Feasibility and toxicity of a single fraction high-dose-rate brachytherapy followed by a course of EBRT for localized prostate cancer, a retrospective study: The Polyclinique Courlancy experience

被引:3
作者
Mallet, F. [1 ]
Wdowczyk, D. [1 ]
Bruna, A. [1 ]
Villena, P. [2 ]
Herard, A. [2 ]
Amory, J. -P. [2 ]
Joffroy, P. [1 ]
Pangrazzi, T. [1 ]
机构
[1] Polyclin Coulancy, Serv Radiotherapie, Ctr Radiotherapie & Oncol, F-51100 Reims, France
[2] Polyclin Coulancy, Cabinet Urol, F-51100 Reims, France
来源
CANCER RADIOTHERAPIE | 2010年 / 14卷 / 01期
关键词
Prostate cancer; Boost; High-dose-rate brachytherapy; Inverse optimization; Side effects; EXTERNAL-BEAM RADIATION; RATE AFTERLOADING BRACHYTHERAPY; RATE IR-192 BRACHYTHERAPY; ANDROGEN SUPPRESSION; HDR BRACHYTHERAPY; RADIOTHERAPY; THERAPY; RISK; IRRADIATION; COMBINATION;
D O I
10.1016/j.canrad.2009.10.003
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose. - Evaluate the feasibility and toxicity of radiation dose escalation delivered with a single fraction high-close-rate (HDR) brachytherapy boost followed by external beam radiotherapy for intermediate and high risk localized prostate cancer - a retrospective study. Patients and methods. - Between December 2004 and December 2008, 61 patients with intermediate risk or high-risk localized prostate cancer received a single 10 Gy fraction of interstitial HDR brachytherapy followed by a 64 Gy course of external beam radiation therapy. Dose Volume histograms. conformity index and side effects were systematically analyzed. Results. - HDR brachytherapy dosimetric criteria were respected. Early side effects (<= 3 months after full treatment): 30% reported grade 2 or grade 3 urinary toxicity and 26% reported grade 2 or grade 3 bowel toxicity were reported. Late side effects (>3 months): 12% reported grade 2 or grade 3 urinary toxicity and 5% reported grade 2 or grade 3 bowel toxicity were reported. No patients reported any grade 4 late toxicity events. Three months after treatment, 7% grade 1,25% grade 2 and 39% grade 3 erectile dysfunction were reported. Conclusion. - Our monofractionation protocol is an easy technique to implement logistically. Acute and late toxicities are acceptable and comparable to those published by Various teams Mostly using multifractionation protocols. A longer follow-up is required to assess the effect of this dose escalation protocol on long-term biological control. (C) 2009 Societe francaise de radiotherapie oncologique (SFRO). Published by Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:11 / 18
页数:8
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