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Dive into the research topics where Shirin A. Enger is active.

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Featured researches published by Shirin A. Enger.


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.


Medical Physics | 2011

An algorithm for efficient metal artifact reductions in permanent seed implants

Chen Xu; Frank Verhaegen; Denis Laurendeau; Shirin A. Enger; Luc Beaulieu

PURPOSEnIn permanent seed implants, 60 to more than 100 small metal capsules are inserted in the prostate, creating artifacts in x-ray computed tomography (CT) imaging. The goal of this work is to develop an automatic method for metal artifact reduction (MAR) from small objects such as brachytherapy seeds for clinical applications.nnnMETHODSnThe approach for MAR is based on the interpolation of missing projections by directly using raw helical CT data (sinogram). First, an initial image is reconstructed from the raw CT data. Then, the metal objects segmented from the reconstructed image are reprojected back into the sinogram space to produce a metal-only sinogram. The Steger method is used to determine precisely the position and edges of the seed traces in the raw CT data. By combining the use of Steger detection and reprojections, the missing projections are detected and replaced by interpolation of non-missing neighboring projections.nnnRESULTSnIn both phantom experiments and patient studies, the missing projections have been detected successfully and the artifacts caused by metallic objects have been substantially reduced. The performance of the algorithm has been quantified by comparing the uniformity between the uncorrected and the corrected phantom images. The results of the artifact reduction algorithm are indistinguishable from the true background value.nnnCONCLUSIONSnAn efficient algorithm for MAR in seed brachytherapy was developed. The test results obtained using raw helical CT data for both phantom and clinical cases have demonstrated that the proposed MAR method is capable of accurately detecting and correcting artifacts caused by a large number of very small metal objects (seeds) in sinogram space. This should enable a more accurate use of advanced brachytherapy dose calculations, such as Monte Carlo simulations.


Physics in Medicine and Biology | 2012

Dose to tissue medium or water cavities as surrogate for the dose to cell nuclei at brachytherapy photon energies

Shirin A. Enger; Anders Ahnesjö; Frank Verhaegen; Luc Beaulieu

It has been suggested that modern dose calculation algorithms should be able to report absorbed dose both as dose to the local medium, D(m,m,) and as dose to a water cavity embedded in the medium, D(w,m), using conversion factors from cavity theory. Assuming that the cell nucleus with its DNA content is the most important target for biological response, the aim of this study is to investigate, by means of Monte Carlo (MC) simulations, the relationship of the dose to a cell nucleus in a medium, D(n,m,) to D(m,m) and D(w,m), for different combinations of cell nucleus compositions and tissue media for different photon energies used in brachytherapy. As D(n,m) is very impractical to calculate directly for routine treatment planning, while D(m,m) and D(w,m) are much easier to obtain, the questions arise which one of these quantities is the best surrogate for D(n,m) and which cavity theory assumptions should one use for its estimate. The Geant4.9.4 MC code was used to calculate D(m,m,) D(w,m) and D(n,m) for photon energies from 20 (representing the lower energy end of brachytherapy for ¹⁰³Pd or ¹²⁵I) to 300 keV (close to the mean energy of (¹⁹²Ir) and for the tissue media adipose, breast, prostate and muscle. To simulate the cell and its nucleus, concentric spherical cavities were placed inside a cubic phantom (10 × 10 × 10 mm³). The diameter of the simulated nuclei was set to 14 µm. For each tissue medium, three different setups were simulated; (a) D(n,m) was calculated with nuclei embedded in tissues (MC-D(n,m)). Four different published elemental compositions of cell nuclei were used. (b) D(w,m) was calculated with MC (MC-D(w,m)) and compared with large cavity theory calculated D(w,m) (LCT-D(w,m)), and small cavity theory calculated D(w,m) (SCT-D(w,m)). (c) D(m,m) was calculated with MC (MC-D(m,m)). MC-D(w,m) is a good substitute for MC-D(n,m) for all photon energies and for all simulated nucleus compositions and tissue types. SCT-D(w,m) can be used for most energies in brachytherapy, while LCT-D(w,m) should only be considered for source spectra well below 50 keV, since contributions to the absorbed dose inside the nucleus to a large degree stem from electrons released in the surrounding medium. MC-D(m,m) is not an appropriate substitute for MC-D(n,m) for the lowest photon energies for adipose and breast tissues. The ratio of MC-D(m,m) to MC-D(n,m) for adipose and breast tissue deviates from unity by 34% and 15% respectively for the lowest photon energy (20 keV), whereas the ratio is close to unity for higher energies. For prostate and muscle tissue MC-D(m,m) is a good substitute for MC-D(n,m). However, for all photon energies and tissue types the nucleus composition with the highest hydrogen content behaves differently than other compositions. Elemental compositions of the tissue and nuclei affect considerably the absorbed dose to the cell nuclei for brachytherapy sources, in particular those at the low-energy end of the spectrum. Thus, there is a need for more accurate data for the elemental compositions of tumours and healthy cells. For the nucleus compositions and tissue types investigated, MC-D(w,m) is a good substitute to MC-D(n,m) for all simulated photon energies. Whether other studied surrogates are good approximations to MC-D(n,m) depends on the target size, target composition, composition of the surrounding tissue and photon energy.


Medical Physics | 2012

Exploring 57Co as a new isotope for brachytherapy applications

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

PURPOSEnThe 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.nnnMETHODSnA 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.nnnRESULTSnThe 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.nnnCONCLUSIONSn(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

PURPOSEnTo 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.nnnMETHODSnGEANT4 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.nnnRESULTSnFor 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.nnnCONCLUSIONSnA (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

SU‐D‐BRB‐06: G4DBR: A Fast Geant4‐Based Monte Carlo Dosimetry Platform for Brachytherapy

Hossein Afsharpour; Jean-François Carrier; M DˈAmours; Shirin A. Enger; Guillaume Landry; Emily Poon; F Verhaegen; Luc Beaulieu

Purpose: To present, G4DBR, a fast Geant4‐based Monte Carlo (MC)dosimetry platform for brachytherapy. The special case of low dose rate (LDR) brachytherapy is considered here. Methods: Geant4 9.3 has been used for designing a new MC platform for calculating the dose distribution in brachytherapy called G4DBR. This code is capable of dealing with the DICOM RT format to build a virtual representation of each patient with the full multi‐seed configuration. The dose is scored both to medium and to water using track‐length estimator. The dose distributions are extracted in 3ddose format for visualization or to calculate the DVHs. Results: One prostate permanent 125I seed (PPSI) and one breast permanent 103Pd seed implant (BSPI) patient have been selected for evaluating the performance of G4DBR on a 2.93 GHz Intel Xeon Nehalem single core. Post‐implant dosimetry of those cases are performed in a 2 mm3 mesh for comparison with BrachyDose and MCPI. 45 seconds were required for G4DBR to reach a statistical uncertainty of 2% on PTV dose in PPSI. Note that for a similar precision, BrachyDose requires 30 seconds on 3 GHz Woodcrest (Thomson et al. Med. Phys. 2010) while MCPI needs 59 seconds on a single 2.4 GHz Pentium 4 CPU (Chibani et al. Med. Phys. 2005). G4DBR takes 114 seconds to attain a statistical uncertainty of less than 2% in the BPSI case. Conclusions: G4DBR is accurate and fast enough for clinical purposes. G4DBR is able to achieve good calculation speeds comparable with BrachyDose and MCPI. Indeed, a statistical uncertainty of less than 2% is attained in 45 seconds in a prostate case while 118 seconds were needed in BPSI to achieve 0.5% of uncertainty. Further developments will include the incorporation of high dose rate (HDR) dosimetry and a user‐friendly GUI for G4DBR.


Medical Physics | 2010

Poster — Thur Eve — 27: Investigation of the Influence of Different Encapsulating Material on 170Tm Brachytherapy Source Spectra

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

The purpose of this work was to investigate the influence of the encapsulating material on different part of the 170Tm decay spectra. A hypothetical 170Tm source with the Flexisource brachytherapy encapsulation was used in the simulations. The active core of the source is a pure thulium cylinder with a length of 3.5 mm, a radius of 0.3 mm and covered with a stainless‐steel or a pure gold cylinder. The length of the capsule is 5 mm, the inner radius is 3.0 mm and the outer radius 0.425 mm. Simulations were performed with and without taking the source encapsulation into account. The simulation utilized GEANT4 Monte Carlo code version 9.2. For the stainless‐steel encapsulation 95.5% of the total brems Strahlung is produced inside the core, 3.8% in the capsule and less than 1% in the water. For the gold capsule 85% is produced inside the core, 14.2% inside the gold capsule and negligible amount (<1%) in water. The range of the beta particles decreases with 1.1 mm with the stainless‐steel encapsulation but the tissue will still receive dose from the beta particles up to 3 mm from the source. The gold encapsulation, if present, absorbs most of the electrons and attenuates low energy photons. The mean energy of the photons escaping the core and the stainless‐steel capsule is 113 keV while for gold capsule the mean energy is 160 keV. TG43 parameters in both cases are extracted.


Medical Physics | 2010

SU-GG-T-438: Dose to Medium or Dose to a Water Cavity Embedded in Medium? A Monte Carlo Study

Shirin A. Enger; Anders Ahnesjö; Luc Beaulieu

Purpose: The target for radiotherapy is to sterilize cells by imposing damage to their DNA content. It is therefore of interest to study the relations between the dose calculated to a tissue medium, D m,m, with an representative average atomic composition versus the doseD n,m specifically absorbed by the cell nuclei, and the doseD w,m to a cell nuclei surrogate represented as a water cavity embedded into tissue. The simulations were performed for six types of tissues and three different brachytherapysources.Methods and Materials: Absorbed dose calculations were performed by GEANT4 MC code version 9.2 using the Penelope physics package. Three different sources,192Ir to represent high energy conditions, 169Yb for intermediate energies and a low energy brachytherapysource125I, were simulated. The photonspectra used in this study were taken from http://www.physics.carleton.ca/clrp/seed_database. The 192Ir spectra was from Nucletron, microSelectron‐HDR v2 and for 125I from Nucletron, SelectSeed, 130.002. Particle spectra for 192Ir and energy spectra for 192I were also scored to calculate the dose with different cavity theories and compare it with MC calculated doses.Results: The MC calculated D m,m , D w,m and D n,m ratio shows the largest value for 125I brachytherapysource and the cortical bone material, adipose tissue and prostate tissues(ICRU). The difference between D w,m and D n,m is also largest for the cortical bone and 125I source. For the 192Ir source, the ratio was 1 for the soft tissues while for the cortical bone it was higher. Conclusion: Monte Carlo calculations made it possible to report the dose as absorbed dose to medium. Accurate reporting of treatment planning requires a stringent standard for dose definition. MC calculations can be used to develop conversion factors to convert dose according to different definitions for different brachytherapysources.


Archive | 2016

The impact on linear-quadratic parameterization of cell survival data from the microdosimetric spread of specific energy for different cell nuclei size distributions.

Fernanda Villegas; Nina Tilly; Gloria Bäckström; Shirin A. Enger; Anders Ahnesjö


Brachytherapy | 2011

Modeling a Hypothetical 57Co Source for Brachytherapy Application

Shirin A. Enger; Luc Beaulieu

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F Verhaegen

McGill University Health Centre

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Anders Ahnesjö

Université catholique de Louvain

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Frank Verhaegen

Maastricht University Medical Centre

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