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Featured researches published by M D'Amours.


Physics in Medicine and Biology | 2012

ALGEBRA: ALgorithm for the heterogeneous dosimetry based on GEANT4 for BRAchytherapy

Hossein Afsharpour; Guillaume Landry; M D'Amours; Shirin A. Enger; Brigitte Reniers; Emily Poon; Jean-François Carrier; F Verhaegen; Luc Beaulieu

Task group 43 (TG43)-based dosimetry algorithms are efficient for brachytherapy dose calculation in water. However, human tissues have chemical compositions and densities different than water. Moreover, the mutual shielding effect of seeds on each other (interseed attenuation) is neglected in the TG43-based dosimetry platforms. The scientific community has expressed the need for an accurate dosimetry platform in brachytherapy. The purpose of this paper is to present ALGEBRA, a Monte Carlo platform for dosimetry in brachytherapy which is sufficiently fast and accurate for clinical and research purposes. ALGEBRA is based on the GEANT4 Monte Carlo code and is capable of handling the DICOM RT standard to recreate a virtual model of the treated site. Here, the performance of ALGEBRA is presented for the special case of LDR brachytherapy in permanent prostate and breast seed implants. However, the algorithm is also capable of handling other treatments such as HDR brachytherapy.


Physics in Medicine and Biology | 2012

Layered mass geometry: a novel technique to overlay seeds and applicators onto patient geometry in Geant4 brachytherapy simulations

Shirin A. Enger; Guillaume Landry; M D'Amours; Frank Verhaegen; Luc Beaulieu; Makoto Asai; J Perl

A problem faced by all Monte Carlo (MC) particle transport codes is how to handle overlapping geometries. The Geant4 MC toolkit allows the user to create parallel geometries within a single application. In Geant4 the standard mass-containing geometry is defined in a simulation volume called the World Volume. Separate parallel geometries can be defined in parallel worlds, that is, alternate three dimensional simulation volumes that share the same coordinate system with the World Volume for geometrical event biasing, scoring of radiation interactions, and/or the creation of hits in detailed readout structures. Until recently, only one of those worlds could contain mass so these parallel worlds provided no solution to simplify a complex geometric overlay issue in brachytherapy, namely the overlap of radiation sources and applicators with a CT based patient geometry. The standard method to handle seed and applicator overlay in MC requires removing CT voxels whose boundaries would intersect sources, placing the sources into the resulting void and then backfilling the remaining space of the void with a relevant material. The backfilling process may degrade the accuracy of patient representation, and the geometrical complexity of the technique precludes using fast and memory-efficient coding techniques that have been developed for regular voxel geometries. The patient must be represented by the less memory and CPU-efficient Geant4 voxel placement technique, G4PVPlacement, rather than the more efficient G4NestedParameterization (G4NestedParam). We introduce for the first time a Geant4 feature developed to solve this issue: Layered Mass Geometry (LMG) whereby both the standard (CT based patient geometry) and the parallel world (seeds and applicators) may now have mass. For any area where mass is present in the parallel world, the parallel mass is used. Elsewhere, the mass of the standard world is used. With LMG the user no longer needs to remove patient CT voxels that would include for example seeds. The patient representation can be a regular voxel grid, conducive to G4NestedParam, and the patient CT derived materials remain exact, avoiding the inaccuracy of the backfilling technique. Post-implant dosimetry for one patient with (125)I permanent seed implant was performed using Geant4 version 9.5.p01 using three different geometrical techniques. The first technique was the standard described above (G4PVPlacement). The second technique placed patient voxels as before, but placed seeds with LMG (G4PVPlacement+LMG). The third technique placed patient voxels through G4NestedParam and seeds through LMG (G4NestedParam+LMG). All the scenarios were calculated with 3 different image compression factors to manipulate the number of voxels. Additionally, the dosimetric impact of the backfilling technique was investigated for the case of calcifications in close proximity of sources. LMG eliminated the need for backfilling and simplified geometry description. Of the two LMG techniques, G4PVPlacement+LMG had no benefit to calculation time or memory use, actually increasing calculation time, but G4NestedParam+LMG reduced both calculation time and memory. The benefits of G4NestedParam+LMG over standard G4PVPlacement increased with increasing voxel numbers. For the case of calcifications in close proximity to sources, LMG not only increased efficiency but also yielded more accurate dose calculation than G4PVPlacement. G4NestedParam in combination with LMG present a new, efficient approach to simulate radiation sources that overlap patient geometry. Cases with brachytherapy applicators would constitute a direct extension of the method.


Medical Physics | 2012

Sub-second high dose rate brachytherapy Monte Carlo dose calculations with bGPUMCD.

Sami Hissoiny; M D'Amours; Benoît Ozell; Philippe Després; Luc Beaulieu

PURPOSE To establish the accuracy and speed ofbGPUMCD, a GPU-oriented Monte Carlo code used for high dose rate brachytherapy dose calculations. The first objective is to evaluate the time required for dose calculation when full Monte Carlo generated dose distribution kernels are used for plan optimization. The second objective is to assess the accuracy and speed when recalculating pre-optimized plans, consisting of many dwell positions. METHODS bGPUMCD is tested with three clinical treatment plans : one prostate case, one breast case, and one rectum case with a shielded applicator. Reference distributions, generated with GEANT4, are used as a basis of comparison. Calculations of full dose distributions of pre-optimized treatment plans as well as single dwell dosimetry are performed. Single source dosimetry, based on TG-43 parameters reproduction, is also presented for the microSelectron V2 (Nucletron, Veenendaal, The Netherlands). RESULTS In timing experiments, the computation of single dwell position dose kernels takes between 0.25 and 0.5 s.bGPUMCD can compute full dose distributions of previously optimized plans in ∼2 s. bGPUMCD is capable of computing pre-optimized brachytherapy plans within 1% for the prostate case and 2% for the breast and shielded applicator cases, when comparing the dosimetric parameters D90 and V100 of the reference (GEANT4) and bGPUMCD distributions. For all voxels within the target, an absolute average difference of approximately 1% is found for the prostate case, less than 2% for the breast case and less than 2% for the rectum case with shielded applicator. Larger point differences (>5%) are found within bony regions in the prostate case, where bGPUMCD underdoses compared to GEANT4. Single source dosimetry results are mostly within 2% for the radial function and within 1%-4% for the anisotropic function. CONCLUSIONS bGPUMCD has the potential to allow for fast MC dose calculation in a clinical setting for all phases of HDR treatment planning, from dose kernel calculations for plan optimization to plan recalculation.PURPOSE To establish the accuracy and speed of bGPUMCD, a GPU-oriented Monte Carlo code used for high dose rate brachytherapy dose calculations. The first objective is to evaluate the time required for dose calculation when full Monte Carlo generated dose distribution kernels are used for plan optimization. The second objective is to assess the accuracy and speed when recalculating pre-optimized plans, consisting of many dwell positions. METHODS bGPUMCD is tested with three clinical treatment plans : one prostate case, one breast case, and one rectum case with a shielded applicator. Reference distributions, generated with GEANT4, are used as a basis of comparison. Calculations of full dose distributions of pre-optimized treatment plans as well as single dwell dosimetry are performed. Single source dosimetry, based on TG-43 parameters reproduction, is also presented for the microSelectron V2 (Nucletron, Veenendaal, The Netherlands). RESULTS In timing experiments, the computation of single dwell position dose kernels takes between 0.25 and 0.5 s. bGPUMCD can compute full dose distributions of previously optimized plans in ∼2 s. bGPUMCD is capable of computing pre-optimized brachytherapy plans within 1% for the prostate case and 2% for the breast and shielded applicator cases, when comparing the dosimetric parameters D90 and V100 of the reference (GEANT4) and bGPUMCD distributions. For all voxels within the target, an absolute average difference of approximately 1% is found for the prostate case, less than 2% for the breast case and less than 2% for the rectum case with shielded applicator. Larger point differences (>5%) are found within bony regions in the prostate case, where bGPUMCD underdoses compared to GEANT4. Single source dosimetry results are mostly within 2% for the radial function and within 1%-4% for the anisotropic function. CONCLUSIONS bGPUMCD has the potential to allow for fast MC dose calculation in a clinical setting for all phases of HDR treatment planning, from dose kernel calculations for plan optimization to plan recalculation.


Medical Physics | 2012

Exploring 57Co as a new isotope for brachytherapy applications

Shirin A. Enger; Hans Lundqvist; M D'Amours; Luc Beaulieu

PURPOSE The characteristics of the radionuclide (57)Co make it interesting for use as a brachytherapy source. (57)Co combines a possible high specific activity with the emission of relatively low-energy photons and a half-life (272 days) suitable for regular source exchanges in an afterloader. (57)Co decays by electron capture to the stable (57)Fe with emission of 136 and 122 keV photons. METHODS A hypothetical (57)Co source based on the Flexisource brachytherapy encapsulation with the active core set as a pure cobalt cylinder (length 3.5 mm and diameter 0.6 mm) covered with a cylindrical stainless-steel capsule (length 5 mm and thickness 0.125 mm) was simulated using Geant4 Monte Carlo (MC) code version 9.4. The radial dose function, g(r), and anisotropy function F(r,θ), for the line source approximation were calculated following the TG-43U1 formalism. The results were compared to well-known (192)Ir and (125)I radionuclides, representing the higher and the lower energy end of brachytherapy, respectively. RESULTS The mean energy of photons in water, after passing through the core and the encapsulation material was 123 keV. This hypothetical (57)Co source has an increasing g(r) due to multiple scatter of low-energy photons, which results in a more uniform dose distribution than (192)Ir. CONCLUSIONS (57)Co has many advantages compared to (192)Ir due to its low-energy gamma emissions without any electron contamination. (57)Co has an increasing g(r) that results in a more uniform dose distribution than (192)Ir due to its multiple scattered photons. The anisotropy of the (57)Co source is comparable to that of (192)Ir. Furthermore, (57)Co has lower shielding requirements than (192)Ir.


Medical Physics | 2011

Modeling a hypothetical 170Tm source for brachytherapy applications.

Shirin A. Enger; M D'Amours; Luc Beaulieu

PURPOSE To perform absorbed dose calculations based on Monte Carlo simulations for a hypothetical (170)Tm source and to investigate the influence of encapsulating material on the energy spectrum of the emitted electrons and photons. METHODS GEANT4 Monte Carlo code version 9.2 patch 2 was used to simulate the decay process of (170)Tm and to calculate the absorbed dose distribution using the GEANT4 Penelope physics models. A hypothetical (170)Tm source based on the Flexisource brachytherapy design with the active core set as a pure thulium cylinder (length 3.5 mm and diameter 0.6 mm) and different cylindrical source encapsulations (length 5 mm and thickness 0.125 mm) constructed of titanium, stainless-steel, gold, or platinum were simulated. The radial dose function for the line source approximation was calculated following the TG-43U1 formalism for the stainless-steel encapsulation. RESULTS For the titanium and stainless-steel encapsulation, 94% of the total bremsstrahlung is produced inside the core, 4.8 and 5.5% in titanium and stainless-steel capsules, respectively, and less than 1% in water. For the gold capsule, 85% is produced inside the core, 14.2% inside the gold capsule, and a negligible amount (<1%) in water. Platinum encapsulation resulted in bremsstrahlung effects similar to those with the gold encapsulation. The range of the beta particles decreases by 1.1 mm with the stainless-steel encapsulation compared to the bare source but the tissue will still receive dose from the beta particles several millimeters from the source capsule. The gold and platinum capsules not only absorb most of the electrons but also attenuate low energy photons. The mean energy of the photons escaping the core and the stainless-steel capsule is 113 keV while for the gold and platinum the mean energy is 160 keV and 165 keV, respectively. CONCLUSIONS A (170)Tm source is primarily a bremsstrahlung source, with the majority of bremsstrahlung photons being generated in the source core and experiencing little attenuation in the source encapsulation. Electrons are efficiently absorbed by the gold and platinum encapsulations. However, for the stainless-steel capsule (or other lower Z encapsulations) electrons will escape. The dose from these electrons is dominant over the photon dose in the first few millimeter but is not taken into account by current standard treatment planning systems. The total energy spectrum of photons emerging from the source depends on the encapsulation composition and results in mean photon energies well above 100 keV. This is higher than the main gamma-ray energy peak at 84 keV. Based on our results, the use of (170)Tm as a brachytherapy source presents notable challenges.


Medical Physics | 2011

Modeling a Hypothetical {sup 170}Tm Source for Brachytherapy Applications

Shirin A. Enger; M D'Amours; Luc Beaulieu

PURPOSE To perform absorbed dose calculations based on Monte Carlo simulations for a hypothetical (170)Tm source and to investigate the influence of encapsulating material on the energy spectrum of the emitted electrons and photons. METHODS GEANT4 Monte Carlo code version 9.2 patch 2 was used to simulate the decay process of (170)Tm and to calculate the absorbed dose distribution using the GEANT4 Penelope physics models. A hypothetical (170)Tm source based on the Flexisource brachytherapy design with the active core set as a pure thulium cylinder (length 3.5 mm and diameter 0.6 mm) and different cylindrical source encapsulations (length 5 mm and thickness 0.125 mm) constructed of titanium, stainless-steel, gold, or platinum were simulated. The radial dose function for the line source approximation was calculated following the TG-43U1 formalism for the stainless-steel encapsulation. RESULTS For the titanium and stainless-steel encapsulation, 94% of the total bremsstrahlung is produced inside the core, 4.8 and 5.5% in titanium and stainless-steel capsules, respectively, and less than 1% in water. For the gold capsule, 85% is produced inside the core, 14.2% inside the gold capsule, and a negligible amount (<1%) in water. Platinum encapsulation resulted in bremsstrahlung effects similar to those with the gold encapsulation. The range of the beta particles decreases by 1.1 mm with the stainless-steel encapsulation compared to the bare source but the tissue will still receive dose from the beta particles several millimeters from the source capsule. The gold and platinum capsules not only absorb most of the electrons but also attenuate low energy photons. The mean energy of the photons escaping the core and the stainless-steel capsule is 113 keV while for the gold and platinum the mean energy is 160 keV and 165 keV, respectively. CONCLUSIONS A (170)Tm source is primarily a bremsstrahlung source, with the majority of bremsstrahlung photons being generated in the source core and experiencing little attenuation in the source encapsulation. Electrons are efficiently absorbed by the gold and platinum encapsulations. However, for the stainless-steel capsule (or other lower Z encapsulations) electrons will escape. The dose from these electrons is dominant over the photon dose in the first few millimeter but is not taken into account by current standard treatment planning systems. The total energy spectrum of photons emerging from the source depends on the encapsulation composition and results in mean photon energies well above 100 keV. This is higher than the main gamma-ray energy peak at 84 keV. Based on our results, the use of (170)Tm as a brachytherapy source presents notable challenges.


Physics in Medicine and Biology | 2014

The use of tetrahedral mesh geometries in Monte Carlo simulation of applicator based brachytherapy dose distributions

Gabriel P. Fonseca; Guillaume Landry; Shane White; M D'Amours; Hélio Yoriyaz; Luc Beaulieu; Brigitte Reniers; Frank Verhaegen

Accounting for brachytherapy applicator attenuation is part of the recommendations from the recent report of AAPM Task Group 186. To do so, model based dose calculation algorithms require accurate modelling of the applicator geometry. This can be non-trivial in the case of irregularly shaped applicators such as the Fletcher Williamson gynaecological applicator or balloon applicators with possibly irregular shapes employed in accelerated partial breast irradiation (APBI) performed using electronic brachytherapy sources (EBS). While many of these applicators can be modelled using constructive solid geometry (CSG), the latter may be difficult and time-consuming. Alternatively, these complex geometries can be modelled using tessellated geometries such as tetrahedral meshes (mesh geometries (MG)). Recent versions of Monte Carlo (MC) codes Geant4 and MCNP6 allow for the use of MG. The goal of this work was to model a series of applicators relevant to brachytherapy using MG. Applicators designed for (192)Ir sources and 50 kV EBS were studied; a shielded vaginal applicator, a shielded Fletcher Williamson applicator and an APBI balloon applicator. All applicators were modelled in Geant4 and MCNP6 using MG and CSG for dose calculations. CSG derived dose distributions were considered as reference and used to validate MG models by comparing dose distribution ratios. In general agreement within 1% for the dose calculations was observed for all applicators between MG and CSG and between codes when considering volumes inside the 25% isodose surface. When compared to CSG, MG required longer computation times by a factor of at least 2 for MC simulations using the same code. MCNP6 calculation times were more than ten times shorter than Geant4 in some cases. In conclusion we presented methods allowing for high fidelity modelling with results equivalent to CSG. To the best of our knowledge MG offers the most accurate representation of an irregular APBI balloon applicator.


Medical Physics | 2008

TH-C-AUD A-03: A New Approach for Afterloading Brachytherapy Inverse Planned Dose Optimization Based On the Accurate Monte Carlo Method

M D'Amours; Jean-François Carrier; Etienne Lessard; Jean Pouliot; Frank Verhaegen; Luc Beaulieu

Purpose: In brachytherapy, considering the perturbations from the heterogeneities in the planning system will give a better dose conformity for specific sites. The goal of this work is to demonstrate the feasibility of replacing the TG43 analytical approach by a Monte Carlo (MC)dose calculation engine in the optimization process. Method and Materials: The novel method is based on pre‐computed 3D dose kernels. The CT clinical images and the dwell positions (DWP) are loaded from the DICOM‐RT files to create a voxel based simulation of the treatment. MCdose calculation is used to create the dose kernel specific for each possible DWP. Density and tissue compositions are fully taken into account in MC. The Inverse Planning Simulated Annealing (IPSA) algorithm is used for the optimization process. IPSA reads and analyzes the MCdose kernels before the beginning of the optimization process; it replaces the TG43 parameterization. A breast interstitial HDR plan is used to demonstrate the approach. Results: Computation of precise 3D‐kernels is the most time consuming portion and is proportional to the number of DWP. However, the optimization process itself takes the same amount of time as a standard (TG43) optimization. The breast, TG43/MC plan shows an underdosage in the CTV relative to the TG43/TG43 plan by 4.3 % on D90 and 3.2 % on D50. For the surgical bed, the difference is 4.2 % and 3.5 % for D90 and D50 respectively. This was corrected in the MC/MC plan, with a minimal dose increase of the skin.Conclusion:MCoptimization improved the dose conformity. The method presented is straightforward and can be applied to any site and any afterloading process (HDR or PDR) using various type of sources, from Ir‐192 to micro‐XRay devices, as long as a precise MC model is made.


Medical Physics | 2009

Sci—Thurs AM: YIS—02: Optimizing Number and Position of Catheters within Inverse Planning Simulated Annealing (IPSA) for Prostate and Breast High Dose Rate Brachytherapy

Guylaine Ayotte; M D'Amours; Sylviane Aubin; Etienne Lessard; Jean Pouliot; Luc Beaulieu

Introduction: In clinical high dose rate (HDR) brachytherapy for prostate and breast, catheters are generally implanted using a template, without considering precise tumor size and shape. In this work, we present a method to optimize the number and position of catheters before the implantation stage. Methods: A research version of IPSA was modified to gradually remove uniformly distributed catheters on target volume, until the desired number of catheters is reached. Criterion for removal is based on the fraction of total treatment time attributable to each catheter. We have applied this method to a clinical prostate case implanted with 18 catheters and a breast implant of 21 catheters. For prostate case, some chosen catheters were fixed to take into account the low, but essential treatment time needed near the urethra. Results: For the studied prostate case, the cost function value is reduced for optimizations with 18 catheters down to 15, compared with the clinical plan. Bladder and urethra receive lower dose for all plans and rectum V75 is independent of the number of catheters. For the breast case, a plan with 19 catheters leads to a similar cost function value than the clinical case and optimized plans lead to a better skin protection, down to 13 catheters. Conclusion: We have devised a simple and efficient method to optimize the locations and number of catheters which could be extended to all types of interstitial HDR brachytherapy. The results indicate that it is possible to obtain clinically optimal treatment plans with fewer catheters.


Journal of Physics: Conference Series | 2008

Monte Carlo iodine brachytherapy dosimetry: study for a clinical application

C Furstoss; Brigitte Reniers; E Poon; M D'Amours; Jean-François Carrier; Luc Beaulieu; Jeffrey F. Williamson; F Verhaegen

At present, all clinical algorithms used in brachytherapy are based on the TG-43 algorithm, which has the advantage to offer very fast calculation time. However, this formalism has many simplifications, assuming for example the patient tissue composition equivalent to water. For low energy brachytherapy seeds such as iodine seeds, it is of interest to evaluate the dosimetric differences between calculations based on Monte Carlo simulations (considered the gold standard) and the TG-43 formalism. For a 6711 model 125I seed calculated photon spectra were compared to spectra measured with a CdTe spectrometer. Good agreement was found except for the lowest energy peak which seems to be over-estimated by the experiment due to the contribution of the spectrometer CdTe diode to the measurement. Dose distributions in water are measured with EBT Gafchromic film and compared to the Monte Carlo calculation. A very good agreement is found. Finally, the method to create a MCNPX input file from computed tomography (CT) scanner images is explained and some preliminary isodose distributions are presented.

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Frank Verhaegen

Maastricht University Medical Centre

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Jean Pouliot

University of California

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F Verhaegen

McGill University Health Centre

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