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前列腺床放疗的替代放射肿瘤学方法(PAROS)-一项前瞻性、多中心、随机 III 期试验。

Prostate bed irradiation with alternative radio-oncological approaches (PAROS) - a prospective, multicenter and randomized phase III trial.

机构信息

Department of Radiation Oncology, Heidelberg University Hospital, Heidelberg, Germany.

National Center for Tumor diseases (NCT), Heidelberg, Germany.

出版信息

Radiat Oncol. 2019 Jul 10;14(1):122. doi: 10.1186/s13014-019-1325-x.

Abstract

BACKGROUND

For patients with treatment-naïve carcinoma of the prostate, hypofractionated irradiation becomes more and more popular. Due to the low α/β value of prostate cancer, increased single dose leading to a shortened treatment period seems to be safe and feasible. However, reliable data is lacking for post-prostatectomy patients so far. Further, the role of proton therapy is still under debate. Two prospective phase II trials with both, hypofractionated photon and proton therapy, provided promising results.

METHODS/ DESIGN: The PAROS trial is a prospective, multicenter and randomized phase III trial for men with localized prostate carcinoma after surgery. Post-prostatectomy patients will be randomized to either normofractionated radiotherapy (nRT) with photons (70.0/ 2.0 Gy), or hypofractionated radiotherapy (hRT) with photons (57.0/ 3.0 Gy) or hRT with protons (57.0/ 3.0 Gy relative biological effectiveness [RBE]). Block randomization is stratified by Gleason Score (≤ 7 vs. > 7) and treatment indication (adjuvant vs. salvage). The trial is planned to enroll 897 patients. The primary objective is to show an improvement in the bowel-score according to EORTC QLQ-PR25 after proton therapy compared to photon irradiation (week 12 vs. baseline). Secondary aims are non-inferiority of hRT compared to nRT with regard to biochemical progression-free survival (bPFS), overall survival (OS), quality of life and toxicity.

DISCUSSION

The present study aims to evaluate the role of hypofractionated radiotherapy to the prostate bed with photons and protons leading to significant impact on future management of operated men with prostate cancer.

TRIAL REGISTRATION

Deutsches Register klinischer Studien: DRKS00015231 ; registered 27 September 2018.

摘要

背景

对于初治前列腺癌患者,分次剂量降低的放疗越来越受欢迎。由于前列腺癌的α/β 值较低,增加单次剂量以缩短治疗时间似乎是安全且可行的。然而,迄今为止,对于前列腺切除术后的患者,还缺乏可靠的数据。此外,质子治疗的作用仍存在争议。两项采用光子和质子低分割放疗的前瞻性 II 期试验提供了有前景的结果。

方法/设计:PAROS 试验是一项针对前列腺癌根治术后局部前列腺癌患者的前瞻性、多中心、随机 III 期试验。前列腺切除术后患者将随机分为光子常规分割放疗(nRT)组(70.0/2.0Gy)、光子低分割放疗(hRT)组(57.0/3.0Gy)或质子低分割放疗(57.0/3.0Gy 相对生物效应[RBE])组。分层随机分组因素为 Gleason 评分(≤7 分与>7 分)和治疗适应证(辅助治疗与挽救性治疗)。该试验计划入组 897 例患者。主要研究目的是比较质子放疗与光子放疗后 EORTC QLQ-PR25 中的肠道评分的改善情况(第 12 周与基线相比),以证明质子放疗的优势。次要研究目的是比较光子 hRT 与 nRT 对生化无进展生存期(bPFS)、总生存期(OS)、生活质量和毒性的非劣效性。

讨论

本研究旨在评估光子和质子低分割放疗对前列腺床的作用,对前列腺癌术后患者的管理产生重大影响。

试验注册

德国临床试验注册中心:DRKS00015231;注册日期:2018 年 9 月 27 日。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/968a/6617634/2cec57cbe527/13014_2019_1325_Fig1_HTML.jpg

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