due to mammographic examinations were assessed using a MIRD-type female phantom and Monte Carlo simulations. Clinical mammographic data, which vary according to the age group of the subject undergoing the examinations, were obtained from the Korea Cancer Center Hospital in Seoul. The tube potential was fixed to 26 kVp, most commonly used in the mammographic examination, and the source-film distance was kept constant at 65 cm. The breast tissue was assumed to have an even composition between glandular tissue and adipose tissue. The nominal breast equivalent doses were in the range from 0.6 to 1.8 mSv and the resulting effective doses ranged from 0.06 to 0.19 mSv depending on the age group and the projection modes. Lower doses were resulted at older ages. Contributions of organs other than the breast to the effective doses were negligible as long as the X-ray beam was adequately collimated and aligned to avoid exposure of other part of the body than the breast. This means that a simple breast-only phantom can be used in dosimetric calculations for mammography. (author)
Applying Monte Carlo Simulation to Launch Vehicle Design and Requirements Verification
Hanson, John M.; Beard, Bernard B.
2010-01-01
This paper is focused on applying Monte Carlo simulation to probabilistic launch vehicle design and requirements verification. The approaches developed in this paper can be applied to other complex design efforts as well. Typically the verification must show that requirement "x" is met for at least "y" % of cases, with, say, 10% consumer risk or 90% confidence. Two particular aspects of making these runs for requirements verification will be explored in this paper. First, there are several types of uncertainties that should be handled in different ways, depending on when they become known (or not). The paper describes how to handle different types of uncertainties and how to develop vehicle models that can be used to examine their characteristics. This includes items that are not known exactly during the design phase but that will be known for each assembled vehicle (can be used to determine the payload capability and overall behavior of that vehicle), other items that become known before or on flight day (can be used for flight day trajectory design and go/no go decision), and items that remain unknown on flight day. Second, this paper explains a method (order statistics) for determining whether certain probabilistic requirements are met or not and enables the user to determine how many Monte Carlo samples are required. Order statistics is not new, but may not be known in general to the GN&C community. The methods also apply to determining the design values of parameters of interest in driving the vehicle design. The paper briefly discusses when it is desirable to fit a distribution to the experimental Monte Carlo results rather than using order statistics.
The Monte Carlo simulation of the absorbed dose in quartz
Energy Technology Data Exchange (ETDEWEB)
Chen Shaowen [School of Physics Science and Engineering, Sun Yat-Sen University, Guangzhou, Guangdong 510275 (China) and Electron Engineering Department, Dongguan University of Technology, Dongguan 523808 (China)], E-mail: siumon@163.com; Liu Xiaowei; Zhang Chunxiang; Tang Qiang [School of Physics Science and Engineering, Sun Yat-Sen University, Guangzhou, Guangdong 510275 (China)
2009-05-15
Regeneration irradiation is a necessary procedure in TL or OSL dating protocol. The accuracy of measuring the absorbed dose is one of the important factors in dating. Since a beta source is often used in the regeneration irradiation process, the size of the quartz sample, pressure of nitrogen gas and the material of the sample holder may cause significant uncertainties in delivering the absorbed dose. In this work, the effects of the size of the quartz sample, the pressure of nitrogen gas and the material of the sample holder are simulated using the Monte Carlo method, and the uncertainties are discussed in these cases. The results show that they need to be considered in the dating.
Micelle hydrogels for three-dimensional dose verification
Babic, S.; Battista, J.; Jordan, K.
2009-05-01
Gelatin hydrogels form a transparent and colourless matrix for polymerization or chromic reactions initiated by absorption of ionizing radiation. Generally, hydrogel chemistries have been limited to water soluble reactants. Work to adapt a water insoluble colourless leuco dye to coloured dye conversion reaction in hydrogels, led to the idea that micelles (i.e. tiny aggregates of surfactant molecules) may provide the necessary polar and nonpolar hybrid environment. Both leucomalachite green and leuco crystal violet radiochromic gels have been developed as three-dimensional (3-D) radiochromic dosimeters for optical computed tomography (CT) scanners. It has been found that the post-irradiation diffusion rates strongly correlate with the solubility of the leuco dyes. Since the crystal violet dye is more soluble in the micelle than in the surrounding water, the dose distribution degrades at the slower rate of micelle diffusion, thus yielding stable images of dose. A dosimetric characterization of leucomalachite green and leuco crystal violet gels, respectively, reveals that tissue equivalent micelle hydrogels are promising dosimeters for radiation therapy 3-D dose verification.
International Nuclear Information System (INIS)
We isolate the most computationally expensive steps of a robust nuclear reactor core Monte Carlo particle transport simulation. The hot kernel is then abstracted into a simplified proxy application, designed to mimic the key performance characteristics of the full application. A series of performance verification tests and analyses are carried out to investigate the low-level performance parameters of both the simplified kernel and the full application. The kernel's performance profile is found to closely match that of the application, making it a convenient test bed for performance analyses on cutting edge platforms and experimental next-generation high performance computing architectures. (author)
Locke, C.; Zavgorodni, S.
2008-01-01
Monte Carlo (MC) methods provide the most accurate to-date dose calculations in heterogeneous media and complex geometries, and this spawns increasing interest in incorporating MC calculations into treatment planning quality assurance process. This involves MC dose calculations for clinically produced treatment plans. To perform these calculations, a number of treatment plan parameters specifying radiation beam and patient geometries need to be transferred to MC codes, such as BEAMnrc and DOS...
Schmitz, Richard M; Townson, Reid W; Zavgorodni, Sergei
2014-01-01
The International Electrotechnical Commission (IEC) has previously defined standard rotation operators for positive gantry, collimator and couch rotations for the radiotherapy DICOM coordinate system that is commonly used by treatment planning systems. Coordinate transformations to the coordinate systems of commonly used Monte Carlo (MC) codes (BEAMnrc/DOSXYZnrc and VMC++) have been derived and published in the literature. However, these coordinate transformations disregard patient orientation during the computed tomography (CT) scan, and assume the most commonly used 'head first, supine' orientation. While less common, other patient orientations are used in clinics - Monte Carlo verification of such treatments can be problematic due to the lack of appropriate coordinate transformations. In this work, a solution has been obtained by correcting the CT-derived phantom orientation and deriving generalized coordinate transformations for field angles in the DOSXYZnrc and VMC++ codes. The rotation operator that inc...
Monte Carlo dose calculation in dental amalgam phantom.
Aziz, Mohd Zahri Abdul; Yusoff, A L; Osman, N D; Abdullah, R; Rabaie, N A; Salikin, M S
2015-01-01
It has become a great challenge in the modern radiation treatment to ensure the accuracy of treatment delivery in electron beam therapy. Tissue inhomogeneity has become one of the factors for accurate dose calculation, and this requires complex algorithm calculation like Monte Carlo (MC). On the other hand, computed tomography (CT) images used in treatment planning system need to be trustful as they are the input in radiotherapy treatment. However, with the presence of metal amalgam in treatment volume, the CT images input showed prominent streak artefact, thus, contributed sources of error. Hence, metal amalgam phantom often creates streak artifacts, which cause an error in the dose calculation. Thus, a streak artifact reduction technique was applied to correct the images, and as a result, better images were observed in terms of structure delineation and density assigning. Furthermore, the amalgam density data were corrected to provide amalgam voxel with accurate density value. As for the errors of dose uncertainties due to metal amalgam, they were reduced from 46% to as low as 2% at d80 (depth of the 80% dose beyond Zmax) using the presented strategies. Considering the number of vital and radiosensitive organs in the head and the neck regions, this correction strategy is suggested in reducing calculation uncertainties through MC calculation. PMID:26500401
Monte carlo dose calculation in dental amalgam phantom
Directory of Open Access Journals (Sweden)
Mohd Zahri Abdul Aziz
2015-01-01
Full Text Available It has become a great challenge in the modern radiation treatment to ensure the accuracy of treatment delivery in electron beam therapy. Tissue inhomogeneity has become one of the factors for accurate dose calculation, and this requires complex algorithm calculation like Monte Carlo (MC. On the other hand, computed tomography (CT images used in treatment planning system need to be trustful as they are the input in radiotherapy treatment. However, with the presence of metal amalgam in treatment volume, the CT images input showed prominent streak artefact, thus, contributed sources of error. Hence, metal amalgam phantom often creates streak artifacts, which cause an error in the dose calculation. Thus, a streak artifact reduction technique was applied to correct the images, and as a result, better images were observed in terms of structure delineation and density assigning. Furthermore, the amalgam density data were corrected to provide amalgam voxel with accurate density value. As for the errors of dose uncertainties due to metal amalgam, they were reduced from 46% to as low as 2% at d80 (depth of the 80% dose beyond Zmax using the presented strategies. Considering the number of vital and radiosensitive organs in the head and the neck regions, this correction strategy is suggested in reducing calculation uncertainties through MC calculation.
Energy Technology Data Exchange (ETDEWEB)
McCaw, T; Culberson, W; DeWerd, L [University of Wisconsin Medical Radiation Research Center, Madison, WI (United States)
2014-06-01
Purpose: To experimentally verify a Monte Carlo (MC) linear accelerator model for the simulation of intensity-modulated radiation therapy (IMRT) treatments of moving targets. Methods: A Varian Clinac™ 21EX linear accelerator was modeled using the EGSnrc user code BEAMnrc. The mean energy, radial-intensity distribution, and divergence of the electron beam incident on the bremsstrahlung target were adjusted to achieve agreement between simulated and measured percentage-depth-dose and transverse field profiles for a 6 MV beam. A seven-field step-and-shoot IMRT lung procedure was prepared using Varian Eclipse™ treatment planning software. The plan was delivered using a Clinac™ 21EX linear accelerator and measured with a Gafchromic™ EBT2 film stack dosimeter (FSD) in two separate static geometries: within a cylindrical water-equivalent-plastic phantom and within an anthropomorphic chest phantom. Two measurements were completed in each setup. The dose distribution for each geometry was simulated using the EGSnrc user code DOSXYZnrc. MC geometries of the treatment couch, cylindrical phantom, and chest phantom were developed by thresholding CT data sets using MATLAB™. The FSD was modeled as water. The measured and simulated dose distributions were normalized to the median dose within the FSD. Results: Using an electron beam with a mean energy of 6.05 MeV, a Gaussian radial-intensity distribution with a full width at half maximum of 1.5 mm, and a divergence of 0°, the measured and simulated dose profiles agree within 1.75% and 1 mm. Measured and simulated dose distributions within both the cylindrical and chest phantoms agree within 3% over 94% of the FSD volume. The overall uncertainty in the FSD measurements is 3.1% (k=1). Conclusion: MC simulations agree with FSD measurements within measurement uncertainty, thereby verifying the accuracy of the linear accelerator model for the simulation of IMRT treatments of static geometries. The experimental verification
Gamma analysis in volumetric dose verification in intensity modulated radiation therapy
International Nuclear Information System (INIS)
IMRT treatments are planned and finalised with predetermined volumetric dose distribution to planning target volume (PTV) and organ at risk (OAR). However dose verification using planer detector and point dose does not suffice to verify the volumetric set dose criteria during the planning of IMRT. 3D dosimetry systems allow volumetric comparisons of planned and delivered dose using the dose volume histogram for organ of interest. In this way we can compare the planned and delivered dose as per the ICRU 83. To be more practical 3D gamma analysis methods make it possible to analyze planned and delivered dose verification by taking into account for small setup errors of the dosimeter phantom and/or detector. This work describes the results of volumetric dose verification using dose at 98%, 95%, 2% to volume of interest and 3D gamma analysis methods in IMRT using computational environment for radiotherapy research software platform by incorporating quantitative 3D gamma analysis tools
Monte Carlo N Particle code - Dose distribution of clinical electron beams in inhomogeneous phantoms
H A Nedaie; Mosleh-Shirazi, M. A.; Allahverdi, M.
2013-01-01
Electron dose distributions calculated using the currently available analytical methods can be associated with large uncertainties. The Monte Carlo method is the most accurate method for dose calculation in electron beams. Most of the clinical electron beam simulation studies have been performed using non- MCNP [Monte Carlo N Particle] codes. Given the differences between Monte Carlo codes, this work aims to evaluate the accuracy of MCNP4C-simulated electron dose distributions in a homogenous...
TH-A-19A-06: Site-Specific Comparison of Analytical and Monte Carlo Based Dose Calculations
Energy Technology Data Exchange (ETDEWEB)
Schuemann, J; Grassberger, C; Paganetti, H [Massachusetts General Hospital and Harvard Medical School, Boston, MA (United States); Dowdell, S [Illawarra Shoalhaven Local Health District, Wollongong (Australia)
2014-06-15
Purpose: To investigate the impact of complex patient geometries on the capability of analytical dose calculation algorithms to accurately predict dose distributions and to verify currently used uncertainty margins in proton therapy. Methods: Dose distributions predicted by an analytical pencilbeam algorithm were compared with Monte Carlo simulations (MCS) using TOPAS. 79 complete patient treatment plans were investigated for 7 disease sites (liver, prostate, breast, medulloblastoma spine and whole brain, lung and head and neck). A total of 508 individual passively scattered treatment fields were analyzed for field specific properties. Comparisons based on target coverage indices (EUD, D95, D90 and D50) were performed. Range differences were estimated for the distal position of the 90% dose level (R90) and the 50% dose level (R50). Two-dimensional distal dose surfaces were calculated and the root mean square differences (RMSD), average range difference (ARD) and average distal dose degradation (ADD), the distance between the distal position of the 80% and 20% dose levels (R80- R20), were analyzed. Results: We found target coverage indices calculated by TOPAS to generally be around 1–2% lower than predicted by the analytical algorithm. Differences in R90 predicted by TOPAS and the planning system can be larger than currently applied range margins in proton therapy for small regions distal to the target volume. We estimate new site-specific range margins (R90) for analytical dose calculations considering total range uncertainties and uncertainties from dose calculation alone based on the RMSD. Our results demonstrate that a reduction of currently used uncertainty margins is feasible for liver, prostate and whole brain fields even without introducing MC dose calculations. Conclusion: Analytical dose calculation algorithms predict dose distributions within clinical limits for more homogeneous patients sites (liver, prostate, whole brain). However, we recommend
Performance testing and dose verification for extremity ring dosimetry
International Nuclear Information System (INIS)
The paper describes the testing performed on an extremity dosimetry system to measure the personal dose equivalent Hp(0.07) in photon and beta reference fields. This research refers to the American National Standard Institute to organize the performance testing for the INER's TLD-100H extremity ring dosimeters. The results show that tolerance level (L), absolute of bias (|B|) and standard deviation (S) for all categories of performance testing meet the ANSI N13.32 performance testing criteria. The performance testing results were suggested to be an important step of an accreditation procedure for the extremity ring dosimetry system in Taiwan. Besides, the dose evaluation of extremity ring dosimeters to measure Hp(0.07) in realistic fields of nuclear medicine is also verified. The reference values of Hp(0.07) were calculated using the Monte Carlo method normalized by the measured activity of the radioactive solution. For nuclear medicine irradiations the relative response to 201Tl and 99mTc radionuclides produced by INER are also satisfactory.
Feasibility of RACT for 3D dose measurement and range verification in a water phantom
Energy Technology Data Exchange (ETDEWEB)
Alsanea, Fahed [School of Health Sciences, Purdue University, 550 Stadium Mall Drive, West Lafayette, Indiana 47907-2051 (United States); Moskvin, Vadim [Radiation Oncology, Indiana University School of Medicine, 535 Barnhill Drive, RT 041, Indianapolis, Indiana 46202-5289 (United States); Stantz, Keith M., E-mail: kstantz@purdue.edu [School of Health Sciences, Purdue University, 550 Stadium Mall Drive, West Lafayette, Indiana 47907-2051 and Radiology and Imaging Sciences, Indiana University School of Medicine, 950 West Walnut Street, Indianapolis, Indiana 46202-5289 (United States)
2015-02-15
Purpose: The objective of this study is to establish the feasibility of using radiation-induced acoustics to measure the range and Bragg peak dose from a pulsed proton beam. Simulation studies implementing a prototype scanner design based on computed tomographic methods were performed to investigate the sensitivity to proton range and integral dose. Methods: Derived from thermodynamic wave equation, the pressure signals generated from the dose deposited from a pulsed proton beam with a 1 cm lateral beam width and a range of 16, 20, and 27 cm in water using Monte Carlo methods were simulated. The resulting dosimetric images were reconstructed implementing a 3D filtered backprojection algorithm and the pressure signals acquired from a 71-transducer array with a cylindrical geometry (30 × 40 cm) rotated over 2π about its central axis. Dependencies on the detector bandwidth and proton beam pulse width were performed, after which, different noise levels were added to the detector signals (using 1 μs pulse width and a 0.5 MHz cutoff frequency/hydrophone) to investigate the statistical and systematic errors in the proton range (at 20 cm) and Bragg peak dose (of 1 cGy). Results: The reconstructed radioacoustic computed tomographic image intensity was shown to be linearly correlated to the dose within the Bragg peak. And, based on noise dependent studies, a detector sensitivity of 38 mPa was necessary to determine the proton range to within 1.0 mm (full-width at half-maximum) (systematic error < 150 μm) for a 1 cGy Bragg peak dose, where the integral dose within the Bragg peak was measured to within 2%. For existing hydrophone detector sensitivities, a Bragg peak dose of 1.6 cGy is possible. Conclusions: This study demonstrates that computed tomographic scanner based on ionizing radiation-induced acoustics can be used to verify dose distribution and proton range with centi-Gray sensitivity. Realizing this technology into the clinic has the potential to significantly
Feasibility of RACT for 3D dose measurement and range verification in a water phantom
International Nuclear Information System (INIS)
Purpose: The objective of this study is to establish the feasibility of using radiation-induced acoustics to measure the range and Bragg peak dose from a pulsed proton beam. Simulation studies implementing a prototype scanner design based on computed tomographic methods were performed to investigate the sensitivity to proton range and integral dose. Methods: Derived from thermodynamic wave equation, the pressure signals generated from the dose deposited from a pulsed proton beam with a 1 cm lateral beam width and a range of 16, 20, and 27 cm in water using Monte Carlo methods were simulated. The resulting dosimetric images were reconstructed implementing a 3D filtered backprojection algorithm and the pressure signals acquired from a 71-transducer array with a cylindrical geometry (30 × 40 cm) rotated over 2π about its central axis. Dependencies on the detector bandwidth and proton beam pulse width were performed, after which, different noise levels were added to the detector signals (using 1 μs pulse width and a 0.5 MHz cutoff frequency/hydrophone) to investigate the statistical and systematic errors in the proton range (at 20 cm) and Bragg peak dose (of 1 cGy). Results: The reconstructed radioacoustic computed tomographic image intensity was shown to be linearly correlated to the dose within the Bragg peak. And, based on noise dependent studies, a detector sensitivity of 38 mPa was necessary to determine the proton range to within 1.0 mm (full-width at half-maximum) (systematic error < 150 μm) for a 1 cGy Bragg peak dose, where the integral dose within the Bragg peak was measured to within 2%. For existing hydrophone detector sensitivities, a Bragg peak dose of 1.6 cGy is possible. Conclusions: This study demonstrates that computed tomographic scanner based on ionizing radiation-induced acoustics can be used to verify dose distribution and proton range with centi-Gray sensitivity. Realizing this technology into the clinic has the potential to significantly
Dosimetry and dose planning in boron neutron capture therapy : Monte Carlo studies
Energy Technology Data Exchange (ETDEWEB)
Koivunoro, H.
2012-07-01
Boron neutron capture therapy (BNCT) is a biologically targeted radiotherapy modality. So far, 249 cancer patients have received BNCT at the Finnish Research Reactor 1 (FiR 1) in Finland. The effectiveness and safety of radiotherapy are dependent on the radiation dose delivered to the tumor and healthy tissues, and on the accuracy of the doses. At FiR 1, patient dose calculations are performed with the Monte Carlo (MC) -based treatmentplanning system (TPS), Simulation Environment for Radiotherapy Applications (SERA). Initially, BNCT was applied to head and neck cancer, brain tumors, and malignant melanoma. To evaluate the applicability of the new target tumors for BNCT, calculation dosimetry studies are needed. So far, clinical BNCT has been performed with the neutrons from a nuclear reactor, while an accelerator based neutron sources applicable for hospital operation would be preferable. In this thesis, BNCT patient dose calculation practice in Finland was evaluated against reference calculations and experimental data in several cases. Calculations with two TPSs applied in clinical BNCT were compared. The suitability of the deuterium-deuterium (DD) and deuterium-tritium (D-T) fusion reaction-based compact neutron sources for BNCT were evaluated. In addition, feasibility of BNCT for noninvasive liver tumor treatments was examined. The deviation between SERA and the reference calculations was within 4% in the phantoms studied and in a brain cancer patient model elsewhere, except on the phantom or skin surface, for the boron, nitrogen, and photon dose components. These dose components produce 99% of the tumor dose and > 90% of the healthy tissue dose at points of relevance for treatment at the FiR 1 facility. The reduced voxel cell size ({<=} 0.5 cm) in the SERA edit mesh improved calculation accuracy on the surface. The erratic biased fastneutron run option in SERA led to significant underestimation (up to 30-60%) of the fastneutron dose, while more accurate fast
An in vivo dose verification method for SBRT–VMAT delivery using the EPID
International Nuclear Information System (INIS)
Purpose: Radiation treatments have become increasingly more complex with the development of volumetric modulated arc therapy (VMAT) and the use of stereotactic body radiation therapy (SBRT). SBRT involves the delivery of substantially larger doses over fewer fractions than conventional therapy. SBRT–VMAT treatments will strongly benefit from in vivo patient dose verification, as any errors in delivery can be more detrimental to the radiobiology of the patient as compared to conventional therapy. Electronic portal imaging devices (EPIDs) are available on most commercial linear accelerators (Linacs) and their documented use for dosimetry makes them valuable tools for patient dose verification. In this work, the authors customize and validate a physics-based model which utilizes on-treatment EPID images to reconstruct the 3D dose delivered to the patient during SBRT–VMAT delivery. Methods: The SBRT Linac head, including jaws, multileaf collimators, and flattening filter, were modeled using Monte Carlo methods and verified with measured data. The simulation provides energy spectrum data that are used by their “forward” model to then accurately predict fluence generated by a SBRT beam at a plane above the patient. This fluence is then transported through the patient and then the dose to the phosphor layer in the EPID is calculated. Their “inverse” model back-projects the EPID measured focal fluence to a plane upstream of the patient and recombines it with the extra-focal fluence predicted by the forward model. This estimate of total delivered fluence is then forward projected onto the patient’s density matrix and a collapsed cone convolution algorithm calculates the dose delivered to the patient. The model was tested by reconstructing the dose for two prostate, three lung, and two spine SBRT–VMAT treatment fractions delivered to an anthropomorphic phantom. It was further validated against actual patient data for a lung and spine SBRT–VMAT plan. The
An in vivo dose verification method for SBRT–VMAT delivery using the EPID
Energy Technology Data Exchange (ETDEWEB)
McCowan, P. M., E-mail: peter.mccowan@cancercare.mb.ca [Department of Physics and Astronomy, University of Manitoba, Winnipeg, Manitoba R3T 2N2 (Canada); Medical Physics Department, CancerCare Manitoba, 675 McDermot Avenue, Winnipeg, Manitoba R3E 0V9 (Canada); Van Uytven, E.; Van Beek, T.; Asuni, G. [Medical Physics Department, CancerCare Manitoba, 675 McDermot Avenue, Winnipeg, Manitoba R3E 0V9 (Canada); McCurdy, B. M. C. [Department of Physics and Astronomy, University of Manitoba, Winnipeg, Manitoba R3T 2N2 (Canada); Medical Physics Department, CancerCare Manitoba, 675 McDermot Avenue, Winnipeg, Manitoba R3E 0V9 (Canada); Department of Radiology, University of Manitoba, 820 Sherbrook Street, Winnipeg, Manitoba R3A 1R9 (Canada)
2015-12-15
Purpose: Radiation treatments have become increasingly more complex with the development of volumetric modulated arc therapy (VMAT) and the use of stereotactic body radiation therapy (SBRT). SBRT involves the delivery of substantially larger doses over fewer fractions than conventional therapy. SBRT–VMAT treatments will strongly benefit from in vivo patient dose verification, as any errors in delivery can be more detrimental to the radiobiology of the patient as compared to conventional therapy. Electronic portal imaging devices (EPIDs) are available on most commercial linear accelerators (Linacs) and their documented use for dosimetry makes them valuable tools for patient dose verification. In this work, the authors customize and validate a physics-based model which utilizes on-treatment EPID images to reconstruct the 3D dose delivered to the patient during SBRT–VMAT delivery. Methods: The SBRT Linac head, including jaws, multileaf collimators, and flattening filter, were modeled using Monte Carlo methods and verified with measured data. The simulation provides energy spectrum data that are used by their “forward” model to then accurately predict fluence generated by a SBRT beam at a plane above the patient. This fluence is then transported through the patient and then the dose to the phosphor layer in the EPID is calculated. Their “inverse” model back-projects the EPID measured focal fluence to a plane upstream of the patient and recombines it with the extra-focal fluence predicted by the forward model. This estimate of total delivered fluence is then forward projected onto the patient’s density matrix and a collapsed cone convolution algorithm calculates the dose delivered to the patient. The model was tested by reconstructing the dose for two prostate, three lung, and two spine SBRT–VMAT treatment fractions delivered to an anthropomorphic phantom. It was further validated against actual patient data for a lung and spine SBRT–VMAT plan. The
Evaluation of MatriXX for IMRT and VMAT dose verifications in peripheral dose regions
International Nuclear Information System (INIS)
Purpose: MatriXX is a two-dimensional ion chamber array designed for IMRT/VMAT (RapidArc, IMAT, etc.) dose verifications. Its dosimetric properties have been characterized for megavoltage beams in a number of studies; however, to the best of the authors' knowledge, there is still a lack of an investigation into its performance in the peripheral or low dose regions. In this work, the authors have carried out a systematic study on this issue. Methods: The authors compare the performance of MatriXX with a cylindrical ion chamber in solid water phantoms in the peripheral dose regions. The comparisons are performed for a number of typical irradiation conditions that involve different gantry and/or MLC motions, field sizes, and distances to the target including static gantry/open fields, static gantry/sweeping MLC gap (mimicking an IMRT delivery), dynamic gantry/oscillating sweeping MLC gap (mimicking a VMAT delivery), as well as clinical IMRT and VMAT plans. Results: MatriXX, when used according to the manufacturer's recommendations, is found to disagree with an ion chamber in peripheral dose regions. This disagreement has been attributed to four types of MatriXX errors, namely, positive bias, over-response to scattered doses, round-off error, and angular dependence, all of which contribute to dose inaccuracies in the peripheral regions. The positive bias, which is independent of the dose level, is cumulative when MatriXX operates in the movie mode. The accumulation is proportional to the number of movie frames (snaps) when the sampling time is greater than 500 ms and is proportional to the overall movie time for a sampling time shorter than 500 ms. This behavior suggests multiple sources of the bias. MatriXX is also found to over-respond to peripheral doses by about 2.0% for the regions investigated in this work (3-15 cm from the field edge), where phantom scatter and collimator scatter dominate. Round-off error is determined to be due to insufficient precision in
Clinical implementation of full Monte Carlo dose calculation in proton beam therapy
Energy Technology Data Exchange (ETDEWEB)
Paganetti, Harald; Jiang, Hongyu; Parodi, Katia; Slopsema, Roelf; Engelsman, Martijn [Department of Radiation Oncology, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114 (United States)
2008-09-07
The goal of this work was to facilitate the clinical use of Monte Carlo proton dose calculation to support routine treatment planning and delivery. The Monte Carlo code Geant4 was used to simulate the treatment head setup, including a time-dependent simulation of modulator wheels (for broad beam modulation) and magnetic field settings (for beam scanning). Any patient-field-specific setup can be modeled according to the treatment control system of the facility. The code was benchmarked against phantom measurements. Using a simulation of the ionization chamber reading in the treatment head allows the Monte Carlo dose to be specified in absolute units (Gy per ionization chamber reading). Next, the capability of reading CT data information was implemented into the Monte Carlo code to model patient anatomy. To allow time-efficient dose calculation, the standard Geant4 tracking algorithm was modified. Finally, a software link of the Monte Carlo dose engine to the patient database and the commercial planning system was established to allow data exchange, thus completing the implementation of the proton Monte Carlo dose calculation engine ('DoC++'). Monte Carlo re-calculated plans are a valuable tool to revisit decisions in the planning process. Identification of clinically significant differences between Monte Carlo and pencil-beam-based dose calculations may also drive improvements of current pencil-beam methods. As an example, four patients (29 fields in total) with tumors in the head and neck regions were analyzed. Differences between the pencil-beam algorithm and Monte Carlo were identified in particular near the end of range, both due to dose degradation and overall differences in range prediction due to bony anatomy in the beam path. Further, the Monte Carlo reports dose-to-tissue as compared to dose-to-water by the planning system. Our implementation is tailored to a specific Monte Carlo code and the treatment planning system XiO (Computerized Medical
Locke, C
2008-01-01
Monte Carlo (MC) method provides the most accurate to-date dose calculations in heterogeneous media and complex geometries, and this spawns increasing interest in incorporating MC calculations to treatment planning quality assurance process. This process involves MC dose calculations for the treatment plans produced clinically. To perform these calculations a number of treatment plan parameters specifying radiation beam and patient geometries needs to be transferred to MC codes such as BEAMnrc and DOSXYZnrc. Extracting these parameters from DICOM files is not a trivial task that has previously been performed mostly using Matlab-based software. This paper describes DICOM tags that contain information required for MC modeling of conformal and IMRT plans, and reports development of an in-house DICOM interface through a library (named Vega) of platform-independent, object-oriented C++ codes. Vega library is small and succinct, offering just the fundamental functions for reading/modifying/writing DICOM files in a ...
Parodi, K.; Ferrari, A.; Sommerer, F.; Paganetti, H.
2007-07-01
Clinical investigations on post-irradiation PET/CT (positron emission tomography/computed tomography) imaging for in vivo verification of treatment delivery and, in particular, beam range in proton therapy are underway at Massachusetts General Hospital (MGH). Within this project, we have developed a Monte Carlo framework for CT-based calculation of dose and irradiation-induced positron emitter distributions. Initial proton beam information is provided by a separate Geant4 Monte Carlo simulation modelling the treatment head. Particle transport in the patient is performed in the CT voxel geometry using the FLUKA Monte Carlo code. The implementation uses a discrete number of different tissue types with composition and mean density deduced from the CT scan. Scaling factors are introduced to account for the continuous Hounsfield unit dependence of the mass density and of the relative stopping power ratio to water used by the treatment planning system (XiO (Computerized Medical Systems Inc.)). Resulting Monte Carlo dose distributions are generally found in good correspondence with calculations of the treatment planning program, except a few cases (e.g. in the presence of air/tissue interfaces). Whereas dose is computed using standard FLUKA utilities, positron emitter distributions are calculated by internally combining proton fluence with experimental and evaluated cross-sections yielding 11C, 15O, 14O, 13N, 38K and 30P. Simulated positron emitter distributions yield PET images in good agreement with measurements. In this paper, we describe in detail the specific implementation of the FLUKA calculation framework, which may be easily adapted to handle arbitrary phase spaces of proton beams delivered by other facilities or include more reaction channels based on additional cross-section data. Further, we demonstrate the effects of different acquisition time regimes (e.g., PET imaging during or after irradiation) on the intensity and spatial distribution of the irradiation
Verification of SMART Neutronics Design Methodology by the MCNAP Monte Carlo Code
International Nuclear Information System (INIS)
SMART is a small advanced integral pressurized water reactor (PWR) of 330 MW(thermal) designed for both electricity generation and seawater desalinization. The CASMO-3/MASTER nuclear analysis system, a design-basis of Korean PWR plants, has been employed for the SMART core nuclear design and analysis because the fuel assembly (FA) characteristics and reactor operating conditions in temperature and pressure are similar to those of PWR plants. However, the SMART FAs are highly poisoned with more than 20 Al2O3-B4C plus additional Gd2O3/UO2 BPRs each FA. The reactor is operated with control rods inserted. Therefore, the flux and power distribution may become more distorted than those of commercial PWR plants. In addition, SMART should produce power from room temperature to hot-power operating condition because it employs nuclear heating from room temperature. This demands reliable predictions of core criticality, shutdown margin, control rod worth, power distributions, and reactivity coefficients at both room temperature and hot operating condition, yet no such data are available to verify the CASMO-3/MASTER (hereafter MASTER) code system. In the absence of experimental verification data for the SMART neutronics design, the Monte Carlo depletion analysis program MCNAP is adopted as near-term alternatives for qualifying MASTER neutronics design calculations. The MCNAP is a personal computer-based continuous energy Monte Carlo neutronics analysis program written in C++ language. We established its qualification by presenting its prediction accuracy on measurements of Venus critical facilities and core neutronics analysis of a PWR plant in operation, and depletion characteristics of integral burnable absorber FAs of the current PWR. Here, we present a comparison of MASTER and MCNAP neutronics design calculations for SMART and establish the qualification of the MASTER system
Monte Carlo calculation of ''skyshine'' neutron dose from ALS [Advanced Light Source
International Nuclear Information System (INIS)
This report discusses the following topics on ''skyshine'' neutron dose from ALS: Sources of radiation; ALS modeling for skyshine calculations; MORSE Monte-Carlo; Implementation of MORSE; Results of skyshine calculations from storage ring; and Comparison of MORSE shielding calculations
Monte Carlo calculation of 60Co γ-ray's albedo-dose rate from the air
International Nuclear Information System (INIS)
The Monte Carlo calculation of 60Co γ-ray's albedo-dose rate from the air is reported. A formula is presented with which the relations of the albedo-doserate with some parameters are simulated and fitted
SU-E-T-602: Patient-Specific Online Dose Verification Based On Transmission Detector Measurements
Energy Technology Data Exchange (ETDEWEB)
Thoelking, J; Yuvaraj, S; Jens, F; Lohr, F; Wenz, F; Wertz, H; Wertz, H [University Medical Center Mannheim, University of Heidelberg, Mannheim, Baden-Wuerttemberg (Germany)
2015-06-15
Purpose: Intensity modulated radiotherapy requires a comprehensive quality assurance program in general and ideally independent verification of dose delivery. Since conventional 2D detector arrays allow only pre-treatment verification, there is a debate concerning the need of online dose verification. This study presents the clinical performance, including dosimetric plan verification in 2D as well as in 3D and the error detection abilities of a new transmission detector (TD) for online dose verification of 6MV photon beam. Methods: To validate the dosimetric performance of the new device, dose reconstruction based on TD measurements were compared to a conventional pre-treatment verification method (reference) and treatment planning system (TPS) for 18 IMRT and VMAT treatment plans. Furthermore, dose reconstruction inside the patient based on TD read-out was evaluated by comparing various dose volume indices and 3D gamma evaluations against independent dose computation and TPS. To investigate the sensitivity of the new device, different types of systematic and random errors for leaf positions and linac output were introduced in IMRT treatment sequences. Results: The 2D gamma index evaluation of transmission detector based dose reconstruction showed an excellent agreement for all IMRT and VMAT plans compared to reference measurements (99.3±1.2)% and TPS (99.1±0.7)%. Good agreement was also obtained for 3D dose reconstruction based on TD read-out compared to dose computation (mean gamma value of PTV = 0.27±0.04). Only a minimal dose underestimation within the target volume was observed when analyzing DVH indices (<1%). Positional errors in leaf banks larger than 1mm and errors in linac output larger than 2% could clearly identified with the TD. Conclusion: Since 2D and 3D evaluations for all IMRT and VMAT treatment plans were in excellent agreement with reference measurements and dose computation, the new TD is suitable to qualify for routine treatment plan
SU-E-T-602: Patient-Specific Online Dose Verification Based On Transmission Detector Measurements
International Nuclear Information System (INIS)
Purpose: Intensity modulated radiotherapy requires a comprehensive quality assurance program in general and ideally independent verification of dose delivery. Since conventional 2D detector arrays allow only pre-treatment verification, there is a debate concerning the need of online dose verification. This study presents the clinical performance, including dosimetric plan verification in 2D as well as in 3D and the error detection abilities of a new transmission detector (TD) for online dose verification of 6MV photon beam. Methods: To validate the dosimetric performance of the new device, dose reconstruction based on TD measurements were compared to a conventional pre-treatment verification method (reference) and treatment planning system (TPS) for 18 IMRT and VMAT treatment plans. Furthermore, dose reconstruction inside the patient based on TD read-out was evaluated by comparing various dose volume indices and 3D gamma evaluations against independent dose computation and TPS. To investigate the sensitivity of the new device, different types of systematic and random errors for leaf positions and linac output were introduced in IMRT treatment sequences. Results: The 2D gamma index evaluation of transmission detector based dose reconstruction showed an excellent agreement for all IMRT and VMAT plans compared to reference measurements (99.3±1.2)% and TPS (99.1±0.7)%. Good agreement was also obtained for 3D dose reconstruction based on TD read-out compared to dose computation (mean gamma value of PTV = 0.27±0.04). Only a minimal dose underestimation within the target volume was observed when analyzing DVH indices (<1%). Positional errors in leaf banks larger than 1mm and errors in linac output larger than 2% could clearly identified with the TD. Conclusion: Since 2D and 3D evaluations for all IMRT and VMAT treatment plans were in excellent agreement with reference measurements and dose computation, the new TD is suitable to qualify for routine treatment plan
International Nuclear Information System (INIS)
This study determined the influence of patient individuality on lung organ doses for chest CT examinations. The aim was a statistical statement on the variability as well as the uncertainty caused by the patient individuality. Furthermore, the reproducibility of the mean organ dose value of the lung using the new ICRP 110 voxelized adult female phantom was determined. Calculation of lung doses for 61 female chest CT studies with identical scan parameters (120 kV, 135 mAs, 100 mm collimation, 1.5 pitch) were done. For all patients, the lung was contoured and the geometry was simulated using the Monte Carlo method without patient table and with its original voxel size. The lungs were completely included in the scan area. A so-called user code CTDOSPP was developed which extends the Monte Carlo package EGSnrc and enables rotational simulation of CT X-ray sources. A developed graphical user interface GMctdospp allows easy handling of simulation parameters and CT studies, which are loaded in the DicomRT struct format. The transformation of CT values to material and density values is carried out with a standard relationship. The ICRP adult female material composition of all organs were directly taken from the publication. The patient table and bed and pillow were assumed to be air in order to be similar to patient pool. All simulations were calibrated for better handling and visualisation to a CTDIair value of 22.9 mGy. Simulation values were grouped into 1 mSv classes. The organ dose classes fit well to a Gaussian distribution (correlation coefficient R2 = 0.97). The fit's mean value is 10 mSv with a standard deviation of 2 mSv. The variability is about ± 30 % with minimum at 8 mSv and maximum at 13 mSv. The calculated organ dose to the lungs of the ICRP adult female phantom is about 11 mSv and thus within the calculated standard deviation of the patient pool. For all simulations the statistical uncertainty was between 2 and 3.5 %. This present study shows good
TPSPET—A TPS-based approach for in vivo dose verification with PET in proton therapy
International Nuclear Information System (INIS)
Since the interest in ion-irradiation for tumour therapy has significantly increased over the last few decades, intensive investigations are performed to improve the accuracy of this form of patient treatment. One major goal is the development of methods for in vivo dose verification. In proton therapy, a PET (positron emission tomography)-based approach measuring the irradiation-induced tissue activation inside the patient has been already clinically implemented. The acquired PET images can be compared to an expectation, derived under the assumption of a correct treatment application, to validate the particle range and the lateral field position in vivo. In the context of this work, TPSPET is introduced as a new approach to predict proton-irradiation induced three-dimensional positron emitter distributions by means of the same algorithms of the clinical treatment planning system (TPS). In order to perform additional activity calculations, reaction-channel-dependent input positron emitter depth distributions are necessary, which are determined from the application of a modified filtering approach to the TPS reference depth dose profiles in water. This paper presents the implementation of TPSPET on the basis of the research treatment planning software treatment planning for particles. The results are validated in phantom and patient studies against Monte Carlo simulations, and compared to β+-emitter distributions obtained from a slightly modified version of the originally proposed one-dimensional filtering approach applied to three-dimensional dose distributions. In contrast to previously introduced methods, TPSPET provides a faster implementation, the results show no sensitivity to lateral field extension and the predicted β+-emitter densities are fully consistent to the planned treatment dose as they are calculated by the same pencil beam algorithms. These findings suggest a large potential of the application of TPSPET for in vivo dose verification in the daily
Implementation of Monte Carlo Dose calculation for CyberKnife treatment planning
Ma, C.-M.; Li, J. S.; Deng, J.; Fan, J.
2008-02-01
Accurate dose calculation is essential to advanced stereotactic radiosurgery (SRS) and stereotactic radiotherapy (SRT) especially for treatment planning involving heterogeneous patient anatomy. This paper describes the implementation of a fast Monte Carlo dose calculation algorithm in SRS/SRT treatment planning for the CyberKnife® SRS/SRT system. A superposition Monte Carlo algorithm is developed for this application. Photon mean free paths and interaction types for different materials and energies as well as the tracks of secondary electrons are pre-simulated using the MCSIM system. Photon interaction forcing and splitting are applied to the source photons in the patient calculation and the pre-simulated electron tracks are repeated with proper corrections based on the tissue density and electron stopping powers. Electron energy is deposited along the tracks and accumulated in the simulation geometry. Scattered and bremsstrahlung photons are transported, after applying the Russian roulette technique, in the same way as the primary photons. Dose calculations are compared with full Monte Carlo simulations performed using EGS4/MCSIM and the CyberKnife treatment planning system (TPS) for lung, head & neck and liver treatments. Comparisons with full Monte Carlo simulations show excellent agreement (within 0.5%). More than 10% differences in the target dose are found between Monte Carlo simulations and the CyberKnife TPS for SRS/SRT lung treatment while negligible differences are shown in head and neck and liver for the cases investigated. The calculation time using our superposition Monte Carlo algorithm is reduced up to 62 times (46 times on average for 10 typical clinical cases) compared to full Monte Carlo simulations. SRS/SRT dose distributions calculated by simple dose algorithms may be significantly overestimated for small lung target volumes, which can be improved by accurate Monte Carlo dose calculations.
Implementation of Monte Carlo Dose calculation for CyberKnife treatment planning
International Nuclear Information System (INIS)
Accurate dose calculation is essential to advanced stereotactic radiosurgery (SRS) and stereotactic radiotherapy (SRT) especially for treatment planning involving heterogeneous patient anatomy. This paper describes the implementation of a fast Monte Carlo dose calculation algorithm in SRS/SRT treatment planning for the CyberKnife (registered) SRS/SRT system. A superposition Monte Carlo algorithm is developed for this application. Photon mean free paths and interaction types for different materials and energies as well as the tracks of secondary electrons are pre-simulated using the MCSIM system. Photon interaction forcing and splitting are applied to the source photons in the patient calculation and the pre-simulated electron tracks are repeated with proper corrections based on the tissue density and electron stopping powers. Electron energy is deposited along the tracks and accumulated in the simulation geometry. Scattered and bremsstrahlung photons are transported, after applying the Russian roulette technique, in the same way as the primary photons. Dose calculations are compared with full Monte Carlo simulations performed using EGS4/MCSIM and the CyberKnife treatment planning system (TPS) for lung, head and neck and liver treatments. Comparisons with full Monte Carlo simulations show excellent agreement (within 0.5%). More than 10% differences in the target dose are found between Monte Carlo simulations and the CyberKnife TPS for SRS/SRT lung treatment while negligible differences are shown in head and neck and liver for the cases investigated. The calculation time using our superposition Monte Carlo algorithm is reduced up to 62 times (46 times on average for 10 typical clinical cases) compared to full Monte Carlo simulations. SRS/SRT dose distributions calculated by simple dose algorithms may be significantly overestimated for small lung target volumes, which can be improved by accurate Monte Carlo dose calculations
Implementation of Monte Carlo Dose calculation for CyberKnife treatment planning
Energy Technology Data Exchange (ETDEWEB)
Ma, C-M; Li, J S; Deng, J; Fan, J [Radiation Oncology Department, Fox Chase Cancer Center, Philadelphia, PA (United States)], E-mail: Charlie.ma@fccc.edu
2008-02-01
Accurate dose calculation is essential to advanced stereotactic radiosurgery (SRS) and stereotactic radiotherapy (SRT) especially for treatment planning involving heterogeneous patient anatomy. This paper describes the implementation of a fast Monte Carlo dose calculation algorithm in SRS/SRT treatment planning for the CyberKnife (registered) SRS/SRT system. A superposition Monte Carlo algorithm is developed for this application. Photon mean free paths and interaction types for different materials and energies as well as the tracks of secondary electrons are pre-simulated using the MCSIM system. Photon interaction forcing and splitting are applied to the source photons in the patient calculation and the pre-simulated electron tracks are repeated with proper corrections based on the tissue density and electron stopping powers. Electron energy is deposited along the tracks and accumulated in the simulation geometry. Scattered and bremsstrahlung photons are transported, after applying the Russian roulette technique, in the same way as the primary photons. Dose calculations are compared with full Monte Carlo simulations performed using EGS4/MCSIM and the CyberKnife treatment planning system (TPS) for lung, head and neck and liver treatments. Comparisons with full Monte Carlo simulations show excellent agreement (within 0.5%). More than 10% differences in the target dose are found between Monte Carlo simulations and the CyberKnife TPS for SRS/SRT lung treatment while negligible differences are shown in head and neck and liver for the cases investigated. The calculation time using our superposition Monte Carlo algorithm is reduced up to 62 times (46 times on average for 10 typical clinical cases) compared to full Monte Carlo simulations. SRS/SRT dose distributions calculated by simple dose algorithms may be significantly overestimated for small lung target volumes, which can be improved by accurate Monte Carlo dose calculations.
Three-dimensional dose prediction based on two-dimensional verification measurements for IMRT.
Sumida, Iori; Yamaguchi, Hajime; Kizaki, Hisao; Aboshi, Keiko; Yamada, Yuji; Yoshioka, Yasuo; Ogawa, Kazuhiko
2014-01-01
Dose verifications for intensity-modulated radiation therapy (IMRT) are generally performed once before treatment. A 39-fraction treatment course for prostate cancer delivers a dose prescription of 78 Gy in eight weeks. Any changes in multileaf collimator leaf position over the treatment course may affect the dosimetry. To evaluate the magnitude of deviations from the predicted dose over an entire treatment course with MLC leaf calibrations performed every two weeks, we tracked weekly changes in relative dose error distributions measured with two-dimensional (2D) beam-by-beam analysis. We compared the dosimetric results from 20 consecutive patient-specific IMRT quality assurance (QA) tests using beam-by-beam analysis and a 2D diode detector array to the dose plans calculated by the treatment planning system (TPS). We added back the resulting relative dose error measured weekly into the original dose grid for each beam. To validate the prediction method, the predicted doses and dose distributions were compared to the measurements using an ionization chamber and film. The predicted doses were in good agreement, within 2% of the measured doses, and the predicted dose distributions also presented good agreement with the measured distributions. Dose verification results measured once as a pretreatment QA test were not completely stable, as results of weekly beam-by-beam analysis showed some variation. Because dosimetric errors throughout the treatment course were averaged, the overall dosimetric impact to patients was small. PMID:25207574
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Hornbeck, Amaury, E-mail: amauryhornbeck@gmail.com, E-mail: tristan.garcia@cea.fr; Garcia, Tristan, E-mail: amauryhornbeck@gmail.com, E-mail: tristan.garcia@cea.fr [CEA, LIST, Laboratoire National Henri Becquerel, 91191 Gif-sur-Yvette Cedex (France); Cuttat, Marguerite; Jenny, Catherine [Radiotherapy Department, Medical Physics Unit, University Hospital Pitié-Salpêtrière, 75013 Paris (France)
2014-06-15
Purpose: Elekta Leksell Gamma Knife{sup ®} (LGK) is a radiotherapy beam machine whose features are not compliant with the international calibration protocols for radiotherapy. In this scope, the Laboratoire National Henri Becquerel and the Pitié-Salpêtrière Hospital decided to conceive a new LKG dose calibration method and to compare it with the currently used one. Furthermore, the accuracy of the dose delivered by the LGK machine was checked using an “end-to-end” test. This study also aims to compare doses delivered by the two latest software versions of the Gammaplan treatment planning system (TPS). Methods: The dosimetric method chosen is the electron paramagnetic resonance (EPR) of alanine. Dose rate (calibration) verification was done without TPS using a spherical phantom. Absolute calibration was done with factors calculated by Monte Carlo simulation (MCNP-X). For “end-to-end” test, irradiations in an anthropomorphic head phantom, close to real treatment conditions, are done using the TPS in order to verify the delivered dose. Results: The comparison of the currently used calibration method with the new one revealed a deviation of +0.8% between the dose rates measured by ion chamber and EPR/alanine. For simple fields configuration (less than 16 mm diameter), the “end-to-end” tests showed out average deviations of −1.7% and −0.9% between the measured dose and the calculated dose by Gammaplan v9 and v10, respectively. Conclusions: This paper shows there is a good agreement between the new calibration method and the currently used one. There is also a good agreement between the calculated and delivered doses especially for Gammaplan v10.
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Wang, Z; Thomas, A; Newton, J; Ibbott, G; Deasy, J; Oldham, M, E-mail: Zhiheng.wang@duke.ed
2010-11-01
Achieving adequate verification and quality-assurance (QA) for radiosurgery treatment of trigeminal-neuralgia (TGN) is particularly challenging because of the combination of very small fields, very high doses, and complex irradiation geometries (multiple gantry and couch combinations). TGN treatments have extreme requirements for dosimetry tools and QA techniques, to ensure adequate verification. In this work we evaluate the potential of Presage/Optical-CT dosimetry system as a tool for the verification of TGN distributions in high-resolution and in 3D. A TGN treatment was planned and delivered to a Presage 3D dosimeter positioned inside the Radiological-Physics-Center (RPC) head and neck IMRT credentialing phantom. A 6-arc treatment plan was created using the iPlan system, and a maximum dose of 80Gy was delivered with a Varian Trilogy machine. The delivered dose to Presage was determined by optical-CT scanning using the Duke Large field-of-view Optical-CT Scanner (DLOS) in 3D, with isotropic resolution of 0.7mm{sup 3}. DLOS scanning and reconstruction took about 20minutes. 3D dose comparisons were made with the planning system. Good agreement was observed between the planned and measured 3D dose distributions, and this work provides strong support for the viability of Presage/Optical-CT as a highly useful new approach for verification of this complex technique.
Wang, Z.; Thomas, A.; Newton, J.; Ibbott, G.; Deasy, J.; Oldham, M.
2010-11-01
Achieving adequate verification and quality-assurance (QA) for radiosurgery treatment of trigeminal-neuralgia (TGN) is particularly challenging because of the combination of very small fields, very high doses, and complex irradiation geometries (multiple gantry and couch combinations). TGN treatments have extreme requirements for dosimetry tools and QA techniques, to ensure adequate verification. In this work we evaluate the potential of Presage/Optical-CT dosimetry system as a tool for the verification of TGN distributions in high-resolution and in 3D. A TGN treatment was planned and delivered to a Presage 3D dosimeter positioned inside the Radiological-Physics-Center (RPC) head and neck IMRT credentialing phantom. A 6-arc treatment plan was created using the iPlan system, and a maximum dose of 80Gy was delivered with a Varian Trilogy machine. The delivered dose to Presage was determined by optical-CT scanning using the Duke Large field-of-view Optical-CT Scanner (DLOS) in 3D, with isotropic resolution of 0.7mm3. DLOS scanning and reconstruction took about 20minutes. 3D dose comparisons were made with the planning system. Good agreement was observed between the planned and measured 3D dose distributions, and this work provides strong support for the viability of Presage/Optical-CT as a highly useful new approach for verification of this complex technique.
International Nuclear Information System (INIS)
Achieving adequate verification and quality-assurance (QA) for radiosurgery treatment of trigeminal-neuralgia (TGN) is particularly challenging because of the combination of very small fields, very high doses, and complex irradiation geometries (multiple gantry and couch combinations). TGN treatments have extreme requirements for dosimetry tools and QA techniques, to ensure adequate verification. In this work we evaluate the potential of Presage/Optical-CT dosimetry system as a tool for the verification of TGN distributions in high-resolution and in 3D. A TGN treatment was planned and delivered to a Presage 3D dosimeter positioned inside the Radiological-Physics-Center (RPC) head and neck IMRT credentialing phantom. A 6-arc treatment plan was created using the iPlan system, and a maximum dose of 80Gy was delivered with a Varian Trilogy machine. The delivered dose to Presage was determined by optical-CT scanning using the Duke Large field-of-view Optical-CT Scanner (DLOS) in 3D, with isotropic resolution of 0.7mm3. DLOS scanning and reconstruction took about 20minutes. 3D dose comparisons were made with the planning system. Good agreement was observed between the planned and measured 3D dose distributions, and this work provides strong support for the viability of Presage/Optical-CT as a highly useful new approach for verification of this complex technique.
Monte Carlo calculation of received dose from ingestion and inhalation of natural uranium
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For the purpose of this study eighty samples are taken from the area Bela Crkva and Vrsac. The activity of radionuclide in the soil is determined by gamma- ray spectrometry. Monte Carlo method is used to calculate effective dose received by population resulting from the inhalation and ingestion of natural uranium. The estimated doses were compared with the legally prescribed levels. (author)
International Nuclear Information System (INIS)
The objective of this study was to evaluate the patient effective dose and scattered dose from recently developed dental mobile equipment in Korea. The MCNPX 2.6 (Los Alamos National Laboratory, USA) was used in a Monte Carlo simulation to calculate both the effective and scattered doses. The MCNPX code was constructed identically as in the general use of equipment and the effective dose and scattered dose were calculated using the KTMAN-2 digital phantom. The effective dose was calculated as 906 μSv. The equivalent doses per organ were calculated via the MCNPX code, and were 32 174 and 19 μSv in the salivary gland and oesophagus, respectively. The scattered dose of 22.5-32.6 μSv of the tube side at 25 cm from the centre in anterior and posterior planes was measured as 1.4-3 times higher than the detector side of 10.5-16.0 μSv. (authors)
PCDOSE-ESTSC, Radioactive Dose Assessment and NRC Verification
International Nuclear Information System (INIS)
1 - Description of program or function: PCDOSE was developed for the Nuclear Regulatory Commission (NRC) to perform calculations to determine radioactive dose due to the annual averaged offsite release of liquid and gaseous effluent by U.S. commercial nuclear power facilities. Using NRC approved dose assessment methodologies, it acts as an inspector's tool for verifying the compliance of the facility's dose assessment software. PCDOSE duplicates the calculations of the GASPAR II mainframe code as well as calculations using the methodologies of Reg. Guide 1.109 Rev. 1 and NUREG-0133 by optional choice. 2 - Method of solution: PCDOSE uses spread-sheet models of the dose assessment mathematical equations. The results appear in table format. 3 - Restrictions on the complexity of the problem: PCDOSE requires Lotus 1-2-3 software
Verification of Calculated Skin Doses in Postmastectomy Helical Tomotherapy
International Nuclear Information System (INIS)
Purpose: To verify the accuracy of calculated skin doses in helical tomotherapy for postmastectomy radiation therapy (PMRT). Methods and Materials: In vivo thermoluminescent dosimeters (TLDs) were used to measure the skin dose at multiple points in each of 14 patients throughout the course of treatment on a TomoTherapy Hi.Art II system, for a total of 420 TLD measurements. Five patients were evaluated near the location of the mastectomy scar, whereas 9 patients were evaluated throughout the treatment volume. The measured dose at each location was compared with calculations from the treatment planning system. Results: The mean difference and standard error of the mean difference between measurement and calculation for the scar measurements was -1.8% ± 0.2% (standard deviation [SD], 4.3%; range, -11.1% to 10.6%). The mean difference and standard error of the mean difference between measurement and calculation for measurements throughout the treatment volume was -3.0% ± 0.4% (SD, 4.7%; range, -18.4% to 12.6%). The mean difference and standard error of the mean difference between measurement and calculation for all measurements was -2.1% ± 0.2% (standard deviation, 4.5%: range, -18.4% to 12.6%). The mean difference between measured and calculated TLD doses was statistically significant at two standard deviations of the mean, but was not clinically significant (i.e., was <5%). However, 23% of the measured TLD doses differed from the calculated TLD doses by more than 5%. Conclusions: The mean of the measured TLD doses agreed with TomoTherapy calculated TLD doses within our clinical criterion of 5%.
Multichannel OSL dosimetry for dose verification in radiotherapy
International Nuclear Information System (INIS)
An innovative multichannel fibre-coupled Optically Stimulated Luminescence (OSL) dosimeter is proposed for on-line in vivo quality assurance in Radiation Therapy (RT). Small Al2O3:C fibre crystals (TLD500) are used as OSL detectors, incorporated into a rugged, radiation-resistant and radiation-transparent OSL fibre sensor design. The temperature and fading dependences of OSL fibre sensors and stability vs cumulated dose have been tested with a X-ray generator. Predosed OSL sensors tested at Institut Gustave Roussy (IGR) show a good repeatability in multichannel operation. Sensor calibration and depth-dose measurements with electron beams have been performed with a Saturne 43 LINAC in reference conditions at CEA-LNHB (ionizing radiation reference laboratory in France). The difference between absorbed doses measured by OSL and an ionization chamber was within ± 0.9 % (for a dose of about 1 Gy) despite a sub linear dose response. Finally, a single calibration curve was used for all beams as energy independence vs electron energy was found in the range [9 MeV, 18 MeV]. Angular independence was found as well in the range [0 degree, 45 degree] when the OSL sensor is equipped with its bolus. (author)
An energy transfer method for 4D Monte Carlo dose calculation
Siebers, Jeffrey V; Zhong, Hualiang
2008-01-01
This article presents a new method for four-dimensional Monte Carlo dose calculations which properly addresses dose mapping for deforming anatomy. The method, called the energy transfer method (ETM), separates the particle transport and particle scoring geometries: Particle transport takes place in the typical rectilinear coordinate system of the source image, while energy deposition scoring takes place in a desired reference image via use of deformable image registration. Dose is the energy ...
Application of the peregrine Monte Carlo dose calculation system to stereotactic radiosurgery
International Nuclear Information System (INIS)
Purpose/Objective: This work describes the capability to perform Monte Carlo dose calculations for stereotactic radiosurgery within the framework of the PEREGRINE dose calculation system. A future study will use this capability to assess the clinical benefits to this technique of higher accuracy in dose calculation. Materials and Methods: PEREGRINE is a first-principles 3D Monte Carlo dose calculation system for clinical radiation therapy treatment planning (RTP) systems. By taking advantage of recent advances in low-cost computer commodity hardware, modern symmetric multiprocessor architectures and state-of-the-art Monte Carlo transport algorithms, PEREGRINE performs high-resolution (1 mm), high accuracy, Monte Carlo RTP calculations in times that are reasonable for clinical use (< 30 minutes.) The PEREGRINE source model provides a compact, accurate representation of the radiation source and the effects of beam modifiers. Our experience in implementing blocks, wedges, and static MLC ports in PEREGRINE as beam modifiers provides physics models that accurately reproduce the transmitted and scattered fluence at the patient surface. Adapting PEREGRINE to calculate stereotactic radiosurgery dose distributions requires extending the PEREGRINE source model to include stereotactic apertures and treatment arcs. The physics models used for other modifiers will accurately determine stereotactic aperture effects. We only need to provide a new geometry module to describe the physical properties of the apertures. Treatment arcs are easily implemented as a probability distribution in beam direction as a function of delivered dose. Results: A comparison of results from PEREGRINE calculations and experimental measurements made at the University of Wisconsin/Madison is presented. The distribution of direct, transmitted and scattered radiation and the resulting contributions to dose from stereotactic apertures are shown. The accuracy and calculational efficiency of the physics
Patient-specific CT dose determination from CT images using Monte Carlo simulations
Liang, Qing
Radiation dose from computed tomography (CT) has become a public concern with the increasing application of CT as a diagnostic modality, which has generated a demand for patient-specific CT dose determinations. This thesis work aims to provide a clinically applicable Monte-Carlo-based CT dose calculation tool based on patient CT images. The source spectrum was simulated based on half-value layer measurements. Analytical calculations along with the measured flux distribution were used to estimate the bowtie-filter geometry. Relative source output at different points in a cylindrical phantom was measured and compared with Monte Carlo simulations to verify the determined spectrum and bowtie-filter geometry. Sensitivity tests were designed with four spectra with the same kVp and different half-value layers, and showed that the relative output at different locations in a phantom is sensitive to different beam qualities. An mAs-to-dose conversion factor was determined with in-air measurements using an Exradin A1SL ionization chamber. Longitudinal dose profiles were measured with thermoluminescent dosimeters (TLDs) and compared with the Monte-Carlo-simulated dose profiles to verify the mAs-to-dose conversion factor. Using only the CT images to perform Monte Carlo simulations would cause dose underestimation due to the lack of a scatter region. This scenario was demonstrated with a cylindrical phantom study. Four different image extrapolation methods from the existing CT images and the Scout images were proposed. The results show that performing image extrapolation beyond the scan region improves the dose calculation accuracy under both step-shoot scan mode and helical scan mode. Two clinical studies were designed and comparisons were performed between the current CT dose metrics and the Monte-Carlo-based organ dose determination techniques proposed in this work. The results showed that the current CT dosimetry failed to show dose differences between patients with the same
Directory of Open Access Journals (Sweden)
Nitin Ramesh Kakade
2015-01-01
Full Text Available Background: Gold nanoparticle (GNP-aided radiation therapy (RT is useful to make the tumor more sensitive to radiation damage because of the enhancement in the dose inside the tumor region. Polymer gel dosimeter (PGD can be a good choice for the physical measurement of dose enhancement produced by GNP inside the gel. Materials and Methods: The present study uses EGSnrc Monte Carlo code to estimate dose enhancement factor (DEF due to the introduction of GNPs inside the PGD at different concentrations (7 and 18 mg Au/g of gel when irradiated by therapeutic X-rays of energy 100 kVp, 150 kVp, 6 MV, and 15 MV. The simulation was also carried out to quantify the dose enhancement in PAGAT gel and tumor for 100 kVp X-rays. Results: For 100 kVp X-rays, average DEF of 1.86 and 2.91 is observed in the PAGAT gel dosimeter with 7 and 18 mg Au/g of gel, respectively. Average DEF of 1.69 and 2.61 is recorded for 150 kVp X-rays with 7 and 18 mg Au/g of gel, respectively. No clinically meaningful DEF was observed for 6 and 15 MV photon beams. Furthermore, the dose enhancement within the PAGAT gel dosimeter and tumor closely matches with each other. Conclusion: The polymer gel dosimetry can be a suitable method of dose estimation and verification for clinical implementation of GNP-aided RT. GNP-aided RT has the potential of delivering high localized tumoricidal dose with significant sparing of normal structures when the treatment is delivered with low energy X-rays.
Gel-layer dosimetry for dose verification in intensity-modulated radiation therapy
Tomatis, S.; Carrara, M.; Gambarini, G.; Marchesini, R.; Valente, M.
2007-09-01
Intensity-modulated radiotherapy (IMRT) is a technique in which the radiation fluence within each of the treatment beams is not uniformly distributed. This allows the patient dose to follow the boundaries even of a target volume of complex shape, and, virtually, to spare critical healthy organs at risk. The agreement between planned and delivered IMRT dose is verified by means of standard dosimetric methods such as film dosimetry or semiconductors array dosimetry. In this paper, we compare the output of a commercial device using an array of diodes for IMRT absolute dose verification with the output of a gel dosimeter, composed by a 10×8 cm 2 rectangular layer of a tissue-equivalent gel matrix in which a proper chemical dosimeter has been incorporated. The dose distribution is derived from the images of visible light transmittance, detected with a CCD camera before and after the gel exposure. The analysis was carried out on a single IMRT field chosen among those archived at the Istituto Nazionale Tumori of Milan. The radiation field was examined in an area common to both dosimeters. The agreement between the two detectors was good, as shown by analysis of dose profiles, especially for doses above 15-20 cGy. Gel dosimeter was in good agreement with the planned dose too, with a percentage of dosimeter points passing a dose to agreement test ranging between 90% and 93%. Although preliminary, our data suggest that gel dosimetry is a reliable method for IMRT dose verification. Due to the good spatial resolution and to the tissue equivalent properties of its composition, it would be suitable also for 3D IMRT dose reconstruction and verification in the form of multiple piled-up gel layers.
Gel-layer dosimetry for dose verification in intensity-modulated radiation therapy
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Tomatis, S.; Carrara, M. [Istituto Nazionale Tumori, Via Venezian 1, Milan 20133 (Italy); Gambarini, G. [Physics Department of University of Milan and INFN - National Institute of Nuclear Physics, Via Celoria 16, Milan 20133 (Italy)], E-mail: grazia.gambarini@mi.infn.it; Marchesini, R. [Istituto Nazionale Tumori, Via Venezian 1, Milan 20133 (Italy); Valente, M. [Physics Department of University of Milan and INFN - National Institute of Nuclear Physics, Via Celoria 16, Milan 20133 (Italy)
2007-09-21
Intensity-modulated radiotherapy (IMRT) is a technique in which the radiation fluence within each of the treatment beams is not uniformly distributed. This allows the patient dose to follow the boundaries even of a target volume of complex shape, and, virtually, to spare critical healthy organs at risk. The agreement between planned and delivered IMRT dose is verified by means of standard dosimetric methods such as film dosimetry or semiconductors array dosimetry. In this paper, we compare the output of a commercial device using an array of diodes for IMRT absolute dose verification with the output of a gel dosimeter, composed by a 10x8 cm{sup 2} rectangular layer of a tissue-equivalent gel matrix in which a proper chemical dosimeter has been incorporated. The dose distribution is derived from the images of visible light transmittance, detected with a CCD camera before and after the gel exposure. The analysis was carried out on a single IMRT field chosen among those archived at the Istituto Nazionale Tumori of Milan. The radiation field was examined in an area common to both dosimeters. The agreement between the two detectors was good, as shown by analysis of dose profiles, especially for doses above 15-20 cGy. Gel dosimeter was in good agreement with the planned dose too, with a percentage of dosimeter points passing a dose to agreement test ranging between 90% and 93%. Although preliminary, our data suggest that gel dosimetry is a reliable method for IMRT dose verification. Due to the good spatial resolution and to the tissue equivalent properties of its composition, it would be suitable also for 3D IMRT dose reconstruction and verification in the form of multiple piled-up gel layers.
Homma, Yuto; Moriwaki, Hiroyuki; Ohki, Shigeo; Ikeda, Kazumi
2014-06-01
This paper deals with verification of three dimensional triangular prismatic discrete ordinates transport calculation code ENSEMBLE-TRIZ by comparison with multi-group Monte Carlo calculation code GMVP in a large fast breeder reactor. The reactor is a 750 MWe electric power sodium cooled reactor. Nuclear characteristics are calculated at beginning of cycle of an initial core and at beginning and end of cycle of equilibrium core. According to the calculations, the differences between the two methodologies are smaller than 0.0002 Δk in the multi-plication factor, relatively about 1% in the control rod reactivity, and 1% in the sodium void reactivity.
Local dose enhancement in radiation therapy: Monte Carlo simulation study
International Nuclear Information System (INIS)
The development of nanotechnology has boosted the use of nanoparticles in radiation therapy in order to achieve greater therapeutic ratio between tumor and healthy tissues. Gold has been shown to be most suitable to this task due to the high biocompatibility and high atomic number, which contributes to a better in vivo distribution and for the local energy deposition. As a result, this study proposes to study, nanoparticle in the tumor cell. At a range of 11 nm from the nanoparticle surface, results have shown an absorbed dose 141 times higher for the medium with the gold nanoparticle compared to the water for an incident energy spectrum with maximum photon energy of 50 keV. It was also noted that when only scattered radiation is interacting with the gold nanoparticles, the dose was 134 times higher compared to enhanced local dose that remained significant even for scattered radiation. (author)
International Nuclear Information System (INIS)
In this work experimental verification of Monte Carlo neutron flux calculations in the carousel facility (CF) of the 250 kW TRIGA Mark II reactor at the Jozef Stefan Institute is presented. Simulations were carried out using the Monte Carlo radiation-transport code, MCNP4B. The objective of the work was to model and verify experimentally the azimuthal variation of neutron flux in the CF for core No. 176, set up in April 2002. '1'9'8Au activities of Al-Au(0.1%) disks irradiated in 11 channels of the CF covering 180'0 around the perimeter of the core were measured. The comparison between MCNP calculation and measurement shows relatively good agreement and demonstrates the overall accuracy with which the detailed spectral characteristics can be predicted by calculations.(author)
International Nuclear Information System (INIS)
Highlights: •Develop the novel Multi-Step CADIS (MS-CADIS) hybrid Monte Carlo/deterministic method for multi-step shielding analyses. •Accurately calculate shutdown dose rates using full-scale Monte Carlo models of fusion energy systems. •Demonstrate the dramatic efficiency improvement of the MS-CADIS method for the rigorous two step calculations of the shutdown dose rate in fusion reactors. -- Abstract: The rigorous 2-step (R2S) computational system uses three-dimensional Monte Carlo transport simulations to calculate the shutdown dose rate (SDDR) in fusion reactors. Accurate full-scale R2S calculations are impractical in fusion reactors because they require calculating space- and energy-dependent neutron fluxes everywhere inside the reactor. The use of global Monte Carlo variance reduction techniques was suggested for accelerating the R2S neutron transport calculation. However, the prohibitive computational costs of these approaches, which increase with the problem size and amount of shielding materials, inhibit their ability to accurately predict the SDDR in fusion energy systems using full-scale modeling of an entire fusion plant. This paper describes a novel hybrid Monte Carlo/deterministic methodology that uses the Consistent Adjoint Driven Importance Sampling (CADIS) method but focuses on multi-step shielding calculations. The Multi-Step CADIS (MS-CADIS) methodology speeds up the R2S neutron Monte Carlo calculation using an importance function that represents the neutron importance to the final SDDR. Using a simplified example, preliminary results showed that the use of MS-CADIS enhanced the efficiency of the neutron Monte Carlo simulation of an SDDR calculation by a factor of 550 compared to standard global variance reduction techniques, and that the efficiency enhancement compared to analog Monte Carlo is higher than a factor of 10,000
Experimental validation of Monte Carlo calculations for organ dose
International Nuclear Information System (INIS)
The problem of validating estimates of absorbed dose due to photon energy deposition is examined. The computational approaches used for the estimation of the photon energy deposition is examined. The limited data for validation of these approaches is discussed and suggestions made as to how better validation information might be obtained
International Nuclear Information System (INIS)
Interventional cardiology consists on a set of medical procedures which are mainly focused on diagnosing and treating patients who suffer cardiovascular diseases. Even though the usage of X-ray is justified on this case, it is greatly advised to evaluate the dose which professionals and patients will be exposed due to the fact that the complexity and length of the procedures often require high doses. The objective of this work is to estimate the radiation dose on both a patient and a physician through conversion coefficient (CCs) of effective dose (E) and equivalent dose (H) during a coronary angiography examination.The dose CCs was estimated using the Visual Monte Carlo code (VMC) and a pair of simulators anthropomorphic voxel (Female Adult VoXel). The CCs were normalized in terms of kerma-area product (KAP). As expected, for all situations studied, the patient in anteroposterior projection (AP) obtained the highest conversion coefficient of equivalent dose and effective dose (author)
Monte Carlo calculations of the impact of a hip prosthesis on the dose distribution
International Nuclear Information System (INIS)
Because of the ageing of the population, an increasing number of patients with hip prostheses are undergoing pelvic irradiation. Treatment planning systems (TPS) currently available are not always able to accurately predict the dose distribution around such implants. In fact, only Monte Carlo simulation has the ability to precisely calculate the impact of a hip prosthesis during radiotherapeutic treatment. Monte Carlo phantoms were developed to evaluate the dose perturbations during pelvic irradiation. A first model, constructed with the DOSXYZnrc usercode, was elaborated to determine the dose increase at the tissue-metal interface as well as the impact of the material coating the prosthesis. Next, CT-based phantoms were prepared, using the usercode CTCreate, to estimate the influence of the geometry and the composition of such implants on the beam attenuation. Thanks to a program that we developed, the study was carried out with CT-based phantoms containing a hip prosthesis without metal artefacts. Therefore, anthropomorphic phantoms allowed better definition of both patient anatomy and the hip prosthesis in order to better reproduce the clinical conditions of pelvic irradiation. The Monte Carlo results revealed the impact of certain coatings such as PMMA on dose enhancement at the tissue-metal interface. Monte Carlo calculations in CT-based phantoms highlighted the marked influence of the implant's composition, its geometry as well as its position within the beam on dose distribution
Jeraj, Robert; Keall, Paul
2000-12-01
The effect of the statistical uncertainty, or noise, in inverse treatment planning for intensity modulated radiotherapy (IMRT) based on Monte Carlo dose calculation was studied. Sets of Monte Carlo beamlets were calculated to give uncertainties at Dmax ranging from 0.2% to 4% for a lung tumour plan. The weights of these beamlets were optimized using a previously described procedure based on a simulated annealing optimization algorithm. Several different objective functions were used. It was determined that the use of Monte Carlo dose calculation in inverse treatment planning introduces two errors in the calculated plan. In addition to the statistical error due to the statistical uncertainty of the Monte Carlo calculation, a noise convergence error also appears. For the statistical error it was determined that apparently successfully optimized plans with a noisy dose calculation (3% 1σ at Dmax ), which satisfied the required uniformity of the dose within the tumour, showed as much as 7% underdose when recalculated with a noise-free dose calculation. The statistical error is larger towards the tumour and is only weakly dependent on the choice of objective function. The noise convergence error appears because the optimum weights are determined using a noisy calculation, which is different from the optimum weights determined for a noise-free calculation. Unlike the statistical error, the noise convergence error is generally larger outside the tumour, is case dependent and strongly depends on the required objectives.
Monte-Carlo Method Python Library for dose distribution Calculation in Brachytherapy
International Nuclear Information System (INIS)
The Cs-137 Brachytherapy treatment is performed in Madagascar since 2005. Time treatment calculation for prescribed dose is made manually. Monte-Carlo Method Python library written at Madagascar INSTN is experimentally used to calculate the dose distribution on the tumour and around it. The first validation of the code was done by comparing the library curves with the Nucletron company curves. To reduce the duration of the calculation, a Grid of PC's is set up with listner patch run on each PC. The library will be used to modelize the dose distribution in the CT scan patient picture for individual and better accuracy time calculation for a prescribed dose.
Feasibility Study of Neutron Dose for Real Time Image Guided Proton Therapy: A Monte Carlo Study
Kim, Jin Sung; Shin, Jung Suk; Kim, Daehyun; Shin, EunHyuk; Chung, Kwangzoo; Cho, Sungkoo; Ahn, Sung Hwan; Ju, Sanggyu; Chung, Yoonsun; Jung, Sang Hoon; Han, Youngyih
2015-01-01
Two full rotating gantry with different nozzles (Multipurpose nozzle with MLC, Scanning Dedicated nozzle) with conventional cyclotron system is installed and under commissioning for various proton treatment options at Samsung Medical Center in Korea. The purpose of this study is to investigate neutron dose equivalent per therapeutic dose, H/D, to x-ray imaging equipment under various treatment conditions with monte carlo simulation. At first, we investigated H/D with the various modifications...
Simulation studies for the in-vivo dose verification of particle therapy
Energy Technology Data Exchange (ETDEWEB)
Rohling, Heide
2015-06-08
An increasing number of cancer patients is treated with proton beams or other light ion beams which allow to deliver dose precisely to the tumor. However, the depth dose distribution of these particles, which enables this precision, is sensitive to deviations from the treatment plan, as e.g. anatomical changes. Thus, to assure the quality of the treatment, a non-invasive in-vivo dose verification is highly desired. This monitoring of particle therapy relies on the detection of secondary radiation which is produced by interactions between the beam particles and the nuclei of the patient's tissue. Up to now, the only clinically applied method for in-vivo dosimetry is Positron Emission Tomography which makes use of the β{sup +}-activity produced during the irradiation (PT-PET). Since from a PT-PET measurement the applied dose cannot be directly deduced, the simulated distribution of β{sup +}-emitting nuclei is used as a basis for the analysis of the measured PT-PET data. Therefore, the reliable modeling of the production rates and the spatial distribution of the β{sup +}-emitters is required. PT-PET applied during instead of after the treatment is referred to as in-beam PET. A challenge concerning in-beam PET is the design of the PET camera, because a standard full-ring scanner is not feasible. Thus, for in-beam PET and PGI dedicated detection systems and, moreover, profound knowledge about the corresponding radiation fields are required. Using various simulation codes, this thesis contributes to the modelling of the β{sup +}-emitters and photons produced during particle irradiation, as well as to the evaluation and optimization of hardware for both techniques. Concerning the modeling of the production of the relevant β{sup +}-emitters, the abilities of the Monte Carlo simulation code PHITS and of the deterministic, one-dimensional code HIBRAC were assessed. HIBRAC was substantially extended to enable the modeling of the depth-dependent yields of specific
Simulation studies for the in-vivo dose verification of particle therapy
International Nuclear Information System (INIS)
An increasing number of cancer patients is treated with proton beams or other light ion beams which allow to deliver dose precisely to the tumor. However, the depth dose distribution of these particles, which enables this precision, is sensitive to deviations from the treatment plan, as e.g. anatomical changes. Thus, to assure the quality of the treatment, a non-invasive in-vivo dose verification is highly desired. This monitoring of particle therapy relies on the detection of secondary radiation which is produced by interactions between the beam particles and the nuclei of the patient's tissue. Up to now, the only clinically applied method for in-vivo dosimetry is Positron Emission Tomography which makes use of the β+-activity produced during the irradiation (PT-PET). Since from a PT-PET measurement the applied dose cannot be directly deduced, the simulated distribution of β+-emitting nuclei is used as a basis for the analysis of the measured PT-PET data. Therefore, the reliable modeling of the production rates and the spatial distribution of the β+-emitters is required. PT-PET applied during instead of after the treatment is referred to as in-beam PET. A challenge concerning in-beam PET is the design of the PET camera, because a standard full-ring scanner is not feasible. Thus, for in-beam PET and PGI dedicated detection systems and, moreover, profound knowledge about the corresponding radiation fields are required. Using various simulation codes, this thesis contributes to the modelling of the β+-emitters and photons produced during particle irradiation, as well as to the evaluation and optimization of hardware for both techniques. Concerning the modeling of the production of the relevant β+-emitters, the abilities of the Monte Carlo simulation code PHITS and of the deterministic, one-dimensional code HIBRAC were assessed. HIBRAC was substantially extended to enable the modeling of the depth-dependent yields of specific nuclides. For proton beams and
Organ doses from medical x-ray examinations calculated using Monte Carlo techniques
Jones, D G
1985-01-01
Monte Carlo techniques were used to calculate the mean doses received by 20 organs during diagnostic X-ray examinations. Results are presented for 22 commonly used radiographic views and for 45 combinations of tube voltage and filtration ranging from 50 to 140 kVp and 1.5 to 4 mm of aluminium, respectively.
Alem-Bezoubiri, A.; Bezoubiri, F.; Badreddine, A.; Mazrou, H.; Lounis-Mokrani, Z.
2014-04-01
A fully detailed Monte Carlo geometrical model of an 18 MV Varian Clinac 2100C medical linear accelerator, lodged at Blida Anti-Cancer Centre in Algeria, was developed during this study to estimate the photoneutrons spectra and doses at the patient table in a radiotherapy treatment room, for radiation protection purposes.
Gamma irradiator dose mapping: a Monte Carlo simulation and experimental measurements
International Nuclear Information System (INIS)
Gamma irradiator facilities can be used in a wide range of applications such as biological and chemical researches, food treatment and sterilization of medical devices and products. Dose mapping must be performed in these equipment in order to establish plant operational parameters, as dose uniformity, source utilization efficiency and maximum and minimum dose positions. The isodoses curves are generally measured using dosimeters distributed throughout the device, and this procedure often consume a large amount of dosimeters, irradiation time and manpower. However, a detailed curve doses identification of the irradiation facility can be performed using Monte Carlo simulation, which reduces significantly the monitoring with dosimeters. The present work evaluates the absorbed dose in the CDTN/CNEN Gammacell Irradiation Facility, using the Monte Carlo N-particles (MCNP) code. The Gammacell 220, serial number 39, was produced by Atomic Energy of Canada Limited and was loaded with sources of 60Co. Dose measurements using TLD and Fricke dosimeters were also performed to validate the calculations. The good agreement of the results shows that Monte Carlo simulations can be used as a predictive tool of irradiation planning for the CDTN/CNEN Gamma Cell Irradiator. (author)
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Lee, Choonsik; Kim, Kwang Pyo; Long, Daniel; Fisher, Ryan; Tien, Chris; Simon, Steven L.; Bouville, Andre; Bolch, Wesley E. [Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institute of Health, Bethesda, Maryland 20852 (United States); Department of Nuclear Engineering, Kyung Hee University, Yongin 446-701 (Korea, Republic of); Department of Nuclear and Radiological Engineering, University of Florida, Gainesville, Florida 32611 (United States); Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institute of Health, Bethesda, Maryland 20852 (United States); Department of Nuclear and Radiological Engineering, University of Florida, Gainesville, Florida 32611 (United States)
2011-03-15
Purpose: To develop a computed tomography (CT) organ dose estimation method designed to readily provide organ doses in a reference adult male and female for different scan ranges to investigate the degree to which existing commercial programs can reasonably match organ doses defined in these more anatomically realistic adult hybrid phantomsMethods: The x-ray fan beam in the SOMATOM Sensation 16 multidetector CT scanner was simulated within the Monte Carlo radiation transport code MCNPX2.6. The simulated CT scanner model was validated through comparison with experimentally measured lateral free-in-air dose profiles and computed tomography dose index (CTDI) values. The reference adult male and female hybrid phantoms were coupled with the established CT scanner model following arm removal to simulate clinical head and other body region scans. A set of organ dose matrices were calculated for a series of consecutive axial scans ranging from the top of the head to the bottom of the phantoms with a beam thickness of 10 mm and the tube potentials of 80, 100, and 120 kVp. The organ doses for head, chest, and abdomen/pelvis examinations were calculated based on the organ dose matrices and compared to those obtained from two commercial programs, CT-EXPO and CTDOSIMETRY. Organ dose calculations were repeated for an adult stylized phantom by using the same simulation method used for the adult hybrid phantom. Results: Comparisons of both lateral free-in-air dose profiles and CTDI values through experimental measurement with the Monte Carlo simulations showed good agreement to within 9%. Organ doses for head, chest, and abdomen/pelvis scans reported in the commercial programs exceeded those from the Monte Carlo calculations in both the hybrid and stylized phantoms in this study, sometimes by orders of magnitude. Conclusions: The organ dose estimation method and dose matrices established in this study readily provides organ doses for a reference adult male and female for different
Experimental verification of radiation dose in mixed neutron/gamma radiation fields
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The TRIGA research reactor at Jozef Stefan Institute is used for irradiation of various samples. The Monte Carlo code for transport of neutrons and photons, MCNP, was used to calculate dose rates in irradiation channels in the operating TRIGA research reactor. Several measurements of dose rates in individual irradiation channels were performed with CaF2 and LiF TLDs. The calculated dose rates significantly differ from the measured ones especially for the neutron dose rate. The second experimental method used was tooth enamel dosimetry. Results indicate that human teeth are suitable for radiation dose assessment in mixed neutron/gamma radiation fields with dose rates of several Gy per second. (author)
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Descalle, M-A; Chuang, C; Pouliot, J
2002-01-30
Patient positioning accuracy remains an issue for external beam radiotherapy. Currently, kilovoltage verification images are used as reference by clinicians to compare the actual patient treatment position with the planned position. These images are qualitatively different from treatment-time megavoltage portal images. This study will investigate the feasibility of using PEREGRINE, a 3D Monte Carlo calculation engine, to create reference images for portal image comparisons. Portal images were acquired using an amorphous-silicon flat-panel EPID for (1) the head and pelvic sections of an anthropomorphic phantom with 7-8 mm displacements applied, and (2) a prostate patient on five treatment days. Planning CT scans were used to generate simulated reference images with PEREGRINE. A correlation algorithm quantified the setup deviations between simulated and portal images. Monte Carlo simulated images exhibit similar qualities to portal images, the phantom slabs appear clearly. Initial positioning differences and applied displacements were detected and quantified. We find that images simulated with Monte Carlo methods can be used as reference images to detect and quantify set-up errors during treatment.
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We evaluated the Monte Carlo Monaco Planner v2.0.3 for calculation between non-homogeneous low density (equivalent to lung), as a complement to the verification of modeling in homogeneous medium and prior to the introduction of the SBRT technique. We performed the same tests on Pinnacle v8.0m, with the same purpose. We compare the results obtained with the algorithm Monte Carlo of Monaco and the Collapsed Cone of Pinnacle. (Author)
Monte Carlo angular dose distribution of the microselectron HDR 192Ir brachytherapy source
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Polar dose profiles around the Nucletron MicroSelectron high dose rate (HDR) 192Ir brachytherapy source were calculated using the Monte Carlo radiation transport code MCNP (Monte Carlo N Particle) version 4A. The geometry modeled consisted of an identical simulation of the construction of the MicroSelectron HDR source located at the centre of a spherical water phantom of 100cm radius. Doses were calculated using a spherical coordinate system at 5 degree intervals (measured relative to the cable) at radii of 0.25, 0.5,1.0, 3.0, 5.0 and 7.0cm. These polar doses were compared to equivalent profiles from the Nucletron PLATO Brachytherapy Planning System (BPS) version 13.X. At 3.0, 5.0 and 7.0cm radii, the Monte Carlo and BPS profiles are generally within 3%. The near field polar dose profiles however, are in significant disagreement. At 1.0cm radius, the discrepancy can exceed 5%. At 0.5cm this figure rises to 15%, and even 60% at 0.25cm radius
Aguirre, Eder; David, Mariano; deAlmeida, Carlos E
2016-01-01
This work studies the impact of systematic uncertainties associated to interaction cross sections on depth dose curves determined by Monte Carlo simulations. The corresponding sensitivity factors are quantified by changing cross sections in a given amount and determining the variation in the dose. The influence of total cross sections for all particles, photons and only for Compton scattering is addressed. The PENELOPE code was used in all simulations. It was found that photon cross section sensitivity factors depend on depth. In addition, they are positive and negative for depths below and above an equilibrium depth, respectively. At this depth, sensitivity factors are null. The equilibrium depths found in this work agree very well with the mean free path of the corresponding incident photon energy. Using the sensitivity factors reported here, it is possible to estimate the impact of photon cross section uncertainties on the uncertainty of Monte Carlo-determined depth dose curves.
Calculation of radiation dose to the lens of the eye using Monte Carlo simulation
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The radiation dose to the lens of the eye of patients undergoing diagnostic and interventional radiological procedures of the lacrimal drainage system has been calculated using a Monte Carlo technique. The technique has also been suggested for the retrospective estimation of the lens dose; when applied to individual patients, good correlation is obtained. In such study, data is required for image acquisition frame numbers and fluoro on-time, mean exposure values for these parameters, and the ratio of lens-to-air dose (viz. the head factor, HF) derived for a standard adult head
SU-E-J-60: Efficient Monte Carlo Dose Calculation On CPU-GPU Heterogeneous Systems
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Purpose: It is well-known that the performance of GPU-based Monte Carlo dose calculation implementations is bounded by memory bandwidth. One major cause of this bottleneck is the random memory writing patterns in dose deposition, which leads to several memory efficiency issues on GPU such as un-coalesced writing and atomic operations. We propose a new method to alleviate such issues on CPU-GPU heterogeneous systems, which achieves overall performance improvement for Monte Carlo dose calculation. Methods: Dose deposition is to accumulate dose into the voxels of a dose volume along the trajectories of radiation rays. Our idea is to partition this procedure into the following three steps, which are fine-tuned for CPU or GPU: (1) each GPU thread writes dose results with location information to a buffer on GPU memory, which achieves fully-coalesced and atomic-free memory transactions; (2) the dose results in the buffer are transferred to CPU memory; (3) the dose volume is constructed from the dose buffer on CPU. We organize the processing of all radiation rays into streams. Since the steps within a stream use different hardware resources (i.e., GPU, DMA, CPU), we can overlap the execution of these steps for different streams by pipelining. Results: We evaluated our method using a Monte Carlo Convolution Superposition (MCCS) program and tested our implementation for various clinical cases on a heterogeneous system containing an Intel i7 quad-core CPU and an NVIDIA TITAN GPU. Comparing with a straightforward MCCS implementation on the same system (using both CPU and GPU for radiation ray tracing), our method gained 2-5X speedup without losing dose calculation accuracy. Conclusion: The results show that our new method improves the effective memory bandwidth and overall performance for MCCS on the CPU-GPU systems. Our proposed method can also be applied to accelerate other Monte Carlo dose calculation approaches. This research was supported in part by NSF under Grants CCF
Clouvas, A; Antonopoulos-Domis, M; Silva, J
2000-01-01
The dose rate conversion factors D/sub CF/ (absorbed dose rate in air per unit activity per unit of soil mass, nGy h/sup -1/ per Bq kg/sup -1/) are calculated 1 m above ground for photon emitters of natural radionuclides uniformly distributed in the soil. Three Monte Carlo codes are used: 1) The MCNP code of Los Alamos; 2) The GEANT code of CERN; and 3) a Monte Carlo code developed in the Nuclear Technology Laboratory of the Aristotle University of Thessaloniki. The accuracy of the Monte Carlo results is tested by the comparison of the unscattered flux obtained by the three Monte Carlo codes with an independent straightforward calculation. All codes and particularly the MCNP calculate accurately the absorbed dose rate in air due to the unscattered radiation. For the total radiation (unscattered plus scattered) the D/sub CF/ values calculated from the three codes are in very good agreement between them. The comparison between these results and the results deduced previously by other authors indicates a good ag...
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The dose rate conversion factors dot DCF (absorbed dose rate in air per unit activity per unit of soil mass, nGy h-1 per Bq kg-1) are calculated 1 m above ground for photon emitters of natural radionuclides uniformly distributed in the soil. Three Monte Carlo codes are used: (1) The MCNP code of Los Alamos; (2) The GEANT code of CERN; and (3) a Monte Carlo code developed in the Nuclear Technology Laboratory of the Aristotle University of Thessaloniki. The accuracy of the Monte Carlo results is tested by the comparison of the unscattered flux obtained by the three Monte Carlo codes with an independent straightforward calculation. All codes and particularly the MCNP calculate accurately the absorbed dose rate in air due to the unscattered radiation. For the total radiation (unscattered plus scattered) the dot DCF values calculated from the three codes are in very good agreement between them. The comparison between these results and the results deduced previously by other authors indicates a good agreement (less than 15% of difference) for photon energies above 1,500 keV. Antithetically, the agreement is not as good (difference of 20--30%) for the low energy photons
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The γ-index test has been commonly adopted to quantify the degree of agreement between a reference dose distribution and an evaluation dose distribution. Monte Carlo (MC) simulation has been widely used for the radiotherapy dose calculation for both clinical and research purposes. The goal of this work is to investigate both theoretically and experimentally the impact of the MC statistical fluctuation on the γ-index test when the fluctuation exists in the reference, the evaluation, or both dose distributions. To the first order approximation, we theoretically demonstrated in a simplified model that the statistical fluctuation tends to overestimate γ-index values when existing in the reference dose distribution and underestimate γ-index values when existing in the evaluation dose distribution given the original γ-index is relatively large for the statistical fluctuation. Our numerical experiments using realistic clinical photon radiation therapy cases have shown that (1) when performing a γ-index test between an MC reference dose and a non-MC evaluation dose, the average γ-index is overestimated and the gamma passing rate decreases with the increase of the statistical noise level in the reference dose; (2) when performing a γ-index test between a non-MC reference dose and an MC evaluation dose, the average γ-index is underestimated when they are within the clinically relevant range and the gamma passing rate increases with the increase of the statistical noise level in the evaluation dose; (3) when performing a γ-index test between an MC reference dose and an MC evaluation dose, the gamma passing rate is overestimated due to the statistical noise in the evaluation dose and underestimated due to the statistical noise in the reference dose. We conclude that the γ-index test should be used with caution when comparing dose distributions computed with MC simulation. (paper)
Poster — Thur Eve — 14: Improving Tissue Segmentation for Monte Carlo Dose Calculation using DECT
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Di Salvio, A.; Bedwani, S.; Carrier, J-F. [Centre hospitalier de l' Université de Montréal (Canada); Bouchard, H. [National Physics Laboratory, Teddington (United Kingdom)
2014-08-15
Purpose: To improve Monte Carlo dose calculation accuracy through a new tissue segmentation technique with dual energy CT (DECT). Methods: Electron density (ED) and effective atomic number (EAN) can be extracted directly from DECT data with a stoichiometric calibration method. Images are acquired with Monte Carlo CT projections using the user code egs-cbct and reconstructed using an FDK backprojection algorithm. Calibration is performed using projections of a numerical RMI phantom. A weighted parameter algorithm then uses both EAN and ED to assign materials to voxels from DECT simulated images. This new method is compared to a standard tissue characterization from single energy CT (SECT) data using a segmented calibrated Hounsfield unit (HU) to ED curve. Both methods are compared to the reference numerical head phantom. Monte Carlo simulations on uniform phantoms of different tissues using dosxyz-nrc show discrepancies in depth-dose distributions. Results: Both SECT and DECT segmentation methods show similar performance assigning soft tissues. Performance is however improved with DECT in regions with higher density, such as bones, where it assigns materials correctly 8% more often than segmentation with SECT, considering the same set of tissues and simulated clinical CT images, i.e. including noise and reconstruction artifacts. Furthermore, Monte Carlo results indicate that kV photon beam depth-dose distributions can double between two tissues of density higher than muscle. Conclusions: A direct acquisition of ED and the added information of EAN with DECT data improves tissue segmentation and increases the accuracy of Monte Carlo dose calculation in kV photon beams.
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Contrast-enhanced stereotactic synchrotron radiation therapy (SSRT) is an innovative technique based on localized dose-enhancement effects obtained by reinforced photoelectric absorption in the tumor. Medium energy monochromatic X-rays (50 - 100 keV) are used for irradiating tumors previously loaded with a high-Z element. Clinical trials of SSRT are being prepared at the European Synchrotron Radiation Facility (ESRF), an iodinated contrast agent will be used. In order to compute the energy deposited in the patient (dose), a dedicated treatment planning system (TPS) has been developed for the clinical trials, based on the ISOgray TPS. This work focuses on the SSRT specific modifications of the TPS, especially to the PENELOPE-based Monte Carlo dose engine. The TPS uses a dedicated Monte Carlo simulation of medium energy polarized photons to compute the deposited energy in the patient. Simulations are performed considering the synchrotron source, the modeled beamline geometry and finally the patient. Specific materials were also implemented in the voxelized geometry of the patient, to consider iodine concentrations in the tumor. The computation process has been optimized and parallelized. Finally a specific computation of absolute doses and associated irradiation times (instead of monitor units) was implemented. The dedicated TPS was validated with depth dose curves, dose profiles and absolute dose measurements performed at the ESRF in a water tank and solid water phantoms with or without bone slabs. (author)
Noblet, C.; Chiavassa, S.; Smekens, F.; Sarrut, D.; Passal, V.; Suhard, J.; Lisbona, A.; Paris, F.; Delpon, G.
2016-05-01
In preclinical studies, the absorbed dose calculation accuracy in small animals is fundamental to reliably investigate and understand observed biological effects. This work investigated the use of the split exponential track length estimator (seTLE), a new kerma based Monte Carlo dose calculation method for preclinical radiotherapy using a small animal precision micro irradiator, the X-RAD 225Cx. Monte Carlo modelling of the irradiator with GATE/GEANT4 was extensively evaluated by comparing measurements and simulations for half-value layer, percent depth dose, off-axis profiles and output factors in water and water-equivalent material for seven circular fields, from 20 mm down to 1 mm in diameter. Simulated and measured dose distributions in cylinders of water obtained for a 360° arc were also compared using dose, distance-to-agreement and gamma-index maps. Simulations and measurements agreed within 3% for all static beam configurations, with uncertainties estimated to 1% for the simulation and 3% for the measurements. Distance-to-agreement accuracy was better to 0.14 mm. For the arc irradiations, gamma-index maps of 2D dose distributions showed that the success rate was higher than 98%, except for the 0.1 cm collimator (92%). Using the seTLE method, MC simulations compute 3D dose distributions within minutes for realistic beam configurations with a clinically acceptable accuracy for beam diameter as small as 1 mm.
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Aim of this study is to examine the feasibility of using the new Gafchromic EBT3 film in a high-dose stereotactic radiosurgery and radiotherapy quality assurance procedure. Owing to the reduced dimensions of the involved lesions, the feasibility of scanning plan verification films on the scanner plate area with the best uniformity rather than using a correction mask was evaluated. For this purpose, signal values dispersion and reproducibility of film scans were investigated. Uniformity was then quantified in the selected area and was found to be within 1.5% for doses up to 8 Gy. A high-dose threshold level for analyses using this procedure was established evaluating the sensitivity of the irradiated films. Sensitivity was found to be of the order of centiGray for doses up to 6.2 Gy and decreasing for higher doses. The obtained results were used to implement a procedure comparing dose distributions delivered with a CyberKnife system to planned ones. The procedure was validated through single beam irradiation on a Gafchromic film. The agreement between dose distributions was then evaluated for 13 patients (brain lesions, 5 Gy/die prescription isodose ~80%) using gamma analysis. Results obtained using Gamma test criteria of 5%/1 mm show a pass rate of 94.3%. Gamma frequency parameters calculation for EBT3 films showed to strongly depend on subtraction of unexposed film pixel values from irradiated ones. In the framework of the described dosimetric procedure, EBT3 films proved to be effective in the verification of high doses delivered to lesions with complex shapes and adjacent to organs at risk
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Cusumano, Davide, E-mail: davide.cusumano@unimi.it [School of Medical Physics, University of Milan, Milan (Italy); Fumagalli, Maria L. [Health Department, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan (Italy); Marchetti, Marcello; Fariselli, Laura [Department of Neurosurgery, Radiotherapy Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan (Italy); De Martin, Elena [Health Department, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan (Italy)
2015-10-01
Aim of this study is to examine the feasibility of using the new Gafchromic EBT3 film in a high-dose stereotactic radiosurgery and radiotherapy quality assurance procedure. Owing to the reduced dimensions of the involved lesions, the feasibility of scanning plan verification films on the scanner plate area with the best uniformity rather than using a correction mask was evaluated. For this purpose, signal values dispersion and reproducibility of film scans were investigated. Uniformity was then quantified in the selected area and was found to be within 1.5% for doses up to 8 Gy. A high-dose threshold level for analyses using this procedure was established evaluating the sensitivity of the irradiated films. Sensitivity was found to be of the order of centiGray for doses up to 6.2 Gy and decreasing for higher doses. The obtained results were used to implement a procedure comparing dose distributions delivered with a CyberKnife system to planned ones. The procedure was validated through single beam irradiation on a Gafchromic film. The agreement between dose distributions was then evaluated for 13 patients (brain lesions, 5 Gy/die prescription isodose ~80%) using gamma analysis. Results obtained using Gamma test criteria of 5%/1 mm show a pass rate of 94.3%. Gamma frequency parameters calculation for EBT3 films showed to strongly depend on subtraction of unexposed film pixel values from irradiated ones. In the framework of the described dosimetric procedure, EBT3 films proved to be effective in the verification of high doses delivered to lesions with complex shapes and adjacent to organs at risk.
Monte Carlo calculation of dose to water of a 106Ru COB-type ophthalmic plaque
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The concave eye applicators with 106Ru/106Rh or 90Sr/90Y beta-ray sources are worldwide used in brachytherapy for treating intraocular tumors. It raises the need to know the exact dose delivered by beta radiation to tumors but measurement of the dose to water (or tissue) is very difficult due to short range of electrons. The Monte Carlo technique provides a powerful tool for calculation of the dose and dose distributions which helps to predict and determine the doses from different shapes of various types of eye applicators more accurately. The Monte Carlo code MCNPX has been used to calculate dose distributions from a COB-type 106Ru/106Rh ophthalmic applicator manufactured by Eckert and Ziegler BEBIG GmbH. This type of a concave eye applicator has a cut-out whose purpose is to protect the eye nerve which makes the dose distribution more complicated. Several calculations have been performed including depth dose along the applicator central axis and various dose distributions. The depth dose along the applicator central axis and the dose distribution on a spherical surface 1 mm above the plaque inner surface have been compared with measurement data provided by the manufacturer. For distances from 0.5 to 4 mm above the surface, the agreement was within 2.5% and from 5 mm the difference increased from 6% up to 25% at 10 mm whereas the uncertainty on manufacturer data is 20% (2s). It is assumed that the difference is caused by nonuniformly distributed radioactivity over the applicator radioactive layer
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Ortiz Lora, A.; Miras del Rio, H.; Terron Leon, J. A.
2013-07-01
Following the recommendations of the IAEA, and as a further check, they have been Monte Carlo simulation of each one of the plates that are arranged at the Hospital. The objective of the work is the verification of the certificates of calibration and intends to establish criteria of action for its acceptance. (Author)
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Purpose: The commercial release of volumetric modulated arc therapy techniques using a conventional linear accelerator and the growing number of helical tomotherapy users have triggered renewed interest in dose verification methods, and also in tools for exploring the impact of machine tolerance and patient motion on dose distributions without the need to approximate time-varying parameters such as gantry position, MLC leaf motion, or patient motion. To this end we have developed a Monte Carlo-based calculation method capable of simulating a wide variety of treatment techniques without the need to resort to discretization approximations. Methods: The ability to perform complete position-probability-sampled Monte Carlo dose calculations was implemented in the BEAMnrc/DOSXZYnrc user codes of EGSnrc. The method includes full accelerator head simulations of our tomotherapy and Elekta linacs, and a realistic representation of continous motion via the sampling of a time variable. The functionality of this algorithm was tested via comparisons with both measurements and treatment planning dose distributions for four types of treatment techniques: 3D conformal, step-shoot intensity modulated radiation therapy, helical tomotherapy, and volumetric modulated arc therapy. Results: For static fields, the absolute dose agreement between the EGSnrc Monte Carlo calculations and measurements is within 2%/1 mm. Absolute dose agreement between Monte Carlo calculations and treatment planning system for the four different treatment techniques is within 3%/3 mm. Discrepancies with the tomotherapy TPS on the order of 10%/5 mm were observed for the extreme example of a small target located 15 cm off-axis and planned with a low modulation factor. The increase in simulation time associated with using position-probability sampling, as opposed to the discretization approach, was less than 2% in most cases. Conclusions: A single Monte Carlo simulation method can be used to calculate patient
SU-E-J-138: On the Ion Beam Range and Dose Verification in Hadron Therapy Using Sound Waves
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Purpose: Accurate range verification is of great importance to fully exploit the potential benefits of ion beam therapies. Current research efforts on this topic include the use of PET imaging of induced activity, detection of emerging prompt gamma rays or secondary particles. It has also been suggested recently to detect the ultrasound waves emitted through the ion energy absorption process. The energy absorbed in a medium is dissipated as heat, followed by thermal expansion that leads to generation of acoustic waves. By using an array of ultrasound transducers the precise spatial location of the Bragg peak can be obtained. The shape and intensity of the emitted ultrasound pulse depend on several variables including the absorbed energy and the pulse length. The main objective of this work is to understand how the ultrasound wave amplitude and shape depend on the initial ion energy and intensity. This would help guide future experiments in ionoacoustic imaging. Methods: The absorbed energy density for protons and carbon ions of different energy and field sizes were obtained using Fluka Monte Carlo code. Subsequently, the system of coupled equations for temperature and pressure is solved for different ion pulse intensities and lengths to obtain the pressure wave shape, amplitude and spectral distribution. Results: The proposed calculations show that the excited pressure wave amplitude is proportional to the absorbed energy density and for longer ion pulses inversely proportional to the ion pulse duration. It is also shown that the resulting ionoacoustic pressure distribution depends on both ion pulse duration and time between the pulses. Conclusion: The Bragg peak localization using ionoacoustic signal may eventually lead to the development of an alternative imaging method with sub-millimeter resolution. It may also open a way for in-vivo dose verification from the measured acoustic signal
Verification of the shift Monte Carlo code with the C5G7 reactor benchmark
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Sly, N. C.; Mervin, B. T. [Dept. of Nuclear Engineering, Univ. of Tennessee, 311 Pasqua Engineering Building, Knoxville, TN 37996-2300 (United States); Mosher, S. W.; Evans, T. M.; Wagner, J. C. [Oak Ridge National Laboratory, PO Box 2008, Oak Ridge, TN 37831 (United States); Maldonado, G. I. [Dept. of Nuclear Engineering, Univ. of Tennessee, 311 Pasqua Engineering Building, Knoxville, TN 37996-2300 (United States)
2012-07-01
Shift is a new hybrid Monte Carlo/deterministic radiation transport code being developed at Oak Ridge National Laboratory. At its current stage of development, Shift includes a parallel Monte Carlo capability for simulating eigenvalue and fixed-source multigroup transport problems. This paper focuses on recent efforts to verify Shift's Monte Carlo component using the two-dimensional and three-dimensional C5G7 NEA benchmark problems. Comparisons were made between the benchmark eigenvalues and those output by the Shift code. In addition, mesh-based scalar flux tally results generated by Shift were compared to those obtained using MCNP5 on an identical model and tally grid. The Shift-generated eigenvalues were within three standard deviations of the benchmark and MCNP5-1.60 values in all cases. The flux tallies generated by Shift were found to be in very good agreement with those from MCNP. (authors)
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Beta-emitters have proved to be appropriate for radioimmunotherapy. The dosimetric characterization of each radionuclide has to be carefully investigated. One usual and practical dosimetric approach is the calculation of dose distribution from a unit point source emitting particles according to any radionuclide of interest, which is known as dose point kernel. Absorbed dose distributions are due to primary and radiation scattering contributions. This work presented a method capable of performing dose distributions for nuclear medicine dosimetry by means of Monte Carlo methods. Dedicated subroutines have been developed in order to separately compute primary and scattering contributions to the total absorbed dose, performing particle transport up to 1 keV or least. Preliminarily, the suitability of the calculation method has been satisfactory, being tested for monoenergetic sources, and it was further applied to the characterization of different beta-minus radionuclides of nuclear medicine interests for radioimmunotherapy. (author)
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The crucial problem for radiation shielding design at heavy ion accelerator facilities with beam energies of several GeV/n is the source term problem. Experimental data on double differential neutron yields from thick targets irradiated with high-energy uranium nuclei are lacking. At present there are not many Monte Carlo multipurpose codes that can work with primary high-energy uranium nuclei. These codes use different physical models for simulating nucleus-nucleus reactions. Therefore, verification of the codes with available experimental data is very important for selection of the most reliable code for practical tasks. This paper presents comparisons of the FLUKA, GEANT4 and SHIELD code simulations with experimental data on neutron production at 1 GeV/n 238U beam interaction with a thick Fe target
A point dose method for in vivo range verification in proton therapy
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Range uncertainty in proton therapy is a recognized concern. For certain treatment sites, less optimal beam directions are used to avoid the potential risk, but also with reduced benefit. In vivo dosimetry, with implanted or intra-cavity dosimeters, has been widely used for treatment verification in photon/electron therapy. The method cannot, however, verify the beam range for proton treatment, unless we deliver the treatment in a different manner. Specifically, we split the spread-out Bragg peaks in a proton field into two separate fields, each delivering a 'sloped' depth-dose distribution, rather than the usual plateau in a typical proton field. The two fields are 'sloped' in opposite directions so that the total depth-dose distribution retains the constant dose plateau covering the target volume. By measuring the doses received from both fields and calculating the ratio, the water-equivalent path length to the location of the implanted dosimeter can be verified, thus limiting range uncertainty to only the remaining part of the beam path. Production of such subfields has been experimented with a passive scattering beam delivery system. Phantom measurements have been performed to illustrate the application for in vivo beam range verification. (note)
High-Dose-Rate 192Ir Brachytherapy Dose Verification: A Phantom Study
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Alireza Nikoofar
2015-05-01
Full Text Available Background: The high-dose-rate (HDR brachytherapy might be an effective tool for palliation of dysphagia. Because of some concerns about adverse effects due to absorbed radiation dose, it is important to estimate absorbed dose in risky organs during this treatment. Objectives: This study aimed to measure the absorbed dose in the parotid, thyroid, and submandibular gland, eye, trachea, spinal cord, and manubrium of sternum in brachytherapy in an anthropomorphic phantom. Materials and Methods: To measure radiation dose, eye, parotid, thyroid, and submandibular gland, spine, and sternum, an anthropomorphic phantom was considered with applicators to set thermoluminescence dosimeters (TLDs. A specific target volume of about 23 cm3 in the upper thoracic esophagus was considered as target, and phantom planned computed tomography (CT for HDR brachytherapy, then with a micro-Selectron HDR (192Ir remote after-loading unit. Results: Absorbed doses were measured with calibrated TLDs and were expressed in centi-Gray (cGy. In regions far from target (≥ 16 cm such as submandibular, parotid and thyroid glands, mean measured dose ranged from 1.65 to 5.5 cGy. In closer regions (≤ 16 cm, the absorbed dose might be as high as 113 cGy. Conclusions: Our study showed similar depth and surface doses; in closer regions, the surface and depth doses differed significantly due to the role of primary radiation that had imposed a high-dose gradient and difference between the plan and measurement, which was more severe because of simplifications in tissue inhomogeneity, considered in TPS relative to phantom.
An automatic dose verification system for adaptive radiotherapy for helical tomotherapy
Mo, Xiaohu; Chen, Mingli; Parnell, Donald; Olivera, Gustavo; Galmarini, Daniel; Lu, Weiguo
2014-03-01
verification system that quantifies treatment doses, and provides necessary information for adaptive planning without impeding clinical workflows.
An automatic dose verification system for adaptive radiotherapy for helical tomotherapy
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dose verification system that quantifies treatment doses, and provides necessary information for adaptive planning without impeding clinical workflows.
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The purpose of this study is to perform a clinical evaluation of the first commercial (MDS Nordion, now Nucletron) treatment planning system for electron beams incorporating Monte Carlo dose calculation module. This software implements Kawrakow's VMC++ voxel-based Monte Carlo calculation algorithm. The accuracy of the dose distribution calculations is evaluated by direct comparisons with extensive sets of measured data in homogeneous and heterogeneous phantoms at different source-to-surface distances (SSDs) and gantry angles. We also verify the accuracy of the Monte Carlo module for monitor unit calculations in comparison with independent hand calculations for homogeneous water phantom at two different SSDs. All electron beams in the range 6-20 MeV are from a Siemens KD-2 linear accelerator. We used 10 000 or 50 000 histories/cm2 in our Monte Carlo calculations, which led to about 2.5% and 1% relative standard error of the mean of the calculated dose. The dose calculation time depends on the number of histories, the number of voxels used to map the patient anatomy, the field size, and the beam energy. The typical run time of the Monte Carlo calculations (10 000 histories/cm2) is 1.02 min on a 2.2 GHz Pentium 4 Xeon computer for a 9 MeV beam, 10x10 cm2 field size, incident on the phantom 15x15x10 cm3 consisting of 31 CT slices and voxels size of 3x3x3 mm3 (total of 486 720 voxels). We find good agreement (discrepancies smaller than 5%) for most of the tested dose distributions. We also find excellent agreement (discrepancies of 2.5% or less) for the monitor unit calculations relative to the independent manual calculations. The accuracy of monitor unit calculations does not depend on the SSD used, which allows the use of one virtual machine for each beam energy for all arbitrary SSDs. In some cases the test results are found to be sensitive to the voxel size applied such that bigger systematic errors (>5%) occur when large voxel sizes interfere with the extensions of
A simulation study of a C-shaped in-beam PET system for dose verification in carbon ion therapy
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The application of hadrons such as carbon ions is being developed for the treatment of cancer. The effectiveness of such a technique is due to the eligibility of charged particles in delivering most of their energy near the end of the range, called the Bragg peak. However, accurate verification of dose delivery is required since misalignment of the hadron beam can cause serious damage to normal tissue. PET scanners can be utilized to track the carbon beam to the tumor by imaging the trail of the hadron-induced positron emitters in the irradiated volume. In this study, we designed and evaluated (through Monte Carlo simulations) an in-beam PET scanner for monitoring patient dose in carbon beam therapy. A C-shaped PET and a partial-ring PET were designed to avoid interference between the PET detectors and the therapeutic carbon beam delivery. Their performance was compared with that of a full-ring PET scanner. The C-shaped, partial-ring, and full-ring scanners consisted of 14, 12, and 16 detector modules, respectively, with a 30.2 cm inner diameter for brain imaging. Each detector module was composed of a 13×13 array of 4.0 mm×4.0 mm×20.0 mm LYSO crystals and four round 25.4 mm diameter PMTs. To estimate the production yield of positron emitters such as 10C, 11C, and 15O, a cylindrical PMMA phantom (diameter, 20 cm; thickness, 20 cm) was irradiated with 170, 290, and 350 AMeV 12C beams using the GATE code. Phantom images of the three types of scanner were evaluated by comparing the longitudinal profile of the positron emitters, measured along the carbon beam as it passed a simulated positron emitter distribution. The results demonstrated that the development of a C-shaped PET scanner to characterize carbon dose distribution for therapy planning is feasible.
Radiation doses in volume-of-interest breast computed tomography—A Monte Carlo simulation study
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Lai, Chao-Jen, E-mail: cjlai3711@gmail.com; Zhong, Yuncheng; Yi, Ying; Wang, Tianpeng; Shaw, Chris C. [Department of Imaging Physics, The University of Texas MD Anderson Cancer Center, Houston, Texas 77030-4009 (United States)
2015-06-15
Purpose: Cone beam breast computed tomography (breast CT) with true three-dimensional, nearly isotropic spatial resolution has been developed and investigated over the past decade to overcome the problem of lesions overlapping with breast anatomical structures on two-dimensional mammographic images. However, the ability of breast CT to detect small objects, such as tissue structure edges and small calcifications, is limited. To resolve this problem, the authors proposed and developed a volume-of-interest (VOI) breast CT technique to image a small VOI using a higher radiation dose to improve that region’s visibility. In this study, the authors performed Monte Carlo simulations to estimate average breast dose and average glandular dose (AGD) for the VOI breast CT technique. Methods: Electron–Gamma-Shower system code-based Monte Carlo codes were used to simulate breast CT. The Monte Carlo codes estimated were validated using physical measurements of air kerma ratios and point doses in phantoms with an ion chamber and optically stimulated luminescence dosimeters. The validated full cone x-ray source was then collimated to simulate half cone beam x-rays to image digital pendant-geometry, hemi-ellipsoidal, homogeneous breast phantoms and to estimate breast doses with full field scans. 13-cm in diameter, 10-cm long hemi-ellipsoidal homogeneous phantoms were used to simulate median breasts. Breast compositions of 25% and 50% volumetric glandular fractions (VGFs) were used to investigate the influence on breast dose. The simulated half cone beam x-rays were then collimated to a narrow x-ray beam with an area of 2.5 × 2.5 cm{sup 2} field of view at the isocenter plane and to perform VOI field scans. The Monte Carlo results for the full field scans and the VOI field scans were then used to estimate the AGD for the VOI breast CT technique. Results: The ratios of air kerma ratios and dose measurement results from the Monte Carlo simulation to those from the physical
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The purpose of this study was to compare dose distributions from three different algorithms with the x-ray Voxel Monte Carlo (XVMC) calculations, in actual computed tomography (CT) scans for use in stereotactic radiotherapy (SRT) of small lung cancers. Slow CT scan of 20 patients was performed and the internal target volume (ITV) was delineated on Pinnacle3. All plans were first calculated with a scatter homogeneous mode (SHM) which is compatible with Clarkson algorithm using Pinnacle3 treatment planning system (TPS). The planned dose was 48 Gy in 4 fractions. In a second step, the CT images, structures and beam data were exported to other treatment planning systems (TPSs). Collapsed cone convolution (CCC) from Pinnacle3, superposition (SP) from XiO, and XVMC from Monaco were used for recalculating. The dose distributions and the Dose Volume Histograms (DVHs) were compared with each other. The phantom test revealed that all algorithms could reproduce the measured data within 1% except for the SHM with inhomogeneous phantom. For the patient study, the SHM greatly overestimated the isocenter (IC) doses and the minimal dose received by 95% of the PTV (PTV95) compared to XVMC. The differences in mean doses were 2.96 Gy (6.17%) for IC and 5.02 Gy (11.18%) for PTV95. The DVH's and dose distributions with CCC and SP were in agreement with those obtained by XVMC. The average differences in IC doses between CCC and XVMC, and SP and XVMC were -1.14% (p = 0.17), and -2.67% (p = 0.0036), respectively. Our work clearly confirms that the actual practice of relying solely on a Clarkson algorithm may be inappropriate for SRT planning. Meanwhile, CCC and SP were close to XVMC simulations and actual dose distributions obtained in lung SRT
Effects of CT based Voxel Phantoms on Dose Distribution Calculated with Monte Carlo Method
Institute of Scientific and Technical Information of China (English)
Chen Chaobin; Huang Qunying; Wu Yican
2005-01-01
A few CT-based voxel phantoms were produced to investigate the sensitivity of Monte Carlo simulations of X-ray beam and electron beam to the proportions of elements and the mass densities of the materials used to express the patient's anatomical structure. The human body can be well outlined by air, lung, adipose, muscle, soft bone and hard bone to calculate the dose distribution with Monte Carlo method. The effects of the calibration curves established by using various CT scanners are not clinically significant based on our investigation. The deviation from the values of cumulative dose volume histogram derived from CT-based voxel phantoms is less than 1% for the given target.
Effects of CT based Voxel Phantoms on Dose Distribution Calculated with Monte Carlo Method
Chen, Chaobin; Huang, Qunying; Wu, Yican
2005-04-01
A few CT-based voxel phantoms were produced to investigate the sensitivity of Monte Carlo simulations of x-ray beam and electron beam to the proportions of elements and the mass densities of the materials used to express the patient's anatomical structure. The human body can be well outlined by air, lung, adipose, muscle, soft bone and hard bone to calculate the dose distribution with Monte Carlo method. The effects of the calibration curves established by using various CT scanners are not clinically significant based on our investigation. The deviation from the values of cumulative dose volume histogram derived from CT-based voxel phantoms is less than 1% for the given target.
Dose conversion coefficients for ICRP110 voxel phantom in the Geant4 Monte Carlo code
Martins, M. C.; Cordeiro, T. P. V.; Silva, A. X.; Souza-Santos, D.; Queiroz-Filho, P. P.; Hunt, J. G.
2014-02-01
The reference adult male voxel phantom recommended by International Commission on Radiological Protection no. 110 was implemented in the Geant4 Monte Carlo code. Geant4 was used to calculate Dose Conversion Coefficients (DCCs) expressed as dose deposited in organs per air kerma for photons, electrons and neutrons in the Annals of the ICRP. In this work the AP and PA irradiation geometries of the ICRP male phantom were simulated for the purpose of benchmarking the Geant4 code. Monoenergetic photons were simulated between 15 keV and 10 MeV and the results were compared with ICRP 110, the VMC Monte Carlo code and the literature data available, presenting a good agreement.
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Lazzeroni, Marta, E-mail: Marta.Lazzeroni@ki.se; Brahme, Anders
2015-09-15
In the present study we develop a new technique for the production of clean quasi-monochromatic {sup 11}C positron emitter beams for accurate radiation therapy and PET–CT dose delivery imaging and treatment verification. The {sup 11}C ion beam is produced by projectile fragmentation using a primary {sup 12}C ion beam. The practical elimination of the energy spread of the secondary {sup 11}C fragments and other beam contaminating fragments is described. Monte Carlo calculation with the SHIELD-HIT10+ code and analytical methods for the transport of the ions in matter are used in the analysis. Production yields, as well as energy, velocity and magnetic rigidity distributions of the fragments generated in a cylindrical target are scored as a function of the depth within 1 cm thick slices for an optimal target consisting of a fixed 20 cm section of liquid hydrogen followed by a variable thickness section of polyethylene. The wide energy and magnetic rigidity spread of the {sup 11}C ion beam can be reduced to values around 1% by using a variable monochromatizing wedge-shaped degrader in the beam line. Finally, magnetic rigidity and particle species selection, as well as discrimination of the particle velocity through a combined Time of Flight and Radio Frequency-driven Velocity filter purify the beam from similar magnetic rigidity contaminating fragments (mainly {sup 7}Be and {sup 3}He fragments). A beam purity of about 99% is expected by the combined method.
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In the present study we develop a new technique for the production of clean quasi-monochromatic 11C positron emitter beams for accurate radiation therapy and PET–CT dose delivery imaging and treatment verification. The 11C ion beam is produced by projectile fragmentation using a primary 12C ion beam. The practical elimination of the energy spread of the secondary 11C fragments and other beam contaminating fragments is described. Monte Carlo calculation with the SHIELD-HIT10+ code and analytical methods for the transport of the ions in matter are used in the analysis. Production yields, as well as energy, velocity and magnetic rigidity distributions of the fragments generated in a cylindrical target are scored as a function of the depth within 1 cm thick slices for an optimal target consisting of a fixed 20 cm section of liquid hydrogen followed by a variable thickness section of polyethylene. The wide energy and magnetic rigidity spread of the 11C ion beam can be reduced to values around 1% by using a variable monochromatizing wedge-shaped degrader in the beam line. Finally, magnetic rigidity and particle species selection, as well as discrimination of the particle velocity through a combined Time of Flight and Radio Frequency-driven Velocity filter purify the beam from similar magnetic rigidity contaminating fragments (mainly 7Be and 3He fragments). A beam purity of about 99% is expected by the combined method
Lazzeroni, Marta; Brahme, Anders
2015-09-01
In the present study we develop a new technique for the production of clean quasi-monochromatic 11C positron emitter beams for accurate radiation therapy and PET-CT dose delivery imaging and treatment verification. The 11C ion beam is produced by projectile fragmentation using a primary 12C ion beam. The practical elimination of the energy spread of the secondary 11C fragments and other beam contaminating fragments is described. Monte Carlo calculation with the SHIELD-HIT10+ code and analytical methods for the transport of the ions in matter are used in the analysis. Production yields, as well as energy, velocity and magnetic rigidity distributions of the fragments generated in a cylindrical target are scored as a function of the depth within 1 cm thick slices for an optimal target consisting of a fixed 20 cm section of liquid hydrogen followed by a variable thickness section of polyethylene. The wide energy and magnetic rigidity spread of the 11C ion beam can be reduced to values around 1% by using a variable monochromatizing wedge-shaped degrader in the beam line. Finally, magnetic rigidity and particle species selection, as well as discrimination of the particle velocity through a combined Time of Flight and Radio Frequency-driven Velocity filter purify the beam from similar magnetic rigidity contaminating fragments (mainly 7Be and 3He fragments). A beam purity of about 99% is expected by the combined method.
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A model of a gamma sterilizer was built using the ITS/ACCEPT Monte Carlo code and verified through dosimetry. Individual dosimetry measurements in homogeneous material were pooled to represent larger bodies that could be simulated in a reasonable time. With the assumptions and simplifications described, dose predictions were within 2-5% of dosimetry. The model was used to simulate product movement through the sterilizer and to predict information useful for process optimization and facility design
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Veltchev, I; Fourkal, E; Doss, M; Ma, C; Meyer, J; Yu, M; Horwitz, E [Fox Chase Cancer Center, Philadelphia, PA (United States)
2014-06-01
Purpose: In the past few years there have been numerous proposals for 3D dose reconstruction from the PET-CT imaging of patients undergoing radioembolization treatment of the liver with yttrium-90 microspheres. One of the most promising techniques uses convolution of the measured PET activity distribution with a pre-calculated Monte Carlo dose deposition kernel. The goal of the present study is to experimentally verify the accuracy of this method and to analyze the significance of various error sources. Methods: Optically stimulated luminescence detectors (OSLD) were used (NanoDot, Landauer) in this experiment. Two detectors were mounted on the central axis of a cylinder filled with water solution of yttrium-90 chloride. The total initial activity was 90mCi. The cylinder was inserted in a larger water phantom and scanned on a Siemens Biograph 16 Truepoint PET-CT scanner. Scans were performed daily over a period of 20 days to build a calibration curve for the measured absolute activity spanning 7 yttrium-90 half-lives. The OSLDs were mounted in the phantom for a predetermined period of time in order to record 2Gy dose. The measured dose was then compared to the dose reconstructed from the activity density at the location of each dosimeter. Results: Thorough error analysis of the dose reconstruction algorithm takes into account the uncertainties in the absolute PET activity, branching ratios, and nonlinearity of the calibration curve. The measured dose for 105-minute exposure on day 10 of the experiment was 219(11)cGy, while the reconstructed dose at the location of the detector was 215(47)cGy. Conclusion: We present the first experimental verification of the accuracy of the convolution algorithm for absolute dose reconstruction of yttrium-90 microspheres. The excellent agreement between the measured and calculated point doses will encourage the broad clinical adoption of the convolution-based dose reconstruction algorithm, making future quantitative dose
Monte Carlo N Particle code - Dose distribution of clinical electron beams in inhomogeneous phantoms
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H A Nedaie
2013-01-01
Full Text Available Electron dose distributions calculated using the currently available analytical methods can be associated with large uncertainties. The Monte Carlo method is the most accurate method for dose calculation in electron beams. Most of the clinical electron beam simulation studies have been performed using non- MCNP [Monte Carlo N Particle] codes. Given the differences between Monte Carlo codes, this work aims to evaluate the accuracy of MCNP4C-simulated electron dose distributions in a homogenous phantom and around inhomogeneities. Different types of phantoms ranging in complexity were used; namely, a homogeneous water phantom and phantoms made of polymethyl methacrylate slabs containing different-sized, low- and high-density inserts of heterogeneous materials. Electron beams with 8 and 15 MeV nominal energy generated by an Elekta Synergy linear accelerator were investigated. Measurements were performed for a 10 cm × 10 cm applicator at a source-to-surface distance of 100 cm. Individual parts of the beam-defining system were introduced into the simulation one at a time in order to show their effect on depth doses. In contrast to the first scattering foil, the secondary scattering foil, X and Y jaws and applicator provide up to 5% of the dose. A 2%/2 mm agreement between MCNP and measurements was found in the homogenous phantom, and in the presence of heterogeneities in the range of 1-3%, being generally within 2% of the measurements for both energies in a "complex" phantom. A full-component simulation is necessary in order to obtain a realistic model of the beam. The MCNP4C results agree well with the measured electron dose distributions.
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Different codes were used for Monte Carlo calculations in radiation therapy. In this study, a new Monte Carlo Simulation Program (MCSP) was developed for the effects of the physical parameters of photons emitted from a Siemens Primus clinical linear accelerator (LINAC) on the dose distribution in water. For MCSP, it was written considering interactions of photons with matter. Here, it was taken into account mainly two interactions: The Compton (or incoherent) scattering and photoelectric effect. Photons which come to water phantom surface emitting from a point source were Bremsstrahlung photons. It should be known the energy distributions of these photons for following photons. Bremsstrahlung photons which have 6 MeV (6 MV photon mode) maximum energies were taken into account. In the 6 MV photon mode, the energies of photons were sampled from using Mohan's experimental energy spectrum (Mohan at al 1985). In order to investigate the performance and accuracy of the simulation, measured and calculated (MCSP) percentage depth dose curves and dose profiles were compared. The Monte Carlo results were shown good agreement with experimental measurements.
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Different codes were used for Monte Carlo calculations in radiation therapy. In this study, a new Monte Carlo Simulation Program (MCSP) was developed for the effects of the physical parameters of photons emitted from a Siemens Primus clinical linear accelerator (LINAC) on the dose distribution in water. For MCSP, it was written considering interactions of photons with matter. Here, it was taken into account mainly two interactions: The Compton (or incoherent) scattering and photoelectric effect. Photons which come to water phantom surface emitting from a point source were Bremsstrahlung photons. It should be known the energy distributions of these photons for following photons. Bremsstrahlung photons which have 6 MeV (6 MV photon mode) maximum energies were taken into account. In the 6 MV photon mode, the energies of photons were sampled from using Mohan's experimental energy spectrum (Mohan at al 1985). In order to investigate the performance and accuracy of the simulation, measured and calculated (MCSP) percentage depth dose curves and dose profiles were compared. The Monte Carlo results were shown good agreement with experimental measurements.
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Wieslander, Elinore; Knoeoes, Tommy [Radiation Physics, Lund University Hospital, SE-221 85 Lund (Sweden)
2003-10-21
An increasing number of patients receiving radiation therapy have metallic implants such as hip prostheses. Therefore, beams are normally set up to avoid irradiation through the implant; however, this cannot always be accomplished. In such situations, knowledge of the accuracy of the used treatment planning system (TPS) is required. Two algorithms, the pencil beam (PB) and the collapsed cone (CC), are implemented in the studied TPS. Comparisons are made with Monte Carlo simulations for 6 and 18 MV. The studied materials are steel, CoCrMo, Orthinox(a stainless steel alloy and registered trademark of Stryker Corporation), TiAlV and Ti. Monte Carlo simulated depth dose curves and dose profiles are compared to CC and PB calculated data. The CC algorithm shows overall a better agreement with Monte Carlo than the PB algorithm. Thus, it is recommended to use the CC algorithm to get the most accurate dose calculation both for the planning target volume and for tissues adjacent to the implants when beams are set up to pass through implants.
International Nuclear Information System (INIS)
An increasing number of patients receiving radiation therapy have metallic implants such as hip prostheses. Therefore, beams are normally set up to avoid irradiation through the implant; however, this cannot always be accomplished. In such situations, knowledge of the accuracy of the used treatment planning system (TPS) is required. Two algorithms, the pencil beam (PB) and the collapsed cone (CC), are implemented in the studied TPS. Comparisons are made with Monte Carlo simulations for 6 and 18 MV. The studied materials are steel, CoCrMo, Orthinox(a stainless steel alloy and registered trademark of Stryker Corporation), TiAlV and Ti. Monte Carlo simulated depth dose curves and dose profiles are compared to CC and PB calculated data. The CC algorithm shows overall a better agreement with Monte Carlo than the PB algorithm. Thus, it is recommended to use the CC algorithm to get the most accurate dose calculation both for the planning target volume and for tissues adjacent to the implants when beams are set up to pass through implants
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Biniam Yohannes Tesfamicael
2014-03-01
Full Text Available Purpose: To construct a dose monitoring system based on an endorectal balloon coupled to thin scintillating fibers to study the dose to the rectum in proton therapy of prostate cancer.Method: A Geant4 Monte Carlo toolkit was used to simulate the proton therapy of prostate cancer, with an endorectal balloon and a set of scintillating fibers for immobilization and dosimetry measurements, respectively.Results: A linear response of the fibers to the dose delivered was observed to within less than 2%. Results obtained show that fibers close to the prostate recorded higher dose, with the closest fiber recording about one-third of the dose to the target. A 1/r2 (r is defined as center-to-center distance between the prostate and the fibers decrease was observed as one goes toward the frontal and distal regions. A very low dose was recorded by the fibers beneath the balloon which is a clear indication that the overall volume of the rectal wall that is exposed to a higher dose is relatively minimized. Further analysis showed a relatively linear relationship between the dose to the target and the dose to the top fibers (total 17, with a slope of (-0.07 ± 0.07 at large number of events per degree of rotation of the modulator wheel (i.e., dose.Conclusion: Thin (1 mm × 1 mm, long (1 m scintillating fibers were found to be ideal for real time in-vivo dose measurement to the rectum during proton therapy of prostate cancer. The linear response of the fibers to the dose delivered makes them good candidates as dosimeters. With thorough calibration and the ability to define a good correlation between the dose to the target and the dose to the fibers, such dosimeters can be used for real time dose verification to the target.-----------------------------------Cite this article as: Tesfamicael BY, Avery S, Gueye P, Lyons D, Mahesh M. Scintillating fiber based in-vivo dose monitoring system to the rectum in proton therapy of prostate cancer: A Geant4 Monte Carlo
Diagnostic X ray dose profiles in molar teeth using Monte Carlo simulation
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The dose profiles in molar teeth from diagnostic X rays was calculated using the Monte Carlo software program MCNP4c2. The information calculated supports needs in EPR retrospective dosimetry to account for diagnostic X ray exposures in teeth. Only tooth positions 6, 7 and 8 were simulated (the three teeth furthest back including the wisdom teeth) using a very detailed model of the pertinent physiology. The lingual and buccal halves of teeth were evaluated as were the crown dentin and roots in tooth position 7. Linear dose profiles through the enamel were also calculated. (author)
Applying graphics processor units to Monte Carlo dose calculation in radiation therapy
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Bakhtiari M
2010-01-01
Full Text Available We investigate the potential in using of using a graphics processor unit (GPU for Monte-Carlo (MC-based radiation dose calculations. The percent depth dose (PDD of photons in a medium with known absorption and scattering coefficients is computed using a MC simulation running on both a standard CPU and a GPU. We demonstrate that the GPU′s capability for massive parallel processing provides a significant acceleration in the MC calculation, and offers a significant advantage for distributed stochastic simulations on a single computer. Harnessing this potential of GPUs will help in the early adoption of MC for routine planning in a clinical environment.
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This study determined the influence of patient individuality on lung organ doses for chest computed tomography (CT) examinations, viewed in the context of the recommendation of the ICRP 103. Within this current recommendation, a more individualized dose estimation is emphasized. The new ICRP 110 voxelized adult phantom was used and compared to calculation of lung doses for chest CT studies with identical scan parameters (120 kV, 135 mAs, 100 mm collimation, 1.5 pitch). For all patient images, the lung was contoured, and the scanning geometry was simulated using the Monte Carlo method. The lungs were completely included in the scan area. A user code was developed for the Monte Carlo package EGSnrc, which enables the simulation of a CT examination procedure and allows an efficient dose scoring within a patient geometry. All simulations were calculated with the same CT source model and calibrated to a realistic CTDIair value. Simulation values were grouped into 1 mSv classes. The organ dose classes fit well to a Gaussian distribution (adjusted correlation coefficient R2 = 0.95). The mean value of the fit was 10 mSv, with a standard deviation of 2 mSv. The variability was about ±30% with a minimum of 8 mSv and maximum of 13 mSv. The calculated lung dose of the ICRP adult female phantom was approximately 11 mSv and thus within the calculated standard deviation of the patient pool. The correlation between lung volume and dose was weak (adjusted correlation coefficient R2 = 0.33). Gender specific differences between the ICRP male and female phantoms were about 17%. In comparison, the differences between the female and a limited set of male patient studies were not statistically significant. Further, the relation between the HU values of CT scans and material/density necessary for the Monte Carlo simulations was investigated. It resulted that the simple but commonly employed relationship leads to significant deviations compared to definite materials in the ICRP phantoms
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A common approach to implementing the Monte Carlo method for the calculation of brachytherapy radiation dose deposition is to use a phase space file containing information on particles emitted from a brachytherapy source. However, the loading of the phase space file during the dose calculation consumes a large amount of computer random access memory, imposing a higher requirement for computer hardware. In this study, we propose a method to parameterize the information (e.g., particle location, direction and energy) stored in the phase space file by using several probability distributions. This method was implemented for dose calculations of a commercial Ir-192 high dose rate source. Dose calculation accuracy of the parameterized source was compared to the results observed using the full phase space file in a simple water phantom and in a clinical breast cancer case. The results showed the parameterized source at a size of 200 kB was as accurate as the phase space file represented source of 1.1 GB. By using the parameterized source representation, a compact Monte Carlo job can be designed, which allows an easy setup for parallel computing in brachytherapy planning. (paper)
Zhang, M.; Zou, W.; Chen, T.; Kim, L.; Khan, A.; Haffty, B.; Yue, N. J.
2014-01-01
A common approach to implementing the Monte Carlo method for the calculation of brachytherapy radiation dose deposition is to use a phase space file containing information on particles emitted from a brachytherapy source. However, the loading of the phase space file during the dose calculation consumes a large amount of computer random access memory, imposing a higher requirement for computer hardware. In this study, we propose a method to parameterize the information (e.g., particle location, direction and energy) stored in the phase space file by using several probability distributions. This method was implemented for dose calculations of a commercial Ir-192 high dose rate source. Dose calculation accuracy of the parameterized source was compared to the results observed using the full phase space file in a simple water phantom and in a clinical breast cancer case. The results showed the parameterized source at a size of 200 kB was as accurate as the phase space file represented source of 1.1 GB. By using the parameterized source representation, a compact Monte Carlo job can be designed, which allows an easy setup for parallel computing in brachytherapy planning.
Effects of human model configuration in Monte Carlo calculations on organ doses from CT examinations
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A new dosimetry system, WAZA-ARI, is being developed to estimate radiation dose from Computed Tomography (CT) examination in Japan. The dose estimation in WAZA-ARI utilizes organ dose data, which have been derived by Monte Carlo calculations using Particle and Heavy Ion Transport code System, PHITS. A Japanese adult male phantom, JM phantom, is adapted as a reference human model in the calculations, because the physique and inner organ masses agree well with the average values for Japanese adult males. On the other hand, each patient has arbitrary physical characteristics. Thus, the effects of human body configuration on organ doses are studied by applying another Japanese male model and the reference phantom by the International Commission on Radiological Protection (ICRP) to PHITS. In addition, this paper describes computation conditions for the three human models, which are constructed in the format of voxel phantom with different resolutions. (author)
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Patient-specific dose verification for treatment planning in helical tomotherapy is routinely performed using a homogeneous virtual water cylindrical phantom of 30 cm diameter and 18 cm length (Cheese phantom). Because of this small length, treatment with total marrow irradiation (TMI) requires multiple deliveries of the dose verification procedures to cover a wide range of the target volumes, which significantly prolongs the dose verification process. We propose a fast, simple, and informative patient-specific dose verification method which reduce dose verification time for TMI with helical tomotherapy. We constructed a two-step solid water slab phantom (length 110 cm, height 8 cm, and two-step width of 30 cm and 15 cm), termed the Whole Body Phantom (WB phantom). Three ionization chambers and three EDR-2 films can be inserted to cover extended field TMI treatment delivery. Three TMI treatment plans were conducted with a TomoTherapy HiArt Planning Station and verified using the WB phantom with ion chambers and films. Three regions simulating the head and neck, thorax, and pelvis were covered in a single treatment delivery. The results were compared to those with the cheese phantom supplied by Accuray, Inc. following three treatment deliveries to cover the body from head to pelvis. Use of the WB phantom provided point doses or dose distributions from head and neck to femur in a single treatment delivery of TMI. Patient-specific dose verification with the WB phantom was 62% faster than with the cheese phantom. The average pass rate in gamma analysis with the criteria of a 3-mm distance-to-agreement and 3% dose differences was 94% ± 2% for the three TMI treatment plans. The differences in pass rates between the WB and cheese phantoms at the upper thorax to abdomen regions were within 2%. The calculated dose agreed with the measured dose within 3% for all points in all five cases in both the WB and cheese phantoms. Our dose verification method with the WB phantom
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Chibani, Omar, E-mail: omar.chibani@fccc.edu; C-M Ma, Charlie [Fox Chase Cancer Center, Philadelphia, Pennsylvania 19111 (United States)
2014-05-15
Purpose: To present a new accelerated Monte Carlo code for CT-based dose calculations in high dose rate (HDR) brachytherapy. The new code (HDRMC) accounts for both tissue and nontissue heterogeneities (applicator and contrast medium). Methods: HDRMC uses a fast ray-tracing technique and detailed physics algorithms to transport photons through a 3D mesh of voxels representing the patient anatomy with applicator and contrast medium included. A precalculated phase space file for the{sup 192}Ir source is used as source term. HDRM is calibrated to calculated absolute dose for real plans. A postprocessing technique is used to include the exact density and composition of nontissue heterogeneities in the 3D phantom. Dwell positions and angular orientations of the source are reconstructed using data from the treatment planning system (TPS). Structure contours are also imported from the TPS to recalculate dose-volume histograms. Results: HDRMC was first benchmarked against the MCNP5 code for a single source in homogenous water and for a loaded gynecologic applicator in water. The accuracy of the voxel-based applicator model used in HDRMC was also verified by comparing 3D dose distributions and dose-volume parameters obtained using 1-mm{sup 3} versus 2-mm{sup 3} phantom resolutions. HDRMC can calculate the 3D dose distribution for a typical HDR cervix case with 2-mm resolution in 5 min on a single CPU. Examples of heterogeneity effects for two clinical cases (cervix and esophagus) were demonstrated using HDRMC. The neglect of tissue heterogeneity for the esophageal case leads to the overestimate of CTV D90, CTV D100, and spinal cord maximum dose by 3.2%, 3.9%, and 3.6%, respectively. Conclusions: A fast Monte Carlo code for CT-based dose calculations which does not require a prebuilt applicator model is developed for those HDR brachytherapy treatments that use CT-compatible applicators. Tissue and nontissue heterogeneities should be taken into account in modern HDR
Verification of Transformer Restricted Earth Fault Protection by using the Monte Carlo Method
KRSTIVOJEVIC, J. P.; DJURIC, M. B.
2015-01-01
The results of a comprehensive investigation of the influence of current transformer (CT) saturation on restricted earth fault (REF) protection during power transformer magnetization inrush are presented. Since the inrush current during switch-on of unloaded power transformer is stochastic, its values are obtained by: (i) laboratory measurements and (ii) calculations based on the input data obtained by the Monte Carlo (MC) simulation. To make a detailed assessment of the curre...
Midplane dose determination and verification of calculated doses in total body irradiation
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Özlem ÖZDEMİR
2014-06-01
Full Text Available OBJECTIVES To compare calculated and measured doses for different regions of anthropomorphic phantom and patients using ion chamber and thermoluminescence dosimetry (TLD for total body irradiation. METHODS Measurements were done for lateral fields with 6 MV, gantry 82º, 40x40 cm2 field and 400 cm source-axis distance (SAD. Entrance-exit and midline doses were measured on anthropomorphic phantom by TLD and entrance-exit doses were measured by TLD and ion chamber on patients. RESULTS For anthropomorphic phantom measurements differences between calculated and measured entrance-exit doses of head, neck, shoulder, lung and thick pelvis were 0.8%, 2.7%, 26.4%, 4.4% and 4.9% and for midline doses were 1.6%, 1.6%, 6.3%, -1.4% and 7.4% respectively. For patients; TLD differences were within -4.13% ile 6.7%, -3.3% ile 3.9%, 5.1% ile 16.6%, -7.8% ile 2.4%, and 3.6% ile 7.1% respectively. For thick pelvis measurements with ion chamber differences were within %0.1-1.9. CONCLUSION Total body irradiation is being applied in limit values in our clinic.
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Verification of calculated lung dose in an anthropomorphic phantom is performed using two dosimetry media. Dosimetry is complicated by factors such as variations in density at slice interfaces and appropriate position on CT scanning slice to accommodate these factors. Dose in lung for a 6 MV and 10 MV anterior-posterior field was calculated with a collapsed cone convolution method using an ADAC Pinnacle, 3D planning system. Up to 5% variations between doses calculated at the centre and near the edge of the 2 cm phantom slice positioned at the beam central axis were seen, due to the composition of each phantom slice. Validation of dose was performed with LiF thermoluminescent dosimeters (TLDs) and X-Omat V radiographic film. Both dosimetry media produced dose results which agreed closely with calculated results nearest their physical positioning in the phantom. The collapsed cone convolution method accurately calculates dose within inhomogeneous lung regions at 6 MV and 10 MV x-ray energy. (author)
Monte Carlo study of electron dose distributions produced by the elekta precise linear accelerator
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Background: Monte Carlo simulation of radiation transport is considered to be one of the most accurate methods of radiation therapy dose calculation and has ability to reduce the uncertainty in the calculated dose to a few percent. Aims: (1) To study the efficacy of the MCNP4C Monte Carlo code to simulate the dose distribution in a homogeneous medium produced by electron beams from the Elekta Precise linear accelerator. (2) To quantify the effect of introduction of various components to the simulated geometry for the above machine. Materials/Methods: Full Monte Carlo simulation of the detailed geometry of the Precise treatment head for 8 and 15 MeV energies and 10 x 10 applicator was performed. Experimental depth dose and lateral profiles at 2 cm depth were measured using a P-type diode detector with a 2.5 mm diameter. To quantify the effects of different parts of the treatment head, seven cases were simulated for a 15 MeV beam to reflect increasing levels of complexity, by step-wise introduction of beam divergence, primary and secondary scattering foils, secondary collimators, applicator, Mirror and Mylar screen. Results: The discrepancy between measured and calculated data is within 2 %/2 mm at both 8 and 15 MeV. In terms of the mean and most probable energies at the surface, the difference was < 0.2 MeV for the majority of cases and the maximum deviation was no more than 0.3 MeV. Conclusions: The results obtained with MCNP4C agree well with measured electron dose distributions. Inclusion of all the main components of the treatment head in the simulated geometry is necessary to avoid discrepancies of about 5 % compared to measurements. (authors)
Makarevich, K. O.; Minenko, V. F.; Verenich, K. A.; Kuten, S. A.
2016-05-01
This work is dedicated to modeling dental radiographic examinations to assess the absorbed doses of patients and effective doses. For simulating X-ray spectra, the TASMIP empirical model is used. Doses are assessed on the basis of the Monte Carlo method by using MCNP code for voxel phantoms of ICRP. The results of the assessment of doses to individual organs and effective doses for different types of dental examinations and features of X-ray tube are presented.
An energy transfer method for 4D Monte Carlo dose calculation.
Siebers, Jeffrey V; Zhong, Hualiang
2008-09-01
This article presents a new method for four-dimensional Monte Carlo dose calculations which properly addresses dose mapping for deforming anatomy. The method, called the energy transfer method (ETM), separates the particle transport and particle scoring geometries: Particle transport takes place in the typical rectilinear coordinate system of the source image, while energy deposition scoring takes place in a desired reference image via use of deformable image registration. Dose is the energy deposited per unit mass in the reference image. ETM has been implemented into DOSXYZnrc and compared with a conventional dose interpolation method (DIM) on deformable phantoms. For voxels whose contents merge in the deforming phantom, the doses calculated by ETM are exactly the same as an analytical solution, contrasting to the DIM which has an average 1.1% dose discrepancy in the beam direction with a maximum error of 24.9% found in the penumbra of a 6 MV beam. The DIM error observed persists even if voxel subdivision is used. The ETM is computationally efficient and will be useful for 4D dose addition and benchmarking alternative 4D dose addition algorithms. PMID:18841862
Evaluation of a new commercial Monte Carlo dose calculation algorithm for electron beams
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Purpose: In this report the authors present the validation of a Monte Carlo dose calculation algorithm (XiO EMC from Elekta Software) for electron beams. Methods: Calculated and measured dose distributions were compared for homogeneous water phantoms and for a 3D heterogeneous phantom meant to approximate the geometry of a trachea and spine. Comparisons of measurements and calculated data were performed using 2D and 3D gamma index dose comparison metrics. Results: Measured outputs agree with calculated values within estimated uncertainties for standard and extended SSDs for open applicators, and for cutouts, with the exception of the 17 MeV electron beam at extended SSD for cutout sizes smaller than 5 × 5 cm2. Good agreement was obtained between calculated and experimental depth dose curves and dose profiles (minimum number of measurements that pass a 2%/2 mm agreement 2D gamma index criteria for any applicator or energy was 97%). Dose calculations in a heterogeneous phantom agree with radiochromic film measurements (>98% of pixels pass a 3 dimensional 3%/2 mm γ-criteria) provided that the steep dose gradient in the depth direction is considered. Conclusions: Clinically acceptable agreement (at the 2%/2 mm level) between the measurements and calculated data for measurements in water are obtained for this dose calculation algorithm. Radiochromic film is a useful tool to evaluate the accuracy of electron MC treatment planning systems in heterogeneous media
A clinical study of lung cancer dose calculation accuracy with Monte Carlo simulation
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The accuracy of dose calculation is crucial to the quality of treatment planning and, consequently, to the dose delivered to patients undergoing radiation therapy. Current general calculation algorithms such as Pencil Beam Convolution (PBC) and Collapsed Cone Convolution (CCC) have shortcomings in regard to severe inhomogeneities, particularly in those regions where charged particle equilibrium does not hold. The aim of this study was to evaluate the accuracy of the PBC and CCC algorithms in lung cancer radiotherapy using Monte Carlo (MC) technology. Four treatment plans were designed using Oncentra Masterplan TPS for each patient. Two intensity-modulated radiation therapy (IMRT) plans were developed using the PBC and CCC algorithms, and two three-dimensional conformal therapy (3DCRT) plans were developed using the PBC and CCC algorithms. The DICOM-RT files of the treatment plans were exported to the Monte Carlo system to recalculate. The dose distributions of GTV, PTV and ipsilateral lung calculated by the TPS and MC were compared. For 3DCRT and IMRT plans, the mean dose differences for GTV between the CCC and MC increased with decreasing of the GTV volume. For IMRT, the mean dose differences were found to be higher than that of 3DCRT. The CCC algorithm overestimated the GTV mean dose by approximately 3% for IMRT. For 3DCRT plans, when the volume of the GTV was greater than 100 cm3, the mean doses calculated by CCC and MC almost have no difference. PBC shows large deviations from the MC algorithm. For the dose to the ipsilateral lung, the CCC algorithm overestimated the dose to the entire lung, and the PBC algorithm overestimated V20 but underestimated V5; the difference in V10 was not statistically significant. PBC substantially overestimates the dose to the tumour, but the CCC is similar to the MC simulation. It is recommended that the treatment plans for lung cancer be developed using an advanced dose calculation algorithm other than PBC. MC can accurately
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Lee, Choonsik; Kim, Kwang Pyo; Long, Daniel J.; Bolch, Wesley E. [Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institute of Health, Bethesda, Maryland 20852 (United States); Department of Nuclear Engineering, Kyung Hee University, Gyeonggi-do, 446906 (Korea, Republic of); J. Crayton Pruitt Family Department of Biomedical Engineering, University of Florida, Gainesville, Florida 32611 (United States)
2012-04-15
Purpose: To establish an organ dose database for pediatric and adolescent reference individuals undergoing computed tomography (CT) examinations by using Monte Carlo simulation. The data will permit rapid estimates of organ and effective doses for patients of different age, gender, examination type, and CT scanner model. Methods: The Monte Carlo simulation model of a Siemens Sensation 16 CT scanner previously published was employed as a base CT scanner model. A set of absorbed doses for 33 organs/tissues normalized to the product of 100 mAs and CTDI{sub vol} (mGy/100 mAs mGy) was established by coupling the CT scanner model with age-dependent reference pediatric hybrid phantoms. A series of single axial scans from the top of head to the feet of the phantoms was performed at a slice thickness of 10 mm, and at tube potentials of 80, 100, and 120 kVp. Using the established CTDI{sub vol}- and 100 mAs-normalized dose matrix, organ doses for different pediatric phantoms undergoing head, chest, abdomen-pelvis, and chest-abdomen-pelvis (CAP) scans with the Siemens Sensation 16 scanner were estimated and analyzed. The results were then compared with the values obtained from three independent published methods: CT-Expo software, organ dose for abdominal CT scan derived empirically from patient abdominal circumference, and effective dose per dose-length product (DLP). Results: Organ and effective doses were calculated and normalized to 100 mAs and CTDI{sub vol} for different CT examinations. At the same technical setting, dose to the organs, which were entirely included in the CT beam coverage, were higher by from 40 to 80% for newborn phantoms compared to those of 15-year phantoms. An increase of tube potential from 80 to 120 kVp resulted in 2.5-2.9-fold greater brain dose for head scans. The results from this study were compared with three different published studies and/or techniques. First, organ doses were compared to those given by CT-Expo which revealed dose
GPUMCD: a new GPU-oriented Monte Carlo dose calculation platform
Hissoiny, Sami; Ozell, Benoît; Després, Philippe
2011-01-01
Purpose: Monte Carlo methods are considered the gold standard for dosimetric computations in radiotherapy. Their execution time is however still an obstacle to the routine use of Monte Carlo packages in a clinical setting. To address this problem, a completely new, and designed from the ground up for the GPU, Monte Carlo dose calculation package for voxelized geometries is proposed: GPUMCD. Method : GPUMCD implements a coupled photon-electron Monte Carlo simulation for energies in the range 0.01 MeV to 20 MeV. An analogue simulation of photon interactions is used and a Class II condensed history method has been implemented for the simulation of electrons. A new GPU random number generator, some divergence reduction methods as well as other optimization strategies are also described. GPUMCD was run on a NVIDIA GTX480 while single threaded implementations of EGSnrc and DPM were run on an Intel Core i7 860. Results : Dosimetric results obtained with GPUMCD were compared to EGSnrc. In all but one test case, 98% o...
Fast Monte Carlo Simulation for Patient-specific CT/CBCT Imaging Dose Calculation
Jia, Xun; Gu, Xuejun; Jiang, Steve B
2011-01-01
Recently, X-ray imaging dose from computed tomography (CT) or cone beam CT (CBCT) scans has become a serious concern. Patient-specific imaging dose calculation has been proposed for the purpose of dose management. While Monte Carlo (MC) dose calculation can be quite accurate for this purpose, it suffers from low computational efficiency. In response to this problem, we have successfully developed a MC dose calculation package, gCTD, on GPU architecture under the NVIDIA CUDA platform for fast and accurate estimation of the x-ray imaging dose received by a patient during a CT or CBCT scan. Techniques have been developed particularly for the GPU architecture to achieve high computational efficiency. Dose calculations using CBCT scanning geometry in a homogeneous water phantom and a heterogeneous Zubal head phantom have shown good agreement between gCTD and EGSnrc, indicating the accuracy of our code. In terms of improved efficiency, it is found that gCTD attains a speed-up of ~400 times in the homogeneous water ...
Research of photon beam dose deposition kernel based on Monte Carlo method
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Using Monte Carlo program BEAMnrc to simulate Siemens accelerator 6 MV photon beam, using BEAMdp program to analyse the energy spectrum distribution and mean energy from phase space data of different field sizes, then building beam source, energy spectrum and mono-energy source, to use DOSXYZnrc program to calculate the dose deposition kernels at dmax in standard water phantom with different beam sources and make comparison with different dose deposition kernels. The results show that the dose difference using energy spectrum source is small, the maximum percentage dose discrepancy is 1.47%, but it is large using mono-energy source, which is 6.28%. The maximum dose difference for the kernels derived from energy spectrum source and mono-energy source of the same field is larger than 9%, up to 13.2%. Thus, dose deposition has dependence on photon energy, it can lead to larger errors only using mono-energy source because of the beam spectrum distribution of accelerator. A good method to calculate dose more accurately is to use deposition kernel of energy spectrum source. (authors)
Experience of total plan dose verification in step and shoot and sliding window IMRT
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Intensity Modulation Radiation Therapy (IMRT) uses radiation beams with non-uniform intensity in order to obtain dose distributions with optimal sparing of organs at risk. The IMRT total plan quality control includes comparison between measured and calculated doses. IMRT quality control should be accurate and reproducible in a fast and easy way. Small sized ionization chambers are recommended for total plan dose verification. However, the smaller the ionization chamber, the smaller the signal, the higher the relative contribution of noise sources such as leakage and the longer the stabilization time required. On the other hand, Farmer type ionization chambers have better signal to noise ratios, but their larger size can lead to problems related to a loss of electronic equilibrium and spatial resolution. The aim of this study is to show our experience during the last 8 years, in the comparison of calculated versus measured doses using a Farmer type ion chamber for 1800 dynamic and step and shoot IMRT plans. For some of the step and shoot IMRT plans the influence of the detector size was studied comparing calculated versus measured doses using PinPoint and Farmer type ion chambers
A comparison of Monte Carlo and analytic first scatter dose spread arrays.
McGary, J E; Boyer, A L; Mackie, T R
1999-05-01
We compare first scattered point dose spread arrays generated by Monte Carlo and an analytic method. The analytic method models energy deposition using Klein-Nishina cross sections for Compton scatter and approximations for electron transport. Assumptions in the analytic method are shown to be valid within a region of the point dose spread kernel in which meaningful comparisons can be made. Differences between the models are less than 10% for the forward scatter directions for radii greater than the electron range associated with the first scattered Compton photon. Differences in the backscatter region are discussed and indicate that the analytic model is useful for identifying large errors that might be present in numerically generated first scatter point dose spread arrays. The analytic method is simple and useful for validating first scatter kernels. PMID:10360537
MO-G-BRF-09: Investigating Magnetic Field Dose Effects in Mice: A Monte Carlo Study
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Rubinstein, A; Guindani, M; Followill, D; Melancon, A; Hazle, J; Court, L [UT MD Anderson Cancer Center, Houston, TX (United States)
2014-06-15
Purpose: In MRI-linac treatments, radiation dose distributions are affected by magnetic fields, especially at high-density/low-density interfaces. Radiobiological consequences of magnetic field dose effects are presently unknown; therefore, preclinical studies are needed to ensure the safe clinical use of MRI-linacs. This study investigates the optimal combination of beam energy and magnetic field strength needed for preclinical murine studies. Methods: The Monte Carlo code MCNP6 was used to simulate the effects of a magnetic field when irradiating a mouse-sized lung phantom with a 1.0cmx1.0cm photon beam. Magnetic field effects were examined using various beam energies (225kVp, 662keV[Cs-137], and 1.25MeV[Co-60]) and magnetic field strengths (0.75T, 1.5T, and 3T). The resulting dose distributions were compared to Monte Carlo results for humans with various field sizes and patient geometries using a 6MV/1.5T MRI-linac. Results: In human simulations, the addition of a 1.5T magnetic field caused an average dose increase of 49% (range:36%–60%) to lung at the soft tissue-to-lung interface and an average dose decrease of 30% (range:25%–36%) at the lung-to-soft tissue interface. In mouse simulations, the magnetic fields had no effect on the 225kVp dose distribution. The dose increases for the Cs-137 beam were 12%, 33%, and 49% for 0.75T, 1.5T, and 3.0T magnetic fields, respectively while the dose decreases were 7%, 23%, and 33%. For the Co-60 beam, the dose increases were 14%, 45%, and 41%, and the dose decreases were 18%, 35%, and 35%. Conclusion: The magnetic field dose effects observed in mouse phantoms using a Co-60 beam with 1.5T or 3T fields and a Cs-137 beam with a 3T field compare well with those seen in simulated human treatments with an MRI-linac. These irradiator/magnet combinations are suitable for preclinical studies investigating potential biological effects of delivering radiation therapy in the presence of a magnetic field. Partially funded by Elekta.
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To report the result of independent absorbed-dose calculations based on a Monte Carlo (MC) algorithm in volumetric modulated arc therapy (VMAT) for various treatment sites. All treatment plans were created by the superposition/convolution (SC) algorithm of SmartArc (Pinnacle V9.2, Philips). The beam information was converted into the format of the Monaco V3.3 (Elekta), which uses the X-ray voxel-based MC (XVMC) algorithm. The dose distribution was independently recalculated in the Monaco. The dose for the planning target volume (PTV) and the organ at risk (OAR) were analyzed via comparisons with those of the treatment plan. Before performing an independent absorbed-dose calculation, the validation was conducted via irradiation from 3 different gantry angles with a 10- × 10-cm2 field. For the independent absorbed-dose calculation, 15 patients with cancer (prostate, 5; lung, 5; head and neck, 3; rectal, 1; and esophageal, 1) who were treated with single-arc VMAT were selected. To classify the cause of the dose difference between the Pinnacle and Monaco TPSs, their calculations were also compared with the measurement data. In validation, the dose in Pinnacle agreed with that in Monaco within 1.5%. The agreement in VMAT calculations between Pinnacle and Monaco using phantoms was exceptional; at the isocenter, the difference was less than 1.5% for all the patients. For independent absorbed-dose calculations, the agreement was also extremely good. For the mean dose for the PTV in particular, the agreement was within 2.0% in all the patients; specifically, no large difference was observed for high-dose regions. Conversely, a significant difference was observed in the mean dose for the OAR. For patients with prostate cancer, the mean rectal dose calculated in Monaco was significantly smaller than that calculated in Pinnacle. There was no remarkable difference between the SC and XVMC calculations in the high-dose regions. The difference observed in the low-dose regions may
Tetrahedral-mesh-based computational human phantom for fast Monte Carlo dose calculations
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Although polygonal-surface computational human phantoms can address several critical limitations of conventional voxel phantoms, their Monte Carlo simulation speeds are much slower than those of voxel phantoms. In this study, we sought to overcome this problem by developing a new type of computational human phantom, a tetrahedral mesh phantom, by converting a polygonal surface phantom to a tetrahedral mesh geometry. The constructed phantom was implemented in the Geant4 Monte Carlo code to calculate organ doses as well as to measure computation speed, the values were then compared with those for the original polygonal surface phantom. It was found that using the tetrahedral mesh phantom significantly improved the computation speed by factors of between 150 and 832 considering all of the particles and simulated energies other than the low-energy neutrons (0.01 and 1 MeV), for which the improvement was less significant (17.2 and 8.8 times, respectively). (paper)
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By the help of a Monte-Carlo program the dose that single organs, organ groups and bigger or smaller parts of body would receive on an average, caused by an irradiation definitely fixed by the geometry of irradiation and photon energy, can be determined. Thus the phantom in connection with the Monte-Carlo program can be used for several considerations as for example - calculation of dose from occupational exposures - calculation of dose from diagnostic procedures - calculation of dose from radiotherapy procedures. (orig.)
SU-E-T-238: Monte Carlo Estimation of Cerenkov Dose for Photo-Dynamic Radiotherapy
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Chibani, O; Price, R; Ma, C [Fox Chase Cancer Center, Philadelphia, PA (United States); Eldib, A [Fox Chase Cancer Center, Philadelphia, PA (United States); University Cairo (Egypt); Mora, G [de Lisboa, Codex, Lisboa (Portugal)
2014-06-01
Purpose: Estimation of Cerenkov dose from high-energy megavoltage photon and electron beams in tissue and its impact on the radiosensitization using Protoporphyrine IX (PpIX) for tumor targeting enhancement in radiotherapy. Methods: The GEPTS Monte Carlo code is used to generate dose distributions from 18MV Varian photon beam and generic high-energy (45-MV) photon and (45-MeV) electron beams in a voxel-based tissueequivalent phantom. In addition to calculating the ionization dose, the code scores Cerenkov energy released in the wavelength range 375–425 nm corresponding to the pick of the PpIX absorption spectrum (Fig. 1) using the Frank-Tamm formula. Results: The simulations shows that the produced Cerenkov dose suitable for activating PpIX is 4000 to 5500 times lower than the overall radiation dose for all considered beams (18MV, 45 MV and 45 MeV). These results were contradictory to the recent experimental studies by Axelsson et al. (Med. Phys. 38 (2011) p 4127), where Cerenkov dose was reported to be only two orders of magnitude lower than the radiation dose. Note that our simulation results can be corroborated by a simple model where the Frank and Tamm formula is applied for electrons with 2 MeV/cm stopping power generating Cerenkov photons in the 375–425 nm range and assuming these photons have less than 1mm penetration in tissue. Conclusion: The Cerenkov dose generated by high-energy photon and electron beams may produce minimal clinical effect in comparison with the photon fluence (or dose) commonly used for photo-dynamic therapy. At the present time, it is unclear whether Cerenkov radiation is a significant contributor to the recently observed tumor regression for patients receiving radiotherapy and PpIX versus patients receiving radiotherapy only. The ongoing study will include animal experimentation and investigation of dose rate effects on PpIX response.
SU-E-T-238: Monte Carlo Estimation of Cerenkov Dose for Photo-Dynamic Radiotherapy
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Purpose: Estimation of Cerenkov dose from high-energy megavoltage photon and electron beams in tissue and its impact on the radiosensitization using Protoporphyrine IX (PpIX) for tumor targeting enhancement in radiotherapy. Methods: The GEPTS Monte Carlo code is used to generate dose distributions from 18MV Varian photon beam and generic high-energy (45-MV) photon and (45-MeV) electron beams in a voxel-based tissueequivalent phantom. In addition to calculating the ionization dose, the code scores Cerenkov energy released in the wavelength range 375–425 nm corresponding to the pick of the PpIX absorption spectrum (Fig. 1) using the Frank-Tamm formula. Results: The simulations shows that the produced Cerenkov dose suitable for activating PpIX is 4000 to 5500 times lower than the overall radiation dose for all considered beams (18MV, 45 MV and 45 MeV). These results were contradictory to the recent experimental studies by Axelsson et al. (Med. Phys. 38 (2011) p 4127), where Cerenkov dose was reported to be only two orders of magnitude lower than the radiation dose. Note that our simulation results can be corroborated by a simple model where the Frank and Tamm formula is applied for electrons with 2 MeV/cm stopping power generating Cerenkov photons in the 375–425 nm range and assuming these photons have less than 1mm penetration in tissue. Conclusion: The Cerenkov dose generated by high-energy photon and electron beams may produce minimal clinical effect in comparison with the photon fluence (or dose) commonly used for photo-dynamic therapy. At the present time, it is unclear whether Cerenkov radiation is a significant contributor to the recently observed tumor regression for patients receiving radiotherapy and PpIX versus patients receiving radiotherapy only. The ongoing study will include animal experimentation and investigation of dose rate effects on PpIX response
SU-E-T-358: Monte Carlo Dose Calculation of Small Field Electron Beams
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Purpose: Dynamic radiotherapy involving electron beams such as Dynamic Electron Arc Radiotherapy (DEAR) requires accurate dose modelling of small field sizes, similar to the requirement of IMRT field on the small photon field. The current commercial electron Monte Carlo algorithms such as eMC v11 in Eclipse were developed for standard field sizes and do not support the planning of dynamic therapy yet. The purpose of this study is to develop a method to accurately model small field electron beam dosimetry using Monte Carlo simulations. Methods: Comparison between eMC, phantom measurements (diode), and Monte Carlo (MC) simulations (BEAMnrc/DOSYZnrc) were performed for a Varian TrueBeam linac. MC simulations utilized Varian TrueBeam phase space files which had been validated in another study. Static single small field was assessed by comparing dose distributions in water for a 16 MeV beam for circular (2 cm diameter) and rectangular (1×10 cm2) cut-out. MC was performed with a resolution of 2.5×2.5×2 mm2 and statistical uncertainty < 4%. The dose distribution was averaged over adjacent bins to improve precision. Depth dose and orthogonal profiles were evaluated. Results: Small field PDDs differ from those with standard cones. For both circular and rectangular cutouts, the difference in range R8 0-R1 0 is less than 2 mm and in dose within 2%. For the orthogonal profiles, field size and penumbra differences were within 1 mm at depth of maximum dose. The eMC displayed a distinctive “step” in the out-field dose profile in disagreement with both measurement and MC results and needs further investigation. Conclusion: MC was able to characterize the small field dosimetry with good agreement with the measurement data, and thus offers the opportunity for treatment planning of dynamic radiotherapy. Analyses for all other electron energies and cut-out sizes are under way and results will be included in the presentation
Monte Carlo calculation of synchrotron x-ray beam dose profiles in a lung phantom
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Full text: Recent advances in synchrotron generated X-ray beams with high fluence rate permit investigation of the application of an array of closely spaced, parallel or converging microplanar beams in radiotherapy. The proposed technique takes advantage of the hypothesized repair mechanism of capillary cells between alternate microbeam zones, which regenerates the lethally irradiated endothelial cells. The lateral and depth doses of 100 keV microplanar beams are investigated for different beam dimensions and spacings in a tissue, lung and tissue/lung/tissue phantom. The EGS4 Monte Carlo code is used to calculate dose profiles at different depth and bundles of beams (up to 20x20 cm square cross section). The maximum dose on the beam axis (peak) and the minimum interbeam dose (valley) are compared at different depths, bundles, heights, widths and beam spacings. Relatively high peak to valley ratios are observed in the lung region, suggesting an ideal environment for microbeam radiotherapy. For a single field, the ratio at the tissue/lung interface will set the maximum dose to the target volume. However, in clinical application, several fields would be involved allowing much greater doses to be applied for the elimination of cancer cells. We conclude therefore that multifield microbeam therapy has the potential to achieve useful therapeutic ratios for the treatment of lung cancer
Postimplant Dosimetry Using a Monte Carlo Dose Calculation Engine: A New Clinical Standard
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Purpose: To use the Monte Carlo (MC) method as a dose calculation engine for postimplant dosimetry. To compare the results with clinically approved data for a sample of 28 patients. Two effects not taken into account by the clinical calculation, interseed attenuation and tissue composition, are being specifically investigated. Methods and Materials: An automated MC program was developed. The dose distributions were calculated for the target volume and organs at risk (OAR) for 28 patients. Additional MC techniques were developed to focus specifically on the interseed attenuation and tissue effects. Results: For the clinical target volume (CTV) D90 parameter, the mean difference between the clinical technique and the complete MC method is 10.7 Gy, with cases reaching up to 17 Gy. For all cases, the clinical technique overestimates the deposited dose in the CTV. This overestimation is mainly from a combination of two effects: the interseed attenuation (average, 6.8 Gy) and tissue composition (average, 4.1 Gy). The deposited dose in the OARs is also overestimated in the clinical calculation. Conclusions: The clinical technique systematically overestimates the deposited dose in the prostate and in the OARs. To reduce this systematic inaccuracy, the MC method should be considered in establishing a new standard for clinical postimplant dosimetry and dose-outcome studies in a near future
Monte Carlo simulation of red bone marrow dose from CT examination
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To evaluate the methods of calculating red bone marrow dose from CT scan, simulating red bone marrow do ses from different CT scan protocols using different energy can provide the basic dose data for patient radiation protection. Method: Monte Carlo software MCNPX and RPI voxel phantom were used for the simulation, by mass absorption coefficient (MEAC) method, energy including 80 kV, 100 kV, 120 kV and 140 kV of the CT device were simulated, and different CT protocols such as chest scan, abdomen scan and body scan were taken into consideration when simulating the red bone marrow dose (mGy/100 mAs). Results: Under the same other conditions, the larger beam energy caused larger red bone marrow dose, the results of 140 kV was two times larger than that of 80 kV for the same protocol; while under the same beam energy, the difference among different protocol was less than 10%. Conclusion: Under the same conditions, the red bone marrow dose from CT scan depends on beam energy (tube voltage) and total effective mAs; if the total effective mAs was constant, the influence of scan protocol to red bone marrow dose was not much. (authors)
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The conversion coefficients, H'(d,α)/φ, for monoenergetic positrons and positron-emitting radionuclides were calculated by using the user code UCICRPM of the Monte Carlo code EGS5 to estimate the radiation dose for medical staff involved in positron emission tomography examinations. From these coefficients, the dose equivalent rates per unit activity at 0.07 and 10 mm depths in a soft tissue for a straight-line source of 2-deoxy-2-[18F]fluoro-d-glucose (18F-FDG) were calculated by using the developed user code UCF18DOSE. The dose equivalent rates per unit activity at 0.07 and 10 mm depths were measured by using a personal dosemeter (DOSE 3) under the same conditions as those considered in the calculation. The calculated dose equivalent rates per unit activity at 0.07 and 10 mm depths were 0.116 and 0.0352 pSv min-1 Bq-1, respectively, at 20 cm from the 18F-FDG injection tube. (authors)
A 3DHZETRN Code in a Spherical Uniform Sphere with Monte Carlo Verification
Wilson, John W.; Slaba, Tony C.; Badavi, Francis F.; Reddell, Brandon D.; Bahadori, Amir A.
2014-01-01
The computationally efficient HZETRN code has been used in recent trade studies for lunar and Martian exploration and is currently being used in the engineering development of the next generation of space vehicles, habitats, and extra vehicular activity equipment. A new version (3DHZETRN) capable of transporting High charge (Z) and Energy (HZE) and light ions (including neutrons) under space-like boundary conditions with enhanced neutron and light ion propagation is under development. In the present report, new algorithms for light ion and neutron propagation with well-defined convergence criteria in 3D objects is developed and tested against Monte Carlo simulations to verify the solution methodology. The code will be available through the software system, OLTARIS, for shield design and validation and provides a basis for personal computer software capable of space shield analysis and optimization.
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After an accidental release of radionuclides to the inhabited environment the external gamma irradiation from deposited radioactivity contributes significantly to the radiation exposure of the population for extended periods. For evaluating this exposure pathway, three main model requirements are needed: (i) to calculate the air kerma value per photon emitted per unit source area, based on Monte Carlo (MC) simulations; (ii) to describe the distribution and dynamics of radionuclides on the diverse urban surfaces; and (iii) to combine all these elements in a relevant urban model to calculate the resulting doses according to the actual scenario. This paper provides an overview about the different approaches to calculate photon transport in urban areas and about several dose calculation codes published. Two types of Monte Carlo simulations are presented using the global and the local approaches of photon transport. Moreover, two different philosophies of the dose calculation, the 'location factor method' and a combination of relative contamination of surfaces with air kerma values are described. The main features of six codes (ECOSYS, EDEM2M, EXPURT, PARATI, TEMAS, URGENT) are highlighted together with a short model-model features intercomparison
Environmental dose rate assessment of ITER using the Monte Carlo method
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Karimian Alireza
2014-01-01
Full Text Available Exposure to radiation is one of the main sources of risk to staff employed in reactor facilities. The staff of a tokamak is exposed to a wide range of neutrons and photons around the tokamak hall. The International Thermonuclear Experimental Reactor (ITER is a nuclear fusion engineering project and the most advanced experimental tokamak in the world. From the radiobiological point of view, ITER dose rates assessment is particularly important. The aim of this study is the assessment of the amount of radiation in ITER during its normal operation in a radial direction from the plasma chamber to the tokamak hall. To achieve this goal, the ITER system and its components were simulated by the Monte Carlo method using the MCNPX 2.6.0 code. Furthermore, the equivalent dose rates of some radiosensitive organs of the human body were calculated by using the medical internal radiation dose phantom. Our study is based on the deuterium-tritium plasma burning by 14.1 MeV neutron production and also photon radiation due to neutron activation. As our results show, the total equivalent dose rate on the outside of the bioshield wall of the tokamak hall is about 1 mSv per year, which is less than the annual occupational dose rate limit during the normal operation of ITER. Also, equivalent dose rates of radiosensitive organs have shown that the maximum dose rate belongs to the kidney. The data may help calculate how long the staff can stay in such an environment, before the equivalent dose rates reach the whole-body dose limits.
A Monte Carlo tool for raster-scanning particle therapy dose computation
Jelen, U.; Radon, M.; Santiago, A.; Wittig, A.; Ammazzalorso, F.
2014-03-01
Purpose of this work was to implement Monte Carlo (MC) dose computation in realistic patient geometries with raster-scanning, the most advanced ion beam delivery technique, combining magnetic beam deflection with energy variation. FLUKA, a Monte Carlo package well-established in particle therapy applications, was extended to simulate raster-scanning delivery with clinical data, unavailable as built-in feature. A new complex beam source, compatible with FLUKA public programming interface, was implemented in Fortran to model the specific properties of raster-scanning, i.e. delivery by means of multiple spot sources with variable spatial distributions, energies and numbers of particles. The source was plugged into the MC engine through the user hook system provided by FLUKA. Additionally, routines were provided to populate the beam source with treatment plan data, stored as DICOM RTPlan or TRiP98's RST format, enabling MC recomputation of clinical plans. Finally, facilities were integrated to read computerised tomography (CT) data into FLUKA. The tool was used to recompute two representative carbon ion treatment plans, a skull base and a prostate case, prepared with analytical dose calculation (TRiP98). Selected, clinically relevant issues influencing the dose distributions were investigated: (1) presence of positioning errors, (2) influence of fiducial markers and (3) variations in pencil beam width. Notable differences in modelling of these challenging situations were observed between the analytical and Monte Carlo results. In conclusion, a tool was developed, to support particle therapy research and treatment, when high precision MC calculations are required, e.g. in presence of severe density heterogeneities or in quality assurance procedures.
SU-E-I-28: Evaluating the Organ Dose From Computed Tomography Using Monte Carlo Calculations
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Purpose: To evaluate organ doses from computed tomography (CT) using Monte Carlo (MC) calculations. Methods: A Philips Brilliance CT scanner (64 slice) was simulated using the GMctdospp (IMPS, Germany) based on the EGSnrc user code. The X-ray spectra and a bowtie filter for MC simulations were determined to coincide with measurements of half-value layer (HVL) and off-center ratio (OCR) profile in air. The MC dose was calibrated from absorbed dose measurements using a Farmer chamber and a cylindrical water phantom. The dose distribution from CT was calculated using patient CT images and organ doses were evaluated from dose volume histograms. Results: The HVLs of Al at 80, 100, and 120 kV were 6.3, 7.7, and 8.7 mm, respectively. The calculated HVLs agreed with measurements within 0.3%. The calculated and measured OCR profiles agreed within 3%. For adult head scans (CTDIvol) =51.4 mGy), mean doses for brain stem, eye, and eye lens were 23.2, 34.2, and 37.6 mGy, respectively. For pediatric head scans (CTDIvol =35.6 mGy), mean doses for brain stem, eye, and eye lens were 19.3, 24.5, and 26.8 mGy, respectively. For adult chest scans (CTDIvol=19.0 mGy), mean doses for lung, heart, and spinal cord were 21.1, 22.0, and 15.5 mGy, respectively. For adult abdominal scans (CTDIvol=14.4 mGy), the mean doses for kidney, liver, pancreas, spleen, and spinal cord were 17.4, 16.5, 16.8, 16.8, and 13.1 mGy, respectively. For pediatric abdominal scans (CTDIvol=6.76 mGy), mean doses for kidney, liver, pancreas, spleen, and spinal cord were 8.24, 8.90, 8.17, 8.31, and 6.73 mGy, respectively. In head scan, organ doses were considerably different from CTDIvol values. Conclusion: MC dose distributions calculated by using patient CT images are useful to evaluate organ doses absorbed to individual patients
SU-E-I-28: Evaluating the Organ Dose From Computed Tomography Using Monte Carlo Calculations
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Ono, T; Araki, F [Faculty of Life Sciences, Kumamoto University, Kumamoto (Japan)
2014-06-01
Purpose: To evaluate organ doses from computed tomography (CT) using Monte Carlo (MC) calculations. Methods: A Philips Brilliance CT scanner (64 slice) was simulated using the GMctdospp (IMPS, Germany) based on the EGSnrc user code. The X-ray spectra and a bowtie filter for MC simulations were determined to coincide with measurements of half-value layer (HVL) and off-center ratio (OCR) profile in air. The MC dose was calibrated from absorbed dose measurements using a Farmer chamber and a cylindrical water phantom. The dose distribution from CT was calculated using patient CT images and organ doses were evaluated from dose volume histograms. Results: The HVLs of Al at 80, 100, and 120 kV were 6.3, 7.7, and 8.7 mm, respectively. The calculated HVLs agreed with measurements within 0.3%. The calculated and measured OCR profiles agreed within 3%. For adult head scans (CTDIvol) =51.4 mGy), mean doses for brain stem, eye, and eye lens were 23.2, 34.2, and 37.6 mGy, respectively. For pediatric head scans (CTDIvol =35.6 mGy), mean doses for brain stem, eye, and eye lens were 19.3, 24.5, and 26.8 mGy, respectively. For adult chest scans (CTDIvol=19.0 mGy), mean doses for lung, heart, and spinal cord were 21.1, 22.0, and 15.5 mGy, respectively. For adult abdominal scans (CTDIvol=14.4 mGy), the mean doses for kidney, liver, pancreas, spleen, and spinal cord were 17.4, 16.5, 16.8, 16.8, and 13.1 mGy, respectively. For pediatric abdominal scans (CTDIvol=6.76 mGy), mean doses for kidney, liver, pancreas, spleen, and spinal cord were 8.24, 8.90, 8.17, 8.31, and 6.73 mGy, respectively. In head scan, organ doses were considerably different from CTDIvol values. Conclusion: MC dose distributions calculated by using patient CT images are useful to evaluate organ doses absorbed to individual patients.
Application of Monte Carlo method for dose calculation in thyroid follicle
International Nuclear Information System (INIS)
The Monte Carlo method is an important tool to simulate radioactive particles interaction with biologic medium. The principal advantage of the method when compared with deterministic methods is the ability to simulate a complex geometry. Several computational codes use the Monte Carlo method to simulate the particles transport and they have the capacity to simulate energy deposition in models of organs and/or tissues, as well models of cells of human body. Thus, the calculation of the absorbed dose to thyroid's follicles (compound of colloid and follicles' cells) have a fundamental importance to dosimetry, because these cells are radiosensitive due to ionizing radiation exposition, in particular, exposition due to radioisotopes of iodine, because a great amount of radioiodine may be released into the environment in case of a nuclear accidents. In this case, the goal of this work was use the code of particles transport MNCP4C to calculate absorbed doses in models of thyroid's follicles, for Auger electrons, internal conversion electrons and beta particles, by iodine-131 and short-lived iodines (131, 132, 133, 134 e 135), with diameters varying from 30 to 500 μm. The results obtained from simulation with the MCNP4C code shown an average percentage of the 25% of total absorbed dose by colloid to iodine- 131 and 75% to short-lived iodine's. For follicular cells, this percentage was of 13% to iodine-131 and 87% to short-lived iodine's. The contributions from particles with low energies, like Auger and internal conversion electrons should not be neglected, to assessment the absorbed dose in cellular level. Agglomerative hierarchical clustering was used to compare doses obtained by codes MCNP4C, EPOTRAN, EGS4 and by deterministic methods. (author)
Study of dose distribution in dental radiology using the Monte Carlo Simulation
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Full text: The purpose of this study was to study the absorbed dose in mouth due to scattering in teeth in dental radiography using the monte carlo simulation. The Electron Gamma Shower (EGS-4) system of computer codes was used, which is a general purpose package for monte carlo simulation of the coupled transport of electrons and photons in an arbitrary geometry for particles with energies above a few keV up to several TeV. In the case of a X ray dental the low energy photons beam, are removed of the spectrum by the filtration. These low energy photons beam do not contribute in the obtaining of the radiographic image, but they will be contribute in the dose to the patient, however when the incident radiation crosses the tooth it generates a scattering radiation that contributes in the dose received by the patient in the oral cavity (cheek, tooth and oral cavity). Dental radiography is one of the largest single groups of radiographic examination accounting for 32% of radiographs taken in the Brazil. A number of relatively recent improvements in technology, equipment and techniques have the potential to reduce patient radiation dose and improve image quality. To optimize radiation protection all reasonable means should be employed to minimize the dose of each exposure. Dentists therefore need to keep up to date with changes in techniques and equipment and modify their own practice. In preliminary analysis could be notice that the energy below the 30 keV (low energy) is deposited in the cheek. To 30 keV photons there is the maximum absorbed energy in the tooth (about 60%). In 40 keV could be notice that deposited energy is same to teeth and cheek, but up to 40 keV just a small part of energy is deposited, e.g., the great part of energy is transmitted to the inner mouth (oral cavity). (orig.)
Monte Carlo 20 and 45 MeV Bremsstrahlung and dose-reduction calculations
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The SANDYL electron-photon coupled Monte Carlo code has been compared with previously published experimental bremsstrahlung data at 20.9 MeV electron energy. The code was then used to calculate forward-directed spectra, angular distributions and dose-reduction factors for three practical configurations. These are: 20 MeV electrons incident on 1 mm of W + 59 mm of Be, 45 MeV electrons of 1 mm of W and 45 MeV electrons on 1 mm of W + 147 mm of Be. The application of these results to flash radiography is discussed. 7 references, 12 figures, 1 table
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Planetary radiation environment modelling is important to assess the habitability of a planetary body. It is also useful when interpreting the γ-ray data produced by natural emissions from radioisotopes or prompt γ-ray activation analysis. γ-ray spectra acquired in orbit or in-situ by a suitable detector can be converted into meaningful estimates of the concentration of certain elements on the surface of a planet. This paper describes the verification of a Monte Carlo model developed using the MCNPX code at University of Leicester. The model predicts the performance of a geophysical package containing a γ-ray spectrometer operating at a depth of up to 5 m. The experimental verification of the Monte Carlo model was performed at the FRM II facility in Munich, Germany. The paper demonstrates that the model is in good agreement with the experimental data and can be used to model the performance of an in-situ γ-ray spectrometer.
Verification for a GEOSHIELD application to the SMART vessel fluence by a Monte Carlo simulation
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In general the two dimensional discrete ordinates transport code DORT has been used for an evaluation of neutron and gamma fluxes during a shielding design of nuclear reactors. It is very complicated and it takes too much time for shielding designers to prepare input data such as a geometrical modeling and a source distribution and to process an output of the results from the shielding analysis. The GEOSHIELD code was developed to save the time spent preparing a geometrical model and an output processing. The GEOSHIELD code is composed of a module for a geometrical modeling by using a combinatorial geometry, a module for a fixed source redistribution, a module for a DORT processing, and a module for a graphical processing of the output activities. The evaluation of an irradiation of a fast neutron which has an energy of higher than 1.0 MeV is very important to verify the integrity of an internal structure including a pressure vessel. The GEOSHIELD code was applied to evaluate a fast neutron fluence distribution on the internal structures inside the reactor pressure vessel of the SMART reactor and the MCNP was used for verification of the result from the GEOSHIELD calculation. Result of the GEOSHIELD and MCNP showed good agreement each other. (author)
Dose measurement using radiochromic lms and Monte Carlo simulation for hadron-therapy
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Because of the increase in dose at the end of the range of ions, dose delivery during patient treatment with hadron-therapy should be controlled with high precision. Monte Carlo codes are now considered mandatory for validation of clinical treatment planning and as a new tool for dosimetry of ion beams. In this work, we aimed to calculate the absorbed dose using Monte Carlo simulation Geant4/Gate. The effect on the dose calculation accuracy of different Geant4 parameters has been studied for mono-energetic carbon ion beams of 300 MeV/u in water. The parameters are: the production threshold of secondary particles and the maximum step limiter of the particle track. Tolerated criterion were chosen to meet the precision required in radiotherapy in term of value and dose localisation (2%, 2 mm respectively) and to obtain the best compromise on dose distribution and computational time. We propose here the values of parameters in order to satisfy the precision required. In the second part of this work, we study the response of radiochromic films MD-v2-55 for quality control in proton and carbon ion beams. We have particularly observed and studied the quenching effect of dosimetric films for high LET (≥20 keV/μm) irradiation in homogeneous and heterogeneous media. This effect is due to the high ionization density around the track of the particle. We have developed a method to predict the response of radiochromic films taking into account the saturation effect. This model is called the RADIS model for 'Radiochromic films Dosimetry for Ions using Simulations'. It is based on the response of films under photon irradiations and the saturation of films due to high linear energy deposit calculated by Monte Carlo. Different beams were used in this study and aimed to validate the model for hadron-therapy applications: carbon ions, protons and photons at different energies. Experiments were performed at Grand Accelerateur National d'Ions Lourds (GANIL), Proton therapy center of
GPU-based Monte Carlo radiotherapy dose calculation using phase-space sources
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A novel phase-space source implementation has been designed for graphics processing unit (GPU)-based Monte Carlo dose calculation engines. Short of full simulation of the linac head, using a phase-space source is the most accurate method to model a clinical radiation beam in dose calculations. However, in GPU-based Monte Carlo dose calculations where the computation efficiency is very high, the time required to read and process a large phase-space file becomes comparable to the particle transport time. Moreover, due to the parallelized nature of GPU hardware, it is essential to simultaneously transport particles of the same type and similar energies but separated spatially to yield a high efficiency. We present three methods for phase-space implementation that have been integrated into the most recent version of the GPU-based Monte Carlo radiotherapy dose calculation package gDPM v3.0. The first method is to sequentially read particles from a patient-dependent phase-space and sort them on-the-fly based on particle type and energy. The second method supplements this with a simple secondary collimator model and fluence map implementation so that patient-independent phase-space sources can be used. Finally, as the third method (called the phase-space-let, or PSL, method) we introduce a novel source implementation utilizing pre-processed patient-independent phase-spaces that are sorted by particle type, energy and position. Position bins located outside a rectangular region of interest enclosing the treatment field are ignored, substantially decreasing simulation time with little effect on the final dose distribution. The three methods were validated in absolute dose against BEAMnrc/DOSXYZnrc and compared using gamma-index tests (2%/2 mm above the 10% isodose). It was found that the PSL method has the optimal balance between accuracy and efficiency and thus is used as the default method in gDPM v3.0. Using the PSL method, open fields of 4 × 4, 10 × 10 and 30 × 30 cm
GPU-based Monte Carlo radiotherapy dose calculation using phase-space sources.
Townson, Reid W; Jia, Xun; Tian, Zhen; Graves, Yan Jiang; Zavgorodni, Sergei; Jiang, Steve B
2013-06-21
A novel phase-space source implementation has been designed for graphics processing unit (GPU)-based Monte Carlo dose calculation engines. Short of full simulation of the linac head, using a phase-space source is the most accurate method to model a clinical radiation beam in dose calculations. However, in GPU-based Monte Carlo dose calculations where the computation efficiency is very high, the time required to read and process a large phase-space file becomes comparable to the particle transport time. Moreover, due to the parallelized nature of GPU hardware, it is essential to simultaneously transport particles of the same type and similar energies but separated spatially to yield a high efficiency. We present three methods for phase-space implementation that have been integrated into the most recent version of the GPU-based Monte Carlo radiotherapy dose calculation package gDPM v3.0. The first method is to sequentially read particles from a patient-dependent phase-space and sort them on-the-fly based on particle type and energy. The second method supplements this with a simple secondary collimator model and fluence map implementation so that patient-independent phase-space sources can be used. Finally, as the third method (called the phase-space-let, or PSL, method) we introduce a novel source implementation utilizing pre-processed patient-independent phase-spaces that are sorted by particle type, energy and position. Position bins located outside a rectangular region of interest enclosing the treatment field are ignored, substantially decreasing simulation time with little effect on the final dose distribution. The three methods were validated in absolute dose against BEAMnrc/DOSXYZnrc and compared using gamma-index tests (2%/2 mm above the 10% isodose). It was found that the PSL method has the optimal balance between accuracy and efficiency and thus is used as the default method in gDPM v3.0. Using the PSL method, open fields of 4 × 4, 10 × 10 and 30 × 30 cm
Monte Carlo Dosimetry of the 60Co BEBIG High Dose Rate for Brachytherapy.
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Luciana Tourinho Campos
Full Text Available The use of high-dose-rate brachytherapy is currently a widespread practice worldwide. The most common isotope source is 192Ir, but 60Co is also becoming available for HDR. One of main advantages of 60Co compared to 192Ir is the economic and practical benefit because of its longer half-live, which is 5.27 years. Recently, Eckert & Ziegler BEBIG, Germany, introduced a new afterloading brachytherapy machine (MultiSource®; it has the option to use either the 60Co or 192Ir HDR source. The source for the Monte Carlo calculations is the new 60Co source (model Co0.A86, which is referred to as the new BEBIG 60Co HDR source and is a modified version of the 60Co source (model GK60M21, which is also from BEBIG.The purpose of this work is to obtain the dosimetry parameters in accordance with the AAPM TG-43U1 formalism with Monte Carlo calculations regarding the BEBIG 60Co high-dose-rate brachytherapy to investigate the required treatment-planning parameters. The geometric design and material details of the source was provided by the manufacturer and was used to define the Monte Carlo geometry. To validate the source geometry, a few dosimetry parameters had to be calculated according to the AAPM TG-43U1 formalism. The dosimetry studies included the calculation of the air kerma strength Sk, collision kerma in water along the transverse axis with an unbounded phantom, dose rate constant and radial dose function. The Monte Carlo code system that was used was EGSnrc with a new cavity code, which is a part of EGS++ that allows calculating the radial dose function around the source. The spectrum to simulate 60Co was composed of two photon energies, 1.17 and 1.33 MeV. Only the gamma part of the spectrum was used; the contribution of the electrons to the dose is negligible because of the full absorption by the stainless-steel wall around the metallic 60Co. The XCOM photon cross-section library was used in subsequent simulations, and the photoelectric effect, pair
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Purpose: Predicted PET images on the basis of analytical filtering approach for proton range verification has been successful developed and validated using FLUKA Monte Carlo (MC) codes and phantom measurements. The purpose of the study is to validate the effectiveness of analytical filtering model for proton range verification on GATE/GEANT4 Monte Carlo simulation codes. Methods: In this study, we performed two experiments for validation of predicted β+-isotope by the analytical model with GATE/GEANT4 simulations. The first experiments to evaluate the accuracy of predicting β+-yields as a function of irradiated proton energies. In second experiment, we simulate homogeneous phantoms of different materials irradiated by a mono-energetic pencil-like proton beam. The results of filtered β+-yields distributions by the analytical model is compared with those of MC simulated β+-yields in proximal and distal fall-off ranges. Results: The results investigate the distribution between filtered β+-yields and MC simulated β+-yields distribution in different conditions. First, we found that the analytical filtering can be applied over the whole range of the therapeutic energies. Second, the range difference between filtered β+-yields and MC simulated β+-yields at the distal fall-off region are within 1.5mm for all materials used. The findings validated the usefulness of analytical filtering model on range verification of proton therapy on GATE Monte Carlo simulations. In addition, there is a larger discrepancy between filtered prediction and MC simulated β+-yields using GATE code, especially in proximal region. This discrepancy might Result from the absence of wellestablished theoretical models for predicting the nuclear interactions. Conclusion: Despite the fact that large discrepancies of the distributions between MC-simulated and predicted β+-yields were observed, the study prove the effectiveness of analytical filtering model for proton range verification using
Direct dose to water dosimetry for pretreatment IMRT verification using a modified EPID
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Gustafsson, Helen; Vial, Philip; Kuncic, Zdenka; Baldock, Clive; Denham, James W.; Greer, Peter B. [Institute of Medical Physics, School of Physics, University of Sydney, Sydney 2006 (Australia) and Northern Sydney Cancer Centre, Royal North Shore Hospital, Sydney 2065 (Australia); Institute of Medical Physics, School of Physics, University of Sydney, Sydney 2006 (Australia) and Department of Medical Physics, Liverpool and Macarthur Cancer Therapy Centres, Sydney 2170 (Australia); Institute of Medical Physics, School of Physics, University of Sydney, Sydney 2006 (Australia); School of Medicine and Public Health, University of Newcastle, Newcastle 2308 (Australia) and Radiation Oncology Department, Calvary Mater Newcastle Hospital, Newcastle 2310 (Australia); School of Mathematical and Physical Sciences, University of Newcastle, Newcastle 2308 (Australia) and Radiation Oncology Department, Calvary Mater Newcastle Hospital, Newcastle 2310 (Australia)
2011-11-15
Purpose: Electronic portal imaging devices (EPIDs) are high resolution systems that produce electronic dose maps with minimal time required for equipment setup, and therefore potentially present a time-saving alternative for intensity modulated radiation therapy (IMRT) pretreatment verification. A modified commercial EPID was investigated operated with an opaque sheet blocking the optical signal produced in the phosphor layer as a precursor to a switched mode dual dosimetry-imaging EPID system. The purpose of this study was to investigate the feasibility of using this system for direct dose to water dosimetry for pretreatment IMRT verification. Methods: A Varian amorphous silicon EPID was modified by placing an opaque sheet between the Gd{sub 2}S{sub 2}O:Tb phosphor layer and the photodiode array to block the optical photons. The EPID was thus converted to a direct-detecting system (dEPID), in which the high energy radiation deposits energy directly in the photodiode array. The copper build-up was replaced with d{sub max} solid water. Sixty-one IMRT beams of varying complexity were delivered to the EPID, to EDR2 dosimetric film and to a 2D ion chamber array (MapCheck). EPID data was compared to film and MapCheck data using gamma analysis with 3%, 3mm pass criteria. Results: The fraction of points that passed the gamma test was on average 98.1% and 98.6%, for the EPID versus film and EPID versus MapCheck comparisons, respectively. In the case of comparison with film, the majority of observed discrepancies were associated with problems related to film sensitivity or processing. Conclusions: The very close agreement between EPID and both film and MapCheck data demonstrates that the modified EPID is suitable for direct dose to water measurement for pretreatment IMRT verification. These results suggest a reconfigured EPID could be an efficient and accurate dosimeter. Alternatively, optical switching methods could be developed to produce a dual-mode EPID with both
Direct dose to water dosimetry for pretreatment IMRT verification using a modified EPID
International Nuclear Information System (INIS)
Purpose: Electronic portal imaging devices (EPIDs) are high resolution systems that produce electronic dose maps with minimal time required for equipment setup, and therefore potentially present a time-saving alternative for intensity modulated radiation therapy (IMRT) pretreatment verification. A modified commercial EPID was investigated operated with an opaque sheet blocking the optical signal produced in the phosphor layer as a precursor to a switched mode dual dosimetry-imaging EPID system. The purpose of this study was to investigate the feasibility of using this system for direct dose to water dosimetry for pretreatment IMRT verification. Methods: A Varian amorphous silicon EPID was modified by placing an opaque sheet between the Gd2S2O:Tb phosphor layer and the photodiode array to block the optical photons. The EPID was thus converted to a direct-detecting system (dEPID), in which the high energy radiation deposits energy directly in the photodiode array. The copper build-up was replaced with dmax solid water. Sixty-one IMRT beams of varying complexity were delivered to the EPID, to EDR2 dosimetric film and to a 2D ion chamber array (MapCheck). EPID data was compared to film and MapCheck data using gamma analysis with 3%, 3mm pass criteria. Results: The fraction of points that passed the gamma test was on average 98.1% and 98.6%, for the EPID versus film and EPID versus MapCheck comparisons, respectively. In the case of comparison with film, the majority of observed discrepancies were associated with problems related to film sensitivity or processing. Conclusions: The very close agreement between EPID and both film and MapCheck data demonstrates that the modified EPID is suitable for direct dose to water measurement for pretreatment IMRT verification. These results suggest a reconfigured EPID could be an efficient and accurate dosimeter. Alternatively, optical switching methods could be developed to produce a dual-mode EPID with both dosimetry and imaging
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Background. Dosimetry in radionuclide therapy estimates delivered absorbed doses to tumours and ensures that absorbed dose levels to normal organs are below tolerance levels. One procedure is to determine time-activity curves in volumes-of-interests from which the absorbed dose is estimated using SPECT with appropriate corrections for attenuation, scatter and collimator response. From corrected SPECT images the absorbed energy can be calculated by (a) assuming kinetic energy deposited in the same voxel where particles were emitted, (b) convolve with point-dose kernels or (c) use full Monte Carlo (MC) methods. A question arises which dosimetry method is optimal given the limitations in reconstruction- and quantification procedures. Methods. Dosimetry methods (a) and (c) were evaluated by comparing dose-rate volume histograms (DrVHs) from simulated SPECT of 111In, 177Lu, 131I and Bremsstrahlung from 90Y to match true dose rate images. The study used a voxel-based phantom with different tumours in the liver. SPECT reconstruction was made using an iterative OSEM method and MC dosimetry was performed using a charged-particle EGS4 program that also was used to determined true absorbed dose rate distributions for the same phantom geometry but without camera limitations. Results. The DrVHs obtained from SPECT differed from true DrVH mainly due to limited spatial resolution. MC dosimetry had a marginal effect because the SPECT spatial resolution is in the same order as the energy distribution caused by the electron track ranges. For 131I, full MC dosimetry made a difference due to the additional contribution from high-energy photons. SPECT-based DrVHs differ significantly from true DrVHs unless the tumours are considerable larger than the spatial resolution. Conclusion. It is important to understand limitations in quantitative SPECT images and the reasons for apparent heterogeneities since these have an impact on dose-volume histograms. A MC-based dosimetry calculation from
Estimation of skyshine dose from turbine building of BWR plant using Monte Carlo code
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The Monte Carlo N-Particle transport code (MCNP) was adopted to calculate the skyshine dose from the turbine building of a BWR plant for obtaining precise estimations at the site boundary. In MCNP calculation, the equipment and piping arranged on the operating floor of the turbine building were considered and modeled in detail. The inner and outer walls of the turbine building, the shielding materials around the high-pressure turbine, and the piping connected from the moisture separator to the low-pressure turbine were all considered. A three-step study was conducted to estimate the applicability of MCNP code. The first step is confirming the propriety of calculation models. The atmospheric relief diaphragms, which are installed on top of the low-pressure turbine exhaust hood, are not considered in the calculation model. There was little difference between the skyshine dose distributions that were considered when using and not using the atmospheric relief diaphragms. The calculated dose rates agreed well with the measurements taken around the turbine. The second step is estimating the dose rates on the outer roof surface of the turbine building. This calculation was made to confirm the dose distribution of gamma-rays on the turbine roof before being scattered into the air. The calculated dose rates agreed well with the measured data. The third step is making a final confirmation by comparing the calculations and measurements of skyshine dose rates around the turbine building. The source terms of the main steam system are based on the measured activity data of N-16 and C-15. As a conclusion, we were able to calculate reasonable skyshine dose rates by using MCNP code. (authors)
Monte Carlo simulations of absorbed dose in a mouse phantom from 18-fluorine compounds
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The purpose of this study was to calculate internal absorbed dose distribution in mice from preclinical small animal PET imaging procedures with fluorine-18 labeled compounds (18FDG, 18FLT, and fluoride ion). The GATE Monte Carlo software and a realistic, voxel-based mouse phantom that included a subcutaneous tumor were used to perform simulations. Discretized time-activity curves obtained from dynamic in vivo studies with each of the compounds were used to set the activity concentration in the simulations. For 18FDG, a realistic range of uptake ratios was considered for the heart and tumor. For each simulated time frame, the biodistribution of the radionuclide in the phantom was considered constant, and a sufficient number of decays were simulated to achieve low statistical uncertainty. Absorbed dose, which was scaled to take into account radioactive decay, integration with time, and changes in biological distribution was reported in mGy per MBq of administered activity for several organs and uptake scenarios. The mean absorbed dose ranged from a few mGy/MBq to hundreds of mGy/MBq. Major organs receive an absorbed dose in a range for which biological effects have been reported. The effects on a given investigation are hard to predict; however, investigators should be aware of potential perturbations especially when the studied organ receives high absorbed dose and when longitudinal imaging protocols are considered
Verification of Transformer Restricted Earth Fault Protection by using the Monte Carlo Method
Directory of Open Access Journals (Sweden)
KRSTIVOJEVIC, J. P.
2015-08-01
Full Text Available The results of a comprehensive investigation of the influence of current transformer (CT saturation on restricted earth fault (REF protection during power transformer magnetization inrush are presented. Since the inrush current during switch-on of unloaded power transformer is stochastic, its values are obtained by: (i laboratory measurements and (ii calculations based on the input data obtained by the Monte Carlo (MC simulation. To make a detailed assessment of the current transformer performance the uncertain input data for the CT model were obtained by applying the MC method. In this way, different levels of remanent flux in CT core are taken into consideration. By the generated CT secondary currents, the algorithm for REF protection based on phase comparison in time domain is tested. On the basis of the obtained results, a method of adjustment of the triggering threshold in order to ensure safe operation during transients, and thereby improve the algorithm security, has been proposed. The obtained results indicate that power transformer REF protection would be enhanced by using the proposed adjustment of triggering threshold in the algorithm which is based on phase comparison in time domain.
Verification of the spectral history correction method with fully coupled Monte Carlo code BGCore
International Nuclear Information System (INIS)
Recently, a new method for accounting for burnup history effects on few-group cross sections was developed and implemented in the reactor dynamic code DYN3D. The method relies on the tracking of the local Pu-239 density which serves as an indicator of burnup spectral history. The validity of the method was demonstrated in PWR and VVER applications. However, the spectrum variation in BWR core is more pronounced due to the stronger coolant density change. Therefore, the purpose of the current work is to further investigate the applicability of the method to BWR analysis. The proposed methodology was verified against recently developed BGCore system, which couples Monte Carlo neutron transport with depletion and thermal hydraulic solvers and thus capable of providing a reference solution for 3D simulations. The results dearly show that neglecting the spectral history effects leads to a very large deviation (e.g. 2000 pcm in reactivity) from fee reference solution. However, a very good agreement between DYN3D and BGCore is observed (on the order of 200 pcm in reactivity), when the. Pu-correction method is applied. (author)
Tsai, Hui-Yu; Lin, Yung-Chieh; Tyan, Yeu-Sheng
2014-11-01
The purpose of this study was to evaluate organ doses for individual patients undergoing interventional transcatheter arterial embolization (TAE) for hepatocellular carcinoma (HCC) using measurement-based Monte Carlo simulation and adaptive organ segmentation. Five patients were enrolled in this study after institutional ethical approval and informed consent. Gafchromic XR-RV3 films were used to measure entrance surface dose to reconstruct the nonuniform fluence distribution field as the input data in the Monte Carlo simulation. XR-RV3 films were used to measure entrance surface doses due to their lower energy dependence compared with that of XR-RV2 films. To calculate organ doses, each patient's three-dimensional dose distribution was incorporated into CT DICOM images with image segmentation using thresholding and k-means clustering. Organ doses for all patients were estimated. Our dose evaluation system not only evaluated entrance surface doses based on measurements, but also evaluated the 3D dose distribution within patients using simulations. When film measurements were unavailable, the peak skin dose (between 0.68 and 0.82 of a fraction of the cumulative dose) can be calculated from the cumulative dose obtained from TAE dose reports. Successful implementation of this dose evaluation system will aid radiologists and technologists in determining the actual dose distributions within patients undergoing TAE.
Vojtyla, P
2005-01-01
The radiological impact of emissions of radioactive substances from accelerator facilities is characterized by a dominant contribution of the external exposure from short-lived radionuclides in the plume. Ventilation outlets of accelerator facilities are often at low emission heights and receptors reside very close to stacks. Simplified exposure models are not appropriate and integration of the dose kernel over the radioactive plume is required. By using Monte Carlo integration with certain biasing, the integrand can be simplified substantially and an optimum spatial resolution can be achieved. Moreover, long-term releases can be modeled by sampling real weather situations. The mathematical formulation does not depend on any particular atmospheric dispersion model and the applicable code parts can be designed separately, which is another advantage. The obtained results agree within ±10% with results calculated for the semi-infinite cloud model by using detailed particle transport codes and human phantoms.
Characterization of 60Co dose distribution using BEAMnrc Monte Carlo code
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In this study BEAMnrc based on EGSnrc as Monte Carlo code has been used for modeling and simulating 60Co machine in radioisotope centre of Khartoum (RICK), Two fields size ( 5 cm x 5 cm and 35 cm x 35 cm), were been studied, to define the characterization of 60Co machine and to investigate the effect of increasing the surface to skin distance (SSD) on the 60Co machine properties, e.g.; beam profile and percentage depth dose (Pdd). For the narrow field size there is a small change observed in the curves representing beam profile and the percentage depth dose when increasing the distance by 5 cm, for the wide fi ld size there relatively clear different in curves. The study results been compared with other previous studies and clear consistence observed. (Author)
The use of Monte Carlo technique to optimize the dose distribution in total skin irradiation
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Poli, M.E.R. E-mail: esmeraldapoli@hotmail.com; Pereira, S.A.; Yoriyaz, H
2001-06-01
Cutaneous T-cell lymphoma (mycosis fungoides) is an indolent disease with a low percentage of cure. Total skin irradiation using an electron beam has become an efficient treatment of mycosis fungoides with curative intention, with success in almost 40% of the patients. In this work, we propose the use of a Monte Carlo technique to simulate the dose distribution in the patients during total skin irradiation treatments. Use was made of MCNP-4B, a well known and established code used to simulate transport of electrons, photons and neutrons through matter, especially in the area of reactor physics, and also finding increasing utility in medical physics. The goal of our work is to simulate different angles between each beam with a fixed treatment distance in order to obtain a uniform dose distribution in the patient.
Monte Carlo calculations for doses in organs and tissues to oral radiography
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Using the MIRD 5 phantom and Monte Carlo technique, organ doses in patients undergoing external dental examination were calculated taking into account the different x-ray beam geometries and the various possible positions of x-ray source with regard to the head of the patient. It was necessary to introduce in the original computer program a new source description specific for dental examinations. To have a realistic evaluation of organ doses during dental examination it was necessary to introduce a new region in the phantom heat which characterizes the teeth and salivary glands. The attenuation of the x-ray beam by the lead shield of the radiographic film was also introduced in the calculation. (author)
Absorbed dose measurements in mammography using Monte Carlo method and ZrO2+PTFE dosemeters
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Mammography test is a central tool for breast cancer diagnostic. In addition, programs are conducted periodically to detect the asymptomatic women in certain age groups; these programs have shown a reduction on breast cancer mortality. Early detection of breast cancer is achieved through a mammography, which contrasts the glandular and adipose tissue with a probable calcification. The parameters used for mammography are based on the thickness and density of the breast, their values depend on the voltage, current, focal spot and anode-filter combination. To achieve an image clear and a minimum dose must be chosen appropriate irradiation conditions. Risk associated with mammography should not be ignored. This study was performed in the General Hospital No. 1 IMSS in Zacatecas. Was used a glucose phantom and measured air Kerma at the entrance of the breast that was calculated using Monte Carlo methods and ZrO2+PTFE thermoluminescent dosemeters, this calculation was completed with calculating the absorbed dose. (author)
GPU-based fast Monte Carlo simulation for radiotherapy dose calculation
Jia, Xun; Graves, Yan Jiang; Folkerts, Michael; Jiang, Steve B
2011-01-01
Monte Carlo (MC) simulation is commonly considered to be the most accurate dose calculation method in radiotherapy. However, its efficiency still requires improvement for many routine clinical applications. In this paper, we present our recent progress towards the development a GPU-based MC dose calculation package, gDPM v2.0. It utilizes the parallel computation ability of a GPU to achieve high efficiency, while maintaining the same particle transport physics as in the original DPM code and hence the same level of simulation accuracy. In GPU computing, divergence of execution paths between threads can considerably reduce the efficiency. Since photons and electrons undergo different physics and hence attain different execution paths, we use a simulation scheme where photon transport and electron transport are separated to partially relieve the thread divergence issue. High performance random number generator and hardware linear interpolation are also utilized. We have also developed various components to hand...
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This research thesis addresses the dosimetric control of radiotherapy treatments by using amorphous silicon digital portal imagery. In a first part, the author reports the analysis of the dosimetric abilities of the imager (iViewGT) which is used in the radiotherapy department. The stability of the imager response on a short and on a long term has been studied. A relationship between the image grey level and the dose has been established for a reference irradiation field. The influence of irradiation parameters on the grey level variation with respect to the dose has been assessed. The obtained results show the possibility to use this system for dosimetry provided that a precise calibration is performed while taking the most influencing irradiation parameters into account, i.e. photon beam nominal energy, field size, and patient thickness. The author reports the development of a Monte Carlo simulation to model the imager response. It models the accelerator head by a generalized source point. Space and energy distributions of photons are calculated. This modelling can also be applied to the calculation of dose distribution within a patient, or to study physical interactions in the accelerator head. Then, the author explores a new approach to dose portal image prediction within the frame of an in vivo dosimetric control. He computes the image transmitted through the patient by Monte Carlo simulation, and measures the portal image of the irradiation field without the patient. Validation experiments are reported, and problems to be solved are highlighted (computation time, improvement of the collimator simulation)
Development of a GPU-based Monte Carlo dose calculation code for coupled electron-photon transport
Jia, Xun; Sempau, Josep; Choi, Dongju; Majumdar, Amitava; Jiang, Steve B
2009-01-01
Monte Carlo simulation is the most accurate method for absorbed dose calculations in radiotherapy. Its efficiency still requires improvement for routine clinical applications, especially for online adaptive radiotherapy. In this paper, we report our recent development on a GPU-based Monte Carlo dose calculation code for coupled electron-photon transport. We have implemented the Dose Planning Method (DPM) Monte Carlo dose calculation package (Sempau et al, Phys. Med. Biol., 45(2000)2263-2291) on GPU architecture under CUDA platform. The implementation has been tested with respect to the original sequential DPM code on CPU in two cases. Our results demonstrate the adequate accuracy of the GPU implementation for both electron and photon beams in radiotherapy energy range. A speed up factor of 4.5 and 5.5 times have been observed for electron and photon testing cases, respectively, using an NVIDIA Tesla C1060 GPU card against a 2.27GHz Intel Xeon CPU processor .
Verification of Burned Core Modeling Method for Monte Carlo Simulation of HANARO
International Nuclear Information System (INIS)
The reactor core has been managed well by the HANARO core management system called HANAFMS. The heterogeneity of the irradiation device and core made the neutronic analysis difficult and sometimes doubtable. To overcome the deficiency, MCNP was utilized in neutron transport calculation of the HANARO. For the most part, a MCNP model with the assumption that all fuels are filled with fresh fuel assembly showed acceptable analysis results for a design of experimental devices and facilities. However, it sometimes revealed insufficient results in the design, which requires good accuracy like neutron transmutation doping (NTD), because it didn't consider the flux variation induced by depletion of the fuel. In this study, a depleted-core modeling method previously proposed was applied to build burned core model of HANARO and verified through a comparison of the calculated result from the depleted-core model and that from an experiment. The modeling method to establish a depleted-core model for the Monte Carlo simulation was verified by comparing the neutron flux distribution obtained by the zirconium activation method and the reaction rate of 30Si(n, γ) 31Si obtained by a resistivity measurement method. As a result, the reaction rate of 30Si(n, γ) 31Si also agreed well with about 3% difference. It was therefore concluded that the modeling method and resulting depleted-core model developed in this study can be a very reliable tool for the design of the planned experimental facility and a prediction of its performance in HANARO
Verification of Burned Core Modeling Method for Monte Carlo Simulation of HANARO
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Cho, Dongkeun; Kim, Myongseop [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)
2014-05-15
The reactor core has been managed well by the HANARO core management system called HANAFMS. The heterogeneity of the irradiation device and core made the neutronic analysis difficult and sometimes doubtable. To overcome the deficiency, MCNP was utilized in neutron transport calculation of the HANARO. For the most part, a MCNP model with the assumption that all fuels are filled with fresh fuel assembly showed acceptable analysis results for a design of experimental devices and facilities. However, it sometimes revealed insufficient results in the design, which requires good accuracy like neutron transmutation doping (NTD), because it didn't consider the flux variation induced by depletion of the fuel. In this study, a depleted-core modeling method previously proposed was applied to build burned core model of HANARO and verified through a comparison of the calculated result from the depleted-core model and that from an experiment. The modeling method to establish a depleted-core model for the Monte Carlo simulation was verified by comparing the neutron flux distribution obtained by the zirconium activation method and the reaction rate of {sup 30}Si(n, γ) {sup 31}Si obtained by a resistivity measurement method. As a result, the reaction rate of {sup 30}Si(n, γ) {sup 31}Si also agreed well with about 3% difference. It was therefore concluded that the modeling method and resulting depleted-core model developed in this study can be a very reliable tool for the design of the planned experimental facility and a prediction of its performance in HANARO.
Adaptation of GEANT4 to Monte Carlo dose calculations based on CT data
International Nuclear Information System (INIS)
The GEANT4 Monte Carlo code provides many powerful functions for conducting particle transport simulations with great reliability and flexibility. However, as a general purpose Monte Carlo code, not all the functions were specifically designed and fully optimized for applications in radiation therapy. One of the primary issues is the computational efficiency, which is especially critical when patient CT data have to be imported into the simulation model. In this paper we summarize the relevant aspects of the GEANT4 tracking and geometry algorithms and introduce our work on using the code to conduct dose calculations based on CT data. The emphasis is focused on modifications of the GEANT4 source code to meet the requirements for fast dose calculations. The major features include a quick voxel search algorithm, fast volume optimization, and the dynamic assignment of material density. These features are ready to be used for tracking the primary types of particles employed in radiation therapy such as photons, electrons, and heavy charged particles. Re-calculation of a proton therapy treatment plan generated by a commercial treatment planning program for a paranasal sinus case is presented as an example
GPU-based Monte Carlo radiotherapy dose calculation using phase-space sources
Townson, Reid; Tian, Zhen; Graves, Yan Jiang; Zavgorodni, Sergei; Jiang, Steve B
2013-01-01
A novel phase-space source implementation has been designed for GPU-based Monte Carlo dose calculation engines. Due to the parallelized nature of GPU hardware, it is essential to simultaneously transport particles of the same type and similar energies but separated spatially to yield a high efficiency. We present three methods for phase-space implementation that have been integrated into the most recent version of the GPU-based Monte Carlo radiotherapy dose calculation package gDPM v3.0. The first method is to sequentially read particles from a patient-dependent phase-space and sort them on-the-fly based on particle type and energy. The second method supplements this with a simple secondary collimator model and fluence map implementation so that patient-independent phase-space sources can be used. Finally, as the third method (called the phase-space-let, or PSL, method) we introduce a novel strategy to pre-process patient-independent phase-spaces and bin particles by type, energy and position. Position bins l...
Construction and performance of a dose-verification scintillation-fiber detector for proton therapy
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A multilayer scintillation-fiber detector has been developed for precision measurement of time-dependent dose verification in proton therapy. In order to achieve the time and position sensitivity required for the precision dose measurements, a prototype detector was constructed with double-clad 1-mm-thick scintillation fibers and 128-channel silicon photodiodes. The hole charges induced in each channel of the silicon photodiodes were amplified and processed with a charge-integration mode. The detector was tested with 45-MeV proton beams provided by the MC50 cyclotron at the Korea Institute of Radiological and Medical Science (KIRAMS). The detector response for a 45-MeV proton beam was agreed fairly well with the predicted by GEANT4 simulations. Furthermore, the quantitative accuracy appearing in the spatial distribution of the detector response measured for 20 s is in the order of 1%, whose accuracy is satisfactory to verify beam-induced dose in proton therapy. We anticipate that the detector composed of scintillation fibers and operating in the charge-integration mode allows us to perform quality measurement of dynamic therapeutic beams
Three dimensional dose verification for clinical treatments of small intracranial tumours
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Full text: Cancers of the brain and central nervous system account for 1.6% of new cancers and 1.8% of cancer deaths globally. The highest rates of all developed nations are observed in Australia and New Zealand. There are known complexities associated with dose measurement of very small radiation fields. Here, 3D dosimetric verification of treatments for small intracranial tumours using gel dosimetry was investigated. An anthropomorphic head phantom with a 43 mm diameter and 63 mm long gel container was filled with PAGAT normoxic radiosensitive gel. In this work, we show results for a 12-field stereotactic radiotherapy treatment delivered using a Varian 21EX with BrainLAB mini-multi leaf collimator. The gel was read out using an Octopus-1Q laser optical CT scanner. Generally good agreement was observed between the measured doses and those calculated with the iPlan treatment planning system (pencil beam convolution); see Fig. I. For gamma criteria of 5%/5 mm the percentage of gamma values less than unity was 95% above the 80% isodose line, indicating good PTV coverage. For lower isodose regions approaching the boundaries of the container poorer agreement was observed. The feasibility of three-dimensional measurement of small field dose distributions in clinical contexts has been demonstrated. Development of this methodology has the potential to overcome many shortcomings of other dosimetric methods, such as limitations of spatial information (typically one- and two-dimensions), volume-averaging effects and perturbation due to poor mediamatching. (author)
Directory of Open Access Journals (Sweden)
Jia-Ming Wu
2013-01-01
Full Text Available Purpose. This study describes how to identify the coincidence of desired planning isodose curves with film experimental results by using a mathematical fractal dimension characteristic method to avoid the errors caused by visual inspection in the intensity modulation radiation therapy (IMRT. Methods and Materials. The isodose curves of the films delivered by linear accelerator according to Plato treatment planning system were acquired using Osiris software to aim directly at a single interested dose curve for fractal characteristic analysis. The results were compared with the corresponding planning desired isodose curves for fractal dimension analysis in order to determine the acceptable confidence level between the planning and the measurement. Results. The film measured isodose curves and computer planning curves were deemed identical in dose distribution if their fractal dimensions are within some criteria which suggested that the fractal dimension is a unique fingerprint of a curve in checking the planning and film measurement results. The dose measured results of the film were presumed to be the same if their fractal dimension was within 1%. Conclusions. This quantitative rather than qualitative comparison done by fractal dimension numerical analysis helps to decrease the quality assurance errors in IMRT dosimetry verification.
Clinical experience with EPID dosimetry for prostate IMRT pre-treatment dose verification.
McDermott, L N; Wendling, M; van Asselen, B; Stroom, J; Sonke, J J; van Herk, M; Mijnheer, B J
2006-10-01
The aim of this study was to demonstrate how dosimetry with an amorphous silicon electronic portal imaging device (a-Si EPID) replaced film and ionization chamber measurements for routine pre-treatment dosimetry in our clinic. Furthermore, we described how EPID dosimetry was used to solve a clinical problem. IMRT prostate plans were delivered to a homogeneous slab phantom. EPID transit images were acquired for each segment. A previously developed in-house back-projection algorithm was used to reconstruct the dose distribution in the phantom mid-plane (intersecting the isocenter). Segment dose images were summed to obtain an EPID mid-plane dose image for each field. Fields were compared using profiles and in two dimensions with the y evaluation (criteria: 3%/3 mm). To quantify results, the average gamma (gamma avg), maximum gamma (gamma max), and the percentage of points with gamma chamber (IC(iso)). The average ratio, (EPID(iso)/IC(iso)), was 1.00 (0.01 SD). Both measurements were systematically lower than planned, with (EPID(iso)/plan(iso)) and (IC(iso)/plan(iso))=0.99 (0.01 SD). EPID mid-plane dose images for each field were also compared with the corresponding plane derived from the three dimensional (3D) dose grid calculated with the phantom CT scan. Comparisons of 100 fields yielded (gamma avg)=0.39, gamma max=2.52, and (P gamma chamber also agreed. The EPID can therefore replace these dosimetry devices for field-by-field and isocenter IMRT pre-treatment verification. Systematic errors were detected using EPID dosimetry, resulting in the adjustment of a TPS parameter and alteration of two clinical patient plans. One set of EPID measurements (i.e., one open and transit image acquired for each segment of the plan) is sufficient to check each IMRT plan field-by-field and at the isocenter, making it a useful, efficient, and accurate dosimetric tool. PMID:17089854
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Purpose: Current procedure guidelines for whole body [18F]fluoro-2-deoxy-D-glucose (FDG)-positron emission tomography (PET) state that studies with visible dose extravasations should be rejected for quantification protocols. Our work is focused on the development and validation of methods for estimating extravasated doses in order to correct standard uptake value (SUV) values for this effect in clinical routine. Methods: One thousand three hundred sixty-seven consecutive whole body FDG-PET studies were visually inspected looking for extravasation cases. Two methods for estimating the extravasated dose were proposed and validated in different scenarios using Monte Carlo simulations. All visible extravasations were retrospectively evaluated using a manual ROI based method. In addition, the 50 patients with higher extravasated doses were also evaluated using a threshold-based method. Results: Simulation studies showed that the proposed methods for estimating extravasated doses allow us to compensate the impact of extravasations on SUV values with an error below 5%. The quantitative evaluation of patient studies revealed that paravenous injection is a relatively frequent effect (18%) with a small fraction of patients presenting considerable extravasations ranging from 1% to a maximum of 22% of the injected dose. A criterion based on the extravasated volume and maximum concentration was established in order to identify this fraction of patients that might be corrected for paravenous injection effect. Conclusions: The authors propose the use of a manual ROI based method for estimating the effectively administered FDG dose and then correct SUV quantification in those patients fulfilling the proposed criterion
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Silva-Rodríguez, Jesús, E-mail: jesus.silva.rodriguez@sergas.es; Aguiar, Pablo, E-mail: pablo.aguiar.fernandez@sergas.es [Fundación Ramón Domínguez, Santiago de Compostela, Galicia (Spain); Servicio de Medicina Nuclear, Complexo Hospitalario Universidade de Santiago de Compostela (USC), 15782, Galicia (Spain); Grupo de Imaxe Molecular, Instituto de Investigación Sanitarias (IDIS), Santiago de Compostela, 15706, Galicia (Spain); Sánchez, Manuel; Mosquera, Javier; Luna-Vega, Víctor [Servicio de Radiofísica y Protección Radiológica, Complexo Hospitalario Universidade de Santiago de Compostela (USC), 15782, Galicia (Spain); Cortés, Julia; Garrido, Miguel [Servicio de Medicina Nuclear, Complexo Hospitalario Universitario de Santiago de Compostela, 15706, Galicia, Spain and Grupo de Imaxe Molecular, Instituto de Investigación Sanitarias (IDIS), Santiago de Compostela, 15706, Galicia (Spain); Pombar, Miguel [Servicio de Radiofísica y Protección Radiológica, Complexo Hospitalario Universitario de Santiago de Compostela, 15706, Galicia (Spain); Ruibal, Álvaro [Servicio de Medicina Nuclear, Complexo Hospitalario Universidade de Santiago de Compostela (USC), 15782, Galicia (Spain); Grupo de Imaxe Molecular, Instituto de Investigación Sanitarias (IDIS), Santiago de Compostela, 15706, Galicia (Spain); Fundación Tejerina, 28003, Madrid (Spain)
2014-05-15
Purpose: Current procedure guidelines for whole body [18F]fluoro-2-deoxy-D-glucose (FDG)-positron emission tomography (PET) state that studies with visible dose extravasations should be rejected for quantification protocols. Our work is focused on the development and validation of methods for estimating extravasated doses in order to correct standard uptake value (SUV) values for this effect in clinical routine. Methods: One thousand three hundred sixty-seven consecutive whole body FDG-PET studies were visually inspected looking for extravasation cases. Two methods for estimating the extravasated dose were proposed and validated in different scenarios using Monte Carlo simulations. All visible extravasations were retrospectively evaluated using a manual ROI based method. In addition, the 50 patients with higher extravasated doses were also evaluated using a threshold-based method. Results: Simulation studies showed that the proposed methods for estimating extravasated doses allow us to compensate the impact of extravasations on SUV values with an error below 5%. The quantitative evaluation of patient studies revealed that paravenous injection is a relatively frequent effect (18%) with a small fraction of patients presenting considerable extravasations ranging from 1% to a maximum of 22% of the injected dose. A criterion based on the extravasated volume and maximum concentration was established in order to identify this fraction of patients that might be corrected for paravenous injection effect. Conclusions: The authors propose the use of a manual ROI based method for estimating the effectively administered FDG dose and then correct SUV quantification in those patients fulfilling the proposed criterion.
Monte Carlo simulations of dose distributions with necrotic tumor targeted radioimmunotherapy
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Radio-resistant hypoxic tumor cells are significant contributors to the locoregional recurrences and distant metastases that mark failure of radiotherapy. Due to restricted tissue oxygenation, chronically hypoxic tumor cells frequently become necrotic and thus there is often an association between chronically hypoxic and necrotic tumor regions. This simulation study is the first in a series to determine the feasibility of hypoxic cell killing after first targeting adjacent areas of necrosis with either an α- or β-emitting radioimmunoconjugate. - Highlights: • A representative necrotic tumor geometry was created in the Geant4 Monte Carlo toolkit. • Custom designed particle tracking was performed allowing for separation of deposited doses from different decay particles. • Post-processing of the data included relative biological effectiveness of the different decay particles and effects of cell oxygenation. • Physical and equivalent doses resulting from 177Lu and 212Pb were compared by means of dose maps and dose profiles. • 212Pb appears to be a promising isotope for necrotic tumor targeted α-therapy and will be pursued in future in vivo studies
PCXMC, a Monte Carlo program for calculating patient doses in medical x-ray examinations
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PCXMC is a Monte Carlo program for calculating patients' organ doses and effective doses in medical x-ray examinations. The organs and tissues considered in the program are: active bone marrow, adrenals, brain, breasts, colon (upper and lower large intestine), extrathoracic airways, gall bladder, heart, kidneys, liver, lungs, lymph nodes, muscle, oesophagus, oral mucosa, ovaries, pancreas, prostate, salivary glands, skeleton, skin, small intestine, spleen, stomach, testicles, thymus, thyroid, urinary bladder and uterus. The program calculates the effective dose with both the present tissue weighting factors of ICRP Publication 103 (2007) and the old tissue weighting factors of ICRP Publication 60 (1991). The anatomical data are based on the mathematical hermaphrodite phantom models of Cristy and Eckerman (1987), which describe patients of six different ages: new-born, 1, 5, 10, 15-year-old and adult patients. Some changes are made to these phantoms in order to make them more realistic for external irradiation conditions and to enable the calculation of the effective dose according to the new ICRP Publication 103 tissue weighting factors. The phantom sizes are adjustable to mimic patients of an arbitrary weight and height. PCXMC allows a free adjustment of the x-ray beam projection and other examination conditions of projection radiography and fluoroscopy
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Lung brachytherapy using high-dose rate 192Ir technique is a well-established technique of radiation therapy. However, many commercial treatment planning systems do not have the ability to consider the inhomogeneity of lung in relation to normal tissue. Under such circumstances dose calculations for tissues and organs at risk close to the target are inaccurate. The purpose of the current study was to estimate the dose difference due to tissue inhomogeneity using the Monte Carlo simulation code MCNP-5. Results showed that there was a relative sub dosage by treatment planning systems calculations in neighbouring tissues around the radioactive source due to inhomogeneity ignorance. The presence of lung instead of normal tissue resulted in an increase in relative dose, which approached 8 % at 4-cm distance from the source. Additionally, the relative increase was small for the lung (2.1 %) and larger for organs at risk such as the heart (6.8 %) and bone marrow (7.6 %). (authors)
Feasibility Study of Neutron Dose for Real Time Image Guided Proton Therapy: A Monte Carlo Study
Kim, Jin Sung; Kim, Daehyun; Shin, EunHyuk; Chung, Kwangzoo; Cho, Sungkoo; Ahn, Sung Hwan; Ju, Sanggyu; Chung, Yoonsun; Jung, Sang Hoon; Han, Youngyih
2015-01-01
Two full rotating gantry with different nozzles (Multipurpose nozzle with MLC, Scanning Dedicated nozzle) with conventional cyclotron system is installed and under commissioning for various proton treatment options at Samsung Medical Center in Korea. The purpose of this study is to investigate neutron dose equivalent per therapeutic dose, H/D, to x-ray imaging equipment under various treatment conditions with monte carlo simulation. At first, we investigated H/D with the various modifications of the beam line devices (Scattering, Scanning, Multi-leaf collimator, Aperture, Compensator) at isocenter, 20, 40, 60 cm distance from isocenter and compared with other research groups. Next, we investigated the neutron dose at x-ray equipments used for real time imaging with various treatment conditions. Our investigation showed the 0.07 ~ 0.19 mSv/Gy at x-ray imaging equipments according to various treatment options and intestingly 50% neutron dose reduction effect of flat panel detector was observed due to multi- lea...
Monte Carlo simulation methods of determining red bone marrow dose from external radiation
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Objective: To provide evidence for a more reasonable method of determining red bone marrow dose by analyzing and comparing existing simulation methods. Methods: By utilizing Monte Carlo simulation software MCNPX, the absorbed doses of red hone marrow of Rensselaer Polytechnic Institute (RPI) adult female voxel phantom were calculated through 4 different methods: direct energy deposition.dose response function (DRF), King-Spiers factor method and mass-energy absorption coefficient (MEAC). The radiation sources were defined as infinite plate.sources with the energy ranging from 20 keV to 10 MeV, and 23 sources with different energies were simulated in total. The source was placed right next to the front of the RPI model to achieve a homogeneous anteroposterior radiation scenario. The results of different simulated photon energy sources through different methods were compared. Results: When the photon energy was lower than 100 key, the direct energy deposition method gave the highest result while the MEAC and King-Spiers factor methods showed more reasonable results. When the photon energy was higher than 150 keV taking into account of the higher absorption ability of red bone marrow at higher photon energy, the result of the King-Spiers factor method was larger than those of other methods. Conclusions: The King-Spiers factor method might be the most reasonable method to estimate the red bone marrow dose from external radiation. (authors)
Fast CPU-based Monte Carlo simulation for radiotherapy dose calculation
Ziegenhein, Peter; Pirner, Sven; Kamerling, Cornelis Ph; Oelfke, Uwe
2015-08-01
Monte-Carlo (MC) simulations are considered to be the most accurate method for calculating dose distributions in radiotherapy. Its clinical application, however, still is limited by the long runtimes conventional implementations of MC algorithms require to deliver sufficiently accurate results on high resolution imaging data. In order to overcome this obstacle we developed the software-package PhiMC, which is capable of computing precise dose distributions in a sub-minute time-frame by leveraging the potential of modern many- and multi-core CPU-based computers. PhiMC is based on the well verified dose planning method (DPM). We could demonstrate that PhiMC delivers dose distributions which are in excellent agreement to DPM. The multi-core implementation of PhiMC scales well between different computer architectures and achieves a speed-up of up to 37× compared to the original DPM code executed on a modern system. Furthermore, we could show that our CPU-based implementation on a modern workstation is between 1.25× and 1.95× faster than a well-known GPU implementation of the same simulation method on a NVIDIA Tesla C2050. Since CPUs work on several hundreds of GB RAM the typical GPU memory limitation does not apply for our implementation and high resolution clinical plans can be calculated.
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Full text of publication follows. Aim: the aim of this study was to perform a critical comparison of 3 dosimetric approaches in Molecular Radiotherapy: phantom based dosimetry, Dose Voxel Kernels (DVKs) and full Monte Carlo (MC) dosimetry. The objective was to establish the impact of the absorbed dose calculation algorithm on the final result. Materials and Methods: we calculated the absorbed dose to various organs in six healthy volunteers injected with a novel 18F-labelled PET radiotracer from GE Healthcare. Each patient underwent from 8 to 10 whole body 3D PET/CT scans. The first 8 scans were acquired dynamically in order to limit co-registration issues. Eleven organs were segmented on the first PET/CT scan by a physician. We analysed this dataset using the OLINDA/EXM software taking into account actual patient's organ masses; the commercial software Stratos by Philips implementing a DVK approach; and performing full MC dosimetry on the basis of a custom application developed with Gate. The calculations performed with these three techniques were based on the cumulated activities calculated at the voxel level by Stratos. Results: all the absorbed doses calculated with Gate were higher than those calculated with OLINDA. The average ratios between the Gate absorbed dose and OLINDA's was 1.38±0.34 σ (from 0.93 to 2.23) considering all patients. The discrepancy was particularly high for the thyroid, with an average Gate/OLINDA ratio of 1.97±0.83 σ for the 6 patients. The lower absorbed doses in OLINDA may be explained considering the inter-organ distances in the MIRD phantom. These are in general overestimated, leading to lower absorbed doses in target organs. The differences between Stratos and Gate resulted to be the highest. The average ratios between Gate and Stratos absorbed doses were 2.51±1.21 σ (from 1.09 to 6.06). The highest differences were found for lungs (average ratio 4.76±2.13 σ), as expected, since Stratos considers unit density
Ding, George X.; Duggan, Dennis M.; Coffey, Charles W.; Shokrani, Parvaneh; Cygler, Joanna E.
2006-06-01
The purpose of this study is to present our experience of commissioning, testing and use of the first commercial macro Monte Carlo based dose calculation algorithm for electron beam treatment planning and to investigate new issues regarding dose reporting (dose-to-water versus dose-to-medium) as well as statistical uncertainties for the calculations arising when Monte Carlo based systems are used in patient dose calculations. All phantoms studied were obtained by CT scan. The calculated dose distributions and monitor units were validated against measurements with film and ionization chambers in phantoms containing two-dimensional (2D) and three-dimensional (3D) type low- and high-density inhomogeneities at different source-to-surface distances. Beam energies ranged from 6 to 18 MeV. New required experimental input data for commissioning are presented. The result of validation shows an excellent agreement between calculated and measured dose distributions. The calculated monitor units were within 2% of measured values except in the case of a 6 MeV beam and small cutout fields at extended SSDs (>110 cm). The investigation on the new issue of dose reporting demonstrates the differences up to 4% for lung and 12% for bone when 'dose-to-medium' is calculated and reported instead of 'dose-to-water' as done in a conventional system. The accuracy of the Monte Carlo calculation is shown to be clinically acceptable even for very complex 3D-type inhomogeneities. As Monte Carlo based treatment planning systems begin to enter clinical practice, new issues, such as dose reporting and statistical variations, may be clinically significant. Therefore it is imperative that a consistent approach to dose reporting is used.
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The purpose of this study is to present our experience of commissioning, testing and use of the first commercial macro Monte Carlo based dose calculation algorithm for electron beam treatment planning and to investigate new issues regarding dose reporting (dose-to-water versus dose-to-medium) as well as statistical uncertainties for the calculations arising when Monte Carlo based systems are used in patient dose calculations. All phantoms studied were obtained by CT scan. The calculated dose distributions and monitor units were validated against measurements with film and ionization chambers in phantoms containing two-dimensional (2D) and three-dimensional (3D) type low- and high-density inhomogeneities at different source-to-surface distances. Beam energies ranged from 6 to 18 MeV. New required experimental input data for commissioning are presented. The result of validation shows an excellent agreement between calculated and measured dose distributions. The calculated monitor units were within 2% of measured values except in the case of a 6 MeV beam and small cutout fields at extended SSDs (>110 cm). The investigation on the new issue of dose reporting demonstrates the differences up to 4% for lung and 12% for bone when 'dose-to-medium' is calculated and reported instead of 'dose-to-water' as done in a conventional system. The accuracy of the Monte Carlo calculation is shown to be clinically acceptable even for very complex 3D-type inhomogeneities. As Monte Carlo based treatment planning systems begin to enter clinical practice, new issues, such as dose reporting and statistical variations, may be clinically significant. Therefore it is imperative that a consistent approach to dose reporting is used
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International standards and guidelines for calibrating high-dose dosimetry systems to be used in industrial radiation processing recommend that dose-rate effects on dosimeters be evaluated under conditions of use. This is important when the irradiation relies on high-current electron accelerators, which usually provide very high dose-rates. However, most dosimeter calibration facilities use low-intensity gamma radiation or low-current electron accelerators, which deliver comparatively low dose-rates. Because of issues of thermal conductivity and response, portable calorimeters cannot be practically used with high-current accelerators, where product conveyor speeds under an electron beam can exceed several meters per second and the calorimeter is not suitable for use with product handling systems. As an alternative, Monte Carlo calculations can give theoretical estimates of the absorbed dose in materials with flat or complex configurations such that the results are independent of dose-rate. Monte Carlo results can then be compared to experimental dose determinations to see whether dose-rate effects in the dosimeters are significant. A Monte Carlo code has been used in this study to calculate the absorbed doses in alanine film dosimeters supported by flat sheets of plywood irradiated with electrons using incident energies extending from 1.0 MeV to 10 MeV with beam currents up to 30 mA. The same process conditions have been used for dose determinations with high-current electron beams using low dose-rate gamma calibrated alanine film dosimeters. The close agreement between these calculations and the dosimeter determinations indicates that the response of this type of dosimeter system is independent of the dose-rate, and provides assurance that Monte Carlo calculations can yield results with sufficient accuracy for many industrial applications
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Dimitriadis, A; Gialousis, G; Karlatira, M; Karaiskos, P; Georgiou, E; Yakoumakis, E [Medical Physics Department, Medical School, University of Athens, 75 Mikras Asias Str., Goudi 11527, Athens (Greece); Makri, T; Papaodysseas, S, E-mail: anestisdim@yahoo.com [Radiological Imaging Department, Ag. Sofia Hospital, Lebadias and Thibon, Goudi 11527, Athens (Greece)
2011-01-21
Organ doses are important quantities in assessing the radiation risk. In the case of children, estimation of this risk is of particular concern due to their significant radiosensitivity and the greater health detriment. The purpose of this study is to estimate the organ doses to paediatric patients undergoing barium meal and micturating cystourethrography examinations by clinical measurements and Monte Carlo simulation. In clinical measurements, dose-area products (DAPs) were assessed during examination of 50 patients undergoing barium meal and 90 patients undergoing cystourethrography examinations, separated equally within three age categories: namely newborn, 1 year and 5 years old. Monte Carlo simulation of photon transport in male and female mathematical phantoms was applied using the MCNP5 code in order to estimate the equivalent organ doses. Regarding the micturating cystourethrography examinations, the organs receiving considerable amounts of radiation doses were the urinary bladder (1.87, 2.43 and 4.7 mSv, the first, second and third value in the parentheses corresponds to neonatal, 1 year old and 5 year old patients, respectively), the large intestines (1.54, 1.8, 3.1 mSv), the small intestines (1.34, 1.56, 2.78 mSv), the stomach (1.46, 1.02, 2.01 mSv) and the gall bladder (1.46, 1.66, 2.18 mSv), depending upon the age of the child. Organs receiving considerable amounts of radiation during barium meal examinations were the stomach (9.81, 9.92, 11.5 mSv), the gall bladder (3.05, 5.74, 7.15 mSv), the rib bones (9.82, 10.1, 11.1 mSv) and the pancreas (5.8, 5.93, 6.65 mSv), depending upon the age of the child. DAPs to organ/effective doses conversion factors were derived for each age and examination in order to be compared with other studies.
GPU-based fast Monte Carlo dose calculation for proton therapy
Jia, Xun; Schümann, Jan; Paganetti, Harald; Jiang, Steve B.
2012-12-01
Accurate radiation dose calculation is essential for successful proton radiotherapy. Monte Carlo (MC) simulation is considered to be the most accurate method. However, the long computation time limits it from routine clinical applications. Recently, graphics processing units (GPUs) have been widely used to accelerate computationally intensive tasks in radiotherapy. We have developed a fast MC dose calculation package, gPMC, for proton dose calculation on a GPU. In gPMC, proton transport is modeled by the class II condensed history simulation scheme with a continuous slowing down approximation. Ionization, elastic and inelastic proton nucleus interactions are considered. Energy straggling and multiple scattering are modeled. Secondary electrons are not transported and their energies are locally deposited. After an inelastic nuclear interaction event, a variety of products are generated using an empirical model. Among them, charged nuclear fragments are terminated with energy locally deposited. Secondary protons are stored in a stack and transported after finishing transport of the primary protons, while secondary neutral particles are neglected. gPMC is implemented on the GPU under the CUDA platform. We have validated gPMC using the TOPAS/Geant4 MC code as the gold standard. For various cases including homogeneous and inhomogeneous phantoms as well as a patient case, good agreements between gPMC and TOPAS/Geant4 are observed. The gamma passing rate for the 2%/2 mm criterion is over 98.7% in the region with dose greater than 10% maximum dose in all cases, excluding low-density air regions. With gPMC it takes only 6-22 s to simulate 10 million source protons to achieve ˜1% relative statistical uncertainty, depending on the phantoms and energy. This is an extremely high efficiency compared to the computational time of tens of CPU hours for TOPAS/Geant4. Our fast GPU-based code can thus facilitate the routine use of MC dose calculation in proton therapy.
Jansen, Jan T. M.; Shrimpton, Paul C.
2016-07-01
The ImPACT (imaging performance assessment of CT scanners) CT patient dosimetry calculator is still used world-wide to estimate organ and effective doses (E) for computed tomography (CT) examinations, although the tool is based on Monte Carlo calculations reflecting practice in the early 1990’s. Subsequent developments in CT scanners, definitions of E, anthropomorphic phantoms, computers and radiation transport codes, have all fuelled an urgent need for updated organ dose conversion factors for contemporary CT. A new system for such simulations has been developed and satisfactorily tested. Benchmark comparisons of normalised organ doses presently derived for three old scanners (General Electric 9800, Philips Tomoscan LX and Siemens Somatom DRH) are within 5% of published values. Moreover, calculated normalised values of CT Dose Index for these scanners are in reasonable agreement (within measurement and computational uncertainties of ±6% and ±1%, respectively) with reported standard measurements. Organ dose coefficients calculated for a contemporary CT scanner (Siemens Somatom Sensation 16) demonstrate potential deviations by up to around 30% from the surrogate values presently assumed (through a scanner matching process) when using the ImPACT CT Dosimetry tool for newer scanners. Also, illustrative estimates of E for some typical examinations and a range of anthropomorphic phantoms demonstrate the significant differences (by some 10’s of percent) that can arise when changing from the previously adopted stylised mathematical phantom to the voxel phantoms presently recommended by the International Commission on Radiological Protection (ICRP), and when following the 2007 ICRP recommendations (updated from 1990) concerning tissue weighting factors. Further simulations with the validated dosimetry system will provide updated series of dose coefficients for a wide range of contemporary scanners.
Comparison between Acuros XB and Brainlab Monte Carlo algorithms for photon dose calculation
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Misslbeck, M.; Kneschaurek, P. [Klinikum rechts der Isar der Technischen Univ. Muenchen (Germany). Klinik und Poliklinik fuer Strahlentherapie und Radiologische Onkologie
2012-07-15
Purpose: The Acuros {sup registered} XB dose calculation algorithm by Varian and the Monte Carlo algorithm XVMC by Brainlab were compared with each other and with the well-established AAA algorithm, which is also from Varian. Methods: First, square fields to two different artificial phantoms were applied: (1) a 'slab phantom' with a 3 cm water layer, followed by a 2 cm bone layer, a 7 cm lung layer, and another 18 cm water layer and (2) a 'lung phantom' with water surrounding an eccentric lung block. For the slab phantom, depth-dose curves along central beam axis were compared. The lung phantom was used to compare profiles at depths of 6 and 14 cm. As clinical cases, the CTs of three different patients were used. The original AAA plans with all three algorithms using open fields were recalculated. Results: There were only minor differences between Acuros and XVMC in all artificial phantom depth doses and profiles; however, this was different for AAA, which had deviations of up to 13% in depth dose and a few percent for profiles in the lung phantom. These deviations did not translate into the clinical cases, where the dose-volume histograms of all algorithms were close to each other for open fields. Conclusion: Only within artificial phantoms with clearly separated layers of simulated tissue does AAA show differences at layer boundaries compared to XVMC or Acuros. In real patient CTs, these differences in the dose-volume histogram of the planning target volume were not observed. (orig.)
The use of Monte Carlo technique to optimize the dose distribution in total skin irradiation
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Cutaneous T-cell lymphoma (Mycosis Fungoides) is an indolent disease with a low percentage of cure. The total skin irradiation with electron beam became an efficient treatment of mycosis fungoides with curative intention, with success in almost 40% of the patients. The classical technique was developed in Stanford, where patients are irradiated in all longitudinal extension. Two angled fields of about 20 degrees are used, above and below the horizontal line, passing through from the waistline of the patient on foot, distant 3 meters from the focus. During the treatment, 4 or 6 pairs of these beams irradiate the patient; being rotated 90 or 60 degrees on his longitudinal axis, respectively. The energy normally used is about 3-7 MeV. The determination of the dose distribution in the patient can be made in many different ways: using three parallel-plate ionization chambers (Victoreen-Holt plus CNMC 206 electrometer) in the air, using dosimetric films and others. In the first case, at least three ionization chambers are necessary, which is unusual in Brazilian hospitals. In the second case, a lot of dosimetric films are necessary, which is too expensive. In this work, we propose the use of the Monte Carlo technique to simulate the dose distribution in the patients during Total Skin Irradiation treatments. The Monte Carlo code used is the MCNP4B, a well known and established code used to perform the transport of electrons, photons and neutrons through matter, especially in reactor physics, but with increasing utilization in medical physics in recent years. The goals of our work is to simulate different angles between each beam with a fixed treatment distance, which is characteristic of each treatment room, in order to obtain a uniform dose distribution in the patient. (author)
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Highlights: • Pu-239 based spectral history method was tested on 3D BWR single assembly case. • Burnup of a BWR fuel assembly was performed with the nodal code DYN3D. • Reference solution was obtained by coupled Monte-Carlo thermal-hydraulic code BGCore. • The proposed method accurately reproduces moderator density history effect for BWR test case. - Abstract: This research focuses on the verification of a recently developed methodology accounting for spectral history effects in 3D full core nodal simulations. The traditional deterministic core simulation procedure includes two stages: (1) generation of homogenized macroscopic cross section sets and (2) application of these sets to obtain a full 3D core solution with nodal codes. The standard approach adopts the branch methodology in which the branches represent all expected combinations of operational conditions as a function of burnup (main branch). The main branch is produced for constant, usually averaged, operating conditions (e.g. coolant density). As a result, the spectral history effects that associated with coolant density variation are not taken into account properly. Number of methods to solve this problem (such as micro-depletion and spectral indexes) were developed and implemented in modern nodal codes. Recently, we proposed a new and robust method to account for history effects. The methodology was implemented in DYN3D and involves modification of the few-group cross section sets. The method utilizes the local Pu-239 concentration as an indicator of spectral history. The method was verified for PWR and VVER applications. However, the spectrum variation in BWR core is more pronounced due to the stronger coolant density change. The purpose of the current work is investigating the applicability of the method to BWR analysis. The proposed methodology was verified against recently developed BGCore system, which couples Monte Carlo neutron transport with depletion and thermal-hydraulic solvers and
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There is renewed interest in film dosimetry for the verification of dose delivery of complex treatments, particularly small fields, compared to treatment planning system calculations. A new radiochromic film, Gafchromic EBT-XD, is available for high-dose treatment verification and we present the first published evaluation of its use. We evaluate the new film for MV photon dosimetry, including calibration curves, performance with single- and triple-channel dosimetry, and comparison to existing EBT3 film. In the verification of a typical 25 Gy stereotactic radiotherapy (SRS) treatment, compared to TPS planned dose distribution, excellent agreement was seen with EBT-XD using triple-channel dosimetry, in isodose overlay, maximum 1.0 mm difference over 200–2400 cGy, and gamma evaluation, mean passing rate 97% at 3% locally-normalised, 1.5 mm criteria. In comparison to EBT3, EBT-XD gave improved evaluation results for the SRS-plan, had improved calibration curve gradients at high doses, and had reduced lateral scanner effect. The dimensions of the two films are identical. The optical density of EBT-XD is lower than EBT3 for the same dose. The effective atomic number for both may be considered water-equivalent in MV radiotherapy. We have validated the use of EBT-XD for high-dose, small-field radiotherapy, for routine QC and a forthcoming multi-centre SRS dosimetry intercomparison. (paper)
Development and application of a dose verification tool using a small field model for TomoTherapy
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Helical TomoTherapy registered is a radiation delivery technique that uses the superposition of many small fields to precisely deliver the prescribed dose to the patient. This work presents a dose verification tool that can be used as part of a quality assurance program for a tomotherapy system. This tool is based on a small field model that takes into account the two main effects that influence the dose distribution in small fields: the extended shape of the radiation source and the loss of lateral charged particle equilibrium (CPE) within the field. The dose verification tool was implemented for simple beam configurations and used to study the influence of temporal beam parameter variations on the delivered dose. After comparing measured and calculated output factors (OFs) and dose profiles for different field configurations, it was found that they agree well to within the globally-defined gamma acceptance criteria of 2%/2mm. The study demonstrated that none of the studied systematic and random variations applied resulted in failed gamma scores using gamma acceptance criteria of 3%/3mm. The developed model implemented in the verification tool allows to evaluate the performance of devices applying narrow photon beams in the treatment delivery and, in particular, to evaluate the delivery performance of a tomotherapy unit.
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. Dose volume histogram (DVH) analyses revealed much smoother DVH curves for the dual resolution sandwich phantom when compared to the SR phantom. In conclusion, MBMC simulations using a dual resolution sandwich phantom improved simulation spatial resolution for skull base IMRS therapy. More detailed dose analyses for small critical structures can be made available to help in clinical judgment. - Highlights: • The measurement-based Monte Carlo (MBMC) simulation can serve as a standard reference for dose verification in intensity-modulated radiosurgery. • This study is the first in literature to describe a dual resolution sandwich phantom for Monte Carlo simulation. • MBMC simulation using the sandwich phantom revealed more dose distribution details for small volume critical organs. • MBMC simulation using the sandwich phantom detected significant dose differences in small organs of the inner ear
Evaluation of an electron Monte Carlo dose calculation algorithm for treatment planning.
Chamberland, Eve; Beaulieu, Luc; Lachance, Bernard
2015-01-01
The purpose of this study is to evaluate the accuracy of the electron Monte Carlo (eMC) dose calculation algorithm included in a commercial treatment planning system and compare its performance against an electron pencil beam algorithm. Several tests were performed to explore the system's behavior in simple geometries and in configurations encountered in clinical practice. The first series of tests were executed in a homogeneous water phantom, where experimental measurements and eMC-calculated dose distributions were compared for various combinations of energy and applicator. More specifically, we compared beam profiles and depth-dose curves at different source-to-surface distances (SSDs) and gantry angles, by using dose difference and distance to agreement. Also, we compared output factors, we studied the effects of algorithm input parameters, which are the random number generator seed, as well as the calculation grid size, and we performed a calculation time evaluation. Three different inhomogeneous solid phantoms were built, using high- and low-density materials inserts, to clinically simulate relevant heterogeneity conditions: a small air cylinder within a homogeneous phantom, a lung phantom, and a chest wall phantom. We also used an anthropomorphic phantom to perform comparison of eMC calculations to measurements. Finally, we proceeded with an evaluation of the eMC algorithm on a clinical case of nose cancer. In all mentioned cases, measurements, carried out by means of XV-2 films, radiographic films or EBT2 Gafchromic films. were used to compare eMC calculations with dose distributions obtained from an electron pencil beam algorithm. eMC calculations in the water phantom were accurate. Discrepancies for depth-dose curves and beam profiles were under 2.5% and 2 mm. Dose calculations with eMC for the small air cylinder and the lung phantom agreed within 2% and 4%, respectively. eMC calculations for the chest wall phantom and the anthropomorphic phantom also
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The aim of this study was to validate the computed tomography dose index (CTDI) and organ doses evaluated by Monte Carlo simulations through comparisons with doses evaluated by in-phantom dosimetry. Organ doses were measured with radio-photoluminescence glass dosemeter (RGD) set at various organ positions within adult and 1-y-old anthropomorphic phantoms. For the dose simulations, the X-ray spectrum and bow-tie filter shape of a CT scanner were estimated and 3D voxelised data of the CTDI and anthropomorphic phantoms from the acquired CT images were derived. Organ dose simulations and measurements were performed with chest and abdomen -pelvis CT examination scan parameters. Relative differences between the simulated and measured doses were within 5 % for the volume CTDI and 13 % for organ doses for organs within the scan range in adult and paediatric CT examinations. The simulation results were considered to be in good agreement with the measured doses. (authors)
Fujii, K; Nomura, K; Muramatsu, Y; Takahashi, K; Obara, S; Akahane, K; Satake, M
2015-07-01
The aim of this study was to validate the computed tomography dose index (CTDI) and organ doses evaluated by Monte Carlo simulations through comparisons with doses evaluated by in-phantom dosimetry. Organ doses were measured with radio-photoluminescence glass dosemeter (RGD) set at various organ positions within adult and 1-y-old anthropomorphic phantoms. For the dose simulations, the X-ray spectrum and bow-tie filter shape of a CT scanner were estimated and 3D voxelised data of the CTDI and anthropomorphic phantoms from the acquired CT images were derived. Organ dose simulations and measurements were performed with chest and abdomen-pelvis CT examination scan parameters. Relative differences between the simulated and measured doses were within 5 % for the volume CTDI and 13 % for organ doses for organs within the scan range in adult and paediatric CT examinations. The simulation results were considered to be in good agreement with the measured doses. PMID:25848103
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To investigate the radiation dose to the fetus using retrospective tube current modulation (TCM) data selected from archived clinical records. This paper describes the calculation of fetal doses using retrospective TCM data and Monte Carlo (MC) simulations. Three TCM schemes were adopted for use with three pregnant patient phantoms. MC simulations were used to model CT scanners, TCM schemes and pregnant patients. Comparisons between organ doses from TCM schemes and those from non-TCM schemes show that these three TCM schemes reduced fetal doses by 14, 18 and 25 %, respectively. These organ doses were also compared with those from ImPACT calculation. It is found that the difference between the calculated fetal dose and the ImPACT reported dose is as high as 46 %. This work demonstrates methods to study organ doses from various TCM protocols and potential ways to improve the accuracy of CT dose calculation for pregnant patients. (authors)
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The treatment planning systems (T.P.S.) occupy a key position in the radiotherapy service: they realize the projected calculation of the dose distribution and the treatment duration. Traditionally, the quality control of the calculated distribution doses relies on their comparisons with dose distributions measured under the device of treatment. This thesis proposes to substitute these dosimetry measures to the profile of reference dosimetry calculations got by the Penelope Monte-Carlo code. The Monte-Carlo simulations give a broad choice of test configurations and allow to envisage a quality control of dosimetry aspects of T.P.S. without monopolizing the treatment devices. This quality control, based on the Monte-Carlo simulations has been tested on a clinical T.P.S. and has allowed to simplify the quality procedures of the T.P.S.. This quality control, in depth, more precise and simpler to implement could be generalized to every center of radiotherapy. (N.C.)
A virtual photon energy fluence model for Monte Carlo dose calculation
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The presented virtual energy fluence (VEF) model of the patient-independent part of the medical linear accelerator heads, consists of two Gaussian-shaped photon sources and one uniform electron source. The planar photon sources are located close to the bremsstrahlung target (primary source) and to the flattening filter (secondary source), respectively. The electron contamination source is located in the plane defining the lower end of the filter. The standard deviations or widths and the relative weights of each source are free parameters. Five other parameters correct for fluence variations, i.e., the horn or central depression effect. If these parameters and the field widths in the X and Y directions are given, the corresponding energy fluence distribution can be calculated analytically and compared to measured dose distributions in air. This provides a method of fitting the free parameters using the measurements for various square and rectangular fields and a fixed number of monitor units. The next step in generating the whole set of base data is to calculate monoenergetic central axis depth dose distributions in water which are used to derive the energy spectrum by deconvolving the measured depth dose curves. This spectrum is also corrected to take the off-axis softening into account. The VEF model is implemented together with geometry modules for the patient specific part of the treatment head (jaws, multileaf collimator) into the XVMC dose calculation engine. The implementation into other Monte Carlo codes is possible based on the information in this paper. Experiments are performed to verify the model by comparing measured and calculated dose distributions and output factors in water. It is demonstrated that open photon beams of linear accelerators from two different vendors are accurately simulated using the VEF model. The commissioning procedure of the VEF model is clinically feasible because it is based on standard measurements in air and water. It is
Dosimetric validation of Acuros XB with Monte Carlo methods for photon dose calculations
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Purpose: The dosimetric accuracy of the recently released Acuros XB advanced dose calculation algorithm (Varian Medical Systems, Palo Alto, CA) is investigated for single radiation fields incident on homogeneous and heterogeneous geometries, and a comparison is made to the analytical anisotropic algorithm (AAA). Methods: Ion chamber measurements for the 6 and 18 MV beams within a range of field sizes (from 4.0x4.0 to 30.0x30.0 cm2) are used to validate Acuros XB dose calculations within a unit density phantom. The dosimetric accuracy of Acuros XB in the presence of lung, low-density lung, air, and bone is determined using BEAMnrc/DOSXYZnrc calculations as a benchmark. Calculations using the AAA are included for reference to a current superposition/convolution standard. Results: Basic open field tests in a homogeneous phantom reveal an Acuros XB agreement with measurement to within ±1.9% in the inner field region for all field sizes and energies. Calculations on a heterogeneous interface phantom were found to agree with Monte Carlo calculations to within ±2.0%(σMC=0.8%) in lung (ρ=0.24 g cm-3) and within ±2.9%(σMC=0.8%) in low-density lung (ρ=0.1 g cm-3). In comparison, differences of up to 10.2% and 17.5% in lung and low-density lung were observed in the equivalent AAA calculations. Acuros XB dose calculations performed on a phantom containing an air cavity (ρ=0.001 g cm-3) were found to be within the range of ±1.5% to ±4.5% of the BEAMnrc/DOSXYZnrc calculated benchmark (σMC=0.8%) in the tissue above and below the air cavity. A comparison of Acuros XB dose calculations performed on a lung CT dataset with a BEAMnrc/DOSXYZnrc benchmark shows agreement within ±2%/2mm and indicates that the remaining differences are primarily a result of differences in physical material assignments within a CT dataset. Conclusions: By considering the fundamental particle interactions in matter based on theoretical interaction cross sections, the Acuros XB algorithm is
Koger, B.; Kirkby, C.
2016-03-01
Gold nanoparticles (GNPs) have shown potential in recent years as a means of therapeutic dose enhancement in radiation therapy. However, a major challenge in moving towards clinical implementation is the exact characterisation of the dose enhancement they provide. Monte Carlo studies attempt to explore this property, but they often face computational limitations when examining macroscopic scenarios. In this study, a method of converting dose from macroscopic simulations, where the medium is defined as a mixture containing both gold and tissue components, to a mean dose-to-tissue on a microscopic scale was established. Monte Carlo simulations were run for both explicitly-modeled GNPs in tissue and a homogeneous mixture of tissue and gold. A dose ratio was obtained for the conversion of dose scored in a mixture medium to dose-to-tissue in each case. Dose ratios varied from 0.69 to 1.04 for photon sources and 0.97 to 1.03 for electron sources. The dose ratio is highly dependent on the source energy as well as GNP diameter and concentration, though this effect is less pronounced for electron sources. By appropriately weighting the monoenergetic dose ratios obtained, the dose ratio for any arbitrary spectrum can be determined. This allows complex scenarios to be modeled accurately without explicitly simulating each individual GNP.
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The purpose of this study was to evaluate organ doses for individual patients undergoing interventional transcatheter arterial embolization (TAE) for hepatocellular carcinoma (HCC) using measurement-based Monte Carlo simulation and adaptive organ segmentation. Five patients were enrolled in this study after institutional ethical approval and informed consent. Gafchromic XR-RV3 films were used to measure entrance surface dose to reconstruct the nonuniform fluence distribution field as the input data in the Monte Carlo simulation. XR-RV3 films were used to measure entrance surface doses due to their lower energy dependence compared with that of XR-RV2 films. To calculate organ doses, each patient's three-dimensional dose distribution was incorporated into CT DICOM images with image segmentation using thresholding and k-means clustering. Organ doses for all patients were estimated. Our dose evaluation system not only evaluated entrance surface doses based on measurements, but also evaluated the 3D dose distribution within patients using simulations. When film measurements were unavailable, the peak skin dose (between 0.68 and 0.82 of a fraction of the cumulative dose) can be calculated from the cumulative dose obtained from TAE dose reports. Successful implementation of this dose evaluation system will aid radiologists and technologists in determining the actual dose distributions within patients undergoing TAE. - Highlights: • An organ dose evaluation system for interventional procedures was successfully established. • Response variation of XR-RV3 due to energy dependence was 2.7%. • Three-dimensional image segmentations utilize thresholding and k-means clustering. • Peak skin doses are the fractions from 0.68 to 0.82 of cumulated doses for interventional TAE of HCC
Tian, Zhen; Folkerts, Michael; Shi, Feng; Jiang, Steve B; Jia, Xun
2015-01-01
Monte Carlo (MC) simulation is considered as the most accurate method for radiation dose calculations. Accuracy of a source model for a linear accelerator is critical for the overall dose calculation accuracy. In this paper, we presented an analytical source model that we recently developed for GPU-based MC dose calculations. A key concept called phase-space-ring (PSR) was proposed. It contained a group of particles that are of the same type and close in energy and radial distance to the center of the phase-space plane. The model parameterized probability densities of particle location, direction and energy for each primary photon PSR, scattered photon PSR and electron PSR. For a primary photon PSRs, the particle direction is assumed to be from the beam spot. A finite spot size is modeled with a 2D Gaussian distribution. For a scattered photon PSR, multiple Gaussian components were used to model the particle direction. The direction distribution of an electron PSRs was also modeled as a 2D Gaussian distributi...
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The purpose of this work was to study and quantify the differences in dose distributions computed with some of the newest dose calculation algorithms available in commercial planning systems. The study was done for clinical cases originally calculated with pencil beam convolution (PBC) where large density inhomogeneities were present. Three other dose algorithms were used: a pencil beam like algorithm, the anisotropic analytic algorithm (AAA), a convolution superposition algorithm, collapsed cone convolution (CCC), and a Monte Carlo program, voxel Monte Carlo (VMC++). The dose calculation algorithms were compared under static field irradiations at 6 MV and 15 MV using multileaf collimators and hard wedges where necessary. Five clinical cases were studied: three lung and two breast cases. We found that, in terms of accuracy, the CCC algorithm performed better overall than AAA compared to VMC++, but AAA remains an attractive option for routine use in the clinic due to its short computation times. Dose differences between the different algorithms and VMC++ for the median value of the planning target volume (PTV) were typically 0.4% (range: 0.0 to 1.4%) in the lung and -1.3% (range: -2.1 to -0.6%) in the breast for the few cases we analysed. As expected, PTV coverage and dose homogeneity turned out to be more critical in the lung than in the breast cases with respect to the accuracy of the dose calculation. This was observed in the dose volume histograms obtained from the Monte Carlo simulations
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The purpose of this work was to study and quantify the differences in dose distributions computed with some of the newest dose calculation algorithms available in commercial planning systems. The study was done for clinical cases where large density inhomogeneities were present. Three dose algorithms were used: a pencil beam like algorithm, the anisotropic analytic algorithm (AAA), a convolution superposition algorithm, collapsed cone convolution (CCC) and a Monte Carlo program, voxel Monte Carlo (VMC++). The dose calculation algorithms were compared under static field irradiations at 6 MV and 15 MV using multileaf collimators and hard wedges where necessary. Five clinical cases were studied: three lung and two breast cases. We found that the CCC algorithm performed overall better than AAA compared to VMC++, but AAA remains an attractive option for routine use in the clinic due to its short computation times. Dose differences between the different algorithms for the median value of the planning target volume (PTV) were typically 0.4% (range: 0.0-1.4%) in the lung and -1.3% (range: -2.1--0.6%) in the breast for the few cases we analysed. As expected, PTV coverage and dose homogeneity turned out to be more critical in the lung than in the breast cases with respect to the accuracy of the dose calculation. This was observed in the dose volume histograms obtained from the Monte Carlo simulations
Zhang, Aizhen; Wen, Ning; Nurushev, Teamour; Burmeister, Jay; Chetty, Indrin J
2013-01-01
A commercial electron Monte Carlo (eMC) dose calculation algorithm has become available in Eclipse treatment planning system. The purpose of this work was to evaluate the eMC algorithm and investigate the clinical implementation of this system. The beam modeling of the eMC algorithm was performed for beam energies of 6, 9, 12, 16, and 20 MeV for a Varian Trilogy and all available applicator sizes in the Eclipse treatment planning system. The accuracy of the eMC algorithm was evaluated in a homogeneous water phantom, solid water phantoms containing lung and bone materials, and an anthropomorphic phantom. In addition, dose calculation accuracy was compared between pencil beam (PB) and eMC algorithms in the same treatment planning system for heterogeneous phantoms. The overall agreement between eMC calculations and measurements was within 3%/2 mm, while the PB algorithm had large errors (up to 25%) in predicting dose distributions in the presence of inhomogeneities such as bone and lung. The clinical implementation of the eMC algorithm was investigated by performing treatment planning for 15 patients with lesions in the head and neck, breast, chest wall, and sternum. The dose distributions were calculated using PB and eMC algorithms with no smoothing and all three levels of 3D Gaussian smoothing for comparison. Based on a routine electron beam therapy prescription method, the number of eMC calculated monitor units (MUs) was found to increase with increased 3D Gaussian smoothing levels. 3D Gaussian smoothing greatly improved the visual usability of dose distributions and produced better target coverage. Differences of calculated MUs and dose distributions between eMC and PB algorithms could be significant when oblique beam incidence, surface irregularities, and heterogeneous tissues were present in the treatment plans. In our patient cases, monitor unit differences of up to 7% were observed between PB and eMC algorithms. Monitor unit calculations were also preformed
Patient-specific Monte Carlo dose calculations for 103Pd breast brachytherapy
Miksys, N.; Cygler, J. E.; Caudrelier, J. M.; Thomson, R. M.
2016-04-01
This work retrospectively investigates patient-specific Monte Carlo (MC) dose calculations for 103Pd permanent implant breast brachytherapy, exploring various necessary assumptions for deriving virtual patient models: post-implant CT image metallic artifact reduction (MAR), tissue assignment schemes (TAS), and elemental tissue compositions. Three MAR methods (thresholding, 3D median filter, virtual sinogram) are applied to CT images; resulting images are compared to each other and to uncorrected images. Virtual patient models are then derived by application of different TAS ranging from TG-186 basic recommendations (mixed adipose and gland tissue at uniform literature-derived density) to detailed schemes (segmented adipose and gland with CT-derived densities). For detailed schemes, alternate mass density segmentation thresholds between adipose and gland are considered. Several literature-derived elemental compositions for adipose, gland and skin are compared. MC models derived from uncorrected CT images can yield large errors in dose calculations especially when used with detailed TAS. Differences in MAR method result in large differences in local doses when variations in CT number cause differences in tissue assignment. Between different MAR models (same TAS), PTV {{D}90} and skin {{D}1~\\text{c{{\\text{m}}3}}} each vary by up to 6%. Basic TAS (mixed adipose/gland tissue) generally yield higher dose metrics than detailed segmented schemes: PTV {{D}90} and skin {{D}1~\\text{c{{\\text{m}}3}}} are higher by up to 13% and 9% respectively. Employing alternate adipose, gland and skin elemental compositions can cause variations in PTV {{D}90} of up to 11% and skin {{D}1~\\text{c{{\\text{m}}3}}} of up to 30%. Overall, AAPM TG-43 overestimates dose to the PTV ({{D}90} on average 10% and up to 27%) and underestimates dose to the skin ({{D}1~\\text{c{{\\text{m}}3}}} on average 29% and up to 48%) compared to the various MC models derived using the post-MAR CT images studied
Monte Carlo dose calculation using a cell processor based PlayStation 3 system
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This study investigates the performance of the EGSnrc computer code coupled with a Cell-based hardware in Monte Carlo simulation of radiation dose in radiotherapy. Performance evaluations of two processor-intensive functions namely, HOWNEAR and RANMARGET in the EGSnrc code were carried out basing on the 20-80 rule (Pareto principle). The execution speeds of the two functions were measured by the profiler gprof specifying the number of executions and total time spent on the functions. A testing architecture designed for Cell processor was implemented in the evaluation using a PlayStation3 (PS3) system. The evaluation results show that the algorithms examined are readily parallelizable on the Cell platform, provided that an architectural change of the EGSnrc was made. However, as the EGSnrc performance was limited by the PowerPC Processing Element in the PS3, PC coupled with graphics processing units or GPCPU may provide a more viable avenue for acceleration.
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Isotope production and Application Division of Bhabha Atomic Research Center developed 32P patch sources for treatment of superficial tumors. Surface dose rate of a newly developed 32P patch source of nominal diameter 25 mm was measured experimentally using standard extrapolation ionization chamber and Gafchromic EBT film. Monte Carlo model of the 32P patch source along with the extrapolation chamber was also developed to estimate the surface dose rates from these sources. The surface dose rates to tissue (cGy/min) measured using extrapolation chamber and radiochromic films are 82.03±4.18 (k=2) and 79.13±2.53 (k=2) respectively. The two values of the surface dose rates measured using the two independent experimental methods are in good agreement to each other within a variation of 3.5%. The surface dose rate to tissue (cGy/min) estimated using the MCNP Monte Carlo code works out to be 77.78±1.16 (k=2). The maximum deviation between the surface dose rates to tissue obtained by Monte Carlo and the extrapolation chamber method is 5.2% whereas the difference between the surface dose rates obtained by radiochromic film measurement and the Monte Carlo simulation is 1.7%. The three values of the surface dose rates of the 32P patch source obtained by three independent methods are in good agreement to one another within the uncertainties associated with their measurements and calculation. This work has demonstrated that MCNP based electron transport simulations are accurate enough for determining the dosimetry parameters of the indigenously developed 32P patch sources for contact brachytherapy applications. - Highlights: • Surface dose rates of 25 mm nominal diameter newly developed 32P patch sources were measured experimentally using extrapolation chamber and Gafchromic EBT2 film. Monte Carlo model of the 32P patch source along with the extrapolation chamber was also developed. • The surface dose rates to tissue (cGy/min) measured using extrapolation chamber and
Shin, Wook-Geun; Shin, Jae-Ik; Jeong, Jong Hwi; Lee, Se Byeong
2015-01-01
For the in vivo range verification in proton therapy, it has been tried to measure the spatial distribution of the prompt gammas generated by the proton-induced interactions with the close relationship with the proton dose distribution. However, the high energy of the prompt gammas and background gammas are still problematic in measuring the distribution. In this study, we suggested a new method determining the in vivo range by utilizing the time structure of the prompt gammas formed with the rotation of a range modulation wheel (RMW) in the passive scattering proton therapy. To validate the Monte Carlo code simulating the proton beam nozzle, axial percent depth doses (PDDs) were compared with the measured PDDs with the varying beam range of 4.73-24.01 cm. And the relationship between the proton dose rate and the time structure of the prompt gammas was assessed and compared in the water phantom. The results of the PDD showed accurate agreement within the relative errors of 1.1% in the distal range and 2.9% in...
Longo, Mariaconcetta; Marchioni, Chiara; Insero, Teresa; Donnarumma, Raffaella; D'Adamo, Alessandro; Lucatelli, Pierleone; Fanelli, Fabrizio; Salvatori, Filippo Maria; Cannavale, Alessandro; Di Castro, Elisabetta
2016-03-01
This study evaluates X-ray exposure in patient undergoing abdominal extra-vascular interventional procedures by means of Digital Imaging and COmmunications in Medicine (DICOM) image headers and Monte Carlo simulation. The main aim was to assess the effective and equivalent doses, under the hypothesis of their correlation with the dose area product (DAP) measured during each examination. This allows to collect dosimetric information about each patient and to evaluate associated risks without resorting to in vivo dosimetry. The dose calculation was performed in 79 procedures through the Monte Carlo simulator PCXMC (A PC-based Monte Carlo program for calculating patient doses in medical X-ray examinations), by using the real geometrical and dosimetric irradiation conditions, automatically extracted from DICOM headers. The DAP measurements were also validated by using thermoluminescent dosemeters on an anthropomorphic phantom. The expected linear correlation between effective doses and DAP was confirmed with an R(2) of 0.974. Moreover, in order to easily calculate patient doses, conversion coefficients that relate equivalent doses to measurable quantities, such as DAP, were obtained. PMID:26211013
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This study evaluates X-ray exposure in patient undergoing abdominal extra-vascular interventional procedures by means of Digital Imaging and Communications in Medicine (DICOM) image headers and Monte Carlo simulation. The main aim was to assess the effective and equivalent doses, under the hypothesis of their correlation with the dose area product (DAP) measured during each examination. This allows to collect dosimetric information about each patient and to evaluate associated risks without resorting to in vivo dosimetry. The dose calculation was performed in 79 procedures through the Monte Carlo simulator PCXMC (A PC-based Monte Carlo program for calculating patient doses in medical X-ray examinations), by using the real geometrical and dosimetric irradiation conditions, automatically extracted from DICOM headers. The DAP measurements were also validated by using thermoluminescent dosemeters on an anthropomorphic phantom. The expected linear correlation between effective doses and DAP was confirmed with an R2 of 0.974. Moreover, in order to easily calculate patient doses, conversion coefficients that relate equivalent doses to measurable quantities, such as DAP, were obtained. (authors)
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To propose and evaluate a method for the central axis dose verification in patients treated with total body irradiation (TBI) of photons using images obtained through a Computed Radiography (CR) system. It was used the Computed Radiography (Fuji) portal imaging cassette readings and correlate with measured of absorbed dose in water using 10 x 10 irradiation fields with ionization chamber in the 60Co equipment. The analytical and graphic expression is obtained through software 'Origin8', the TBI patient portal verification images were processed using software ImageJ, to obtain the patient dose. To validate the results, the absorbed dose in RW3 models was measured with ionization chamber with different thickness, simulating TBI real conditions. Finally it was performed a retrospective study over the last 4 years obtaining the patients absorbed dose based on the reading in the image and comparing with the planned dose. The analytical equation obtained permits estimate the absorbed dose using image pixel value and the dose measured with ionization chamber and correlated with patient clinical records. Those results are compared with reported evidence obtaining a difference less than 02%, the 3 methods were compared and the results are within 10%. (Author)
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We evaluated the Monte Carlo Monaco Planner v2.0.3 by planners of the SEFM Protocol [1] to the modeling of the photon beam of 6 MV of a linear accelerator Elekta Synergy with collimator MLC Beam Modulator. We compare the Monte Carlo calculation with profiles on water measurement DFS = 100 cm, absorbed dose and dose levels for rectangular, asymmetric fields and different DFS. We compare the results with those obtained with the algorithm Collapsed Cone of Pinnacle Scheduler v8.0m. (Author)
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Iqbal Al Amri
2012-01-01
Full Text Available Inversely planned intensity-modulated radiotherapy (IMRT and stereotactic small field radiotherapy should be verified before treatment execution. A second verification is carried out for planned treatments in IMRT and 3D conformal radiotherapy (3D-CRT using a monitor verification commercial dose calculation management software (DCMS. For the same reference point the ion-chamber measured doses are compared for IMRT plans. DCMS (Diamond computes dose based on modified Clarkson integration, accounting for multi-leaf collimators (MLC transmission and measured collimator scatter factors. DCMS was validated with treatment planning system (TPS (Eclipse 6.5 Version, Varian, USA separately. Treatment plans computed from TPS are exported to DCMS using DICOM interface. Doses are re-calculated at selected points for fields delivered to IMRT phantom (IBA Scanditronix Wellhofer in high-energy linac (Clinac 2300 CD, Varian. Doses measured at central axis, for the same points using CC13 (0.13 cc ion chamber with Dose 1 Electrometer (Scanditronix Wellhofer are compared with calculated data on DCMS and TPS. The data of 53 IMRT patients with fields ranging from 5 to 9 are reported. The computed dose for selected monitor units (MU by Diamond showed good agreement with planned doses by TPS. DCMS dose prediction matched well in 3D-CRT forward plans (0.8 ± 1.3%, n = 37 and in IMRT inverse plans (−0.1 ± 2.2%, n = 37. Ion chamber measurements agreed well with Eclipse planned doses (−2.1 ± 2.0%, n = 53 and re-calculated DCMS doses (−1.5 ± 2.6%, n = 37 in phantom. DCMS dose validation is in reasonable agreement with TPS. DCMS calculations corroborate well with ionometric measured doses in most of the treatment plans.
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Purpose: The objective of this work is to assess the sensitivity of Monte Carlo (MC) dose calculations to uncertainties in human tissue composition for a range of low photon energy brachytherapy sources: 125I, 103Pd, 131Cs, and an electronic brachytherapy source (EBS). The low energy photons emitted by these sources make the dosimetry sensitive to variations in tissue atomic number due to the dominance of the photoelectric effect. This work reports dose to a small mass of water in medium Dw,m as opposed to dose to a small mass of medium in medium Dm,m. Methods: Mean adipose, mammary gland, and breast tissues (as uniform mixture of the aforementioned tissues) are investigated as well as compositions corresponding to one standard deviation from the mean. Prostate mean compositions from three different literature sources are also investigated. Three sets of MC simulations are performed with the GEANT4 code: (1) Dose calculations for idealized TG-43-like spherical geometries using point sources. Radial dose profiles obtained in different media are compared to assess the influence of compositional uncertainties. (2) Dose calculations for four clinical prostate LDR brachytherapy permanent seed implants using 125I seeds (Model 2301, Best Medical, Springfield, VA). The effect of varying the prostate composition in the planning target volume (PTV) is investigated by comparing PTV D90 values. (3) Dose calculations for four clinical breast LDR brachytherapy permanent seed implants using 103Pd seeds (Model 2335, Best Medical). The effects of varying the adipose/gland ratio in the PTV and of varying the elemental composition of adipose and gland within one standard deviation of the assumed mean composition are investigated by comparing PTV D90 values. For (2) and (3), the influence of using the mass density from CT scans instead of unit mass density is also assessed. Results: Results from simulation (1) show that variations in the mean compositions of tissues affect low energy
Choi, Chang Heon; Jung, Seongmoon; Choi, Kanghyuk; Son, Kwang-Jae; Lee, Jun Sig; Ye, Sung-Joon
2016-04-01
This study aims to determine the activity of a sealed pure beta-source by measuring the surface dose rate using an extrapolation chamber. A conversion factor (cGy s-1 Bq-1), which was defined as the ratio of surface dose rate to activity, can be calculated by Monte Carlo simulations of the extrapolation chamber measurement. To validate this hypothesis the certified activities of two standard pure beta-sources of Sr/Y-90 and Si/P-32 were compared with those determined by this method. In addition, a sealed test source of Sr/Y-90 was manufactured by the HANARO reactor group of KAERI (Korea Atomic Energy Research Institute) and used to further validate this method. The measured surface dose rates of the Sr/Y-90 and Si/P-32 standard sources were 4.615×10-5 cGy s-1 and 2.259×10-5 cGy s-1, respectively. The calculated conversion factors of the two sources were 1.213×10-8 cGy s-1 Bq-1 and 1.071×10-8 cGy s-1 Bq-1, respectively. Therefore, the activity of the standard Sr/Y-90 source was determined to be 3.995 kBq, which was 2.0% less than the certified value (4.077 kBq). For Si/P-32 the determined activity was 2.102 kBq, which was 6.6% larger than the certified activity (1.971 kBq). The activity of the Sr/Y-90 test source was determined to be 4.166 kBq, while the apparent activity reported by KAERI was 5.803 kBq. This large difference might be due to evaporation and diffusion of the source liquid during preparation and uncertainty in the amount of weighed aliquot of source liquid. The overall uncertainty involved in this method was determined to be 7.3%. We demonstrated that the activity of a sealed pure beta-source could be conveniently determined by complementary combination of measuring the surface dose rate and Monte Carlo simulations.
2010-01-01
Purpose: To investigate the clinical usage of dose verification of Helical Tomotherapy plans by using 2D-array ion chambers, and to develop an efficient way to validate the dose delivered for the patients during treatments. Materials and Methods: A pixel-segmented ionisation chamber device, IMRT MatriXX™ and Multicube™ phantom from IBA were used on ten selected Tomotherapy IMRT/IGRT head and neck plans in this study. The combined phantom was set up to measure the dose distribution from corona...
Preliminary studies of PQS PET detector module for dose verification of carbon beam therapy
Kim, H.-I.; An, S. Jung; Lee, C. Y.; Jo, W. J.; Min, E.; Lee, K.; Kim, Y.; Joung, J.; Chung, Y. H.
2014-05-01
PET imaging can be used to verify dose distributions of therapeutic particle beams such as carbon ion beams. The purpose of this study was to develop a PET detector module which was designed for an in-beam PET scanner geometry integrated into a carbon beam therapy system, and to evaluate its feasibility as a monitoring system of patient dose distribution. A C-shaped PET geometry was proposed to avoid blockage of the carbon beam by the detector modules. The proposed PET system consisted of 14 detector modules forming a bore with 30.2 cm inner diameter for brain imaging. Each detector module is composed of a 9 × 9 array of 4.0 mm × 4.0 mm × 20.0 mm LYSO crystal module optically coupled with four 29 mm diameter PMTs using Photomultiplier-quadrant-sharing (PQS) technique. Because the crystal pixel was identified based upon the distribution of scintillation lights of four PMTs, the design of the reflector between crystal elements should be well optimized. The optical design of reflectors was optimized using DETECT2000, a Monte Carlo code for light photon transport. A laser-cut reflector set was developed using the Enhanced Specular Reflector (ESR, 3M Co.) mirror-film with a high reflectance of 98% and a thickness of 0.064 mm. All 81 crystal elements of detector module were identified. Our result demonstrates that the C-shaped PET system is under development and we present the first reconstructed image.
Preliminary studies of PQS PET detector module for dose verification of carbon beam therapy
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PET imaging can be used to verify dose distributions of therapeutic particle beams such as carbon ion beams. The purpose of this study was to develop a PET detector module which was designed for an in-beam PET scanner geometry integrated into a carbon beam therapy system, and to evaluate its feasibility as a monitoring system of patient dose distribution. A C-shaped PET geometry was proposed to avoid blockage of the carbon beam by the detector modules. The proposed PET system consisted of 14 detector modules forming a bore with 30.2 cm inner diameter for brain imaging. Each detector module is composed of a 9 × 9 array of 4.0 mm × 4.0 mm × 20.0 mm LYSO crystal module optically coupled with four 29 mm diameter PMTs using Photomultiplier-quadrant-sharing (PQS) technique. Because the crystal pixel was identified based upon the distribution of scintillation lights of four PMTs, the design of the reflector between crystal elements should be well optimized. The optical design of reflectors was optimized using DETECT2000, a Monte Carlo code for light photon transport. A laser-cut reflector set was developed using the Enhanced Specular Reflector (ESR, 3M Co.) mirror-film with a high reflectance of 98% and a thickness of 0.064 mm. All 81 crystal elements of detector module were identified. Our result demonstrates that the C-shaped PET system is under development and we present the first reconstructed image
Spatial fractionation of the dose using neon and heavier ions: A Monte Carlo study
Energy Technology Data Exchange (ETDEWEB)
Peucelle, C.; Martínez-Rovira, I.; Prezado, Y., E-mail: prezado@imnc.in2p3.fr [IMNC-UMR 8165, CNRS Paris 7 and Paris 11 Universities, 15 rue Georges Clemenceau, Orsay Cedex 91406 (France)
2015-10-15
Purpose: This work explores a new radiation therapy approach which might trigger a renewed use of neon and heavier ions to treat cancers. These ions were shown to be extremely efficient in radioresistant tumor killing. Unfortunately, the efficient region also extends into the normal tissue in front of the tumor. The strategy the authors propose is to profit from the well-established sparing effect of thin spatially fractionated beams, so that the impact on normal tissues might be minimized while a high tumor control is achieved. The main goal of this work is to provide a proof of concept of this new approach. With that aim, a dosimetric study was carried out as a first step to evaluate the interest of further explorations of this avenue. Methods: The GATE/GEANT4 v.6.1 Monte Carlo simulation platform was employed to simulate arrays of rectangular minibeams (700 μm × 2 cm) of four ions (Ne, Si, Ar, and Fe). The irradiations were performed with a 2 cm-long spread-out Bragg peak centered at 7 cm-depth. Dose distributions in a water phantom were scored considering two minibeams center-to-center distances: 1400 and 3500 μm. Peak and valley doses, peak-to-valley dose ratios (PVDRs), beam penumbras, and relative contribution of nuclear fragments and electromagnetic processes were assessed as figures of merit. In addition, the type and proportion of the secondary nuclear fragments were evaluated in both peak and valley regions. Results: Extremely high PVDR values (>100) and low valley doses were obtained. The higher the atomic number (Z) of the primary ion is, the lower the valleys and the narrower the penumbras. Although the yield of secondary nuclear products increases with Z, the actual dose being deposited by the secondary nuclear fragments in the valleys starts to be the dominant contribution at deeper points, helping in the sparing of proximal normal tissues. Additionally, a wider center-to-center distance leads to a minimized contribution of heavier secondary
Omar, Artur; Benmakhlouf, Hamza; Marteinsdottir, Maria; Bujila, Robert; Nowik, Patrik; Andreo, Pedro
2014-03-01
Complex interventional and diagnostic x-ray angiographic (XA) procedures may yield patient skin doses exceeding the threshold for radiation induced skin injuries. Skin dose is conventionally determined by converting the incident air kerma free-in-air into entrance surface air kerma, a process that requires the use of backscatter factors. Subsequently, the entrance surface air kerma is converted into skin kerma using mass energy-absorption coefficient ratios tissue-to-air, which for the photon energies used in XA is identical to the skin dose. The purpose of this work was to investigate how the cranial bone affects backscatter factors for the dosimetry of interventional neuroradiology procedures. The PENELOPE Monte Carlo system was used to calculate backscatter factors at the entrance surface of a spherical and a cubic water phantom that includes a cranial bone layer. The simulations were performed for different clinical x-ray spectra, field sizes, and thicknesses of the bone layer. The results show a reduction of up to 15% when a cranial bone layer is included in the simulations, compared with conventional backscatter factors calculated for a homogeneous water phantom. The reduction increases for thicker bone layers, softer incident beam qualities, and larger field sizes, indicating that, due to the increased photoelectric crosssection of cranial bone compared to water, the bone layer acts primarily as an absorber of low-energy photons. For neurointerventional radiology procedures, backscatter factors calculated at the entrance surface of a water phantom containing a cranial bone layer increase the accuracy of the skin dose determination.
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Purpose: To provide commissioning and acceptance test data of the Varian Eclipse electron Monte Carlo model (eMC v.11) for TrueBeam linac. We also investigated the uncertainties in beam model parameters and dose calculation results for different geometric configurations. Methods: For beam commissioning, PTW CC13 thimble chamber and IBA Blue Phantom2 were used to collect PDD and dose profiles in air. Cone factors were measured with a parallel plate chamber (PTW N23342) in solid water. GafChromic EBT3 films were used for dose calculation verifications to compare with parallel plate chamber results in the following test geometries: oblique incident, extended distance, small cutouts, elongated cutouts, irregular surface, and heterogeneous layers. Results: Four electron energies (6e, 9e, 12e, and 15e) and five cones (6×6, 10×10, 15×15, 20×20, and 25×25) with standard cutouts were calculated for different grid sizes (1, 1.5,2, and 2.5 mm) and compared with chamber measurements. The results showed calculations performed with a coarse grid size underestimated the absolute dose. The underestimation decreased as energy increased. For 6e, the underestimation (max 3.3 %) was greater than the statistical uncertainty level (3%) and was systematically observed for all cone sizes. By using a 1mm grid size, all the calculation results agreed with measurements within 5% for all test configurations. The calculations took 21s and 46s for 6e and 15e (2.5mm grid size) respectively distributed on 4 calculation servants. Conclusion: In general, commissioning the eMC dose calculation model on TrueBeam is straightforward and thedose calculation is in good agreement with measurements for all test cases. Monte Carlo dose calculation provides more accurate results which improves treatment planning quality. However, the normal acceptable grid size (2.5mm) would cause systematic underestimation in absolute dose calculation for lower energies, such as 6e. Users need to be cautious in this
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The interpretation of data obtained from fixed, ground-based dose rate monitoring stations of environmental networks, in terms of deposited radionuclide activity per unit area, requires not only the knowledge of the nuclide spectrum and the deposition mechanism, but also the knowledge of the situation in the vicinity at the probe if it significantly differs from ideal conditions, which are defined to be an infinitely-extended plane surface. Distance-dependent calibration factors for different gamma-ray energies and depth profiles are calculated with the new Monte Carlo code PENELOPE. How these distance-dependent calibration factors can take inhomogeneous surface types in the vicinity of the probe into account will also be discussed. In addition, calibration factors for different detector heights and calibration factors for gamma sources in the air will also be calculated. The main irregularities that, in practice, occur in the vicinity of such probes are discussed. Their impact on the representativeness of the site is assessed. For some typical irregularities parameterized calibration factors are calculated and discussed. Sewage plants and sandboxes are discussed as further special examples. The application of these results to real sites allows for the improved interpretation of data and the quantitative assessment of the representativeness of the site. A semi-quantitative scoring scheme helps to decide to what extent irregularities can be tolerated. Its application is straightforward and provides a coarse but objective description of the site-specific conditions of a dose rate probe. (orig.)
Dose to drivers during drive-through cargo scanning using GEANT4 Monte Carlo simulation
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Gomes, Rogerio S.; Gomes, Joana D' Arc R.L.; Costa, Mara Lucia L., E-mail: rogeriog@cnen.gov.br, E-mail: jlopes@cnen.gov.br, E-mail: mara@cnen.gov.br [Comissao Nacional de Energia Nuclear (CNEN-RJ), Rio de Janeiro, RJ (Brazil). Diretoria de Radioprotecao e Seguranca muclear; Miranda, Valeria F.E.S., E-mail: mvaleria@cnen.gov.br [Centro Regional de Ciencias Nucleares do Nordeste (CRCN-NE/CNEN-PE), Recife, PE (Brazil)
2013-07-01
The use of radiation technologies to perform screening for cargo containers has been increased due to security issues, mainly, as a consequence of the United States (US) legislation which requires, from 2013, the scanning of all intermodal cargo containers which arrive at US ports. Currently, systems to cargo inspections, using accelerator-driven high energy X-rays, between 4 and 9 MeV, are available for scanning operations. It is expected that, in the future, the use of these systems will be widely spread on roads, ports and airports in Brazil. However, in order to improve the productivity and reduce the costs of acquisition, operation and maintenance these systems require that the driver drives its vehicle through irradiation area, in a situation where members of the public (the truck drivers) enter in controlled area and are deliberately exposed to high-energy beam. Some manufacturers justifies this procedure arguing that the drivers are exposed briefly, and only to the scattered beam, since there are safety systems in order to avoid that the drivers are exposed to direct beam. In this work, it is presented the preliminary results of Monte Carlo simulations concerning the dose of drivers during scanning operations, including the dose due to a failure of safety system, producing an exposure of drivers to the direct beam, as well as, an analysis of the justification of practice, mainly related to the drive-through operational procedure. (author)
Analysis of portal dose prediction verification results: Small clinic practical view
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Patient-specific quality assurance results with Portal Dose Calculation (PDC, EclipseTM 8.1, Varian Medical Systems, Palo Alto, CA) for pre-treatment verification of 243 sliding window IMRT fields were analyzed for a linear accelerator Clinac iX (Varian Medical Systems) with nominal 6 MV energy and Millenium MLC incorporating 120 leaves. The linac is equipped with a flat panel amorphous silicon (a-Si) electronic portal imaging device (EPID) a-SlOOO with image detection unit (IDU) and image acquisition software (IAS) versions IDU-20/IAS3. Data were collected during an approximately one-year period around 2009. The properties of the Varian PDC method and the gamma evaluation method that it exploits as an error detection method have been described elsewhere. All the plans were calculated with a dose rate of 300 MU/min, source to detector distance (SDD) 105 cm, for 4 to 7 (before automatic split) field IMRT plans with different treatment doses in the range of 14 to 70 Gy (mean 52.9 Gy). The measurements were made with no additional build-up with gantry angle reset to zero. One field was excluded because the imager was not aligned to the correct distance before measurement. Three fields were excluded because the PDC routine did not correctly deal with artificial reference images for split fields that were divided into more than two subfields. Twenty-one fields were excluded because the fields extended over the detector area (crossplane axis > 14.2 cm). The remaining fields were divided into groups firstly by field size, because for field axes less than 7.5 cm the effect of nonuniform backscatter is minimal, secondly by split or non-split carriage property and thirdly by treatment site. The fields were analyzed using ROI covering 1 cm around the collimator positions and gamma index 3% global dose difference and 3 mm distance to agreement as acceptance values. Maximum gamma, average gamma and percentage of area with gamma >1.0 values were recorded. All fields were also
PCXMC. A PC-based Monte Carlo program for calculating patient doses in medical x-ray examinations
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The report describes PCXMC, a Monte Carlo program for calculating patients' organ doses and the effective dose in medical x-ray examinations. The organs considered are: the active bone marrow, adrenals, brain, breasts, colon (upper and lower large intestine), gall bladder, heats, kidneys, liver, lungs, muscle, oesophagus, ovaries, pancreas, skeleton, skin, small intestine, spleen, stomach, testes, thymes, thyroid, urinary bladder, and uterus. (42 refs.)
Kumar, Sudhir; Srinivasan, P; Sharma, S D; Saxena, Sanjay Kumar; Bakshi, A K; Dash, Ashutosh; Babu, D A R; Sharma, D N
2015-09-01
Isotope production and Application Division of Bhabha Atomic Research Center developed (32)P patch sources for treatment of superficial tumors. Surface dose rate of a newly developed (32)P patch source of nominal diameter 25 mm was measured experimentally using standard extrapolation ionization chamber and Gafchromic EBT film. Monte Carlo model of the (32)P patch source along with the extrapolation chamber was also developed to estimate the surface dose rates from these sources. The surface dose rates to tissue (cGy/min) measured using extrapolation chamber and radiochromic films are 82.03±4.18 (k=2) and 79.13±2.53 (k=2) respectively. The two values of the surface dose rates measured using the two independent experimental methods are in good agreement to each other within a variation of 3.5%. The surface dose rate to tissue (cGy/min) estimated using the MCNP Monte Carlo code works out to be 77.78±1.16 (k=2). The maximum deviation between the surface dose rates to tissue obtained by Monte Carlo and the extrapolation chamber method is 5.2% whereas the difference between the surface dose rates obtained by radiochromic film measurement and the Monte Carlo simulation is 1.7%. The three values of the surface dose rates of the (32)P patch source obtained by three independent methods are in good agreement to one another within the uncertainties associated with their measurements and calculation. This work has demonstrated that MCNP based electron transport simulations are accurate enough for determining the dosimetry parameters of the indigenously developed (32)P patch sources for contact brachytherapy applications. PMID:26086681
Radiation dose verification using real tissue phantom in modern radiotherapy techniques
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In vitro dosimetric verification prior to patient treatment has a key role in accurate and precision radiotherapy treatment delivery. Most of commercially available dosimetric phantoms have almost homogeneous density throughout their volume, while real interior of patient body has variable and varying densities inside. In this study an attempt has been made to verify the physical dosimetry in actual human body scenario by using goat head as 'head phantom' and goat meat as 'tissue phantom'. The mean percentage variation between planned and measured doses was found to be 2.48 (standard deviation (SD): 0.74), 2.36 (SD: 0.77), 3.62 (SD: 1.05), and 3.31 (SD: 0.78) for three-dimensional conformal radiotherapy (3DCRT) (head phantom), intensity modulated radiotherapy (IMRT; head phantom), 3DCRT (tissue phantom), and IMRT (tissue phantom), respectively. Although percentage variations in case of head phantom were within tolerance limit (< ± 3%), but still it is higher than the results obtained by using commercially available phantoms. And the percentage variations in most of cases of tissue phantom were out of tolerance limit. On the basis of these preliminary results it is logical and rational to develop radiation dosimetry methods based on real human body and also to develop an artificial phantom which should truly represent the interior of human body. (author)
Radiation dose verification using real tissue phantom in modern radiotherapy techniques
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Om Prakash Gurjar
2014-01-01
Full Text Available In vitro dosimetric verification prior to patient treatment has a key role in accurate and precision radiotherapy treatment delivery. Most of commercially available dosimetric phantoms have almost homogeneous density throughout their volume, while real interior of patient body has variable and varying densities inside. In this study an attempt has been made to verify the physical dosimetry in actual human body scenario by using goat head as "head phantom" and goat meat as "tissue phantom". The mean percentage variation between planned and measured doses was found to be 2.48 (standard deviation (SD: 0.74, 2.36 (SD: 0.77, 3.62 (SD: 1.05, and 3.31 (SD: 0.78 for three-dimensional conformal radiotherapy (3DCRT (head phantom, intensity modulated radiotherapy (IMRT; head phantom, 3DCRT (tissue phantom, and IMRT (tissue phantom, respectively. Although percentage variations in case of head phantom were within tolerance limit (< ± 3%, but still it is higher than the results obtained by using commercially available phantoms. And the percentage variations in most of cases of tissue phantom were out of tolerance limit. On the basis of these preliminary results it is logical and rational to develop radiation dosimetry methods based on real human body and also to develop an artificial phantom which should truly represent the interior of human body.
Patient dose reduction in CT screening of nasal sinuses: results of clinical verification
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Screening examinations of the nasal sinuses using computed tomography (CT) has become a more common diagnostic procedure. The aim of the study was clinical verification of the possibility of patient dose reduction in CT screening of nasal sinuses. A Siemens Somatom AR Star was used for the investigations. First, image quality indicators (contrast and spatial resolution) were analyzed in relation to the intensity of the scanning x-ray beam using a Catphan phantom. Dosimetric evaluation was also performed. The results showed no worsening in the visualization of low-contrast objects when the anode current was lowered from 105 mA to 63 mA; only the size of the smallest detectable object was slightly greater. Spatial resolution was also not changed. The clinical study involved examination of the sinuses of 100 patients. Five details of the image of diagnostic value were analyzed. The routine value of anode current was applied in 50 patients, while the other 50 had the reduced current. The diagnostic images were scored by two independent radiologists who did not know the parameters used during the examinations. To make the results objective, semiquantitative analysis was used. Diagnostic images obtained with the routinely used and at the reduced anode current did not show ny differences in the visualization of the selected image details. Screening CT examinations of nasal sinuses can be performed at a reduced anode current with no loss of diagnostic significance of the examination. The dose to the patient is reduced by 40% when the modified protocol is implemented. (author)
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MCNP and Monte Carlo method was used to calculate dose rate in the air-space of irradiation room at Hanoi Irradiation Center. Experiment measurements were also carried out to investigate the real distribution of dose field in air of the irradiator as well as the distribution of absorbed dose in sample product containers. The results show that there is a deviation between calculated data given by MCNP and measurements. The data of MCNP give a symmetric distribution of dose field against the axes going through the center of the source rack meanwhile the experiment data show that dose rate get higher values in the lower part of the space. Going to lower position to the floor dose rate getting higher value. This phenomenon was also occurred for the measurements of absorbed dose in sample product container. (author)
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There has been some evidence that cervical cancer patients who were treated by radiotherapy, had an increased incidence of second primary cancers noticeable 15 years or more after the radiotherapy. The data suggested that high dose pelvic irradiation was associated with increase in cancers of the bladder, kidneys, rectum, ovaries, corpus uteri, and non-Hodgkin's lymphoma but not leukemia (Kleinerman et al., 1982, Morton 1973). The aim of the present work is to estimate the absorbed dose, due to radiotherapy treatment for cervival cancer, to various organs and tissues in the body. Monte Carlo calculations were performed to calculate the organ absorbed doses resulting from intracavitary sources such as ovoids and applicators filled or loaded with radium, Co-60 and Cs-137. For that purpose a routine which simulates an internal source was constructed and added to the existing Monte Carlo code (GSF-Bericht S-885, Kramer et al.). Calculations were also made for external beam therapy. Various anterior, posterior and lateral fields were applied, resulting from megavoltage, Co-60 and Cs-137 therapy machines. The calculated organ doses are tabulated in three different ways: as organ dose per air Kerma in the reference field, according to the recommendations of the International Commission on Radiation Units and Measurements (ICRU Report No 38, 1985); as organ dose per surface dose and as organ dose per tissue dose at Point B. (orig.)
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A method for the calculation of the transit doses in HDR brachytherapy based on Monte Carlo simulations has been presented. The transit doses resulting from a linear implant with seven dwell positions is simulated by performing calculations at all positions in which, the moving 192Ir source, instantaneously, had its geometrical centre located exactly between two adjacent dwell positions. Discrete step sizes of 0.25 cm were used to calculate the dose rates and the total transit dose at any of the calculation points evaluated. By comparing this method to the results obtained from Sievert Integrals, we observed dose calculation errors ranging from 32 to 21% for the examples considered. The errors could be much higher for longer treatment lengths where contributions from points near the longitudinal axis of the source become more important. To date, the most accurate method of calculating doses in radiotherapy is by Monte Carlo Simulations but the long computational times associated with it renders its use in treatment planning impracticable. The Sievert Integral algorithms on the other hand are simple, versatile and very easy to use but its accuracy had been repeatedly put into question for low energy isotopes like iridium. We therefore advocate a modification of the Sievert Integral algorithms by superimposing the output from Monte Carlo Simulations on the Sievert Integrals when dealing with low energy isotopes. In this way, we would be combining accuracy, simplicity and reasonable computational times (author)
An analytic linear accelerator source model for GPU-based Monte Carlo dose calculations
Tian, Zhen; Li, Yongbao; Folkerts, Michael; Shi, Feng; Jiang, Steve B.; Jia, Xun
2015-10-01
Recently, there has been a lot of research interest in developing fast Monte Carlo (MC) dose calculation methods on graphics processing unit (GPU) platforms. A good linear accelerator (linac) source model is critical for both accuracy and efficiency considerations. In principle, an analytical source model should be more preferred for GPU-based MC dose engines than a phase-space file-based model, in that data loading and CPU-GPU data transfer can be avoided. In this paper, we presented an analytical field-independent source model specifically developed for GPU-based MC dose calculations, associated with a GPU-friendly sampling scheme. A key concept called phase-space-ring (PSR) was proposed. Each PSR contained a group of particles that were of the same type, close in energy and reside in a narrow ring on the phase-space plane located just above the upper jaws. The model parameterized the probability densities of particle location, direction and energy for each primary photon PSR, scattered photon PSR and electron PSR. Models of one 2D Gaussian distribution or multiple Gaussian components were employed to represent the particle direction distributions of these PSRs. A method was developed to analyze a reference phase-space file and derive corresponding model parameters. To efficiently use our model in MC dose calculations on GPU, we proposed a GPU-friendly sampling strategy, which ensured that the particles sampled and transported simultaneously are of the same type and close in energy to alleviate GPU thread divergences. To test the accuracy of our model, dose distributions of a set of open fields in a water phantom were calculated using our source model and compared to those calculated using the reference phase-space files. For the high dose gradient regions, the average distance-to-agreement (DTA) was within 1 mm and the maximum DTA within 2 mm. For relatively low dose gradient regions, the root-mean-square (RMS) dose difference was within 1.1% and the maximum
Liu, Han; Zhuang, Tingliang; Stephans, Kevin; Videtic, Gregory; Raithel, Stephen; Djemil, Toufik; Xia, Ping
2015-01-01
For patients with medically inoperable early-stage non-small cell lung cancer (NSCLC) treated with stereotactic body radiation therapy, early treatment plans were based on a simpler dose calculation algorithm, the pencil beam (PB) calculation. Because these patients had the longest treatment follow-up, identifying dose differences between the PB calculated dose and Monte Carlo calculated dose is clinically important for understanding of treatment outcomes. Previous studies found significant dose differences between the PB dose calculation and more accurate dose calculation algorithms, such as convolution-based or Monte Carlo (MC), mostly for three-dimensional conformal radiotherapy (3D CRT) plans. The aim of this study is to investigate whether these observed dose differences also exist for intensity-modulated radiotherapy (IMRT) plans for both centrally and peripherally located tumors. Seventy patients (35 central and 35 peripheral) were retrospectively selected for this study. The clinical IMRT plans that were initially calculated with the PB algorithm were recalculated with the MC algorithm. Among these paired plans, dosimetric parameters were compared for the targets and critical organs. When compared to MC calculation, PB calculation overestimated doses to the planning target volumes (PTVs) of central and peripheral tumors with different magnitudes. The doses to 95% of the central and peripheral PTVs were overestimated by 9.7% ± 5.6% and 12.0% ± 7.3%, respectively. This dose overestimation did not affect doses to the critical organs, such as the spinal cord and lung. In conclusion, for NSCLC treated with IMRT, dose differences between the PB and MC calculations were different from that of 3D CRT. No significant dose differences in critical organs were observed between the two calculations. PMID:26699560
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Purpose: To monitor the secondary dose distribution originating from a water phantom during proton therapy of prostate cancer using scintillating fibers. Methods: The Geant4 Monte Carlo toolkit version 9.6.p02 was used to simulate prostate cancer proton therapy based treatments. Two cases were studied. In the first case, 8 × 8 = 64 equally spaced fibers inside three 4 × 4 × 2.54 cmm3 DuPont™ Delrin blocks were used to monitor the emission of secondary particles in the transverse (left and right) and distal regions relative to the beam direction. In the second case, a scintillating block with a thickness of 2.54 cm and equal vertical and longitudinal dimensions as the water phantom was used. Geometrical cuts were used to extract the energy deposited in each fiber and the scintillating block. Results: The transverse dose distributions from secondary particles in both cases agree within <5% and with a very good symmetry. The energy deposited not only gradually increases as one moves from the peripheral row fibers towards the center of the block (aligned with the center of the prostate) but also decreases as one goes from the frontal to distal region of the block. The ratio of the doses from the prostate to the ones in the middle two rows of fibers showed a linear relationship with a slope (−3.55±2.26) × 10−5 MeV per treatment Gy. The distal detectors recorded a very small energy deposited due to water attenuation. Conclusion: With a good calibration and the ability to define a good correlation between the dose to the external fibers and the prostate, such fibers can be used for real time dose verification to the target
A GPU-based Monte Carlo dose calculation code for photon transport in a voxel phantom
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Bellezzo, M.; Do Nascimento, E.; Yoriyaz, H., E-mail: mbellezzo@gmail.br [Instituto de Pesquisas Energeticas e Nucleares / CNEN, Av. Lineu Prestes 2242, Cidade Universitaria, 05508-000 Sao Paulo (Brazil)
2014-08-15
As the most accurate method to estimate absorbed dose in radiotherapy, Monte Carlo method has been widely used in radiotherapy treatment planning. Nevertheless, its efficiency can be improved for clinical routine applications. In this paper, we present the CUBMC code, a GPU-based Mc photon transport algorithm for dose calculation under the Compute Unified Device Architecture platform. The simulation of physical events is based on the algorithm used in Penelope, and the cross section table used is the one generated by the Material routine, als present in Penelope code. Photons are transported in voxel-based geometries with different compositions. To demonstrate the capabilities of the algorithm developed in the present work four 128 x 128 x 128 voxel phantoms have been considered. One of them is composed by a homogeneous water-based media, the second is composed by bone, the third is composed by lung and the fourth is composed by a heterogeneous bone and vacuum geometry. Simulations were done considering a 6 MeV monoenergetic photon point source. There are two distinct approaches that were used for transport simulation. The first of them forces the photon to stop at every voxel frontier, the second one is the Woodcock method, where the photon stop in the frontier will be considered depending on the material changing across the photon travel line. Dose calculations using these methods are compared for validation with Penelope and MCNP5 codes. Speed-up factors are compared using a NVidia GTX 560-Ti GPU card against a 2.27 GHz Intel Xeon CPU processor. (Author)
A GPU-based Monte Carlo dose calculation code for photon transport in a voxel phantom
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As the most accurate method to estimate absorbed dose in radiotherapy, Monte Carlo method has been widely used in radiotherapy treatment planning. Nevertheless, its efficiency can be improved for clinical routine applications. In this paper, we present the CUBMC code, a GPU-based Mc photon transport algorithm for dose calculation under the Compute Unified Device Architecture platform. The simulation of physical events is based on the algorithm used in Penelope, and the cross section table used is the one generated by the Material routine, als present in Penelope code. Photons are transported in voxel-based geometries with different compositions. To demonstrate the capabilities of the algorithm developed in the present work four 128 x 128 x 128 voxel phantoms have been considered. One of them is composed by a homogeneous water-based media, the second is composed by bone, the third is composed by lung and the fourth is composed by a heterogeneous bone and vacuum geometry. Simulations were done considering a 6 MeV monoenergetic photon point source. There are two distinct approaches that were used for transport simulation. The first of them forces the photon to stop at every voxel frontier, the second one is the Woodcock method, where the photon stop in the frontier will be considered depending on the material changing across the photon travel line. Dose calculations using these methods are compared for validation with Penelope and MCNP5 codes. Speed-up factors are compared using a NVidia GTX 560-Ti GPU card against a 2.27 GHz Intel Xeon CPU processor. (Author)
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Monte Carlo (MC) simulation has been commonly used in the dose evaluation of radiation accidents and for medical purposes. The accuracy of simulated results is affected by the particle-tracking algorithm, cross-sectional database, random number generator and statistical error. The differences among MC simulation software packages must be validated. This study simulated the dose point kernel (DPK) and the cellular S-values of monoenergetic electrons ranging from 0.01 to 2 MeV and the radionuclides of 90Y, 177Lu and 103mmRh, using Fluktuierende Kaskade (FLUKA) and MC N-Particle Transport Code Version 5 (MCNP5). A 6-μm-radius cell model consisting of the cell surface, cytoplasm and cell nucleus was constructed for cellular S-value calculation. The mean absolute percentage errors (MAPEs) of the scaled DPKs, simulated using FLUKA and MCNP5, were 7.92, 9.64, 4.62, 3.71 and 3.84 % for 0.01, 0.1, 0.5, 1 and 2 MeV, respectively. For the three radionuclides, the MAPEs of the scaled DPKs were within 5 %. The maximum deviations of S(N<-N), S(N<-Cy) and S(N<-CS) for the electron energy larger than 10 keV were 6.63, 6.77 and 5.24 %, respectively. The deviations for the self-absorbed S-values and cross-dose S-values of the three radionuclides were within 4 %. On the basis of the results of this study, it was concluded that the simulation results are consistent between FLUKA and MCNP5. However, there is a minor inconsistency for low energy range. The DPK and the cellular S-value should be used as the quality assurance tools before the MC simulation results are adopted as the gold standard. (authors)
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The analysis of depth-dose distributions in bricks sampled from walls in areas with nuclear waste or accident contamination has the potential of providing information on the energy and source configuration of the γ-radiation that had been incident on the brick. In this study, a brick from a mill facing a shallow water reservoir of the contaminated Techa river in the South Ural region is investigated. Thermoluminescene (TL) methods were used to measure the accumulated dose at several depths in the brick. The accidental external γ-dose is obtained by subtracting the natural radiation background dose from the total accumulated dose. In the first segment of the brick, at a depth of about 1.5 cm, the accident dose was found to be roughly 3.5 Gy. Monte-Carlo simulations of the photon transport form the reservoir bed contaminated with 137Cs were calculated for different depths in the brick. The calculations were made assuming different attenuating water levels. It is found that the depth-dose distribution determined by measurements corresponds to a water level between 20 and 50 cm. The results indicate that the TL measurements combined with Monte-Carlo modelling calculations are highly promising for external γ-dose reconstruction applications. (Author)
Dual-energy CT-based material extraction for tissue segmentation in Monte Carlo dose calculations
Bazalova, Magdalena; Carrier, Jean-François; Beaulieu, Luc; Verhaegen, Frank
2008-05-01
Monte Carlo (MC) dose calculations are performed on patient geometries derived from computed tomography (CT) images. For most available MC codes, the Hounsfield units (HU) in each voxel of a CT image have to be converted into mass density (ρ) and material type. This is typically done with a (HU; ρ) calibration curve which may lead to mis-assignment of media. In this work, an improved material segmentation using dual-energy CT-based material extraction is presented. For this purpose, the differences in extracted effective atomic numbers Z and the relative electron densities ρe of each voxel are used. Dual-energy CT material extraction based on parametrization of the linear attenuation coefficient for 17 tissue-equivalent inserts inside a solid water phantom was done. Scans of the phantom were acquired at 100 kVp and 140 kVp from which Z and ρe values of each insert were derived. The mean errors on Z and ρe extraction were 2.8% and 1.8%, respectively. Phantom dose calculations were performed for 250 kVp and 18 MV photon beams and an 18 MeV electron beam in the EGSnrc/DOSXYZnrc code. Two material assignments were used: the conventional (HU; ρ) and the novel (HU; ρ, Z) dual-energy CT tissue segmentation. The dose calculation errors using the conventional tissue segmentation were as high as 17% in a mis-assigned soft bone tissue-equivalent material for the 250 kVp photon beam. Similarly, the errors for the 18 MeV electron beam and the 18 MV photon beam were up to 6% and 3% in some mis-assigned media. The assignment of all tissue-equivalent inserts was accurate using the novel dual-energy CT material assignment. As a result, the dose calculation errors were below 1% in all beam arrangements. Comparable improvement in dose calculation accuracy is expected for human tissues. The dual-energy tissue segmentation offers a significantly higher accuracy compared to the conventional single-energy segmentation.
Effect of elemental compositions on Monte Carlo dose calculations in proton therapy of eye tumors
Rasouli, Fatemeh S.; Farhad Masoudi, S.; Keshazare, Shiva; Jette, David
2015-12-01
Recent studies in eye plaque brachytherapy have found considerable differences between the dosimetric results by using a water phantom, and a complete human eye model. Since the eye continues to be simulated as water-equivalent tissue in the proton therapy literature, a similar study for investigating such a difference in treating eye tumors by protons is indispensable. The present study inquires into this effect in proton therapy utilizing Monte Carlo simulations. A three-dimensional eye model with elemental compositions is simulated and used to examine the dose deposition to the phantom. The beam is planned to pass through a designed beam line to moderate the protons to the desired energies for ocular treatments. The results are compared with similar irradiation to a water phantom, as well as to a material with uniform density throughout the whole volume. Spread-out Bragg peaks (SOBPs) are created by adding pristine peaks to cover a typical tumor volume. Moreover, the corresponding beam parameters recommended by the ICRU are calculated, and the isodose curves are computed. The results show that the maximum dose deposited in ocular media is approximately 5-7% more than in the water phantom, and about 1-1.5% less than in the homogenized material of density 1.05 g cm-3. Furthermore, there is about a 0.2 mm shift in the Bragg peak due to the tissue composition difference between the models. It is found that using the weighted dose profiles optimized in a water phantom for the realistic eye model leads to a small disturbance of the SOBP plateau dose. In spite of the plaque brachytherapy results for treatment of eye tumors, it is found that the differences between the simplified models presented in this work, especially the phantom containing the homogenized material, are not clinically significant in proton therapy. Taking into account the intrinsic uncertainty of the patient dose calculation for protons, and practical problems corresponding to applying patient
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Purpose: The aim of the study was to evaluate the dosimetric impact of low-Z and high-Z metallic implants on IMRT plans. Methods: Computed tomography (CT) scans of three patients were analyzed to study effects due to the presence of Titanium (low-Z), Platinum and Gold (high-Z) inserts. To eliminate artifacts in CT images, a sinogram-based metal artifact reduction algorithm was applied. IMRT dose calculations were performed on both the uncorrected and corrected images using a commercial planning system (convolution/superposition algorithm) and an in-house Monte Carlo platform. Dose differences between uncorrected and corrected datasets were computed and analyzed using gamma index (Pγ) and setting 2 mm and 2% as distance to agreement and dose difference criteria, respectively. Beam specific depth dose profiles across the metal were also examined. Results: Dose discrepancies between corrected and uncorrected datasets were not significant for low-Z material. High-Z materials caused under-dosage of 20%–25% in the region surrounding the metal and over dosage of 10%–15% downstream of the hardware. Gamma index test yielded Pγ>99% for all low-Z cases; while for high-Z cases it returned 91% < 99%. Analysis of the depth dose curve of a single beam for low-Z cases revealed that, although the dose attenuation is altered inside the metal, it does not differ downstream of the insert. However, for high-Z metal implants the dose is increased up to 10%–12% around the insert. In addition, Monte Carlo method was more sensitive to the presence of metal inserts than superposition/convolution algorithm. Conclusions: The reduction in terms of dose of metal artifacts in CT images is relevant for high-Z implants. In this case, dose distribution should be calculated using Monte Carlo algorithms, given their superior accuracy in dose modeling in and around the metal. In addition, the knowledge of the composition of metal inserts improves the accuracy of the Monte Carlo dose
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The Monte Carlo (MC) method provides the most accurate to-date dose calculations in heterogeneous media and complex geometries, and this spawns increasing interest in incorporating MC calculations in the treatment planning quality assurance process. This process involves MC dose calculations for the treatment plans produced clinically. Commonly used in radiotherapy, MC codes are BEAMnrc and DOSXYZnrc, which transport particles in a coordinate system (c.s.) that has been established historically and does not correspond to the c.s. of treatment planning systems (TPSs). Relative rotations of these c.s. are not straightforward, especially for non-coplanar treatments. Transformation equations are therefore required to re-calculate a treatment plan using BEAM/DOSXYZnrc codes. This paper presents such transformations for beam angles defined in a DICOM-compliant treatment planning coordinate system. Verification of the derived transformations with two three-field plans simulated on a phantom using TPS as well as MC codes has been performed demonstrating exact geometrical agreement of the MC treatment fields' placement. (note)
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Ahad Ollah Ezzati
2014-08-01
Full Text Available Introduction In this study, we aimed to calculate dose enhancement factor (DEF for gold (Au and iron (Fe nanoparticles (NPs in brachytherapy and teletherapy, using Monte Carlo (MC method. Materials and Methods In this study, a new algorithm was introduced to calculate dose enhancement by AuNPs and FeNPs for Iridium-192 (Ir-192 brachytherapy and Cobalt-60 (Co-60 teletherapy sources, using the MC method. In this algorithm, the semi-random distribution of NPs was used instead of the regular distribution. Diameters were assumed to be 15, 30, and 100 nm in brachytherapy and 15 and 30 nm in teletherapy. Monte Carlo MCNP4C code was used for simulations, and NP density values were 0.107 mg/ml and 0.112 mg/ml in brachytherapy and teletherapy, respectively. Results AuNPs significantly enhanced the radiation dose in brachytherapy (approximately 60%, and 100 nm diameter NPs showed the most uniform dose distribution. AuNPs had an insignificant effect on teletherapy radiation field, with a dose enhancement ratio of 3% (about the calculation uncertainty or less. In addition, FeNPs had an insignificant effect on both brachytherapy and teletherapy radiation fields. FeNPs dose enhancement was 3% in brachytherapy and 6% (about the calculation uncertainty or less in teletherapy. Conclusion It can be concluded that AuNPs can significantly increase the absorbed dose in brachytherapy; however, FeNPs do not have a noticeable effect on the absorbed dose
Design optimization of a 2D prompt-gamma measurement system for proton dose verification
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To verify in-vivo proton dose distribution, a 2-dimensional (2D) prompt-gamma measurement system, comprised of a multi-hole collimation system, a 2D array of CsI(Tl) scintillators, and a position-sensitive photomultiplier tube (PS-PMT), is under development. In the present study, to determine the optimal dimension of the measurement system, we employed a series of Monte Carlo simulations with the MCNPX code. To effectively measure the high-energy prompt gammas while minimizing background gammas, we determined the collimator hole size, collimator thickness, and scintillator length to be 0.4 x 0.4 cm2, 15 cm, and 5 cm, respectively. Thereafter, the performance of the optimized measurement system was estimated for monoenergetic proton pencil beams. The peak locations of the prompt-gamma distributions for 80- and 150-MeV proton beams were clearly distinguished, and the correlation between the beam range and the peak location was confirmed by using the measurement system. For a 200-MeV proton beam, however, the peak location could not be determined due to the dominance of background gammas and the lateral dispersion of the proton beam at the end of the beam range. Based on these simulation results, a prototype 2D prompt-gamma measurement system currently is under construction and, upon completion, will be tested with therapeutic proton beams.
Kim, Sangroh; Yoshizumi, Terry T; Toncheva, Greta; Frush, Donald P; Yin, Fang-Fang
2010-03-01
The purpose of this study was to establish a dose estimation tool with Monte Carlo (MC) simulations. A 5-y-old paediatric anthropomorphic phantom was computed tomography (CT) scanned to create a voxelised phantom and used as an input for the abdominal cone-beam CT in a BEAMnrc/EGSnrc MC system. An X-ray tube model of the Varian On-Board Imager((R)) was built in the MC system. To validate the model, the absorbed doses at each organ location for standard-dose and low-dose modes were measured in the physical phantom with MOSFET detectors; effective doses were also calculated. In the results, the MC simulations were comparable to the MOSFET measurements. This voxelised phantom approach could produce a more accurate dose estimation than the stylised phantom method. This model can be easily applied to multi-detector CT dosimetry. PMID:19889800
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In order to apply the Monte Carlo simulation technique for usual radiological examinations we developed a Pc program, 'IradMed', written entirely in Java. The main purpose of this program is to compute the organ doses and the effective dose of patients, which are exposed at a X-ray beam having photon energies in 10 to 150 keV radiodiagnostic range. Three major radiological procedures are considered, namely mammography, radiography and CT. The fluoroscopy implies an irregular geometry and therefore it is neglected. Nevertheless, a gross estimation of patient doses can be made taking into account the fluoroscopy as being composed of several radiographic examinations applied in different anatomical regions. The interactions between radiation and matter are well-known, and the accuracy of the calculation is limited by the accuracy of the anatomical model used to describe actual patients and by characterisation of the radiation field applied. In this version of IradMed, it is assumed that the absorbed dose is equal with kerma for all tissues. No procedure has been used to take account of the finite range of the secondary electrons that are produced by photoelectric or Compton interactions. These ranges are small compared with the dimensions of the organs, and the absorbed dose will not change abruptly with distance except at boundary where composition and density change. However these boundary effects would have little effect in the determination of the average doses to almost all organs, except the active bone marrow which is treated separately. Another justification for this kerma approximation is the fact that the sum of all electron energies that exit the organ is statistically equal with the sum of all electron energies that enter in that particular organ. In this version of program, it is considered the following interactions: the Rayleigh scattering, the Compton scattering and the photoelectric effect. The Compton scattering is modeled by several methods which
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Fulea, D. [Institute of Public Health ' Prof.Dr.Iuliu Moldovan' , Cluj-Napoca (Romania); Cosma, C. [Babes-Bolyai Univ., Faculty of Physics, Cluj-Napoca (Romania)
2006-07-01
In order to apply the Monte Carlo simulation technique for usual radiological examinations we developed a Pc program, 'IradMed', written entirely in Java. The main purpose of this program is to compute the organ doses and the effective dose of patients, which are exposed at a X-ray beam having photon energies in 10 to 150 keV radiodiagnostic range. Three major radiological procedures are considered, namely mammography, radiography and CT. The fluoroscopy implies an irregular geometry and therefore it is neglected. Nevertheless, a gross estimation of patient doses can be made taking into account the fluoroscopy as being composed of several radiographic examinations applied in different anatomical regions. The interactions between radiation and matter are well-known, and the accuracy of the calculation is limited by the accuracy of the anatomical model used to describe actual patients and by characterisation of the radiation field applied. In this version of IradMed, it is assumed that the absorbed dose is equal with kerma for all tissues. No procedure has been used to take account of the finite range of the secondary electrons that are produced by photoelectric or Compton interactions. These ranges are small compared with the dimensions of the organs, and the absorbed dose will not change abruptly with distance except at boundary where composition and density change. However these boundary effects would have little effect in the determination of the average doses to almost all organs, except the active bone marrow which is treated separately. Another justification for this kerma approximation is the fact that the sum of all electron energies that exit the organ is statistically equal with the sum of all electron energies that enter in that particular organ. In this version of program, it is considered the following interactions: the Rayleigh scattering, the Compton scattering and the photoelectric effect. The Compton scattering is modeled by several
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Çatlı, Serap, E-mail: serapcatli@hotmail.com [Gazi University, Faculty of Sciences, 06500 Teknikokullar, Ankara (Turkey); Tanır, Güneş [Gazi University, Faculty of Sciences, 06500 Teknikokullar, Ankara (Turkey)
2013-10-01
The present study aimed to investigate the effects of titanium, titanium alloy, and stainless steel hip prostheses on dose distribution based on the Monte Carlo simulation method, as well as the accuracy of the Eclipse treatment planning system (TPS) at 6 and 18 MV photon energies. In the present study the pencil beam convolution (PBC) method implemented in the Eclipse TPS was compared to the Monte Carlo method and ionization chamber measurements. The present findings show that if high-Z material is used in prosthesis, large dose changes can occur due to scattering. The variance in dose observed in the present study was dependent on material type, density, and atomic number, as well as photon energy; as photon energy increased back scattering decreased. The dose perturbation effect of hip prostheses was significant and could not be predicted accurately by the PBC method for hip prostheses. The findings show that for accurate dose calculation the Monte Carlo-based TPS should be used in patients with hip prostheses.
New approach based on tetrahedral-mesh geometry for accurate 4D Monte Carlo patient-dose calculation
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In the present study, to achieve accurate 4D Monte Carlo dose calculation in radiation therapy, we devised a new approach that combines (1) modeling of the patient body using tetrahedral-mesh geometry based on the patient’s 4D CT data, (2) continuous movement/deformation of the tetrahedral patient model by interpolation of deformation vector fields acquired through deformable image registration, and (3) direct transportation of radiation particles during the movement and deformation of the tetrahedral patient model. The results of our feasibility study show that it is certainly possible to construct 4D patient models (= phantoms) with sufficient accuracy using the tetrahedral-mesh geometry and to directly transport radiation particles during continuous movement and deformation of the tetrahedral patient model. This new approach not only produces more accurate dose distribution in the patient but also replaces the current practice of using multiple 3D voxel phantoms and combining multiple dose distributions after Monte Carlo simulations. For routine clinical application of our new approach, the use of fast automatic segmentation algorithms is a must. In order to achieve, simultaneously, both dose accuracy and computation speed, the number of tetrahedrons for the lungs should be optimized. Although the current computation speed of our new 4D Monte Carlo simulation approach is slow (i.e. ∼40 times slower than that of the conventional dose accumulation approach), this problem is resolvable by developing, in Geant4, a dedicated navigation class optimized for particle transportation in tetrahedral-mesh geometry. (paper)
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The present report describes a computer code DEEP which calculates the organ dose equivalents and the effective dose equivalent for external photon exposure by the Monte Carlo method. MORSE-CG, Monte Carlo radiation transport code, is incorporated into the DEEP code to simulate photon transport phenomena in and around a human body. The code treats an anthropomorphic phantom represented by mathematical formulae and user has a choice for the phantom sex: male, female and unisex. The phantom can wear personal dosimeters on it and user can specify their location and dimension. This document includes instruction and sample problem for the code as well as the general description of dose calculation, human phantom and computer code. (author)
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Asuni, G; Beek, T van; Van Utyven, E [Medical Physics Department, CancerCare Manitoba, Winnipeg, Manitoba (Canada); McCowan, P [Medical Physics Department, CancerCare Manitoba, Winnipeg, Manitoba (Canada); Department of Physics and Astronomy, University of Manitoba, Winnipeg, Manitoba (Canada); McCurdy, B.M.C. [Medical Physics Department, CancerCare Manitoba, Winnipeg, Manitoba (Canada); Department of Physics and Astronomy, University of Manitoba, Winnipeg, Manitoba (Canada); Department of Radiology, University of Manitoba, Winnipeg Manitoba (Canada)
2014-08-15
Radical treatment techniques such as stereotactic body radiation therapy (SBRT) are becoming popular and they involve delivery of large doses in fewer fractions. Due to this feature of SBRT, a high-resolution, pre-treatment dose verification method that makes use of a 3D patient representation would be appropriate. Such a technique will provide additional information about dose delivered to the target volume(s) and organs-at-risk (OARs) in the patient volume compared to 2D verification methods. In this work, we investigate an electronic portal imaging device (EPID) based pre-treatment QA method which provides an accurate reconstruction of the 3D-dose distribution in the patient model. Customized patient plans are delivered ‘in air’ and the portal images are collected using the EPID in cine mode. The images are then analysed to determine an estimate of the incident energy fluence. This is then passed to a collapsed-cone convolution dose algorithm which reconstructs a 3D patient dose estimate on the CT imaging dataset. To date, the method has been applied to 5 SBRT patient plans. Reconstructed doses were compared to those calculated by the TPS. Reconstructed mean doses were mostly within 3% of those in the TPS. DVHs of target volumes and OARs compared well. The Chi pass rates using 3%/3mm in the high dose region are greater than 97% in all cases. These initial results demonstrate clinical feasibility and utility of a robust, efficient, effective and convenient pre-treatment QA method using EPID. Research sponsored in part by Varian Medical Systems.
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Radical treatment techniques such as stereotactic body radiation therapy (SBRT) are becoming popular and they involve delivery of large doses in fewer fractions. Due to this feature of SBRT, a high-resolution, pre-treatment dose verification method that makes use of a 3D patient representation would be appropriate. Such a technique will provide additional information about dose delivered to the target volume(s) and organs-at-risk (OARs) in the patient volume compared to 2D verification methods. In this work, we investigate an electronic portal imaging device (EPID) based pre-treatment QA method which provides an accurate reconstruction of the 3D-dose distribution in the patient model. Customized patient plans are delivered ‘in air’ and the portal images are collected using the EPID in cine mode. The images are then analysed to determine an estimate of the incident energy fluence. This is then passed to a collapsed-cone convolution dose algorithm which reconstructs a 3D patient dose estimate on the CT imaging dataset. To date, the method has been applied to 5 SBRT patient plans. Reconstructed doses were compared to those calculated by the TPS. Reconstructed mean doses were mostly within 3% of those in the TPS. DVHs of target volumes and OARs compared well. The Chi pass rates using 3%/3mm in the high dose region are greater than 97% in all cases. These initial results demonstrate clinical feasibility and utility of a robust, efficient, effective and convenient pre-treatment QA method using EPID. Research sponsored in part by Varian Medical Systems
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The simulation and verification framework developed by the RD53 collaboration is a powerful tool for global architecture optimization and design verification of next generation hybrid pixel readout chips. In this paper the framework is used for studying digital pixel chip architectures at behavioral level. This is carried out by simulating a dedicated, highly parameterized pixel chip description, which makes it possible to investigate different grouping strategies between pixels and different latency buffering and arbitration schemes. The pixel hit information used as simulation input can be either generated internally in the framework or imported from external Monte Carlo detector simulation data. The latter have been provided by both the CMS and ATLAS experiments, featuring HL-LHC operating conditions and the specifications related to the Phase 2 upgrade. Pixel regions and double columns were simulated using such Monte Carlo data as inputs: the performance of different latency buffering architectures was compared and the compliance of different link speeds with the expected column data rate was verified
Brons, S; Elsässer, T; Ferrari, A; Gadioli, E; Mairani, A; Parodi, K; Sala, P; Scholz, M; Sommerer, F
2010-01-01
Monte Carlo codes are rapidly spreading among hadron therapy community due to their sophisticated nuclear/electromagnetic models which allow an improved description of the complex mixed radiation field produced by nuclear reactions in therapeutic irradiation. In this contribution results obtained with the Monte Carlo code FLUKA are presented focusing on the production of secondary fragments in carbon ion interaction with water and on CT-based calculations of absorbed and biological effective dose for typical clinical situations. The results of the simulations are compared with the available experimental data and with the predictions of the GSI analytical treatment planning code TRiP.
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Valente, Mauro [CONICET - Consejo Nacional de Investigaciones Cientificas y Tecnicas de La Republica Argentina (Conicet), Buenos Aires, AR (Brazil); Botta, Francesca; Pedroli, Guido [European Institute of Oncology, Milan (Italy). Medical Physics Department; Perez, Pedro, E-mail: valente@famaf.unc.edu.ar [Universidad Nacional de Cordoba, Cordoba (Argentina). Fac. de Matematica, Astronomia y Fisica (FaMAF)
2012-07-01
Beta-emitters have proved to be appropriate for radioimmunotherapy. The dosimetric characterization of each radionuclide has to be carefully investigated. One usual and practical dosimetric approach is the calculation of dose distribution from a unit point source emitting particles according to any radionuclide of interest, which is known as dose point kernel. Absorbed dose distributions are due to primary and radiation scattering contributions. This work presented a method capable of performing dose distributions for nuclear medicine dosimetry by means of Monte Carlo methods. Dedicated subroutines have been developed in order to separately compute primary and scattering contributions to the total absorbed dose, performing particle transport up to 1 keV or least. Preliminarily, the suitability of the calculation method has been satisfactory, being tested for monoenergetic sources, and it was further applied to the characterization of different beta-minus radionuclides of nuclear medicine interests for radioimmunotherapy. (author)
A study of potential numerical pitfalls in GPU-based Monte Carlo dose calculation
Magnoux, Vincent; Ozell, Benoît; Bonenfant, Éric; Després, Philippe
2015-07-01
The purpose of this study was to evaluate the impact of numerical errors caused by the floating point representation of real numbers in a GPU-based Monte Carlo code used for dose calculation in radiation oncology, and to identify situations where this type of error arises. The program used as a benchmark was bGPUMCD. Three tests were performed on the code, which was divided into three functional components: energy accumulation, particle tracking and physical interactions. First, the impact of single-precision calculations was assessed for each functional component. Second, a GPU-specific compilation option that reduces execution time as well as precision was examined. Third, a specific function used for tracking and potentially more sensitive to precision errors was tested by comparing it to a very high-precision implementation. Numerical errors were found in two components of the program. Because of the energy accumulation process, a few voxels surrounding a radiation source end up with a lower computed dose than they should. The tracking system contained a series of operations that abnormally amplify rounding errors in some situations. This resulted in some rare instances (less than 0.1%) of computed distances that are exceedingly far from what they should have been. Most errors detected had no significant effects on the result of a simulation due to its random nature, either because they cancel each other out or because they only affect a small fraction of particles. The results of this work can be extended to other types of GPU-based programs and be used as guidelines to avoid numerical errors on the GPU computing platform.
Directory of Open Access Journals (Sweden)
Karimian Alireza
2014-01-01
Full Text Available Nowadays, dual energy X-ray absorptiometry is used in bone mineral density systems to assess the amount of osteoporosis. The purpose of this research is to evaluate patient organ doses from dual X-ray absorptiometry by thermoluminescence dosimeters chips and Monte Carlo method. To achieve this goal, in the first step, the surface dose of the cervix, kidney, abdomen region, and thyroid were measured by using TLD-GR 200 at various organ locations. Then, to evaluate the absorbed dose by simulation, the BMD system, patient's body, X-ray source and radiosensitive tissues were simulated by the Monte Carlo method. The results showed, for the spine (left femur bone mineral density scan by using thermoluminescence dosimeters, the absorbed doses of the cervix and kidney were 4.5 (5.64 and 162.17 (3.99(mGy, respectively. For spine (left femur bone mineral density scan in simulation, the absorbed doses of the cervix and kidney were 4.19 (5.88 and 175 (3.68(mGy, respectively. The data obtained showed that the absorbed dose of the kidney in the spine scan is noticeable. Furthermore, because of the small relative difference between the simulation and experimental results, the radiation absorbed dose may be assessed by simulation and software, especially for internal organs, and at different depths of otherwise inaccessible organs which is not possible in experiments.
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Monte Carlo simulation has been used by many researchers to calculate organ and effective dose of patients arising from conventional X-ray examinations. In this study the radiation transport code, MCNP4C, has been used to perform Monte Carlo simulations to estimate radiation dose delivered to different organs in conventional X-ray examinations. Materials and Methods: In this work we have made use of ORNL mathematical phantoms with few modifications which have been made. The source has been defined as a point source, emitting photons into a solid angle. The X-ray beam was shaped by a collimator to produce a rectangular field at the midline of the phantom. Results: to validate the simulation executed in this study normalized organs doses to unit ESD for hermaphrodite phantom were computed. Our results were compared with corresponding values presented by NRPB. In general organs doses obtained by application of MCNP-4C (present study) and corresponding values presented in NRPB were in good agreement. For further evaluation of our phantom, the values acquired for organ and effective doses by MCNP-4C and ODS-60 were compared. Conclusion: the technique we have developed is capable of estimating organ and effective doses with a better accuracy than dose values obtained by employment of NRPB and ODS-60 technique
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Purpose: The electronic portal imaging device (EPID) is a system for checking the patient setup; as a result of its integration with the linear accelerator and software customized for dosimetry, it is increasingly used for verification of the delivery of fixed-field intensity-modulated radiation therapy (IMRT). In order to extend such an approach to intensity-modulated arc therapy (IMAT), the combined use of an EPID system and a portal dose image prediction (PDIP) tool has been investigated. Methods: The dosimetric behavior of an EPID system, mechanically reinforced to maintain its positional stability during the accelerator gantry rotation, has been studied to assess its ability to measure portal dose distributions for IMAT treatment beams. In addition, the PDIP tool of a commercial treatment planning system, commonly used for static IMRT dosimetry, has been validated for simulating the PDIs of IMAT treatment fields. The method has been applied to the delivery verification of 23 treatment fields that were measured in their dual mode of IMRT and IMAT modalities. Results: The EPID system has proved to be appropriate for measuring the PDIs of IMAT fields; additionally the PDIP tool was able to simulate these accurately. The results are quite similar to those obtained for static IMRT treatment verification, although it was necessary to investigate the dependence of the EPID signal and of the accelerator monitor chamber response on variable dose rate. Conclusions: Our initial tests indicate that the EPID system, together with the PDIP tool, is a suitable device for the verification of IMAT plan delivery; however, additional tests are necessary to confirm these results.
The effects of incidence angle on film dosimetry and their consequences in IMRT dose verification
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Purpose: The dosimetric accuracy of EDR2 radiographic film has been rigorously assessed in regular and intensity modulated beams for various incidence angles, including the parallel and perpendicular orientation. There clearly exists confusion in literature regarding the effect of film orientation. The primary aim is to clarify potential sources of the confusion and to gain physical insight into the film orientation effect with a link to radiochromic film as well. Methods: An inverse pyramid IMRT field, consisting of six regular and elongated 3 × 20 cm2 field segments, was studied in perpendicular and parallel orientation. Assessment of film self-perturbation and intrinsic directional sensitivity were also included in the experiments. Finally, the authors investigated the orientational effect in composite beams in the two extreme orientations, i.e., perpendicular and parallel. Results: The study of an inverse pyramid dose profile revealed good agreement between the perpendicular film and the diamond detector within 0.5% in the low-scatter regions for both 6 and 18 MV. The parallel oriented film demonstrated a 3% under-response at 5-cm (6 MV) depth against the perpendicular orientation, but both orientations over responded equally in the central region, which received only scattered dose, at both 5- and 20-cm depths. In a regular 6-MV 5 × 5 cm2 field, a 4.1% lower film response was observed in the parallel orientation compared to perpendicular orientation. The under response gradually increased to 6% when reducing the field size to 0.5 × 5 cm2. On the other hand, the film showed a 1.7% lower response in parallel orientation for the large field size of 20 × 20 cm2 at 5-cm depth but the difference disappeared at 10 cm. At 18 MV, similar but somewhat lower differences were found between the two orientations. The directional sensitivity of the film diminishes with increasing field size and depth. Surprisingly a composite IMRT beam consisting of 20 adjacent strip
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Purpose: To construct a dose monitoring system based on an endorectal balloon coupled to thin scintillating fibers to study the dose delivered to the rectum during prostate cancer proton therapy Methods: The Geant4 Monte Carlo toolkit version 9.6p02 was used to simulate prostate cancer proton therapy treatments of an endorectal balloon (for immobilization of a 2.9 cm diameter prostate gland) and a set of 34 scintillating fibers symmetrically placed around the balloon and perpendicular to the proton beam direction (for dosimetry measurements) Results: A linear response of the fibers to the dose delivered was observed within <2%, a property that makes them good candidates for real time dosimetry. Results obtained show that the closest fiber recorded about 1/3 of the dose to the target with a 1/r2 decrease in the dose distribution as one goes toward the frontal and distal top fibers. Very low dose was recorded by the bottom fibers (about 45 times comparatively), which is a clear indication that the overall volume of the rectal wall that is exposed to a higher dose is relatively minimized. Further analysis indicated a simple scaling relationship between the dose to the prostate and the dose to the top fibers (a linear fit gave a slope of −0.07±0.07 MeV per treatment Gy) Conclusion: Thin (1 mm × 1 mm × 100 cm) long scintillating fibers were found to be ideal for real time in-vivo dose measurement to the rectum for prostate cancer proton therapy. The linear response of the fibers to the dose delivered makes them good candidates of dosimeters. With thorough calibration and the ability to define a good correlation between the dose to the target and the dose to the fibers, such dosimeters can be used for real time dose verification to the target
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Water in soil affects the dose rate in sedimentary media. First it dilutes the radioelements, and second the mass stopping power as well as photon interaction cross sections are greater in water than in typical sediment constituents (). Here the effect of moisture on the gamma dose rate is investigated using Monte Carlo simulations based on the GEANT4 toolkit. Dose deposition processes are studied on the scale of individual grains in modelled well-sorted sediments: detailed tracking of gamma rays and secondary electrons shed light on the relative importance of the different interaction modes at stake, as a function of grain size, porosity and fraction of saturation of the sediments, as well as the energy of gamma rays. A description of the specifically designed GEANT4 codes is provided, followed by a comprehensive analysis of the phenomena. It is shown that geometry effects, specifically grain size and compactness, have a great impact on gamma dose rates received by sediment grains and that these can be quantified in the case of very simple grain assemblages. For a better accuracy in retrospective dosimetry dating methods, morphological features of the sediments that influence dose rates should be characterized and their influence on dose rate studied; Monte Carlo transport codes seem to be the favoured tools for that purpose.
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Lucas Paixão
2015-12-01
Full Text Available Abstract Objective: Derive filtered tungsten X-ray spectra used in digital mammography systems by means of Monte Carlo simulations. Materials and Methods: Filtered spectra for rhodium filter were obtained for tube potentials between 26 and 32 kV. The half-value layer (HVL of simulated filtered spectra were compared with those obtained experimentally with a solid state detector Unfors model 8202031-H Xi R/F & MAM Detector Platinum and 8201023-C Xi Base unit Platinum Plus w mAs in a Hologic Selenia Dimensions system using a direct radiography mode. Results: Calculated HVL values showed good agreement as compared with those obtained experimentally. The greatest relative difference between the Monte Carlo calculated HVL values and experimental HVL values was 4%. Conclusion: The results show that the filtered tungsten anode X-ray spectra and the EGSnrc Monte Carlo code can be used for mean glandular dose determination in mammography.
Paixão, Lucas; Oliveira, Bruno Beraldo; Viloria, Carolina; de Oliveira, Marcio Alves; Teixeira, Maria Helena Araújo; Nogueira, Maria do Socorro
2015-01-01
Objective Derive filtered tungsten X-ray spectra used in digital mammography systems by means of Monte Carlo simulations. Materials and Methods Filtered spectra for rhodium filter were obtained for tube potentials between 26 and 32 kV. The half-value layer (HVL) of simulated filtered spectra were compared with those obtained experimentally with a solid state detector Unfors model 8202031-H Xi R/F & MAM Detector Platinum and 8201023-C Xi Base unit Platinum Plus w mAs in a Hologic Selenia Dimensions system using a direct radiography mode. Results Calculated HVL values showed good agreement as compared with those obtained experimentally. The greatest relative difference between the Monte Carlo calculated HVL values and experimental HVL values was 4%. Conclusion The results show that the filtered tungsten anode X-ray spectra and the EGSnrc Monte Carlo code can be used for mean glandular dose determination in mammography. PMID:26811553
IMRT dose delivery effects in radiotherapy treatment planning using Monte Carlo methods
Tyagi, Neelam
Inter- and intra-leaf transmission and head scatter can play significant roles in Intensity Modulated Radiation Therapy (IMRT)-based treatment deliveries. In order to accurately calculate the dose in the IMRT planning process, it is therefore important that the detailed geometry of the multi-leaf collimator (MLC), in addition to other components in the accelerator treatment head be accurately modeled. In this thesis Monte Carlo (MC) methods have been used to model the treatment head of a Varian linear accelerator. A comprehensive model of the Varian 120-leaf MLC has been developed within the DPM MC code and has been verified against measurements in homogeneous and heterogeneous phantom geometries under different IMRT delivery circumstances. Accuracy of the MLC model in simulating details in the leaf geometry has been established over a range of arbitrarily shaped fields and IMRT fields. A sensitivity analysis of the effect of the electron-on-target parameters and the structure of the flattening filter on the accuracy of calculated dose distributions has been conducted. Adjustment of the electron-on-target parameters resulting in optimal agreement with measurements was an iterative process, with the final parameters representing a tradeoff between small (3x3 cm2) and large (40x40 cm2) field sizes. A novel method based on adaptive kernel density estimation, in the phase space simulation process is also presented as an alternative to particle recycling. Using this model dosimetric differences between MLC-based static (SMLC) and dynamic (DMLC) deliveries have been investigated. Differences between SMLC and DMLC, possibly related to fluence and/or spectral changes, appear to vary systematically with the density of the medium. The effect of fluence modulation due to leaf sequencing shows differences, up to 10% between plans developed with 1% and 10% fluence intervals for both SMLC and DMLC-delivered sequences. Dose differences between planned and delivered leaf sequences
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Organ doses from environmental γ-rays (U-238, Th-232, K-40) were calculated using Monte Carlo methods for three typical sources of a semi-infinite volume source in the air, an infinite plane source in the ground and a volume source in the ground. γ-ray fields in the natural environment were simulated rigourously without approximations or simplifications in the intermediate steps except for the disturbance of the radiation field by the human body which was neglected. Organ doses were calculated for four anthropomorphic phantoms representing a baby, a child, a female and a male adult. The dose of a fetus is given by the dose to the uterus of the adult female. Air kerma and dose conversion factors normalised to air kerma and to source intensity are given for monoenergetic sources and for the natural radionuclides. (orig./HP)
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Consideration is given to the implications of parameter uncertainty on the output of a mathematical model describing the atmospheric dispersion of 131I, transport through the food chain into milk and the subsequent dose to the thyroid gland of infants resulting from milk ingestion. The approach used was a Monte-Carlo procedure which calculates the dose to the thyroid based on parameters whose values were randomly selected from a normal distribution about their means, stores the results and then repeats the process for other randomly selected parameter values. Predicted doses to the thyroid are log-normally distributed, with the mode strongly shifting to the left and a long tail extending to higher doses. Given parameter uncertainties, the present model predicts that it is possible to receive a dose that is an order of magnitude higher than the prediction obtained by inserting the mean value for each parameter into the model, i.e. the deterministic prediction. (U.K.)
Indian Academy of Sciences (India)
V C Petwal; J N Rao; Jishnu Dwivedi; V K Senecha; K V Subbaiah
2010-03-01
A prototype pulsed electron beam irradiation facility for radiation processing of food and medical products is being commissioned at our centre in Indore, India. Analysis of surface dose and uniformity for a pulsed beam facility is of crucial importance because it is influenced by various operating parameters such as beam current, pulse repetition rate (PRR), scanning current profile and frequency, scanning width and product conveying speed. A large number of experiments are required to determine the harmonized setting of these operating parameters for achieving uniform dose. Since there is no readily available tool to set these parameters, use of Monte Carlo methods and computational tools can prove to be the most viable and time saving technique to support the assessment of the dose distribution. In the present study, Monte Carlo code, MCNP, is used to simulate the transport of 10 MeV electron beam through various mediums coming into the beam path and generate an equivalent dose profile in a polystyrene phantom for stationary state. These results have been verified with experimentally measured dose profile, showing that results are in good agreement within 4%. The Monte Carlo simulation further has been used to optimize the overlapping between the successive pulses of a scan to achieve ± 5% dose uniformity along the scanning direction. A mathematical model, which uses the stationary state data, is developed to include the effect of conveyor speed. The algorithm of the model is discussed and the results are compared with the experimentally measured values, which show that the agreement is better than 15%. Finally, harmonized setting for operating parameters of the accelerator are derived to deliver uniform surface dose in the range of 1–13 kGy/pass.
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Purpose: A unique method of delivering radiation dose to the coronary vessel wall to prevent restenosis is by direct injection of radioactive compounds into the vessel wall using a specially designed angioplasty balloon catheter. The radiation dose distribution resulting from such intramural delivery was investigated using Monte Carlo simulations. Materials and methods: The radioisotope source distribution was modeled for two configurations within the vessel wall: (1) uniform to a depth of 0.5 mm and (2) confined to discrete pools surrounding the delivery injection ports. Monte Carlo MCNP4B computer simulations were utilized to estimate the associated radiation dose distribution for the following radioisotopes: 188Re, 186Re, 32P, 153Sm, 111In, 123I, and 99mTc. Results: For the uniform case where the radioisotopes are distributed uniformly to the depth of 0.5 mm into the vessel wall, an essentially constant radiation dose is delivered within the source distribution. Outside of the source volume, the dose falls off at a rate depending on the emission properties of the particular radioisotope. The nonuniform case involving discrete pools of activity showed the dose distribution being confined largely to the regions surrounding the delivery ports with significant regions between these ports receiving very little dose. Conclusions: Direct injection of selected radioisotopes into the arterial wall appears to represent a potentially effective method for delivering radiation dose for the prevention of restenosis. Sufficiently high doses may be obtained from relatively low activity and the dose falls off rapidly outside of the target area for certain radioisotopes
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With the rapidly growing number of CT examinations, the consequential radiation risk has aroused more and more attention. The average dose in each organ during CT scans can only be obtained by using Monte Carlo simulation with computational phantoms. Since children tend to have higher radiation sensitivity than adults, the radiation dose of pediatric CT examinations requires special attention and needs to be assessed accurately. So far, studies on organ doses from CT exposures for pediatric patients are still limited. In this work, a 1-year-old computational phantom was constructed. The body contour was obtained from the CT images of a 1-year-old physical phantom and the internal organs were deformed from an existing Chinese reference adult phantom. To ensure the organ locations in the 1-year-old computational phantom were consistent with those of the physical phantom, the organ locations in 1-year-old computational phantom were manually adjusted one by one, and the organ masses were adjusted to the corresponding Chinese reference values. Moreover, a CT scanner model was developed using the Monte Carlo technique and the 1-year-old computational phantom was applied to estimate organ doses derived from simulated CT exposures. As a result, a database including doses to 36 organs and tissues from 47 single axial scans was built. It has been verified by calculation that doses of axial scans are close to those of helical scans; therefore, this database could be applied to helical scans as well. Organ doses were calculated using the database and compared with those obtained from the measurements made in the physical phantom for helical scans. The differences between simulation and measurement were less than 25% for all organs. The result shows that the 1-year-old phantom developed in this work can be used to calculate organ doses in CT exposures, and the dose database provides a method for the estimation of 1-year-old patient doses in a variety of CT examinations. (paper)
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This report presents a tabulation of organ and tissue equivalent dose as well as effective dose conversion coefficients, normalised to air kerma free in air, for occupational exposures and environmental exposures of the public to external photon radiation. For occupational exposures, whole-body irradiation with idealised geometries, i.e. broad parallel beams and fully isotropic radiation incidence, is considered. The directions of incidence for the parallel beams are anterior-posterior, posterior-anterior, left lateral, right lateral and a full 360 rotation around the body's longitudinal axis. The influence of beam divergence on the body doses is also considered as well as the dependence of effective dose on the angle of radiation incidence. Regarding exposure of the public to environmental sources, three source geometries are considered: exposure from a radioactive cloud, from ground contamination and from the natural radionuclides distributed homogeneously in the ground. The precise angular and energy distributions of the gamma rays incident on the human body were taken into account. The organ dose conversion coefficients given in this catalogue were calculated using a Monte Carlo code simulating the photon transport in mathematical models of an adult male and an adult female, respectively. Conversion coefficients are given for the equivalent dose of 23 organs and tissues as well as for effective dose and the equivalent dose of the so-called 'remainder'. The organ equivalent dose conversion coefficients are given separately for the adult male and female models and - as arithmetic mean of the conversion coefficients of both - for an average adult. Fitted data of the coefficients are presented in tables; the primary raw data as resulting from the Monte Carlo calculation are shown in figures together with the fitted data. (orig.)
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100 monitor units. Over this range, the prototype and standard EPID central axis responses agreed to within 1.6%. Images taken with the prototype EPID were noisier than those taken with the standard EPID, with fractional uncertainties of 0.2% and 0.05% within the central 1 cm2, respectively. For all dosimetry measurements, the prototype EPID exhibited a near water-equivalent response whereas the standard EPID did not. The CNR and spatial resolution of images taken with the standard EPID were greater than those taken with the prototype EPID.Conclusions: A prototype EPID employing an array of PS fibers has been developed and the first experimental measurements are reported. The prototype EPID demonstrated a much morewater-equivalent dose response than the standard EPID. While the imaging performance of the standard EPID was superior to that of the prototype, the prototype EPID has many design characteristics that may be optimized to improve imaging performance. This investigation demonstrates the feasibility of a new detector design for simultaneous imaging and dosimetry treatment verification in radiotherapy
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Knowing the depth dose at the central axis is fundamental for the accurate planning of medical treatment systems involving ionizing radiation. With the evolution of the informatics it is possible the utilization of various computational tools such as GEANT4 and the MCNPX, which use the Monte Carlo Method for simulation of such situations, This paper makes a comparative between the two tools for the this type of application
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Long, Daniel J.; Lee, Choonsik; Tien, Christopher; Fisher, Ryan; Hoerner, Matthew R.; Hintenlang, David; Bolch, Wesley E. [J Crayton Pruitt Family Department of Biomedical Engineering, University of Florida, Gainesville, Florida 32611-6131 (United States); National Cancer Institute, National Institute of Health, Bethesda, Maryland 20892-1502 (United States); J Crayton Pruitt Family Department of Biomedical Engineering, University of Florida, Gainesville, Florida 32611-6131 (United States); Department of Radiology, University of Florida, Gainesville, Florida 32610-0374 (United States); J Crayton Pruitt Family Department of Biomedical Engineering, University of Florida, Gainesville, Florida 32611-6131 (United States)
2013-01-15
Purpose: To validate the accuracy of a Monte Carlo source model of the Siemens SOMATOM Sensation 16 CT scanner using organ doses measured in physical anthropomorphic phantoms. Methods: The x-ray output of the Siemens SOMATOM Sensation 16 multidetector CT scanner was simulated within the Monte Carlo radiation transport code, MCNPX version 2.6. The resulting source model was able to perform various simulated axial and helical computed tomographic (CT) scans of varying scan parameters, including beam energy, filtration, pitch, and beam collimation. Two custom-built anthropomorphic phantoms were used to take dose measurements on the CT scanner: an adult male and a 9-month-old. The adult male is a physical replica of University of Florida reference adult male hybrid computational phantom, while the 9-month-old is a replica of University of Florida Series B 9-month-old voxel computational phantom. Each phantom underwent a series of axial and helical CT scans, during which organ doses were measured using fiber-optic coupled plastic scintillator dosimeters developed at University of Florida. The physical setup was reproduced and simulated in MCNPX using the CT source model and the computational phantoms upon which the anthropomorphic phantoms were constructed. Average organ doses were then calculated based upon these MCNPX results. Results: For all CT scans, good agreement was seen between measured and simulated organ doses. For the adult male, the percent differences were within 16% for axial scans, and within 18% for helical scans. For the 9-month-old, the percent differences were all within 15% for both the axial and helical scans. These results are comparable to previously published validation studies using GE scanners and commercially available anthropomorphic phantoms. Conclusions: Overall results of this study show that the Monte Carlo source model can be used to accurately and reliably calculate organ doses for patients undergoing a variety of axial or helical CT
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Purpose: To validate the accuracy of a Monte Carlo source model of the Siemens SOMATOM Sensation 16 CT scanner using organ doses measured in physical anthropomorphic phantoms. Methods: The x-ray output of the Siemens SOMATOM Sensation 16 multidetector CT scanner was simulated within the Monte Carlo radiation transport code, MCNPX version 2.6. The resulting source model was able to perform various simulated axial and helical computed tomographic (CT) scans of varying scan parameters, including beam energy, filtration, pitch, and beam collimation. Two custom-built anthropomorphic phantoms were used to take dose measurements on the CT scanner: an adult male and a 9-month-old. The adult male is a physical replica of University of Florida reference adult male hybrid computational phantom, while the 9-month-old is a replica of University of Florida Series B 9-month-old voxel computational phantom. Each phantom underwent a series of axial and helical CT scans, during which organ doses were measured using fiber-optic coupled plastic scintillator dosimeters developed at University of Florida. The physical setup was reproduced and simulated in MCNPX using the CT source model and the computational phantoms upon which the anthropomorphic phantoms were constructed. Average organ doses were then calculated based upon these MCNPX results. Results: For all CT scans, good agreement was seen between measured and simulated organ doses. For the adult male, the percent differences were within 16% for axial scans, and within 18% for helical scans. For the 9-month-old, the percent differences were all within 15% for both the axial and helical scans. These results are comparable to previously published validation studies using GE scanners and commercially available anthropomorphic phantoms. Conclusions: Overall results of this study show that the Monte Carlo source model can be used to accurately and reliably calculate organ doses for patients undergoing a variety of axial or helical CT
Investigation of a MOSFET dosimetry system for midpoint dose verification in prostate 3D CRT/IMRT.
Wiese, T; Bezak, E; Nelligan, R
2008-09-01
The suitability of MOSFETs (Metal Oxide Semiconductor Field Effect Transistors) for use in in-vivo dosimetry for IMRT prostate treatment and patient setup errors has been investigated in this work. MOSFETs were placed on entrance and exit surfaces of a number of different phantoms (with varying complexities from homogeneous to anthropomorphic). Dose measurements were then used to calculate a midpoint dose, which was compared with an IC placed at the isocentre. The agreements found between the calculated (MOSFETs) and the measured midpoint dose (IC) was: 0.7% for a prostate treatment verification and 3.5% for an IMRT treatment. MOSFETs placed on entry and exit surfaces can detect patient setup offsets of 2 cm, but do not have the sensitivity to confidently detect offsets of 1 cm or smaller. PMID:18946975
The implementation in-house dose verification for IMRT and VMAT on breast cancer and NPC cases
Azzi, A.; Dimitri, F. Y.; Pawiro, S. A.
2016-03-01
IMRT and VMAT have been widely implemented on breast cancer and NPC cases. Dose verification was conducted to ensure the comparison between dose delivered and prescribe dose in TPS to obtain optimal results and the dose delivered. The gafchromic films measurement was done for breast and NPC simulation on RANDO Phantom, irradiating film by 6 MV photon with 200 cGy and scanned with EPSON V700 using 72 dpi. Dose distribution was calculated using the MATLAB-based in-house algorithm. In order to evaluate the gamma index, gafchromic films and MatriXX 2D array were placed in the Multi Cube and irradiated with EPID in same position. Dose distribution differences for IMRT and VMAT with modalities to TPS on film was 5.34% and 6.68% for NPC PTV70; 12.81% and 6.15% for NPC PTV50; 11.14% and 10.80% for breast cancer. Gamma index differences on IMRT with modalities to MatriXX 2D array and EPID was -0.09% and 5.13% for NPC; 0.51% and 2.28% for breast cancer. On the other hand, gamma index difference on VMAT was -1.65% and 1.43% for NPC; 0.19% and 4.38% for breast cancer. This measurement method can be used to verify dose for breast cancer and NPC cases in IMRT and VMAT.
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Computed tomography (CT) is a technique which offers a high diagnostic capability; however, the dose to the patient is high compared to conventional radiography. This report provides a catalogue of organ doses resulting from CT examinations. The organ doses were calculated for the type of CT scanners most commonly used in the FRG and for three different radiation qualities. For the dose calculations, the patients were represented by the adult mathematical phantoms Adam and Eva. The radiation transport in the body was simulated using a Monte Carlo method. The doses were calculated as conversion factors of mean organ doses per air kerma free in air on the axis of rotation. Mean organ dose conversion factors are given per organ and per single CT slice of 1 cm width. The mean dose to an organ resulting from a particular CT examination can be estimated by summing up the contribution to the organ dose from each relevant slice. In order to facilitate the selection of the appropriate slices, a table is given which relates the mathematical phantoms' coordinates to certain anatomical landmarks in the human body. (orig.)
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Digital breast tomosynthesis (DBT) is a screening and diagnostic modality that acquires images of the breast at multiple angles during a short scan. The Selenia Dimensions (Hologic, Bedford, Mass) DBT system can perform both full-field digital mammography and DBT. The system acquires 15 projections over a 15 deg. angular range (from -7.5 deg. to +7.5 deg.). An important factor in determining the optimal imaging technique for breast tomosynthesis is the radiation dose. In breast imaging, the radiation dose of concern is that deposited in the glandular tissue of the breast because this is the tissue that has a risk of developing cancer. The concept of the normalised mean glandular dose (DgN) has been introduced as the metric for the dose in breast imaging. The DgN is difficult to measure. The Monte Carlo techniques offer an alternative method for a realistic estimation of the radiation dose. The purpose of this work was to use the Monte Carlo code MCNPX technique to generate monoenergetic glandular dose data for estimating the breast tissue dose in tomosynthesis for arbitrary spectra as well as to observe the deposited radiation dose by projection on the glandular portion of the breast in a Selenia Dimensions DBT system. A Monte Carlo simulation of the system was developed to compute the DgN in a craniocaudal view. Monoenergetic X-ray beams from 10 to 49 keV in 1-keV increments were used. The simulation utilised the assumption of a homogeneous breast composition and three compositions (0 % glandular, 50 % glandular and 100 % glandular). The glandular and adipose tissue compositions were specified according ICRU Report 44. A skin layer of 4 mm was assumed to encapsulate the breast on all surfaces. The breast size was varied using the chest wall-to-nipple distance (CND) and compressed breast thickness (t). In this work, the authors assumed a CND of 5 cm and the thicknesses ranged from 2 to 8 cm, in steps of 2 cm. The fractional energy absorption increases (up to 44
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The four primary radiation measurement systems considered to be necessary for the modern radionuclide measurement laboratory are gas-flow proportional counters, liquid scintillation counters, Si spectrometer systems, and Ge spectrometer systems. A national institute of standards recognized by BIPM (Bureau International des Poids et Mesures) use these measurement systems have some limitation. For a gas-filled detector, the source size should not be larger than that determined by the counter geometry and the measurements are limited to sources with the activities of less than 20,000 Bq. A liquid scintillation detector can only be used to measure an activity of liquid mixture isotope. Therefore it can't be used to measure activities of sealed sources. Further it is quite difficult to measure a radioactivity of beta-isotope accurately due to self-absorption and scattering. In particular an radioactivity generated by a nuclear reactor is approximately calculated by using target material compositions, cross-sections, and neutron flux, which the nuclear reactor. However, the results from this approach involve a high uncertainty. We develop a Monte Carlo applied radioactivity determination for beta sources. The extrapolation ion-chamber was used to measure the surface dose rate for a standard source. The Sr/Y-90 standard source is calibrated by NIST used for this study. There was about 1.7% difference in the reference dose rates measured by the two techniques. These difference and relative errors were comparable to those of other studies. It should be noticed that the area of collecting electrode was nine times larger than that of radiation field. It the diameter of the source is smaller than the area of collecting electrode, the source should be located at a sufficiently large distance from the detector surface so that the radiation field at the detector surface was larger than the area of collecting electrode. In addition, beta particles from the applicator interact
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Monte-Carlo simulation is one of the most essential computational tools to study the particle transport and interaction of radiation with matter as well as radiation protection and dosimetry. In this paper it was used to calculate percent depth doses in the water phantom for two Co-60 beam irradiation cases with using the MCNP-4C2 code. The simulation results was validated by comparison with those of measurements. Application of the MCNP-4C2 code for dose calculations in Co-60 beam treatment planning was recommended. (author)
Gharibian, Katherine N; Mueller, Bruce A
2016-07-01
Fluconazole is a renally-eliminated antifungal commonly used to treat Candida species infections. In critically-ill patients receiving prolonged intermittent renal replacement therapy (PIRRT), limited pharmacokinetic (PK) data are available to guide fluconazole dosing. We used previously-published fluconazole clearance data and PK data of critically-ill patients with acute kidney injury to develop a PK model with the goal of determining a therapeutic dosing regimen for critically-ill patients receiving PIRRT. Monte Carlo simulations were performed to create a virtual cohort of patients receiving different fluconazole dosing regimens. Plasma drug concentration-time profiles were evaluated on the probability of attaining a mean 24-hour area under the drug concentration-time curve to minimum inhibitory concentration ratio (AUC24h : MIC) of 100 during the initial 48 hours of antifungal therapy. At the susceptibility breakpoint of Candida albicans (2 mg/L), 93 - 96% of simulated subjects receiving PIRRT attained the pharmacodynamic target with a fluconazole 800-mg loading dose plus 400 mg twice daily (q12h or pre and post PIRRT) regimen. Monte Carlo simulations of a PK model of PIRRT provided a basis for the development of an informed fluconazole dosing recommendation when PK data was limited. This finding should be validated in the clinical setting. PMID:27251341
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The aim of this study was to quantify the dose enhancement by gadolinium and gold nanoparticles in brachytherapy. MCNPX Monte Carlo code was used to simulate four brachytherapy sources: 60Co, 198Au, 192Ir, 169Yb. To verify the accuracy of our simulations, the obtained values of dose rate constants and radial dose functions were compared with corresponding published values for these sources. To study dose enhancements, a spherical soft tissue phantom with 15 cm in radius was simulated. Gadolinium and gold nanoparticles at 10, 20 and 30 mg/ml concentrations were separately assumed in a 1 × 1 × 1 cm3 volume simulating tumour. The simulated dose to the tumour with the impurity was compared to the dose without impurity, as a function of radial distance and concentration of the impurity, to determine the enhancement of dose due to the presence of the impurity. Dose enhancements in the tumour obtained in the presence of gadolinium and gold nanoparticles with concentration of 30 mg/ml, were found to be in the range of −0.5–106.1 and 0.4–153.1 % respectively. In addition, at higher radial distances from the source center, higher dose enhancements were observed. GdNPs can be used as a high atomic number material to enhance dose in tumour volume with dose enhancements up to 106.1 % when used in brachytherapy. Regardless considering the clinical limitations of the here-in presented model, for a similar source and concentration of nanoparticles, gold nanoparticles show higher dose enhancement than gadolinium nanoparticles and can have more clinical usefulness as dose enhancer material.
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This report considers the contribution from scattered radiation to the dose to organs and tissues which lie outside the useful therapy beams. The results presented are the product of Monte Carlo studies used to determine the tissue doses due to internal scattering of the useful beams only. General cases are calculated in which central target volumes in the trunk are treated with 10 x 14 cm2 and 14 x 14 cm2 fields from 200 kV, Co-60, 8 MV and 25 MV therapy equipment. Target volumes in the neck are considered to be treated with 5 x 5 cm2 fields. Different treatment plans are calculated including rotational therapy. Also two specific cases are more fully analysed, namely for Ankylosing Spondylitis and central abdomen malignant disease in the region of the head of the pancreas. The calculated organ doses are presented in tables as a percentage of the target volume dose. (orig.)
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The purpose of this paper is to report a set of experimental values of patient and staff doses in a cardiac catheterisation laboratory using the range of radiographic and geometric parameters from routine clinical practice. The data obtained will be available for validation of Monte Carlo calculations and for training purposes. They will also help optimise radiation protection for patients and staff. Experimental measurements were made with an anthropomorphic phantom, and a monoplane flat detector-based X-ray system was used for interventional cardiology procedures. Standard operational protocols used in clinical practice were applied. Around 1000 patient dose and 5000 staff dose values were measured for different operational conditions (angulations, distances, collimation and wedge filter, magnification, phantom thicknesses, using Copper absorber, etc.). Uncertainties were also estimated. Increase factors of 3-10 for patients and staff doses were measured for the different C-arm angulations. (authors)
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Silva, Laura E. da; Nicolucci, Patricia, E-mail: laura.emilia.fm@gmail.com [Universidade de Sao Paulo (USP), Ribeirao Preto, SP (Brazil). Faculdade de Filosofia, Ciencias e Letras
2014-04-15
The development of nanotechnology has boosted the use of nanoparticles in radiation therapy in order to achieve greater therapeutic ratio between tumor and healthy tissues. Gold has been shown to be most suitable to this task due to the high biocompatibility and high atomic number, which contributes to a better in vivo distribution and for the local energy deposition. As a result, this study proposes to study, nanoparticle in the tumor cell. At a range of 11 nm from the nanoparticle surface, results have shown an absorbed dose 141 times higher for the medium with the gold nanoparticle compared to the water for an incident energy spectrum with maximum photon energy of 50 keV. It was also noted that when only scattered radiation is interacting with the gold nanoparticles, the dose was 134 times higher compared to enhanced local dose that remained significant even for scattered radiation. (author)
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Highlights: → The MCNP5 code has been used to model a radiotherapy room of a 18 MV linear accelerator. → The neutron and the secondary gamma ray dose equivalents were evaluated at various points inside the treatment room and along the the maze. → To reduce the neutron and gamma ray doses, we have also investigated the radiotherapy room shielding performance. → The use of paraffin wax containing boron carbide indicates much better shielding effects. - Abstract: Medical accelerators operating above 10 MV are a source of undesirable neutron radiations which contaminate the therapeutic photon beam. These photoneutrons can also generate secondary gamma rays which increases undesirable dose to the patient body and to personnel and general public. In this study, the Monte Carlo N-Particle MCNP5 code has been used to model the radiotherapy room of a medical linear accelerator operating at 18 MV and to calculate the neutron and the secondary gamma ray energy spectra and the dose equivalents at various points inside the treatment room and along the maze. To validate our Monte Carlo simulation we compared our results with those evaluated by the recommended analytical methods of IAEA Report No. 47, and with experimental and simulated values published in the literature. After validation, the Monte Carlo simulation has been used to evaluate the shielding performance of the radiotherapy room. The obtained results showed that the use of paraffin wax containing boron carbide, in the lining of the radiotherapy room walls, presents enough effectiveness to reduce both neutron and gamma ray doses inside the treatment room and at the maze entrance. Such evaluation cannot be performed by the analytical methods since room material and wall surface lining are not taken into consideration.
Kim, Sangroh; Yoshizumi, Terry; Toncheva, Greta; Yoo, Sua; Yin, Fang-Fang; Frush, Donald
2010-05-01
To address the lack of accurate dose estimation method in cone beam computed tomography (CBCT), we performed point dose metal oxide semiconductor field-effect transistor (MOSFET) measurements and Monte Carlo (MC) simulations. A Varian On-Board Imager (OBI) was employed to measure point doses in the polymethyl methacrylate (PMMA) CT phantoms with MOSFETs for standard and low dose modes. A MC model of the OBI x-ray tube was developed using BEAMnrc/EGSnrc MC system and validated by the half value layer, x-ray spectrum and lateral and depth dose profiles. We compared the weighted computed tomography dose index (CTDIw) between MOSFET measurements and MC simulations. The CTDIw was found to be 8.39 cGy for the head scan and 4.58 cGy for the body scan from the MOSFET measurements in standard dose mode, and 1.89 cGy for the head and 1.11 cGy for the body in low dose mode, respectively. The CTDIw from MC compared well to the MOSFET measurements within 5% differences. In conclusion, a MC model for Varian CBCT has been established and this approach may be easily extended from the CBCT geometry to multi-detector CT geometry. PMID:20386198
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Skyt, Peter S. [Dept. of Medical Physics, Aarhus Univ./Aarhus Univ. Hospital, Aarhus (Denmark); Dept. of Physics and Astronomy, Aarhus Univ., Aarhus (Denmark)], e-mail: skyt@phys.au.dk; Petersen, Joergen B. B.; Yates, Esben S.; Muren, Ludvig P. [Dept. of Medical Physics, Aarhus Univ./Aarhus Univ. Hospital, Aarhus (Denmark); Poulsen, Per R.; Ravkilde, Thomas L. [Dept. of Oncology, Aarhus Univ. Hospital, Aarhus (Denmark); Balling, Peter [Dept. of Physics and Astronomy, Aarhus Univ., Aarhus (Denmark)
2013-10-15
Background: The increasing complexity of radiotherapy (RT) has motivated research into three-dimensional (3D) dosimetry. In this study we investigate the use of 3D dosimetry with polymerizing gels and optical computed tomography (optical CT) as a verification tool for complex RT: dose painting and target tracking. Materials and Methods: For the dose painting studies, two dosimeters were irradiated with a seven-field intensity modulated radiotherapy (IMRT) plan with and without dose prescription based on a hypoxia image dataset of a head and neck patient. In the tracking experiments, two dosimeters were irradiated with a volumetric modulated arc therapy (VMAT) plan with and without clinically measured prostate motion and a third with both motion and target tracking. To assess the performance, 3D gamma analyses were performed between measured and calculated stationary dose distributions. Results: Gamma pass-rates of 95.3 % and 97.3 % were achieved for the standard and dose-painted IMRT plans. Gamma pass-rates of 91.4 % and 54.4 % were obtained for the stationary and moving dosimeter, respectively, while tracking increased the pass-rate for the moving dosimeter to 90.4 %. Conclusions: This study has shown that the 3D dosimetry system can reproduce and thus verify complex dose distributions, also when influenced by motion.
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Background: The increasing complexity of radiotherapy (RT) has motivated research into three-dimensional (3D) dosimetry. In this study we investigate the use of 3D dosimetry with polymerizing gels and optical computed tomography (optical CT) as a verification tool for complex RT: dose painting and target tracking. Materials and Methods: For the dose painting studies, two dosimeters were irradiated with a seven-field intensity modulated radiotherapy (IMRT) plan with and without dose prescription based on a hypoxia image dataset of a head and neck patient. In the tracking experiments, two dosimeters were irradiated with a volumetric modulated arc therapy (VMAT) plan with and without clinically measured prostate motion and a third with both motion and target tracking. To assess the performance, 3D gamma analyses were performed between measured and calculated stationary dose distributions. Results: Gamma pass-rates of 95.3 % and 97.3 % were achieved for the standard and dose-painted IMRT plans. Gamma pass-rates of 91.4 % and 54.4 % were obtained for the stationary and moving dosimeter, respectively, while tracking increased the pass-rate for the moving dosimeter to 90.4 %. Conclusions: This study has shown that the 3D dosimetry system can reproduce and thus verify complex dose distributions, also when influenced by motion
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The crucial problem for radiation shielding design at heavy-ion accelerator facilities with beam energies to several GeV/n is the source term problem. Experimental data on double differential neutron yields from thick target irradiated with high-energy uranium nuclei are lacking. At present, there are not many Monte-Carlo multipurpose codes that can work with primary high-energy uranium nuclei. These codes use different physical models for simulation of nucleus-nucleus reactions. Therefore, verification of the codes with available experimental data is very important for selection of the most reliable code for practical tasks. This paper presents comparisons of the FLUKA, GEANT4 and SHIELD codes simulations with the experimental data on neutron production at 1 GeV/n 238U beam interaction with thick Fe target
Vanderstraeten, Barbara; Reynaert, Nick; Paelinck, Leen; Madani, Indira; De Wagter, Carlos; De Gersem, Werner; De Neve, Wilfried; Thierens, Hubert
2006-09-01
The accuracy of dose computation within the lungs depends strongly on the performance of the calculation algorithm in regions of electronic disequilibrium that arise near tissue inhomogeneities with large density variations. There is a lack of data evaluating the performance of highly developed analytical dose calculation algorithms compared to Monte Carlo computations in a clinical setting. We compared full Monte Carlo calculations (performed by our Monte Carlo dose engine MCDE) with two different commercial convolution/superposition (CS) implementations (Pinnacle-CS and Helax-TMS's collapsed cone model Helax-CC) and one pencil beam algorithm (Helax-TMS's pencil beam model Helax-PB) for 10 intensity modulated radiation therapy (IMRT) lung cancer patients. Treatment plans were created for two photon beam qualities (6 and 18 MV). For each dose calculation algorithm, patient, and beam quality, the following set of clinically relevant dose-volume values was reported: (i) minimal, median, and maximal dose (Dmin, D50, and Dmax) for the gross tumor and planning target volumes (GTV and PTV); (ii) the volume of the lungs (excluding the GTV) receiving at least 20 and 30 Gy (V20 and V30) and the mean lung dose; (iii) the 33rd percentile dose (D33) and Dmax delivered to the heart and the expanded esophagus; and (iv) Dmax for the expanded spinal cord. Statistical analysis was performed by means of one-way analysis of variance for repeated measurements and Tukey pairwise comparison of means. Pinnacle-CS showed an excellent agreement with MCDE within the target structures, whereas the best correspondence for the organs at risk (OARs) was found between Helax-CC and MCDE. Results from Helax-PB were unsatisfying for both targets and OARs. Additionally, individual patient results were analyzed. Within the target structures, deviations above 5% were found in one patient for the comparison of MCDE and Helax-CC, while all differences between MCDE and Pinnacle-CS were below 5%. For both
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The accuracy of dose computation within the lungs depends strongly on the performance of the calculation algorithm in regions of electronic disequilibrium that arise near tissue inhomogeneities with large density variations. There is a lack of data evaluating the performance of highly developed analytical dose calculation algorithms compared to Monte Carlo computations in a clinical setting. We compared full Monte Carlo calculations (performed by our Monte Carlo dose engine MCDE) with two different commercial convolution/superposition (CS) implementations (Pinnacle-CS and Helax-TMS's collapsed cone model Helax-CC) and one pencil beam algorithm (Helax-TMS's pencil beam model Helax-PB) for 10 intensity modulated radiation therapy (IMRT) lung cancer patients. Treatment plans were created for two photon beam qualities (6 and 18 MV). For each dose calculation algorithm, patient, and beam quality, the following set of clinically relevant dose-volume values was reported: (i) minimal, median, and maximal dose (Dmin, D50, and Dmax) for the gross tumor and planning target volumes (GTV and PTV); (ii) the volume of the lungs (excluding the GTV) receiving at least 20 and 30 Gy (V20 and V30) and the mean lung dose; (iii) the 33rd percentile dose (D33) and Dmax delivered to the heart and the expanded esophagus; and (iv) Dmax for the expanded spinal cord. Statistical analysis was performed by means of one-way analysis of variance for repeated measurements and Tukey pairwise comparison of means. Pinnacle-CS showed an excellent agreement with MCDE within the target structures, whereas the best correspondence for the organs at risk (OARs) was found between Helax-CC and MCDE. Results from Helax-PB were unsatisfying for both targets and OARs. Additionally, individual patient results were analyzed. Within the target structures, deviations above 5% were found in one patient for the comparison of MCDE and Helax-CC, while all differences between MCDE and Pinnacle-CS were below 5%. For both
TU-F-18A-03: Improving Tissue Segmentation for Monte Carlo Dose Calculation Using DECT Data
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Di, Salvio A; Bedwani, S; Carrier, J [CHUM - Notre-Dame, Montreal, QC (Canada)
2014-06-15
Purpose: To develop a new segmentation technique using dual energy CT (DECT) to overcome limitations related to segmentation from a standard Hounsfield unit (HU) to electron density (ED) calibration curve. Both methods are compared with a Monte Carlo analysis of dose distribution. Methods: DECT allows a direct calculation of both ED and effective atomic number (EAN) within a given voxel. The EAN is here defined as a function of the total electron cross-section of a medium. These values can be effectively acquired using a calibrated method from scans at two different energies. A prior stoichiometric calibration on a Gammex RMI phantom allows us to find the parameters to calculate EAN and ED within a voxel. Scans from a Siemens SOMATOM Definition Flash dual source system provided the data for our study. A Monte Carlo analysis compares dose distribution simulated by dosxyz-nrc, considering a head phantom defined by both segmentation techniques. Results: Results from depth dose and dose profile calculations show that materials with different atomic compositions but similar EAN present differences of less than 1%. Therefore, it is possible to define a short list of basis materials from which density can be adapted to imitate interaction behavior of any tissue. Comparison of the dose distributions on both segmentations shows a difference of 50% in dose in areas surrounding bone at low energy. Conclusion: The presented segmentation technique allows a more accurate medium definition in each voxel, especially in areas of tissue transition. Since the behavior of human tissues is highly sensitive at low energies, this reduces the errors on calculated dose distribution. This method could be further developed to optimize the tissue characterization based on anatomic site.
TU-F-18A-03: Improving Tissue Segmentation for Monte Carlo Dose Calculation Using DECT Data
International Nuclear Information System (INIS)
Purpose: To develop a new segmentation technique using dual energy CT (DECT) to overcome limitations related to segmentation from a standard Hounsfield unit (HU) to electron density (ED) calibration curve. Both methods are compared with a Monte Carlo analysis of dose distribution. Methods: DECT allows a direct calculation of both ED and effective atomic number (EAN) within a given voxel. The EAN is here defined as a function of the total electron cross-section of a medium. These values can be effectively acquired using a calibrated method from scans at two different energies. A prior stoichiometric calibration on a Gammex RMI phantom allows us to find the parameters to calculate EAN and ED within a voxel. Scans from a Siemens SOMATOM Definition Flash dual source system provided the data for our study. A Monte Carlo analysis compares dose distribution simulated by dosxyz-nrc, considering a head phantom defined by both segmentation techniques. Results: Results from depth dose and dose profile calculations show that materials with different atomic compositions but similar EAN present differences of less than 1%. Therefore, it is possible to define a short list of basis materials from which density can be adapted to imitate interaction behavior of any tissue. Comparison of the dose distributions on both segmentations shows a difference of 50% in dose in areas surrounding bone at low energy. Conclusion: The presented segmentation technique allows a more accurate medium definition in each voxel, especially in areas of tissue transition. Since the behavior of human tissues is highly sensitive at low energies, this reduces the errors on calculated dose distribution. This method could be further developed to optimize the tissue characterization based on anatomic site
Oliver, Mike; Staruch, Robert; Gladwish, Adam; Craig, Jeff; Chen, Jeff; Wong, Eugene
2008-05-01
Respiratory gating is emerging as a tool to limit the effect of motion for liver and lung tumors. In order to study the impact of target motion and gated intensity modulated radiation therapy (IMRT) delivery, a computer program was developed to simulate segmental IMRT delivery to a moving phantom. Two distinct plans were delivered to a rigid-motion phantom with a film insert in place under four conditions: static, sinusoidal motion, gated sinusoidal motion with a duty cycle of 25% and gated sinusoidal motion with duty cycle of 50% under motion conditions of a typical patient (A = 1 cm, T = 4 s). The MLC controller log files and gating log files were retained to perform a retrospective Monte Carlo dose calculation of the plans. Comparison of the 2D planar dose distributions between simulation and measurement demonstrated that our technique had at least 94% of the points passing gamma criteria of 3% for dose difference and 3 mm as the distance to agreement. This note demonstrates that the use of dynamic multi-leaf collimator and respiratory monitoring system log files together with a fast Monte Carlo dose calculation algorithm is an accurate and efficient way to study the dosimetric effect of motion for gated or non-gated IMRT delivery on a rigidly-moving body.
Investigation of geometrical and scoring grid resolution for Monte Carlo dose calculations for IMRT
DeSmedt, B.; Vanderstraeten, B.; Reynaert, N.; DeNeve, W.; Thierens, H.
2005-09-01
Monte Carlo based treatment planning of two different patient groups treated with step-and-shoot IMRT (head-and-neck and lung treatments) with different CT resolutions and scoring methods is performed to determine the effect of geometrical and scoring voxel sizes on DVHs and calculation times. Dose scoring is performed in two different ways: directly into geometrical voxels (or in a number of grouped geometrical voxels) or into scoring voxels defined by a separate scoring grid superimposed on the geometrical grid. For the head-and-neck cancer patients, more than 2% difference is noted in the right optical nerve when using voxel dimensions of 4 × 4 × 4 mm3 compared to the reference calculation with 1 × 1 × 2 mm3 voxel dimensions. For the lung cancer patients, 2% difference is noted in the spinal cord when using voxel dimensions of 4 × 4 × 10 mm3 compared to the 1 × 1 × 5 mm3 calculation. An independent scoring grid introduces several advantages. In cases where a relatively high geometrical resolution is required and where the scoring resolution is less important, the number of scoring voxels can be limited while maintaining a high geometrical resolution. This can be achieved either by grouping several geometrical voxels together into scoring voxels or by superimposing a separate scoring grid of spherical voxels with a user-defined radius on the geometrical grid. For the studied lung cancer cases, both methods produce accurate results and introduce a speed increase by a factor of 10-36. In cases where a low geometrical resolution is allowed, but where a high scoring resolution is required, superimposing a separate scoring grid on the geometrical grid allows a reduction in geometrical voxels while maintaining a high scoring resolution. For the studied head-and-neck cancer cases, calculations performed with a geometrical resolution of 2 × 2 × 2 mm3 and a separate scoring grid containing spherical scoring voxels with a radius of 2 mm produce accurate results
WE-A-17A-04: Development of An Ultra-Fast Monte Carlo Dose Engine for High Dose Rate Brachytherapy
International Nuclear Information System (INIS)
Purpose: Current clinical brachytherapy dose calculations are based on AAPM TG43 guidelines, which approximate the patient geometry as a large water phantom. This ignores heterogeneities and tends to overestimate skin dose. Although Monte Carlo (MC) dose calculations have been recognized as the most accurate method, its associated long computational time is a major bottleneck for routine clinical applications. This work aims to develop a GPU-based ultra-fast MC dose engine (gBMC) for HDR brachytherapy to provide clinical users with accurate sub-minute dose calculations. Methods: Standard photon transport with discrete events including: Compton scattering, Rayleigh scattering and Photoelectric effect, was implemented. Secondary electrons were transported under the continuous slowing down approximation. To reduce the GPU thread divergence, photons and electrons were separately transported. Transport of photons was grouped according to energy. The source model in gBMC can be either a phase-space file generated using Geant4 or a parameterized source model. This dose engine was validated against TG43 in a water phantom and against Geant4 calculations in heterogeneous patient geometries. Results: A phase space file was generated for the Varian VS2000 Ir-192 source. In a water phantom, the calculated radial dose function was within 0.6% of the TG43 calculations for radial distances from 1 cm to 20 cm. The anisotropy functions were within 1% for radial distances from 1 cm to 20 cm except for polar angles larger than 173°. Local point-dose differences were within 2%. In a Mammosite breast cancer case with 22 dwell locations, gBMC and Geant4 isodose lines compared well. The computation time was about 28 seconds using the phase-space file source and 20 seconds using the parameterized source to simulate 1 billion particles, yielding less than 1% statistical uncertainty. Conclusion: The gBMC dose engine makes it possible to use fast and accurate MC dose calculations for
Mairani, A; Valente, M; Battistoni, G; Botta, F; Pedroli, G; Ferrari, A; Cremonesi, M; Di Dia, A; Ferrari, M; Fasso, A
2011-01-01
Purpose: The calculation of patient-specific dose distribution can be achieved by Monte Carlo simulations or by analytical methods. In this study, FLUKA Monte Carlo code has been considered for use in nuclear medicine dosimetry. Up to now, FLUKA has mainly been dedicated to other fields, namely high energy physics, radiation protection, and hadrontherapy. When first employing a Monte Carlo code for nuclear medicine dosimetry, its results concerning electron transport at energies typical of nuclear medicine applications need to be verified. This is commonly achieved by means of calculation of a representative parameter and comparison with reference data. Dose point kernel (DPK), quantifying the energy deposition all around a point isotropic source, is often the one. Methods: FLUKA DPKS have been calculated in both water and compact bone for monoenergetic electrons (10-3 MeV) and for beta emitting isotopes commonly used for therapy ((89)Sr, (90)Y, (131)I, (153)Sm, (177)Lu, (186)Re, and (188)Re). Point isotropic...
Matsumoto, Shinnosuke; Koba, Yusuke; Kohno, Ryosuke; Lee, Choonsik; Bolch, Wesley E; Kai, Michiaki
2016-04-01
Proton therapy has the physical advantage of a Bragg peak that can provide a better dose distribution than conventional x-ray therapy. However, radiation exposure of normal tissues cannot be ignored because it is likely to increase the risk of secondary cancer. Evaluating secondary neutrons generated by the interaction of the proton beam with the treatment beam-line structure is necessary; thus, performing the optimization of radiation protection in proton therapy is required. In this research, the organ dose and energy spectrum were calculated from secondary neutrons using Monte Carlo simulations. The Monte Carlo code known as the Particle and Heavy Ion Transport code System (PHITS) was used to simulate the transport proton and its interaction with the treatment beam-line structure that modeled the double scattering body of the treatment nozzle at the National Cancer Center Hospital East. The doses of the organs in a hybrid computational phantom simulating a 5-y-old boy were calculated. In general, secondary neutron doses were found to decrease with increasing distance to the treatment field. Secondary neutron energy spectra were characterized by incident neutrons with three energy peaks: 1×10, 1, and 100 MeV. A block collimator and a patient collimator contributed significantly to organ doses. In particular, the secondary neutrons from the patient collimator were 30 times higher than those from the first scatter. These results suggested that proactive protection will be required in the design of the treatment beam-line structures and that organ doses from secondary neutrons may be able to be reduced. PMID:26910030
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Ramirez Ros, J. C.; Jerez Sainz, M. I.; Lobato Munoz, M.; Jodar Lopez, C. A.; Ruiz Lopez, M. A.; Carrasco rodriguez, J. L.; Pamos Urena, M.
2013-07-01
We evaluated the Monte Carlo Monaco Planner v2.0.3 for calculation between non-homogeneous low density (equivalent to lung), as a complement to the verification of modeling in homogeneous medium and prior to the introduction of the SBRT technique. We performed the same tests on Pinnacle v8.0m, with the same purpose. We compare the results obtained with the algorithm Monte Carlo of Monaco and the Collapsed Cone of Pinnacle. (Author)
Feasibility study of the neutron dose for real-time image-guided proton therapy: A Monte Carlo study
Kim, Jin Sung; Shin, Jung Suk; Kim, Daehyun; Shin, Eunhyuk; Chung, Kwangzoo; Cho, Sungkoo; Ahn, Sung Hwan; Ju, Sanggyu; Chung, Yoonsun; Jung, Sang Hoon; Han, Youngyih
2015-07-01
Two full rotating gantries with different nozzles (multipurpose nozzle with MLC, scanning dedicated nozzle) for a conventional cyclotron system are installed and being commissioned for various proton treatment options at Samsung Medical Center in Korea. The purpose of this study is to use Monte Carlo simulation to investigate the neutron dose equivalent per therapeutic dose, H/D, for X-ray imaging equipment under various treatment conditions. At first, we investigated the H/D for various modifications of the beamline devices (scattering, scanning, multi-leaf collimator, aperture, compensator) at the isocenter and at 20, 40 and 60 cm distances from the isocenter, and we compared our results with those of other research groups. Next, we investigated the neutron dose at the X-ray equipment used for real-time imaging under various treatment conditions. Our investigation showed doses of 0.07 ~ 0.19 mSv/Gy at the X-ray imaging equipment, depending on the treatment option and interestingly, the 50% neutron dose reduction was observed due to multileaf collimator during proton scanning treatment with the multipurpose nozzle. In future studies, we plan to measure the neutron dose experimentally and to validate the simulation data for X-ray imaging equipment for use as an additional neutron dose reduction method.
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Habib, B.; Poumarede, B.; Tola, F.; Barthe, J. [CEA, LIST, Dept Technol Capteur et Signal, F-91191 Gif Sur Yvette, (France)
2010-07-01
The aim of the present study is to demonstrate the potential of accelerated dose calculations, using the fast Monte Carlo (MC) code referred to as PENFAST, rather than the conventional MC code PENELOPE, without losing accuracy in the computed dose. For this purpose, experimental measurements of dose distributions in homogeneous and inhomogeneous phantoms were compared with simulated results using both PENELOPE and PENFAST. The simulations and experiments were performed using a Saturne 43 linac operated at 12 MV (photons), and at 18 MeV (electrons). Pre-calculated phase space files (PSFs) were used as input data to both the PENELOPE and PENFAST dose simulations. Since depth-dose and dose profile comparisons between simulations and measurements in water were found to be in good agreement (within {+-} 1% to 1 mm), the PSF calculation is considered to have been validated. In addition, measured dose distributions were compared to simulated results in a set of clinically relevant, inhomogeneous phantoms, consisting of lung and bone heterogeneities in a water tank. In general, the PENFAST results agree to within a 1% to 1 mm difference with those produced by PENELOPE, and to within a 2% to 2 mm difference with measured values. Our study thus provides a pre-clinical validation of the PENFAST code. It also demonstrates that PENFAST provides accurate results for both photon and electron beams, equivalent to those obtained with PENELOPE. CPU time comparisons between both MC codes show that PENFAST is generally about 9-21 times faster than PENELOPE. (authors)
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of the physical and internal grid alignment yielded a maximum discrepancy of 2.67 ± 0.01 mm at position 6A on the template. The probe retraction test produced no discrepancies in the “clicks” and corresponding distances. Meanwhile the depth of penetration and axial and lateral resolution test at the time performing the tests were no available standard measurements for comparison. The dose verification test consisted of three tests, the calibration point test, the source strength verification and the TPS dose verification. The calibration point test indicated that distance for maximum ionization chamber sensitivity is 3cm, so seeds can be calibrated at this point. The source strength verification were within the tolerances recommended by ICRU report 38 (ICRU, 1985). The average source strength measured was 0.651450 U ± 0.001052 U deviating from the manufacturer value of 0.64989 U by 0.242 % ± 0. 164 %. The TPS dose verification test produced results with significant errors which occurred due to post irradiation development of film with time but the doses obtained by both TPS and film followed the same pattern. The outcome of the performance evaluations indicate that for patient work, the ultrasound system and prostate brachytherapy system can provide the mechanism for accurate positioning of the brachytherapy seeds facilitating reliable identification of the target volume for accurate effective treatment. (au)
Institute of Scientific and Technical Information of China (English)
Ahmed Shawky Shawata; Tarek El Nimr; Reda Ahmed Morsy; Khaled M. Elshahat
2013-01-01
Objective: This study aimed to evaluate of the accuracy and efficiency of the in-vivo dosimetry systems for routine cancer patient dose verification. Methods: In vivo dosimetry, using diodes and thermoluminescent dosimeters (TLD) is performed in many radiotherapy departments to verify the dose delivered during treatment. A total of 40 TLD divided into two batches (one of 20 and other of 20 TLD) were used. Different doses of Co60 beam were delivered to the TLD chips at different depths. Diodes were irradiated at different depths in a (30 × 30 × 30) cm3 water slab phantom with various conditions of Field sizes, monitor units and SSDs. Results: The limitation of the in-vivo dosimetry technique is that dose can only be in system readout difficulty and type of readout (TLD system and diode) as the patient dose is directly measured. Several authors have investigated the measurements was 1.3%, with a standard deviation of 2.6%. Results were normally distributed around a both eyes were 1.8%, with a standard deviation of 2.7%. These results are similar to studies conducted with diodes and TLD's. Conclusion: The diode is superior to TLD, since the diode measurements can be obtained on line and allows an immediate check. Other advantages of diodes include high sensitivity, good spatial resolution, and small size, simplicity of used.
On-board Dose Measurement and its Monte Carlo Analysis in a Low Level Waste Shipping Vessel
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On-board dose measurements were made in a shipping vessel for low level radioactive wastes, the Seiei Maru. The measured values are much smaller than the regulation values both on the hatch covers and in the accommodation area. The dose equivalent rates on the hatch cover are analysed by using a continuous energy Monte Carlo code, MCNP 4B, with two kinds of calculational models. One is the detailed model with the geometry of containers and LLW drums, and an asymmetrical source distribution. The results of the detailed calculation approached the shape of the measured dose rate distribution graphs. The other is the simplified model that mixes source volume uniformly. The calculated values obtained with the simplified model are twice as large as those calculated with the detailed model. (author)
Influencing factors of dose equivalence for X and γ rays with different energy based on Monte Carlo
International Nuclear Information System (INIS)
Background: The accuracy of dosimeter measurement of X and γ rays needs to be resolved. Purpose: The aim is to study the correction term of the equivalent process of low energy X-ray and the natural radioactive source. Methods: Instead of the standard sources, X-ray machine was adopted on the dose instrument calibration. The influence factors of the equivalence between low-energy X-ray and high-energy X or γ rays were simulated using Monte Carlo (MCNP) software. Results: The influences of distance, space scattering, response of detector on dose equivalence were obtained. The simulation results were also analyzed. Conclusion: The method can be used in dose equivalent correction for low-energy X-ray, high-energy X or γ rays, which is significant for the widespread use of X rays. (authors)
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Sikora, M [Section for Biomedical Physics, University Hospital for Radiation Oncology, Hoppe-Seyler-Str. 3, 72076 Tuebingen (Germany); Dohm, O [Section for Biomedical Physics, University Hospital for Radiation Oncology, Hoppe-Seyler-Str. 3, 72076 Tuebingen (Germany); Alber, M [Section for Biomedical Physics, University Hospital for Radiation Oncology, Hoppe-Seyler-Str. 3, 72076 Tuebingen (Germany)
2007-08-07
A dedicated, efficient Monte Carlo (MC) accelerator head model for intensity modulated stereotactic radiosurgery treatment planning is needed to afford a highly accurate simulation of tiny IMRT fields. A virtual source model (VSM) of a mini multi-leaf collimator (MLC) (the Elekta Beam Modulator (EBM)) is presented, allowing efficient generation of particles even for small fields. The VSM of the EBM is based on a previously published virtual photon energy fluence model (VEF) (Fippel et al 2003 Med. Phys. 30 301) commissioned with large field measurements in air and in water. The original commissioning procedure of the VEF, based on large field measurements only, leads to inaccuracies for small fields. In order to improve the VSM, it was necessary to change the VEF model by developing (1) a method to determine the primary photon source diameter, relevant for output factor calculations (2) a model of the influence of the flattening filter on the secondary photon spectrum and (3) a more realistic primary photon spectrum. The VSM model is used to generate the source phase space data above the mini-MLC. Later the particles are transmitted through the mini-MLC by a passive filter function which significantly speeds up the time of generation of the phase space data after the mini-MLC, used for calculation of the dose distribution in the patient. The improved VSM model was commissioned for 6 and 15 MV beams. The results of MC simulation are in very good agreement with measurements. Less than 2% of local difference between the MC simulation and the diamond detector measurement of the output factors in water was achieved. The X, Y and Z profiles measured in water with an ion chamber (V = 0.125 cm{sup 3}) and a diamond detector were used to validate the models. An overall agreement of 2%/2 mm for high dose regions and 3%/2 mm in low dose regions between measurement and MC simulation for field sizes from 0.8 x 0.8 cm{sup 2} to 16 x 21 cm{sup 2} was achieved. An IMRT plan film
SU-E-T-117: Dose to Organs Outside of CT Scan Range- Monte Carlo and Hybrid Phantom Approach
International Nuclear Information System (INIS)
Purpose: Epidemiological study of second cancer risk for cancer survivors often requires the dose to normal tissues located outside the anatomy covered by radiological imaging, which is usually limited to tumor and organs at risk. We have investigated the feasibility of using whole body computational human phantoms for estimating out-of-field organ doses for patients treated by Intensity Modulated Radiation Therapy (IMRT). Methods: Identical 7-field IMRT prostate plans were performed using X-ray Voxel Monte Carlo (XVMC), a radiotherapy-specific Monte Carlo transport code, on the computed tomography (CT) images of the torso of an adult male patient (175 cm height, 66 kg weight) and an adult male hybrid computational phantom with the equivalent body size. Dose to the liver, right lung, and left lung were calculated and compared. Results: Considerable differences are seen between the doses calculated by XVMC for the patient CT and the hybrid phantom. One major contributing factor is the treatment method, deep inspiration breath hold (DIBH), used for this patient. This leads to significant differences in the organ position relative to the treatment isocenter. The transverse distances from the treatment isocenter to the inferior border of the liver, left lung, and right lung are 19.5cm, 29.5cm, and 30.0cm, respectively for the patient CT, compared with 24.3cm, 36.6cm, and 39.1cm, respectively, for the hybrid phantom. When corrected for the distance, the mean doses calculated using the hybrid phantom are within 28% of those calculated using the patient CT. Conclusion: This study showed that mean dose to the organs located in the missing CT coverage can be reconstructed by using whole body computational human phantoms within reasonable dosimetric uncertainty, however appropriate corrections may be necessary if the patient is treated with a technique that will significantly deform the size or location of the organs relative to the hybrid phantom
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Brualla, Lorenzo, E-mail: lorenzo.brualla@uni-due.de [NCTeam, Strahlenklinik, Universitaetsklinikum Essen, Essen (Germany); Zaragoza, Francisco J.; Sempau, Josep [Institut de Tecniques Energetiques, Universitat Politecnica de Catalunya, Barcelona (Spain); Wittig, Andrea [Department of Radiation Oncology, University Hospital Giessen and Marburg, Philipps-University Marburg, Marburg (Germany); Sauerwein, Wolfgang [NCTeam, Strahlenklinik, Universitaetsklinikum Essen, Essen (Germany)
2012-07-15
Purpose: External beam radiotherapy is the only conservative curative approach for Stage I non-Hodgkin lymphomas of the conjunctiva. The target volume is geometrically complex because it includes the eyeball and lid conjunctiva. Furthermore, the target volume is adjacent to radiosensitive structures, including the lens, lacrimal glands, cornea, retina, and papilla. The radiotherapy planning and optimization requires accurate calculation of the dose in these anatomical structures that are much smaller than the structures traditionally considered in radiotherapy. Neither conventional treatment planning systems nor dosimetric measurements can reliably determine the dose distribution in these small irradiated volumes. Methods and Materials: The Monte Carlo simulations of a Varian Clinac 2100 C/D and human eye were performed using the PENELOPE and PENEASYLINAC codes. Dose distributions and dose volume histograms were calculated for the bulbar conjunctiva, cornea, lens, retina, papilla, lacrimal gland, and anterior and posterior hemispheres. Results: The simulated results allow choosing the most adequate treatment setup configuration, which is an electron beam energy of 6 MeV with additional bolus and collimation by a cerrobend block with a central cylindrical hole of 3.0 cm diameter and central cylindrical rod of 1.0 cm diameter. Conclusions: Monte Carlo simulation is a useful method to calculate the minute dose distribution in ocular tissue and to optimize the electron irradiation technique in highly critical structures. Using a voxelized eye phantom based on patient computed tomography images, the dose distribution can be estimated with a standard statistical uncertainty of less than 2.4% in 3 min using a computing cluster with 30 cores, which makes this planning technique clinically relevant.
International Nuclear Information System (INIS)
Purpose: External beam radiotherapy is the only conservative curative approach for Stage I non-Hodgkin lymphomas of the conjunctiva. The target volume is geometrically complex because it includes the eyeball and lid conjunctiva. Furthermore, the target volume is adjacent to radiosensitive structures, including the lens, lacrimal glands, cornea, retina, and papilla. The radiotherapy planning and optimization requires accurate calculation of the dose in these anatomical structures that are much smaller than the structures traditionally considered in radiotherapy. Neither conventional treatment planning systems nor dosimetric measurements can reliably determine the dose distribution in these small irradiated volumes. Methods and Materials: The Monte Carlo simulations of a Varian Clinac 2100 C/D and human eye were performed using the PENELOPE and PENEASYLINAC codes. Dose distributions and dose volume histograms were calculated for the bulbar conjunctiva, cornea, lens, retina, papilla, lacrimal gland, and anterior and posterior hemispheres. Results: The simulated results allow choosing the most adequate treatment setup configuration, which is an electron beam energy of 6 MeV with additional bolus and collimation by a cerrobend block with a central cylindrical hole of 3.0 cm diameter and central cylindrical rod of 1.0 cm diameter. Conclusions: Monte Carlo simulation is a useful method to calculate the minute dose distribution in ocular tissue and to optimize the electron irradiation technique in highly critical structures. Using a voxelized eye phantom based on patient computed tomography images, the dose distribution can be estimated with a standard statistical uncertainty of less than 2.4% in 3 min using a computing cluster with 30 cores, which makes this planning technique clinically relevant.
SU-E-T-117: Dose to Organs Outside of CT Scan Range- Monte Carlo and Hybrid Phantom Approach
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Pelletier, C; Jung, J [East Carolina University, Greenville, NC (United States); Lee, C [University of Michigan, Ann Arbor, MI (United States); Kim, J [University of Pittsburgh Medical Center, Pittsburgh, PA (United States); Lee, C [National Cancer Institute, Rockville, MD (United States)
2014-06-01
Purpose: Epidemiological study of second cancer risk for cancer survivors often requires the dose to normal tissues located outside the anatomy covered by radiological imaging, which is usually limited to tumor and organs at risk. We have investigated the feasibility of using whole body computational human phantoms for estimating out-of-field organ doses for patients treated by Intensity Modulated Radiation Therapy (IMRT). Methods: Identical 7-field IMRT prostate plans were performed using X-ray Voxel Monte Carlo (XVMC), a radiotherapy-specific Monte Carlo transport code, on the computed tomography (CT) images of the torso of an adult male patient (175 cm height, 66 kg weight) and an adult male hybrid computational phantom with the equivalent body size. Dose to the liver, right lung, and left lung were calculated and compared. Results: Considerable differences are seen between the doses calculated by XVMC for the patient CT and the hybrid phantom. One major contributing factor is the treatment method, deep inspiration breath hold (DIBH), used for this patient. This leads to significant differences in the organ position relative to the treatment isocenter. The transverse distances from the treatment isocenter to the inferior border of the liver, left lung, and right lung are 19.5cm, 29.5cm, and 30.0cm, respectively for the patient CT, compared with 24.3cm, 36.6cm, and 39.1cm, respectively, for the hybrid phantom. When corrected for the distance, the mean doses calculated using the hybrid phantom are within 28% of those calculated using the patient CT. Conclusion: This study showed that mean dose to the organs located in the missing CT coverage can be reconstructed by using whole body computational human phantoms within reasonable dosimetric uncertainty, however appropriate corrections may be necessary if the patient is treated with a technique that will significantly deform the size or location of the organs relative to the hybrid phantom.
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Purpose: We describe computer software that performs, quickly and accurately, secondary dose calculations for high-dose-rate (HDR) treatment plans, including those employed for prostate treatments. Methods: The program takes as primary input the data file used by the HDR remote afterloader console for treatment. Dosimetric calculations are performed using the Meisberger polynomial and the anisotropy table for the HDR Iridium-192 source. For standard applicators, treatment geometry is automatically reconstructed and the dose is calculated at relevant reference point(s). Template-based treatment plans (e.g., prostate) require additional user input; the dose calculation is then performed at user-selected reference points. A total dwell time calculation for volume and planar implants using the Manchester tables was also implemented. Results: For fixed-geometry HDR procedures, secondary dose calculations are within 2% of the treatment plan, and results are available for review instantly. For more general applications, the calculated and planned doses are typically within 3% at the prescription isodose line. The Manchester-based dwell time calculation is within 10% of the planned time
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Purpose: To use 3D printers to design and construct complex geometrical phantoms for commissioning treatment planning systems, dose calculation algorithms, quality assurance (QA), dose delivery, and patient dose verifications. Methods: In radiotherapy, complex geometrical phantoms are often required for dose verification, dose delivery and calculation algorithm validation. Presently, fabrication of customized phantoms is limited due to time, expense and challenges in machining of complex shapes. In this work, we designed and utilized 3D printers to fabricate two phantoms for QA purposes. One phantom includes hills and valleys (HV) for verification of intensity modulated radiotherapy for photons, and protons (IMRT and IMPT). The other phantom includes cylindrical cavities (CC) of various sizes for dose verification of inhomogeneities. We evaluated the HV phantoms for an IMPT beam, and the CC phantom to study various inhomogeneity configurations using photon, electron, and proton beams. Gafcromic ™ films were used to quantify the dose distributions delivered to the phantoms. Results: The HV phantom has dimensions of 12 cm × 12 cm and consists of one row and one column of five peaks with heights ranging from 2 to 5 cm. The CC phantom has a size 10 cm × 14 cm and includes 6 cylindrical cavities with length of 7.2 cm and diameters ranging from 0.6 to 1.2 cm. The IMPT evaluation using the HV phantom shows good agreement as compared to the dose distribution calculated with treatment planning system. The CC phantom also shows reasonable agreements for using different algorithms for each beam modalities. Conclusion: 3D printers with submillimiter resolutions are capable of printing complex phantoms for dose verification and QA in radiotherapy. As printing costs decrease and the technology becomes widely available, phantom design and construction will be readily available to any clinic for testing geometries that were not previously feasible
Directory of Open Access Journals (Sweden)
Nilseia Aparecida Barbosa
2014-08-01
Full Text Available Purpose: Melanoma at the choroid region is the most common primary cancer that affects the eye in adult patients. Concave ophthalmic applicators with 106Ru/106Rh beta sources are the more used for treatment of these eye lesions, mainly lesions with small and medium dimensions. The available treatment planning system for 106Ru applicators is based on dose distributions on a homogeneous water sphere eye model, resulting in a lack of data in the literature of dose distributions in the eye radiosensitive structures, information that may be crucial to improve the treatment planning process, aiming the maintenance of visual acuity. Methods: The Monte Carlo code MCNPX was used to calculate the dose distribution in a complete mathematical model of the human eye containing a choroid melanoma; considering the eye actual dimensions and its various component structures, due to an ophthalmic brachytherapy treatment, using 106Ru/106Rh beta-ray sources. Two possibilities were analyzed; a simple water eye and a heterogeneous eye considering all its structures. Two concave applicators, CCA and CCB manufactured by BEBIG and a complete mathematical model of the human eye were modeled using the MCNPX code. Results and Conclusion: For both eye models, namely water model and heterogeneous model, mean dose values simulated for the same eye regions are, in general, very similar, excepting for regions very distant from the applicator, where mean dose values are very low, uncertainties are higher and relative differences may reach 20.4%. For the tumor base and the eye structures closest to the applicator, such as sclera, choroid and retina, the maximum difference observed was 4%, presenting the heterogeneous model higher mean dose values. For the other eye regions, the higher doses were obtained when the homogeneous water eye model is taken into consideration. Mean dose distributions determined for the homogeneous water eye model are similar to those obtained for the
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This study aims to compare the doses received for patients submitted to brachytherapy High Dose Rate (HDR) brachytherapy, a method of treatment of the cervix carcinoma, performed in the planning system PLATO BPS with the doses obtained by Monte Carlo simulation using the radiation transport code MCNP 5 and one female anthropomorphic phantom based on voxel, the FAX. The implementation of HDR brachytherapy treatment for the cervix carcinoma consists of the insertion of an intrauterine probe and an intravaginal probe (ring or ovoid) and then two radiographs are obtained, anteroposterior (AP) and lateral (LAT) to confirm the position of the applicators in the patient and to allow the treatment planning and the determination of the absorbed dose at points of interest: rectum, bladder, sigmoid and point A, which corresponds anatomically to the crossings of the uterine arteries with ureters The absorbed doses obtained with the code MCNP 5, with the exception of the absorbed dose in the rectum and sigmoid for the simulation considering a point source of 192Ir, are lower than the absorbed doses from PLATO BPS calculations because the MCNP 5 considers the chemical compositions and densities of FAX body, not considering the medium as water. When considering the Monte Carlo simulation for a source with dimensions equal to that used in the brachytherapy irradiator used in this study, the values of calculated absorbed dose to the bladder, to the rectum, to the right point A and to the left point A were respectively lower than those determined by the treatment planning system in 33.29, 5.01, 22.93 and 19.04%. These values are almost all larger than the maximum acceptable deviation between patient planned and administered doses (5 %). With regard to the rectum and bladder, which are organs that must be protected, the present results are in favor of the radiological protection of patients. The point A, that is on the isodose of 100%, used to tumor treatment, the results indicate an
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Full text of publication follows. Purpose: a 3D-Personalized Monte Carlo Dosimetry (PMCD) was developed for treatment planning in nuclear medicine. The method was applied to Selective Internal Radiation Therapy (SIRT) using 90Y-microspheres for unresectable hepatic cancers. Methods: The PMCD method was evaluated for 20 patients treated for hepatic metastases or hepatocellular carcinoma at the European Hospital Georges Pompidou (Paris). First, regions of interest were outlined on the patient CT images. Using the OEDIPE software, patient-specific voxel phantoms were created. 99mTc-MAA SPECT data were then used to generate 3D-matrices of cumulated activity. Absorbed doses and Biologically Effective Dose (BED) were calculated at the voxel scale using the MCNPX Monte Carlo transport code. Finally, OEDIPE was used to determine the maximum injectable activity (MIA) for tolerance criteria on organs at risk (OARs), i.e. the lungs and non tumoral liver (NTL). Tolerance criteria based on mean absorbed doses, mean BED, Dose-Volume Histograms (DVHs) or BED-Volume Histograms (BVHs) were considered. Those MIAs were compared to the Partition Model with tolerance criteria on mean absorbed doses, which is a conventional method applied in clinical practice. Results: compared to Partition Model recommendations, performing dosimetry using the PMCD method enables to increase the activity prescription while ensuring OARs' radiation protection. Moreover, tolerance criteria based on DVHs allow us to enhance treatment planning efficiency by taking advantage of the parallel characteristic of the liver and the lungs, whose functions are not impaired if the level of irradiation to a fraction of the organ is kept sufficiently low. Finally, multi-cycle treatments based on tolerance criteria on mean BED and BVHs, were considered to go further in the dose optimization, taking into account biological considerations such as cell repair or radiosensitivity. Conclusion: besides its feasibility
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This paper discusses the simulation of contemporary computed tomography (CT) scanners using Monte Carlo calculation methods to derive normalized organ doses, which enable hospital physicists to estimate typical organ and effective doses for CT examinations. The hardware used in a small PC-cluster at the Health Protection Agency (HPA) for these calculations is described. Investigations concerning optimization of software, including the radiation transport codes MCNP5 and MCNPX, and the Intel and PGI FORTRAN compilers, are presented in relation to results and calculation speed. Differences in approach for modelling the X-ray source are described and their influences are analysed. Comparisons with previously published calculations at HPA from the early 1990's proved satisfactory for the purposes of quality assurance and are presented in terms of organ dose ratios for whole body exposure and differences in organ location. Influences on normalized effective dose are discussed in relation to choice of cross section library, CT scanner technology (contemporary multi slice versus single slice), definition for effective dose (1990 and 2007 versions) and anthropomorphic phantom (mathematical and voxel). The results illustrate the practical need for the updated scanner-specific dose coefficients presently being calculated at HPA, in order to facilitate improved dosimetry for contemporary CT practice. (authors)
An OpenCL-based Monte Carlo dose calculation engine (oclMC) for coupled photon-electron transport
Tian, Zhen; Folkerts, Michael; Qin, Nan; Jiang, Steve B; Jia, Xun
2015-01-01
Monte Carlo (MC) method has been recognized the most accurate dose calculation method for radiotherapy. However, its extremely long computation time impedes clinical applications. Recently, a lot of efforts have been made to realize fast MC dose calculation on GPUs. Nonetheless, most of the GPU-based MC dose engines were developed in NVidia CUDA environment. This limits the code portability to other platforms, hindering the introduction of GPU-based MC simulations to clinical practice. The objective of this paper is to develop a fast cross-platform MC dose engine oclMC using OpenCL environment for external beam photon and electron radiotherapy in MeV energy range. Coupled photon-electron MC simulation was implemented with analogue simulations for photon transports and a Class II condensed history scheme for electron transports. To test the accuracy and efficiency of our dose engine oclMC, we compared dose calculation results of oclMC and gDPM, our previously developed GPU-based MC code, for a 15 MeV electron ...
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This study aims to investigate the effects of oblique incidence, small field size and inhomogeneous media on the electron dose distribution, and to compare calculated (Elekta/CMS XiO) and measured results. All comparisons were done in terms of absolute dose. A new measuring method was developed for high resolution, absolute dose measurement of non-standard beams using Gafchromic® EBT3 film. A portable U-shaped holder was designed and constructed to hold EBT3 films vertically in a reproducible setup submerged in a water phantom. The experimental film method was verified with ionisation chamber measurements and agreed to within 2% or 1 mm. Agreement between XiO electron Monte Carlo (eMC) and EBT3 was within 2% or 2 mm for most standard fields and 3% or 3 mm for the non-standard fields. Larger differences were seen in the build-up region where XiO eMC overestimates dose by up to 10% for obliquely incident fields and underestimates the dose for small circular fields by up to 5% when compared to measurement. Calculations with inhomogeneous media mimicking ribs, lung and skull tissue placed at the side of the film in water agreed with measurement to within 3% or 3 mm. Gafchromic film in water proved to be a convenient high spatial resolution method to verify dose distributions from electrons in non-standard conditions including irradiation in inhomogeneous media. (paper)
Stratis, Andreas; Zhang, Guozhi; Jacobs, Reinhilde; Bogaerts, Ria; Bosmans, Hilde
2015-03-01
The aim of this work was to investigate the influence of backscatter radiation from the orbital bone and the intraorbital fat on the eye lens dose in the dental CBCT energy range. To this end we conducted three different yet interrelated studies; A preliminary simulation study was conducted to examine the impact of a bony layer situated underneath a soft tissue layer on the amount of backscatter radiation. We compared the Percentage Depth Dose (PDD) curves in soft tissue with and without the bone layer and we estimated the depth in tissue where the decrease in backscatter caused by the presence of the bone is noticeable. In a supplementary study, an eye voxel phantom was designed with the DOSxyznrc code. Simulations were performed exposing the phantom at different x-ray energies sequentially in air, in fat tissue and in realistic anatomy with the incident beam perpendicular to the phantom. Finally, a virtual head phantom was implemented into a validated hybrid Monte Carlo (MC) framework to simulate a large Field of View protocol of a real CBCT scanner and examine the influence of scattered dose to the eye lens during the whole rotation of the paired tube-detector system. The results indicated an increase in the dose to the lens due to the fatty tissue in the surrounding anatomy. There is a noticeable dose reduction close to the bone-tissue interface which weakens with increasing distance from the interface, such that the impact of the orbital bone in the eye lens dose becomes small.
Monte Carlo evaluation of hand and finger doses due to exposure to 18F in PET procedures
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The increasing number of PET procedures performed in nuclear medicine, and, consequently, of workers handling radiopharmaceuticals, is a potential hazard in radiation protection. It is then necessary to evaluate the doses of workers employed in the practice of PET. In this work, the Geant4 Monte Carlo code was used to evaluate doses to fingers and hands of those workers. A geometric phantom, representing the hand of the professional inserted in the clinical procedure, was implemented in the simulation code, with dimensions of a standard man's forearm, which in this case will assess the exposure of the extremities. The geometric phantom is designed so that a simple definition of joint angles configures the fingers, allowing investigations into alternative configurations. Thus, it was possible the placement of the phantom fingers, to simulate all forms of manipulation of a syringe, and subsequently obtain exposure data, relating to the administration procedure of the PET radiopharmaceutical to the patient. The simulation was validated by the irradiation of a REMABR hand phantom, consisting of a human skeleton hand covered by a tenite II shell, which can be filled with water. Air Kerma values were obtained from the beam dosimetry, which was done with a calibrated ionization chamber. The reading of TLD's, placed on certain points of the surface of the phantom, were compared with the values obtained in the Monte Carlo simulation. After validation of the program, we obtained dose values for the PET procedure, simulating syringes with and without shielding. (author)
Directory of Open Access Journals (Sweden)
Ilić Radovan D.
2004-01-01
Full Text Available This paper describes the application of SRNA Monte Carlo package for proton transport simulations in complex geometry and different material composition. SRNA package was developed for 3D dose distribution calculation in proton therapy and dosimetry and it was based on the theory of multiple scattering. The compound nuclei decay was simulated by our own and the Russian MSDM models using ICRU 63 data. The developed package consists of two codes SRNA-2KG, which simulates proton transport in the combinatorial geometry and SRNA-VOX, which uses the voxelized geometry using the CT data and conversion of the Hounsfield’s data to tissue elemental composition. Transition probabilities for both codes are prepared by the SRNADAT code. The simulation of proton beam characterization by Multi-Layer Faraday Cup, spatial distribution of positron emitters obtained by SRNA-2KG code, and intercomparison of computational codes in radiation dosimetry, indicate the immediate application of the Monte Carlo techniques in clinical practice. In this paper, we briefly present the physical model implemented in SRNA pack age, the ISTAR proton dose planning software, as well as the results of the numerical experiments with proton beams to obtain 3D dose distribution in the eye and breast tumor.
Monte Carlo evaluation of hand and finger doses due to exposure to {sup 18}F in PET procedures
Energy Technology Data Exchange (ETDEWEB)
Pessanha, Paula R.; Queiroz Filho, Pedro P.; Santos, Denison S.; Mauricio, Claudia L.P., E-mail: paula@ird.gov.br, E-mail: queiroz@ird.gov.br, E-mail: santosd@ird.gov.br, E-mail: claudia@ird.gov.br [Instituto de Radioprotecao e Dosimetria (IRD/CNEN-RJ), Rio de Janeiro, RJ (Brazil)
2011-07-01
The increasing number of PET procedures performed in nuclear medicine, and, consequently, of workers handling radiopharmaceuticals, is a potential hazard in radiation protection. It is then necessary to evaluate the doses of workers employed in the practice of PET. In this work, the Geant4 Monte Carlo code was used to evaluate doses to fingers and hands of those workers. A geometric phantom, representing the hand of the professional inserted in the clinical procedure, was implemented in the simulation code, with dimensions of a standard man's forearm, which in this case will assess the exposure of the extremities. The geometric phantom is designed so that a simple definition of joint angles configures the fingers, allowing investigations into alternative configurations. Thus, it was possible the placement of the phantom fingers, to simulate all forms of manipulation of a syringe, and subsequently obtain exposure data, relating to the administration procedure of the PET radiopharmaceutical to the patient. The simulation was validated by the irradiation of a REMAB{sup R} hand phantom, consisting of a human skeleton hand covered by a tenite II shell, which can be filled with water. Air Kerma values were obtained from the beam dosimetry, which was done with a calibrated ionization chamber. The reading of TLD's, placed on certain points of the surface of the phantom, were compared with the values obtained in the Monte Carlo simulation. After validation of the program, we obtained dose values for the PET procedure, simulating syringes with and without shielding. (author)
International Nuclear Information System (INIS)
A novel procedure for the generation of a realistic virtual Computed Tomography (CT) image of a patient, using the advanced Boundary RE Presentation (BREP)-based model MASH, has been implemented. This method can be used in radiotherapy assessment. It is shown that it is possible to introduce an artificial cancer, which can be modeled using mesh surfaces. The use of virtual CT images based on BREP models presents several advantages with respect to CT images of actual patients, such as automation, control and flexibility. As an example, two artificial cases, namely a brain and a prostate cancer, were created through the generation of images and tumor/organ contours. As a secondary objective, the described methodology has been used to generate input files for treatment planning system (TPS) and Monte Carlo code dose evaluation. In this paper, we consider treatment plans generated assuming a dose delivery via an active proton beam scanning performed with the INFN-IBA TPS kernel. Additionally, Monte Carlo simulations of the two treatment plans were carried out with GATE/GEANT4. The work demonstrates the feasibility of the approach based on the BREP modeling to produce virtual CT images. In conclusion, this study highlights the benefits in using digital phantom model capable of representing different anatomical structures and varying tumors across different patients. These models could be useful for assessing radiotherapy treatment planning systems (TPS) and computer simulations for the evaluation of the adsorbed dose. (author)
Energy Technology Data Exchange (ETDEWEB)
Milian, F. M.; Attili, A.; Russo, G; Marchetto, F.; Cirio, R., E-mail: felix_mas_milian@yahoo.com, E-mail: attili@to.infn.it, E-mail: russo@to.infn.it, E-mail: fmarchet@to.infn.it, E-mail: cirio@to.infn.it [Istituto Nazionale di Fisica Nucleare (INFN), Torino, TO (Italy); Bourhaleb, F., E-mail: bourhale@to.infn.it [Universita di Torino (UNITO), Torino, TO (Italy)
2013-07-01
A novel procedure for the generation of a realistic virtual Computed Tomography (CT) image of a patient, using the advanced Boundary RE Presentation (BREP)-based model MASH, has been implemented. This method can be used in radiotherapy assessment. It is shown that it is possible to introduce an artificial cancer, which can be modeled using mesh surfaces. The use of virtual CT images based on BREP models presents several advantages with respect to CT images of actual patients, such as automation, control and flexibility. As an example, two artificial cases, namely a brain and a prostate cancer, were created through the generation of images and tumor/organ contours. As a secondary objective, the described methodology has been used to generate input files for treatment planning system (TPS) and Monte Carlo code dose evaluation. In this paper, we consider treatment plans generated assuming a dose delivery via an active proton beam scanning performed with the INFN-IBA TPS kernel. Additionally, Monte Carlo simulations of the two treatment plans were carried out with GATE/GEANT4. The work demonstrates the feasibility of the approach based on the BREP modeling to produce virtual CT images. In conclusion, this study highlights the benefits in using digital phantom model capable of representing different anatomical structures and varying tumors across different patients. These models could be useful for assessing radiotherapy treatment planning systems (TPS) and computer simulations for the evaluation of the adsorbed dose. (author)
International Nuclear Information System (INIS)
This paper describes the application of SRNA Monte Carlo package for proton transport simulations in complex geometry and different material composition. SRNA package was developed for 3D dose distribution calculation in proton therapy and dosimetry and it was based on the theory of multiple scattering. The compound nuclei decay was simulated by our own and the Russian MSDM models using ICRU 63 data. The developed package consists of two codes: SRNA-2KG, which simulates proton transport in the combinatorial geometry and SRNA-VOX, which uses the voxelized geometry using the CT data and conversion of the Hounsfield's data to tissue elemental composition. Transition probabilities for both codes are prepared by the SRNADAT code. The simulation of proton beam characterization by Multi-Layer Faraday Cup, spatial distribution of positron emitters obtained by SRNA-2KG code, and intercomparison of computational codes in radiation dosimetry, indicate the immediate application of the Monte Carlo techniques in clinical practice. In this paper, we briefly present the physical model implemented in SRNA package, the ISTAR proton dose planning software, as well as the results of the numerical experiments with proton beams to obtain 3D dose distribution in the eye and breast tumor. (author)
The Monte Carlo SRNA-VOX code for 3D proton dose distribution in voxelized geometry using CT data
Energy Technology Data Exchange (ETDEWEB)
Ilic, Radovan D [Laboratory of Physics (010), Vinca Institute of Nuclear Sciences, PO Box 522, 11001 Belgrade (Serbia and Montenegro); Spasic-Jokic, Vesna [Laboratory of Physics (010), Vinca Institute of Nuclear Sciences, PO Box 522, 11001 Belgrade (Serbia and Montenegro); Belicev, Petar [Laboratory of Physics (010), Vinca Institute of Nuclear Sciences, PO Box 522, 11001 Belgrade (Serbia and Montenegro); Dragovic, Milos [Center for Nuclear Medicine MEDICA NUCLEARE, Bulevar Despota Stefana 69, 11000 Belgrade (Serbia and Montenegro)
2005-03-07
This paper describes the application of the SRNA Monte Carlo package for proton transport simulations in complex geometry and different material compositions. The SRNA package was developed for 3D dose distribution calculation in proton therapy and dosimetry and it was based on the theory of multiple scattering. The decay of proton induced compound nuclei was simulated by the Russian MSDM model and our own using ICRU 63 data. The developed package consists of two codes: the SRNA-2KG, which simulates proton transport in combinatorial geometry and the SRNA-VOX, which uses the voxelized geometry using the CT data and conversion of the Hounsfield's data to tissue elemental composition. Transition probabilities for both codes are prepared by the SRNADAT code. The simulation of the proton beam characterization by multi-layer Faraday cup, spatial distribution of positron emitters obtained by the SRNA-2KG code and intercomparison of computational codes in radiation dosimetry, indicate immediate application of the Monte Carlo techniques in clinical practice. In this paper, we briefly present the physical model implemented in the SRNA package, the ISTAR proton dose planning software, as well as the results of the numerical experiments with proton beams to obtain 3D dose distribution in the eye and breast tumour.
The Monte Carlo SRNA-VOX code for 3D proton dose distribution in voxelized geometry using CT data
Ilic, Radovan D.; Spasic-Jokic, Vesna; Belicev, Petar; Dragovic, Milos
2005-03-01
This paper describes the application of the SRNA Monte Carlo package for proton transport simulations in complex geometry and different material compositions. The SRNA package was developed for 3D dose distribution calculation in proton therapy and dosimetry and it was based on the theory of multiple scattering. The decay of proton induced compound nuclei was simulated by the Russian MSDM model and our own using ICRU 63 data. The developed package consists of two codes: the SRNA-2KG, which simulates proton transport in combinatorial geometry and the SRNA-VOX, which uses the voxelized geometry using the CT data and conversion of the Hounsfield's data to tissue elemental composition. Transition probabilities for both codes are prepared by the SRNADAT code. The simulation of the proton beam characterization by multi-layer Faraday cup, spatial distribution of positron emitters obtained by the SRNA-2KG code and intercomparison of computational codes in radiation dosimetry, indicate immediate application of the Monte Carlo techniques in clinical practice. In this paper, we briefly present the physical model implemented in the SRNA package, the ISTAR proton dose planning software, as well as the results of the numerical experiments with proton beams to obtain 3D dose distribution in the eye and breast tumour.
The Monte Carlo SRNA-VOX code for 3D proton dose distribution in voxelized geometry using CT data
International Nuclear Information System (INIS)
This paper describes the application of the SRNA Monte Carlo package for proton transport simulations in complex geometry and different material compositions. The SRNA package was developed for 3D dose distribution calculation in proton therapy and dosimetry and it was based on the theory of multiple scattering. The decay of proton induced compound nuclei was simulated by the Russian MSDM model and our own using ICRU 63 data. The developed package consists of two codes: the SRNA-2KG, which simulates proton transport in combinatorial geometry and the SRNA-VOX, which uses the voxelized geometry using the CT data and conversion of the Hounsfield's data to tissue elemental composition. Transition probabilities for both codes are prepared by the SRNADAT code. The simulation of the proton beam characterization by multi-layer Faraday cup, spatial distribution of positron emitters obtained by the SRNA-2KG code and intercomparison of computational codes in radiation dosimetry, indicate immediate application of the Monte Carlo techniques in clinical practice. In this paper, we briefly present the physical model implemented in the SRNA package, the ISTAR proton dose planning software, as well as the results of the numerical experiments with proton beams to obtain 3D dose distribution in the eye and breast tumour
Energy Technology Data Exchange (ETDEWEB)
Kang, Sei-Kwon; Yoon, Jai-Woong; Hwang, Taejin; Park, Soah; Cheong, Kwang-Ho; Jin Han, Tae; Kim, Haeyoung; Lee, Me-Yeon; Ju Kim, Kyoung, E-mail: kjkim@hallym.or.kr; Bae, Hoonsik
2015-10-01
A metallic contact eye shield has sometimes been used for eyelid treatment, but dose distribution has never been reported for a patient case. This study aimed to show the shield-incorporated CT-based dose distribution using the Pinnacle system and Monte Carlo (MC) calculation for 3 patient cases. For the artifact-free CT scan, an acrylic shield machined as the same size as that of the tungsten shield was used. For the MC calculation, BEAMnrc and DOSXYZnrc were used for the 6-MeV electron beam of the Varian 21EX, in which information for the tungsten, stainless steel, and aluminum material for the eye shield was used. The same plan was generated on the Pinnacle system and both were compared. The use of the acrylic shield produced clear CT images, enabling delineation of the regions of interest, and yielded CT-based dose calculation for the metallic shield. Both the MC and the Pinnacle systems showed a similar dose distribution downstream of the eye shield, reflecting the blocking effect of the metallic eye shield. The major difference between the MC and the Pinnacle results was the target eyelid dose upstream of the shield such that the Pinnacle system underestimated the dose by 19 to 28% and 11 to 18% for the maximum and the mean doses, respectively. The pattern of dose difference between the MC and the Pinnacle systems was similar to that in the previous phantom study. In conclusion, the metallic eye shield was successfully incorporated into the CT-based planning, and the accurate dose calculation requires MC simulation.
International Nuclear Information System (INIS)
A metallic contact eye shield has sometimes been used for eyelid treatment, but dose distribution has never been reported for a patient case. This study aimed to show the shield-incorporated CT-based dose distribution using the Pinnacle system and Monte Carlo (MC) calculation for 3 patient cases. For the artifact-free CT scan, an acrylic shield machined as the same size as that of the tungsten shield was used. For the MC calculation, BEAMnrc and DOSXYZnrc were used for the 6-MeV electron beam of the Varian 21EX, in which information for the tungsten, stainless steel, and aluminum material for the eye shield was used. The same plan was generated on the Pinnacle system and both were compared. The use of the acrylic shield produced clear CT images, enabling delineation of the regions of interest, and yielded CT-based dose calculation for the metallic shield. Both the MC and the Pinnacle systems showed a similar dose distribution downstream of the eye shield, reflecting the blocking effect of the metallic eye shield. The major difference between the MC and the Pinnacle results was the target eyelid dose upstream of the shield such that the Pinnacle system underestimated the dose by 19 to 28% and 11 to 18% for the maximum and the mean doses, respectively. The pattern of dose difference between the MC and the Pinnacle systems was similar to that in the previous phantom study. In conclusion, the metallic eye shield was successfully incorporated into the CT-based planning, and the accurate dose calculation requires MC simulation
Energy Technology Data Exchange (ETDEWEB)
Reynaldo, S. R. [Development Centre of Nuclear Technology, Posgraduate Course in Science and Technology of Radiations, Minerals and Materials / CNEN, Av. Pte. Antonio Carlos 6627, 31270-901 Belo Horizonte, Minas Gerais (Brazil); Benavente C, J. A.; Da Silva, T. A., E-mail: sirr@cdtn.br [Development Centre of Nuclear Technology / CNEN, Av. Pte. Antonio Carlos 6627, 31270-901 Belo Horizonte, Minas Gerais (Brazil)
2015-10-15
Beta Secondary Standard 2 (Bss 2) provides beta radiation fields with certified values of absorbed dose to tissue and the derived operational radiation protection quantities. As part of the quality assurance, metrology laboratories are required to verify the reliability of the Bss-2 system by performing additional verification measurements. In the CDTN Calibration Laboratory, the absorbed dose rates and their angular variation in the {sup 90}Sr/{sup 90}Y and {sup 85}Kr beta radiation fields were studied. Measurements were done with a 23392 model PTW extrapolation chamber and with Gafchromic radiochromic films on a PMMA slab phantom. In comparison to the certificate values provided by the Bss-2, absorbed dose rates measured with the extrapolation chamber differed from -1.4 to 2.9% for the {sup 90}Sr/{sup 90}Y and -0.3% for the {sup 85}Kr fields; their angular variation showed differences lower than 2% for incidence angles up to 40-degrees and it reached 11% for higher angles, when compared to ISO values. Measurements with the radiochromic film showed an asymmetry of the radiation field that is caused by a misalignment. Differences between the angular variations of absorbed dose rates determined by both dosimetry systems suggested that some correction factors for the extrapolation chamber that were not considered should be determined. (Author)
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Purpose: The recently activated Radiation Therapy Oncology Group (RTOG) studies of stereotactic body radiation therapy (SBRT) for non-small-cell lung cancer (NSCLC) require tissue density heterogeneity correction, where the high and intermediate dose compliance criteria were established based on superposition algorithm dose calculations. The study was aimed at comparing superposition algorithm dose calculations with Monte Carlo (MC) dose calculations for SBRT for NSCLC and to evaluate whether compliance criteria need to be adjusted for MC dose calculations. Methods and Materials: Fifteen RTOG 0236 study sets were used. The planning tumor volumes (PTV) ranged from 10.7 to 117.1 cm3. SBRT conformal treatment plans were generated using XiO (CMS Inc.) treatment planning software with superposition algorithm to meet the dosimetric high and intermediate compliance criteria recommended by the RTOG 0813 protocol. Plans were recalculated using the MC algorithm of a Monaco (CMS, Inc.) treatment planning system. Tissue density heterogeneity correction was applied in both calculations. Results: Overall, the dosimetric quantities of the MC calculations have larger magnitudes than those of the superposition calculations. On average, R100% (ratio of prescription isodose volume to PTV), R50% (ratio of 50% prescription isodose volume to PTV), D2cm (maximal dose 2 cm from PTV in any direction as a percentage of prescription dose), and V20 (percentage of lung receiving dose equal to or larger than 20 Gy) increased by 9%, 12%, 7%, and 18%, respectively. In the superposition plans, 3 cases did not meet criteria for R50% or D2cm. In the MC-recalculated plans, 8 cases did not meet criteria for R100%, R50%, or D2cm. After reoptimization with MC calculations, 5 cases did not meet the criteria for R50% or D2cm. Conclusions: Results indicate that the dosimetric criteria, e.g., the criteria for R50% recommended by RTOG 0813 protocol, may need to be adjusted when the MC dose calculation
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Rodrigues, Anna; Yin, Fang-Fang; Wu, Qiuwen, E-mail: Qiuwen.Wu@Duke.edu [Department of Radiation Oncology, Duke University Medical Center, Durham, North Carolina 27710 and Medical Physics Graduate Program, Duke University Medical Center, Durham, North Carolina 27705 (United States); Sawkey, Daren [Varian Medical Systems, Palo Alto, California 94304 (United States)
2015-05-15
Purpose: To develop a framework for accurate electron Monte Carlo dose calculation. In this study, comprehensive validations of vendor provided electron beam phase space files for Varian TrueBeam Linacs against measurement data are presented. Methods: In this framework, the Monte Carlo generated phase space files were provided by the vendor and used as input to the downstream plan-specific simulations including jaws, electron applicators, and water phantom computed in the EGSnrc environment. The phase space files were generated based on open field commissioning data. A subset of electron energies of 6, 9, 12, 16, and 20 MeV and open and collimated field sizes 3 × 3, 4 × 4, 5 × 5, 6 × 6, 10 × 10, 15 × 15, 20 × 20, and 25 × 25 cm{sup 2} were evaluated. Measurements acquired with a CC13 cylindrical ionization chamber and electron diode detector and simulations from this framework were compared for a water phantom geometry. The evaluation metrics include percent depth dose, orthogonal and diagonal profiles at depths R{sub 100}, R{sub 50}, R{sub p}, and R{sub p+} for standard and extended source-to-surface distances (SSD), as well as cone and cut-out output factors. Results: Agreement for the percent depth dose and orthogonal profiles between measurement and Monte Carlo was generally within 2% or 1 mm. The largest discrepancies were observed within depths of 5 mm from phantom surface. Differences in field size, penumbra, and flatness for the orthogonal profiles at depths R{sub 100}, R{sub 50}, and R{sub p} were within 1 mm, 1 mm, and 2%, respectively. Orthogonal profiles at SSDs of 100 and 120 cm showed the same level of agreement. Cone and cut-out output factors agreed well with maximum differences within 2.5% for 6 MeV and 1% for all other energies. Cone output factors at extended SSDs of 105, 110, 115, and 120 cm exhibited similar levels of agreement. Conclusions: We have presented a Monte Carlo simulation framework for electron beam dose calculations for
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Purpose: To develop a framework for accurate electron Monte Carlo dose calculation. In this study, comprehensive validations of vendor provided electron beam phase space files for Varian TrueBeam Linacs against measurement data are presented. Methods: In this framework, the Monte Carlo generated phase space files were provided by the vendor and used as input to the downstream plan-specific simulations including jaws, electron applicators, and water phantom computed in the EGSnrc environment. The phase space files were generated based on open field commissioning data. A subset of electron energies of 6, 9, 12, 16, and 20 MeV and open and collimated field sizes 3 × 3, 4 × 4, 5 × 5, 6 × 6, 10 × 10, 15 × 15, 20 × 20, and 25 × 25 cm2 were evaluated. Measurements acquired with a CC13 cylindrical ionization chamber and electron diode detector and simulations from this framework were compared for a water phantom geometry. The evaluation metrics include percent depth dose, orthogonal and diagonal profiles at depths R100, R50, Rp, and Rp+ for standard and extended source-to-surface distances (SSD), as well as cone and cut-out output factors. Results: Agreement for the percent depth dose and orthogonal profiles between measurement and Monte Carlo was generally within 2% or 1 mm. The largest discrepancies were observed within depths of 5 mm from phantom surface. Differences in field size, penumbra, and flatness for the orthogonal profiles at depths R100, R50, and Rp were within 1 mm, 1 mm, and 2%, respectively. Orthogonal profiles at SSDs of 100 and 120 cm showed the same level of agreement. Cone and cut-out output factors agreed well with maximum differences within 2.5% for 6 MeV and 1% for all other energies. Cone output factors at extended SSDs of 105, 110, 115, and 120 cm exhibited similar levels of agreement. Conclusions: We have presented a Monte Carlo simulation framework for electron beam dose calculations for Varian TrueBeam Linacs. Electron beam energies of 6
SU-E-T-505: CT-Based Independent Dose Verification for RapidArc Plan as a Secondary Check
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Tachibana, H; Baba, H [The National Cancer Center Hospital East, Kashiwa, Chiba (Japan); Kamima, T; Takahashi, R [The Cancer Institute Hospital of JFCR, Koto, Tokyo (Japan)
2014-06-01
Purpose: To design and develop a CT-based independent dose verification for the RapidArc plan and also to show the effectiveness of inhomogeneous correction in the secondary check for the plan. Methods: To compute the radiological path from the body surface to the reference point and equivalent field sizes from the multiple MLC aperture shapes in the RapidArc MLC sequences independently, DICOM files of CT image, structure and RapidArc plan were imported to our in-house software. The radiological path was computed using a three-dimensional CT arrays for each segment. The multiple MLC aperture shapes were used to compute tissue maximum ratio and phantom scatter factor using the Clarkson-method. In this study, two RapidArc plans for oropharynx cancer were used to compare the doses in CT-based calculation and water-equivalent phantom calculation using the contoured body structure to the dose in a treatment planning system (TPS). Results: The comparison in the one plan shows good agreement in both of the calculation (within 1%). However, in the other case, the CT-based calculation shows better agreement compared to the water-equivalent phantom calculation (CT-based: -2.8% vs. Water-based: -3.8%). Because there were multiple structures along the multiple beam paths and the radiological path length in the CT-based calculation and the path in the water-homogenous phantom calculation were comparatively different. Conclusion: RapidArc treatments are performed in any sites (from head, chest, abdomen to pelvis), which includes inhomogeneous media. Therefore, a more reliable CT-based calculation may be used as a secondary check for the independent verification.
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The Project Design of a detection system to verify 2D dose maps for Intensity Modulated Radiation Therapy (IMRT) treatment is one of the 22 sub-projects of the optimization of Particle Accelerator (oPAC) European network. This work is part of a wide scientific collaboration established under the name RADIA. It involves the Department of Atomic, Molecular and Nuclear Physics and the Department of Electronical Engineering of the University of Seville, the National Accelerator Centre (CNA) and also the Virgen Macarena University Hospital. Such a work aims to produce a novel optimized online readout system to obtain 2D dose maps at axial planes for radiotherapy treatment verification, based on silicon technology. This system is being developed following clinical requirements and couples a novel dual single sided silicon strip detectors (SSSSD) chip, designed and developed in collaboration with the company Micron Semiconductor Ltd., to its in-house developed electronics, mechanical phantoms, data acquisition and analysis systems. First measurements have been performed at the Virgen Macarena Hospital in Seville by using a slab phantom (made out of polyethylene, similar in density to human tissue), designed in order to house the detector. Such system has been irradiated with a 6MV photon beam produced by a Siemens linac.This setup has been used to determine important parameters related to the required quality assurance (Q A) protocols such as: linearity of the detector response, reproducibility, penumbra, output factors, percent depth dose (Pdd). The goodness of these results is compared to a feasibility study that was carried out by employing a commercial W1-SS 500 detector, for complex radiotherapy treatment verification. Data acquisition and processing software is also being developed in order to obtain a system that could be directly operated by the medical staff
Monte Carlo simulations of the dose from imaging with GE eXplore 120 micro-CT using GATE
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Bretin, Florian; Bahri, Mohamed Ali; Luxen, André; Phillips, Christophe; Plenevaux, Alain; Seret, Alain, E-mail: aseret@ulg.ac.be [Cyclotron Research Centre, University of Liège, Sart Tilman B30, Liège 4000 (Belgium)
2015-10-15
Purpose: Small animals are increasingly used as translational models in preclinical imaging studies involving microCT, during which the subjects can be exposed to large amounts of radiation. While the radiation levels are generally sublethal, studies have shown that low-level radiation can change physiological parameters in mice. In order to rule out any influence of radiation on the outcome of such experiments, or resulting deterministic effects in the subjects, the levels of radiation involved need to be addressed. The aim of this study was to investigate the radiation dose delivered by the GE eXplore 120 microCT non-invasively using Monte Carlo simulations in GATE and to compare results to previously obtained experimental values. Methods: Tungsten X-ray spectra were simulated at 70, 80, and 97 kVp using an analytical tool and their half-value layers were simulated for spectra validation against experimentally measured values of the physical X-ray tube. A Monte Carlo model of the microCT system was set up and four protocols that are regularly applied to live animal scanning were implemented. The computed tomography dose index (CTDI) inside a PMMA phantom was derived and multiple field of view acquisitions were simulated using the PMMA phantom, a representative mouse and rat. Results: Simulated half-value layers agreed with experimentally obtained results within a 7% error window. The CTDI ranged from 20 to 56 mGy and closely matched experimental values. Derived organ doses in mice reached 459 mGy in bones and up to 200 mGy in soft tissue organs using the highest energy protocol. Dose levels in rats were lower due to the increased mass of the animal compared to mice. The uncertainty of all dose simulations was below 14%. Conclusions: Monte Carlo simulations proved a valuable tool to investigate the 3D dose distribution in animals from microCT. Small animals, especially mice (due to their small volume), receive large amounts of radiation from the GE eXplore 120
Monte Carlo simulations of the dose from imaging with GE eXplore 120 micro-CT using GATE
International Nuclear Information System (INIS)
Purpose: Small animals are increasingly used as translational models in preclinical imaging studies involving microCT, during which the subjects can be exposed to large amounts of radiation. While the radiation levels are generally sublethal, studies have shown that low-level radiation can change physiological parameters in mice. In order to rule out any influence of radiation on the outcome of such experiments, or resulting deterministic effects in the subjects, the levels of radiation involved need to be addressed. The aim of this study was to investigate the radiation dose delivered by the GE eXplore 120 microCT non-invasively using Monte Carlo simulations in GATE and to compare results to previously obtained experimental values. Methods: Tungsten X-ray spectra were simulated at 70, 80, and 97 kVp using an analytical tool and their half-value layers were simulated for spectra validation against experimentally measured values of the physical X-ray tube. A Monte Carlo model of the microCT system was set up and four protocols that are regularly applied to live animal scanning were implemented. The computed tomography dose index (CTDI) inside a PMMA phantom was derived and multiple field of view acquisitions were simulated using the PMMA phantom, a representative mouse and rat. Results: Simulated half-value layers agreed with experimentally obtained results within a 7% error window. The CTDI ranged from 20 to 56 mGy and closely matched experimental values. Derived organ doses in mice reached 459 mGy in bones and up to 200 mGy in soft tissue organs using the highest energy protocol. Dose levels in rats were lower due to the increased mass of the animal compared to mice. The uncertainty of all dose simulations was below 14%. Conclusions: Monte Carlo simulations proved a valuable tool to investigate the 3D dose distribution in animals from microCT. Small animals, especially mice (due to their small volume), receive large amounts of radiation from the GE eXplore 120
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Purpose: To develop a comprehensive end-to-end test for Varian's TrueBeam linear accelerator for head and neck IMRT using a custom phantom designed to utilize multiple dosimetry devices. Purpose: To commission a multiple-source Monte Carlo model of Elekta linear accelerator beams of nominal energies 6MV and 10MV. Methods: A three source, Monte Carlo model of Elekta 6 and 10MV therapeutic x-ray beams was developed. Energy spectra of two photon sources corresponding to primary photons created in the target and scattered photons originating in the linear accelerator head were determined by an optimization process that fit the relative fluence of 0.25 MeV energy bins to the product of Fatigue-Life and Fermi functions to match calculated percent depth dose (PDD) data with that measured in a water tank for a 10x10cm2 field. Off-axis effects were modeled by a 3rd degree polynomial used to describe the off-axis half-value layer as a function of off-axis angle and fitting the off-axis fluence to a piecewise linear function to match calculated dose profiles with measured dose profiles for a 40×40cm2 field. The model was validated by comparing calculated PDDs and dose profiles for field sizes ranging from 3×3cm2 to 30×30cm2 to those obtained from measurements. A benchmarking study compared calculated data to measurements for IMRT plans delivered to anthropomorphic phantoms. Results: Along the central axis of the beam 99.6% and 99.7% of all data passed the 2%/2mm gamma criterion for 6 and 10MV models, respectively. Dose profiles at depths of dmax, through 25cm agreed with measured data for 99.4% and 99.6% of data tested for 6 and 10MV models, respectively. A comparison of calculated dose to film measurement in a head and neck phantom showed an average of 85.3% and 90.5% of pixels passing a 3%/2mm gamma criterion for 6 and 10MV models respectively. Conclusion: A Monte Carlo multiple-source model for Elekta 6 and 10MV therapeutic x-ray beams has been developed as a
Directory of Open Access Journals (Sweden)
Biniam Tesfamicael
2016-03-01
Full Text Available Purpose: The main purpose of this study was to monitor the secondary dose distribution originating from a water phantom during proton therapy of prostate cancer using scintillating fibers.Methods: The Geant4 Monte Carlo toolkit version 9.6.p02 was used to simulate a proton therapy of prostate cancer. Two cases were studied. In the first case, 8 × 8 = 64 equally spaced fibers inside three 4 × 4 × 2.54 cm3 Delrin® blocks were used to monitor the emission of secondary particles in the transverse (left and right and distal regions relative to the beam direction. In the second case, a scintillating block with a thickness of 2.54 cm and equal vertical and longitudinal dimensions as the water phantom was used. Geometrical cuts were implemented to extract the energy deposited in each fiber and inside the scintillating block.Results: The transverse dose distributions from the detected secondary particles in both cases are symmetric and agree to within <3.6%. The energy deposited gradually increases as one moves from the peripheral row of fibers towards the center of the block (aligned with the center of the prostate by a factor of approximately 5. The energy deposited was also observed to decrease as one goes from the frontal to distal region of the block. The ratio of the energy deposited in the prostate to the energy deposited in the middle two rows of fibers showed a linear relationship with a slope of (-3.55±2.26 × 10-5 MeV per treatment Gy delivered. The distal detectors recorded a negligible amount of energy deposited due to higher attenuation of the secondary particles by the water in that direction.Conclusion: With a good calibration and with the ability to define a good correlation between the radiation flux recorded by the external fibers and the dose delivered to the prostate, such fibers can be used for real time dose verification to the target. The system was also observed to respond to the series of Bragg Peaks used to generate the
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Blazy-Aubignac, L
2007-09-15
The treatment planning systems (T.P.S.) occupy a key position in the radiotherapy service: they realize the projected calculation of the dose distribution and the treatment duration. Traditionally, the quality control of the calculated distribution doses relies on their comparisons with dose distributions measured under the device of treatment. This thesis proposes to substitute these dosimetry measures to the profile of reference dosimetry calculations got by the Penelope Monte-Carlo code. The Monte-Carlo simulations give a broad choice of test configurations and allow to envisage a quality control of dosimetry aspects of T.P.S. without monopolizing the treatment devices. This quality control, based on the Monte-Carlo simulations has been tested on a clinical T.P.S. and has allowed to simplify the quality procedures of the T.P.S.. This quality control, in depth, more precise and simpler to implement could be generalized to every center of radiotherapy. (N.C.)
Karimian, A; Nikparvar, B; Jabbari, I
2014-11-01
Renal angiography is one of the medical imaging methods in which patient and physician receive high equivalent doses due to long duration of fluoroscopy. In this research, equivalent doses of some radiosensitive tissues of patient (adult and child) and physician during renal angiography have been calculated by using adult and child Oak Ridge National Laboratory phantoms and Monte Carlo method (MCNPX). The results showed, in angiography of right kidney in a child and adult patient, that gall bladder with the amounts of 2.32 and 0.35 mSv, respectively, has received the most equivalent dose. About the physician, left hand, left eye and thymus absorbed the most amounts of doses, means 0.020 mSv. In addition, equivalent doses of the physician's lens eye, thyroid and knees were 0.023, 0.007 and 7.9E-4 mSv, respectively. Although these values are less than the reported thresholds by ICRP 103, it should be noted that these amounts are related to one examination. PMID:25063788
International Nuclear Information System (INIS)
Renal angiography is one of the medical imaging methods in which patient and physician receive high equivalent doses due to long duration of fluoroscopy. In this research, equivalent doses of some radiosensitive tissues of patient (adult and child) and physician during renal angiography have been calculated by using adult and child Oak Ridge National Laboratory phantoms and Monte Carlo method (MCNPX). The results showed, in angiography of right kidney in a child and adult patient, that gall bladder with the amounts of 2.32 and 0.35 mSv, respectively, has received the most equivalent dose. About the physician, left hand, left eye and thymus absorbed the most amounts of doses, means 0.020 mSv. In addition, equivalent doses of the physician's lens eye, thyroid and knees were 0.023, 0.007 and 7.9 - 4 mSv, respectively. Although these values are less than the reported thresholds by ICRP 103, it should be noted that these amounts are related to one examination. (authors)
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Garcia, Marie-Paule, E-mail: marie-paule.garcia@univ-brest.fr; Villoing, Daphnée [UMR 1037 INSERM/UPS, CRCT, 133 Route de Narbonne, 31062 Toulouse (France); McKay, Erin [St George Hospital, Gray Street, Kogarah, New South Wales 2217 (Australia); Ferrer, Ludovic [ICO René Gauducheau, Boulevard Jacques Monod, St Herblain 44805 (France); Cremonesi, Marta; Botta, Francesca; Ferrari, Mahila [European Institute of Oncology, Via Ripamonti 435, Milano 20141 (Italy); Bardiès, Manuel [UMR 1037 INSERM/UPS, CRCT, 133 Route de Narbonne, Toulouse 31062 (France)
2015-12-15
Purpose: The TestDose platform was developed to generate scintigraphic imaging protocols and associated dosimetry by Monte Carlo modeling. TestDose is part of a broader project (www.dositest.com) whose aim is to identify the biases induced by different clinical dosimetry protocols. Methods: The TestDose software allows handling the whole pipeline from virtual patient generation to resulting planar and SPECT images and dosimetry calculations. The originality of their approach relies on the implementation of functional segmentation for the anthropomorphic model representing a virtual patient. Two anthropomorphic models are currently available: 4D XCAT and ICRP 110. A pharmacokinetic model describes the biodistribution of a given radiopharmaceutical in each defined compartment at various time-points. The Monte Carlo simulation toolkit GATE offers the possibility to accurately simulate scintigraphic images and absorbed doses in volumes of interest. The TestDose platform relies on GATE to reproduce precisely any imaging protocol and to provide reference dosimetry. For image generation, TestDose stores user’s imaging requirements and generates automatically command files used as input for GATE. Each compartment is simulated only once and the resulting output is weighted using pharmacokinetic data. Resulting compartment projections are aggregated to obtain the final image. For dosimetry computation, emission data are stored in the platform database and relevant GATE input files are generated for the virtual patient model and associated pharmacokinetics. Results: Two samples of software runs are given to demonstrate the potential of TestDose. A clinical imaging protocol for the Octreoscan™ therapeutical treatment was implemented using the 4D XCAT model. Whole-body “step and shoot” acquisitions at different times postinjection and one SPECT acquisition were generated within reasonable computation times. Based on the same Octreoscan™ kinetics, a dosimetry
International Nuclear Information System (INIS)
Purpose: The TestDose platform was developed to generate scintigraphic imaging protocols and associated dosimetry by Monte Carlo modeling. TestDose is part of a broader project (www.dositest.com) whose aim is to identify the biases induced by different clinical dosimetry protocols. Methods: The TestDose software allows handling the whole pipeline from virtual patient generation to resulting planar and SPECT images and dosimetry calculations. The originality of their approach relies on the implementation of functional segmentation for the anthropomorphic model representing a virtual patient. Two anthropomorphic models are currently available: 4D XCAT and ICRP 110. A pharmacokinetic model describes the biodistribution of a given radiopharmaceutical in each defined compartment at various time-points. The Monte Carlo simulation toolkit GATE offers the possibility to accurately simulate scintigraphic images and absorbed doses in volumes of interest. The TestDose platform relies on GATE to reproduce precisely any imaging protocol and to provide reference dosimetry. For image generation, TestDose stores user’s imaging requirements and generates automatically command files used as input for GATE. Each compartment is simulated only once and the resulting output is weighted using pharmacokinetic data. Resulting compartment projections are aggregated to obtain the final image. For dosimetry computation, emission data are stored in the platform database and relevant GATE input files are generated for the virtual patient model and associated pharmacokinetics. Results: Two samples of software runs are given to demonstrate the potential of TestDose. A clinical imaging protocol for the Octreoscan™ therapeutical treatment was implemented using the 4D XCAT model. Whole-body “step and shoot” acquisitions at different times postinjection and one SPECT acquisition were generated within reasonable computation times. Based on the same Octreoscan™ kinetics, a dosimetry
International Nuclear Information System (INIS)
Over the last decade, there was a substantial increase in the number of interventional cardiology procedures worldwide, and the corresponding ionizing radiation doses for both the medical staff and patients became a subject of concern. Interventional procedures in cardiology are normally very complex, resulting in long exposure times. Also, these interventions require the operator to work near the patient and, consequently, close to the primary X-ray beam. Moreover, due to the scattered radiation from the patient and the equipment, the medical staff is also exposed to a non-uniform radiation field that can lead to a significant exposure of sensitive body organs and tissues, such as the eye lens, the thyroid and the extremities. In order to better understand the spatial variation of the dose and dose rate distributions during an interventional cardiology procedure, the dose distribution around a C-arm fluoroscopic system, in operation in a cardiac cath lab at Portuguese Hospital, was estimated using both Monte Carlo (MC) simulations and dosimetric measurements. To model and simulate the cardiac cath lab, including the fluoroscopic equipment used to execute interventional procedures, the state-of-the-art MC radiation transport code MCNPX 2.7.0 was used. Subsequently, Thermo-Luminescent Detector (TLD) measurements were performed, in order to validate and support the simulation results obtained for the cath lab model. The preliminary results presented in this study reveal that the cardiac cath lab model was successfully validated, taking into account the good agreement between MC calculations and TLD measurements. The simulated results for the isodose curves related to the C-arm fluoroscopic system are also consistent with the dosimetric information provided by the equipment manufacturer (Siemens). The adequacy of the implemented computational model used to simulate complex procedures and map dose distributions around the operator and the medical staff is discussed, in
Tomotherapy dose distribution verification using MAGIC-f polymer gel dosimetry
Energy Technology Data Exchange (ETDEWEB)
Pavoni, J. F.; Pike, T. L.; Snow, J.; DeWerd, L.; Baffa, O. [Departamento de Fisica, Faculdade de Filosofia Ciencias e Letras de Ribeirao Preto-Universidade de Sao Paulo, Av. Bandeirantes, 3900 - CEP 14040-901 - Bairro Monte Alegre - Ribeirao Preto, SP (Brazil); Medical Radiation Research Center, Department of Medical Physics, University of Wisconsin, 1111 Highland Avenue, B1002 WIMR, Madison, Wisconsin 53705-2275 (United States); Departamento de Fisica, Faculdade de Filosofia Ciencias e Letras de Ribeirao Preto-Universidade de Sao Paulo, Av. Bandeirantes, 3900 - CEP 14040-901 - Bairro Monte Alegre - Ribeirao Preto, SP (Brazil)
2012-05-15
Purpose: This paper presents the application of MAGIC-f gel in a three-dimensional dose distribution measurement and its ability to accurately measure the dose distribution from a tomotherapy unit. Methods: A prostate intensity-modulated radiation therapy (IMRT) irradiation was simulated in the gel phantom and the treatment was delivered by a TomoTherapy equipment. Dose distribution was evaluated by the R2 distribution measured in magnetic resonance imaging. Results: A high similarity was found by overlapping of isodoses of the dose distribution measured with the gel and expected by the treatment planning system (TPS). Another analysis was done by comparing the relative absorbed dose profiles in the measured and in the expected dose distributions extracted along indicated lines of the volume and the results were also in agreement. The gamma index analysis was also applied to the data and a high pass rate was achieved (88.4% for analysis using 3%/3 mm and of 96.5% using 4%/4 mm). The real three-dimensional analysis compared the dose-volume histograms measured for the planning volumes and expected by the treatment planning, being the results also in good agreement by the overlapping of the curves. Conclusions: These results show that MAGIC-f gel is a promise for tridimensional dose distribution measurements.
Dosimetric verification of calculated D max dose rate in half-blocked cobalt beams
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The central beam in half-blocked irradiations passes through the edge of the marked skin field instead of the geometrical centre, hence any point in the skin field receives the same primary radiation as for the full field (at collimator) due to dose uniformity across the field. The backscatter radiation should be assessed accurately in order to arrive at dose rate
Tomotherapy dose distribution verification using MAGIC-f polymer gel dosimetry
International Nuclear Information System (INIS)
Purpose: This paper presents the application of MAGIC-f gel in a three-dimensional dose distribution measurement and its ability to accurately measure the dose distribution from a tomotherapy unit. Methods: A prostate intensity-modulated radiation therapy (IMRT) irradiation was simulated in the gel phantom and the treatment was delivered by a TomoTherapy equipment. Dose distribution was evaluated by the R2 distribution measured in magnetic resonance imaging. Results: A high similarity was found by overlapping of isodoses of the dose distribution measured with the gel and expected by the treatment planning system (TPS). Another analysis was done by comparing the relative absorbed dose profiles in the measured and in the expected dose distributions extracted along indicated lines of the volume and the results were also in agreement. The gamma index analysis was also applied to the data and a high pass rate was achieved (88.4% for analysis using 3%/3 mm and of 96.5% using 4%/4 mm). The real three-dimensional analysis compared the dose-volume histograms measured for the planning volumes and expected by the treatment planning, being the results also in good agreement by the overlapping of the curves. Conclusions: These results show that MAGIC-f gel is a promise for tridimensional dose distribution measurements.
International Nuclear Information System (INIS)
The dose distribution calculation is one of major steps in cancer radiotherapy. This paper applies Monte Carlo code, MCNP5, in simulation 15 MV photon beams from linear accelerator of General Hospital of Kien Giang in a case treatment of lung cancer. The settings for beam direction, field size and isocenter position used in MCNP5 must be the same as in treatment plan at hospital to ensure the results from MCNP5 are accurate. We also built a program CODIM by using MATLAB® programming software. This program is used to construct digital voxel phantoms from lung CT images obtained from cancer treatment cases at Kien Giang hospital and then simulate the delivered dose of linac in these phantoms by using MCNP5 simulation code. The results show that there is a difference of 5% in comparison to Prowess Panther program - a semi-empirical simulation program which is being used for treatment planning in Kien Giang hospital. (author)
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The present paper reports on the structure and first results from a new Monte Carlo programme for calculations of energy distributions within tissue equivalent phantoms irradiated from π--beams. Each pion or generated secondary particle is transported until to the complete loss of its kinetic energy taking into account pion processes like multiple Coulomb scattering, pion reactions in flight and absorption of stopped pions. The code uses mainly data from experiments, and physical models have been added only in cases of lacking data. Depth dose curves for a pensil beam of 170 MeV/c within a water phantom are discussed as a function of various parameters. Isodose contours are plotted resulting from a convolution of an extended beam profile and the dose distribution of a pencil beams. (orig.)
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Purpose: Volumetric modulated arc therapy (VMAT) treatment planning studies have been reported to provide good target coverage and organs at risk (OARs) sparing in total marrow irradiation (TMI). A comprehensive dosimetric study simulating the clinical situation as close as possible is a norm in radiotherapy before a technique can be used to treat a patient. Without such a study, it would be difficult to make a reliable and safe clinical transition especially with a technique as complicated as VMAT-TMI. To this end, the dosimetric feasibility of VMAT-TMI technique in terms of treatment planning, delivery efficiency, and the most importantly three dimensional dose distribution accuracy was investigated in this study. The VMAT-TMI dose distribution inside a humanlike Rando phantom was measured and compared to the dose calculated using RapidArc especially in the field junctions and the inhomogeneous tissues including the lungs, which is the dose-limiting organ in TMI. Methods: Three subplans with a total of nine arcs were used to treat the planning target volume (PTV), which was determined as all the bones plus the 3 mm margin. Thermoluminescent detectors (TLDs) were placed at 39 positions throughout the phantom. The measured TLD doses were compared to the calculated plan doses. Planar dose for each arc was verified using mapcheck. Results: TLD readings demonstrated accurate dose delivery, with a median dose difference of 0.5% (range: -4.3% and 6.6%) from the calculated dose in the junctions and in the inhomogeneous medium including the lungs. Conclusions: The results from this study suggest that RapidArc VMAT technique is dosimetrically accurate, safe, and efficient in delivering TMI within clinically acceptable time frame.
A GPU OpenCL based cross-platform Monte Carlo dose calculation engine (goMC)
International Nuclear Information System (INIS)
Monte Carlo (MC) simulation has been recognized as the most accurate dose calculation method for radiotherapy. However, the extremely long computation time impedes its clinical application. Recently, a lot of effort has been made to realize fast MC dose calculation on graphic processing units (GPUs). However, most of the GPU-based MC dose engines have been developed under NVidia’s CUDA environment. This limits the code portability to other platforms, hindering the introduction of GPU-based MC simulations to clinical practice. The objective of this paper is to develop a GPU OpenCL based cross-platform MC dose engine named goMC with coupled photon–electron simulation for external photon and electron radiotherapy in the MeV energy range. Compared to our previously developed GPU-based MC code named gDPM (Jia et al 2012 Phys. Med. Biol. 57 7783–97), goMC has two major differences. First, it was developed under the OpenCL environment for high code portability and hence could be run not only on different GPU cards but also on CPU platforms. Second, we adopted the electron transport model used in EGSnrc MC package and PENELOPE’s random hinge method in our new dose engine, instead of the dose planning method employed in gDPM. Dose distributions were calculated for a 15 MeV electron beam and a 6 MV photon beam in a homogenous water phantom, a water-bone-lung-water slab phantom and a half-slab phantom. Satisfactory agreement between the two MC dose engines goMC and gDPM was observed in all cases. The average dose differences in the regions that received a dose higher than 10% of the maximum dose were 0.48–0.53% for the electron beam cases and 0.15–0.17% for the photon beam cases. In terms of efficiency, goMC was ∼4–16% slower than gDPM when running on the same NVidia TITAN card for all the cases we tested, due to both the different electron transport models and the different development environments. The code portability of our new dose engine goMC was
A GPU OpenCL based cross-platform Monte Carlo dose calculation engine (goMC)
Tian, Zhen; Shi, Feng; Folkerts, Michael; Qin, Nan; Jiang, Steve B.; Jia, Xun
2015-09-01
Monte Carlo (MC) simulation has been recognized as the most accurate dose calculation method for radiotherapy. However, the extremely long computation time impedes its clinical application. Recently, a lot of effort has been made to realize fast MC dose calculation on graphic processing units (GPUs). However, most of the GPU-based MC dose engines have been developed under NVidia’s CUDA environment. This limits the code portability to other platforms, hindering the introduction of GPU-based MC simulations to clinical practice. The objective of this paper is to develop a GPU OpenCL based cross-platform MC dose engine named goMC with coupled photon-electron simulation for external photon and electron radiotherapy in the MeV energy range. Compared to our previously developed GPU-based MC code named gDPM (Jia et al 2012 Phys. Med. Biol. 57 7783-97), goMC has two major differences. First, it was developed under the OpenCL environment for high code portability and hence could be run not only on different GPU cards but also on CPU platforms. Second, we adopted the electron transport model used in EGSnrc MC package and PENELOPE’s random hinge method in our new dose engine, instead of the dose planning method employed in gDPM. Dose distributions were calculated for a 15 MeV electron beam and a 6 MV photon beam in a homogenous water phantom, a water-bone-lung-water slab phantom and a half-slab phantom. Satisfactory agreement between the two MC dose engines goMC and gDPM was observed in all cases. The average dose differences in the regions that received a dose higher than 10% of the maximum dose were 0.48-0.53% for the electron beam cases and 0.15-0.17% for the photon beam cases. In terms of efficiency, goMC was ~4-16% slower than gDPM when running on the same NVidia TITAN card for all the cases we tested, due to both the different electron transport models and the different development environments. The code portability of our new dose engine goMC was validated by
A GPU OpenCL based cross-platform Monte Carlo dose calculation engine (goMC).
Tian, Zhen; Shi, Feng; Folkerts, Michael; Qin, Nan; Jiang, Steve B; Jia, Xun
2015-10-01
Monte Carlo (MC) simulation has been recognized as the most accurate dose calculation method for radiotherapy. However, the extremely long computation time impedes its clinical application. Recently, a lot of effort has been made to realize fast MC dose calculation on graphic processing units (GPUs). However, most of the GPU-based MC dose engines have been developed under NVidia's CUDA environment. This limits the code portability to other platforms, hindering the introduction of GPU-based MC simulations to clinical practice. The objective of this paper is to develop a GPU OpenCL based cross-platform MC dose engine named goMC with coupled photon-electron simulation for external photon and electron radiotherapy in the MeV energy range. Compared to our previously developed GPU-based MC code named gDPM (Jia et al 2012 Phys. Med. Biol. 57 7783-97), goMC has two major differences. First, it was developed under the OpenCL environment for high code portability and hence could be run not only on different GPU cards but also on CPU platforms. Second, we adopted the electron transport model used in EGSnrc MC package and PENELOPE's random hinge method in our new dose engine, instead of the dose planning method employed in gDPM. Dose distributions were calculated for a 15 MeV electron beam and a 6 MV photon beam in a homogenous water phantom, a water-bone-lung-water slab phantom and a half-slab phantom. Satisfactory agreement between the two MC dose engines goMC and gDPM was observed in all cases. The average dose differences in the regions that received a dose higher than 10% of the maximum dose were 0.48-0.53% for the electron beam cases and 0.15-0.17% for the photon beam cases. In terms of efficiency, goMC was ~4-16% slower than gDPM when running on the same NVidia TITAN card for all the cases we tested, due to both the different electron transport models and the different development environments. The code portability of our new dose engine goMC was validated by
International Nuclear Information System (INIS)
Purpose: This work forms part of an ongoing study to develop a next-generation electronic portal imaging device (EPID) for simultaneous imaging and dose verification in radiotherapy. Monte Carlo (MC) simulations were used to characterize the imaging performance of a novel EPID that has previously been demonstrated to exhibit a water-equivalent response. The EPID ' s response was quantified in several configurations and model parameters were empirically validated against experimental measurements. Methods: A MC model of a novel a-Si EPID incorporating an array of plastic scintillating fibers was developed. Square BCF-99-06A scintillator fibers with PMMA cladding (Saint-Gobain Crystals) were modelled in a matrix with total area measuring 150×150 mm2. The standard electromagnetic and optical physics Geant4 classes were used to simulate radiation transport from an angled slit source (6 MV energy spectrum) through the EPID and optical photons reaching the photodiodes were scored. The prototype's modulation transfer function (MTF) was simulated and validated against experimental measurements. Several optical transport parameters, fiber lengths and thicknesses of an air gap between the scintillator and photodiodes were investigated to quantify their effects on the prototype's detection efficiency, sensitivity and MTF. Results: Simulated EPID response was more sensitive to variations in geometry than in the optical parameters studied. The MTF was particularly sensitive to the introduction of a 0.5–1.0 mm air gap between the scintillator and photodiodes, which lowered the MTF relative to that simulated without the gap. As expected, increasing the fiber length increased the detector efficiency and sensitivity while decreasing the MTF. Conclusion: A model of a novel water-equivalent EPID has been developed and benchmarked against measurements using a physical prototype. We have demonstrated the feasibility of this new device and are continuing to optimize
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Radiation exposure of patients during endovascular aneurysm repair (EVAR) procedures ranks in the upper sector of medical exposure. Thus, estimation of radiation doses achieved during EVAR is of great importance. Organ doses (OD) and effective doses (ED) administered to 17 patients receiving EVAR were determined (1) from the exposure parameters by performing Monte Carlo simulations in mathematical phantoms and (2) by measurements with thermoluminescent dosimeters in a physical anthropomorphic phantom. The mean fluoroscopy time was 26 min, the mean dose area product was 24995 cGy cm2. The mean ED was 34.8 mSv, ODs up to 626 mSv were found. Whereas digital subtraction angiographies (DSA) and fluoroscopies each contributed about 50 % to the cumulative ED, the ED rates of DSAs were found to be ten times higher than those of fluoroscopies. Doubling of the field size caused an ED rate enhancement up to a factor of 3. EVAR procedures cause high radiation exposure levels that exceed the values published thus far. As a consequence, (1) DSAs should be only performed when necessary and with a low image rate, (2) fluoroscopies should be kept as short as possible, and (3) field sizes should be minimized. (orig.)
Energy Technology Data Exchange (ETDEWEB)
Foerth, Monika; Treitl, Karla Maria; Treitl, Marcus [Ludwig Maximilians University of Munich, Institute for Clinical Radiology, Munich (Germany); Seidenbusch, Michael C. [Ludwig Maximilians University of Munich, Institute for Clinical Radiology, Munich (Germany); Clinical Centre of the Ludwig Maximilian University of Munich, Institute for Clinical Radiology, Munich (Germany); Sadeghi-Azandaryani, Mojtaba [Clinical Centre of the County of Erding, Department of Vascular Surgery, Erding (Germany); Lechel, Ursula [Federal Office for Radiation Protection, Department of Medical and Occupational Radiation Protection, Oberschleissheim (Germany)
2015-09-15
Radiation exposure of patients during endovascular aneurysm repair (EVAR) procedures ranks in the upper sector of medical exposure. Thus, estimation of radiation doses achieved during EVAR is of great importance. Organ doses (OD) and effective doses (ED) administered to 17 patients receiving EVAR were determined (1) from the exposure parameters by performing Monte Carlo simulations in mathematical phantoms and (2) by measurements with thermoluminescent dosimeters in a physical anthropomorphic phantom. The mean fluoroscopy time was 26 min, the mean dose area product was 24995 cGy cm2. The mean ED was 34.8 mSv, ODs up to 626 mSv were found. Whereas digital subtraction angiographies (DSA) and fluoroscopies each contributed about 50 % to the cumulative ED, the ED rates of DSAs were found to be ten times higher than those of fluoroscopies. Doubling of the field size caused an ED rate enhancement up to a factor of 3. EVAR procedures cause high radiation exposure levels that exceed the values published thus far. As a consequence, (1) DSAs should be only performed when necessary and with a low image rate, (2) fluoroscopies should be kept as short as possible, and (3) field sizes should be minimized. (orig.)
Energy Technology Data Exchange (ETDEWEB)
Chisela, W; Yao, R; Dorbu, G [Columbus Regional Healthcare, Columbus, GA (United States)
2014-06-01
Purpose: To verify dose delivered with HDR Accuboost applicators using TLD, ion chamber and Gafchromic film measurements and to examine applicator leakage. Methods: A microSelectron HDR unit was used to deliver a dose of 50cGy to the mid-plane of a 62mm thick solid water phantom using dwell times from Monte Carlo pre-calculated nomograms for a 60mm, 70mm Round and 60mm Skin-Dose Optimized (SDO) applicators respectively. GafChromic EBT3+ film was embedded in the phantom midplane horizontally to measure dose distribution. Absolute dose was also measured with TLDs and an ADCL calibrated parallel-plate ion chamber placed in the film plane at field center for each applicator. The film was calibrated using 6MV x-ray beam. TLDs were calibrated in a Cs-137 source at UW-Madison calibration laboratory. Radiation leakage through the tungsten alloy shell was measured with a film wrapped around outside surface of a 60mm Round applicator. Results: Measured maximum doses at field center are consistently lower than predicated by 5.8% for TLD, 8.8% for ion chamber, and 2.6% for EBT3+ film on average, with measurement uncertainties of 2.2%, 0.3%, and 2.9% for TLD, chamber, film respectively. The total standard uncertainties for ion chamber and Gafchromic film measurement are 4.9% and 4.6% respectively[1]. The area defined by the applicator aperture was covered by 80% of maximum dose for 62mm compression thickness. When 100cGy is delivered to mid-plane with a 60mm Round applicator, surface dose ranges from 60cGy to a maximum of 145cGy, which occurs at source entrance to the applicator. Conclusion: Measured doses by all three techniques are consistently lower than predicted in our measurements. For a compression thickness of 62 mm, the field size defined by the applicator is only covered by 80% of prescribed dose. Radiation leakage of up to 145cGy was found at the source entrance of applicators.
Çatli, Serap
2015-01-01
High atomic number and density of dental implants leads to major problems at providing an accurate dose distribution in radiotherapy and contouring tumors and organs caused by the artifact in head and neck tumors. The limits and deficiencies of the algorithms using in the treatment planning systems can lead to large errors in dose calculation, and this may adversely affect the patient's treatment. In the present study, four commercial dental implants were used: pure titanium, titanium alloy (Ti-6Al-4V), amalgam, and crown. The effects of dental implants on dose distribution are determined with two methods: pencil beam convolution (PBC) algorithm and Monte Carlo code for 6 MV photon beam. The central axis depth doses were calculated on the phantom for a source-skin distance (SSD) of 100 cm and a 10 × 10 cm2 field using both of algorithms. The results of Monte Carlo method and Eclipse TPS were compared to each other and to those previously reported. In the present study, dose increases in tissue at a distance of 2 mm in front of the dental implants were seen due to the backscatter of electrons for dental implants at 6 MV using the Monte Carlo method. The Eclipse treatment planning system (TPS) couldn't precisely account for the backscatter radiation caused by the dental prostheses. TPS underestimated the back scatter dose and overestimated the dose after the dental implants. The large errors found for TPS in this study are due to the limits and deficiencies of the algorithms. The accuracy of the PBC algorithm of Eclipse TPS was evaluated in comparison to Monte Carlo calculations in consideration of the recommendations of the American Association of Physicists in Medicine Radiation Therapy Committee Task Group 65. From the comparisons of the TPS and Monte Carlo calculations, it is verified that the Monte Carlo simulation is a good approach to derive the dose distribution in heterogeneous media. PMID:26699323
Monte Carlo Calculations of Dose to Medium and Dose to Water for Carbon Ion Beams in Various Media
DEFF Research Database (Denmark)
Herrmann, Rochus; Petersen, Jørgen B.B.; Jäkel, Oliver;
materials exposed to carbon ion beams. The scored track-length fluence spectrum Φi for a given particle i at the energy E, is multiplied with the mass stopping power for target material for calculating Dm . Similarly, Dw is calculated by multiplying the same fluence spectrum with the mass stopping power...... the PSTAR, ASTAR stopping power routines available at NIST1 and MSTAR2 provided by H. Paul et al. 3 Results For a pristine carbon ion beam we encountered a maximum deviation between Dw and Dm up to 8% for bone. In addition we investigate spread out Bragg peak configurations which dilutes the effect......1 Background In clinical practice the quantity dose to water (Dw ) is used as a reference standard for dosimeters and treatment planning systems. Treatment planning systems usually rely on analytical representation of the particle beam, which are normally expressed as dose with respect to water...
Estimation of staff doses in complex radiological examinations using a Monte Carlo computer code
International Nuclear Information System (INIS)
The protection of medical personnel in interventional radiology is an important issue of radiological protection. The irradiation of the worker is largely non-uniform, and a large part of his body is shielded by a lead apron. The estimation of effective dose (E) under these conditions is difficult and several approaches are used to estimate effective dose involving such a protective apron. This study presents a summary from an extensive series of simulations to determine scatter-dose distribution around the patient and staff effective dose from personal dosimeter readings. The influence of different parameters (like beam energy and size, patient size, irradiated region, worker position and orientation) on the staff doses has been determined. Published algorithms that combine readings of an unshielded and a shielded dosimeter to estimate effective dose have been applied and a new algorithm, that gives more accurate dose estimates for a wide range of situations was proposed. A computational approach was used to determine the dose distribution in the worker's body. The radiation transport and energy deposition was simulated using the MCNP4B code. The human bodies of the patient and radiologist were generated with the Body Builder anthropomorphic model-generating tool. The radiologist is protected with a lead apron (0.5 mm lead equivalent in the front and 0.25 mm lead equivalent in the back and sides) and a thyroid collar (0.35 mm lead equivalent). The lower-arms of the worker were folded to simulate the arms position during clinical examinations. This realistic situation of the folded arms affects the effective dose to the worker. Depending on the worker position and orientation (and of course the beam energy), the difference can go up to 25 percent. A total of 12 Hp(10) dosimeters were positioned above and under the lead apron at the neck, chest and waist levels. Extra dosimeters for the skin dose were positioned at the forehead, the forearms and the front surface of
Mohammadyari, Parvin; Faghihi, Reza; Mosleh-Shirazi, Mohammad Amin; Lotfi, Mehrzad; Hematiyan, Mohammad Rahim; Koontz, Craig; Meigooni, Ali S
2015-12-01
Compression is a technique to immobilize the target or improve the dose distribution within the treatment volume during different irradiation techniques such as AccuBoost(®) brachytherapy. However, there is no systematic method for determination of dose distribution for uncompressed tissue after irradiation under compression. In this study, the mechanical behavior of breast tissue between compressed and uncompressed states was investigated. With that, a novel method was developed to determine the dose distribution in uncompressed tissue after irradiation of compressed breast tissue. Dosimetry was performed using two different methods, namely, Monte Carlo simulations using the MCNP5 code and measurements using thermoluminescent dosimeters (TLD). The displacement of the breast elements was simulated using a finite element model and calculated using ABAQUS software. From these results, the 3D dose distribution in uncompressed tissue was determined. The geometry of the model was constructed from magnetic resonance images of six different women volunteers. The mechanical properties were modeled by using the Mooney-Rivlin hyperelastic material model. Experimental dosimetry was performed by placing the TLD chips into the polyvinyl alcohol breast equivalent phantom. The results determined that the nodal displacements, due to the gravitational force and the 60 Newton compression forces (with 43% contraction in the loading direction and 37% expansion in the orthogonal direction) were determined. Finally, a comparison of the experimental data and the simulated data showed agreement within 11.5% ± 5.9%. PMID:26572554
Calculation of dose distribution in compressible breast tissues using finite element modeling, Monte