Postimplant dosimetry using a Monte Carlo dose calculation engine:: A new clinical standard

被引:61
|
作者
Carrier, Jean-Francois
D'Amours, Michel
Verhaegen, Frank
Reniers, Brigitte
Martin, Andre-Guy
Vigneault, Eric
Beaulieu, Luc
机构
[1] CHUM, Hop Notre Dame de Bon Secours, Dept Radiooncol, Montreal, PQ H2L 4M1, Canada
[2] CHUM, Hop Notre Dame de Bon Secours, Ctr Rech, Montreal, PQ H2L 4M1, Canada
[3] Univ Laval, Dept Radiooncol, Hotel Dieu, Laval, PQ, Canada
[4] Univ Laval, Ctr Rech & Cancerol, Hotel Dieu, Laval, PQ, Canada
[5] McGill Univ, Med Phys Unit, Montreal, PQ, Canada
关键词
prostate cancer; low-dose-rate brachytherapy; permanent seed implants; iodine-125; postimplant dosimetry; Monte Carlo;
D O I
10.1016/j.ijrobp.2007.02.036
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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) D-90 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. (C) 2007 Elsevier Inc.
引用
收藏
页码:1190 / 1198
页数:9
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