Academic Department of Radiation Oncology, Centre Oscar Lambret, Lille, France; CRIStAL UMR CNRS 9189, Lille University, Lille, France.
Département de Physique Médicale, Centre Oscar Lambret, Lille, France.
Eur Urol Oncol. 2023 Aug;6(4):399-405. doi: 10.1016/j.euo.2023.01.009. Epub 2023 Feb 7.
There is no consensus on the best local salvage treatment for prostate cancer recurrence after primary external beam radiotherapy. Prospective data on stereotactic body radiation therapy (SBRT) are very scarce.
To determine the optimal dose regimen for salvage SBRT.
DESIGN, SETTING, AND PARTICIPANTS: The present report concerns the phase 1 part of the GETUG-AFU 31 multicenter open-label study. The main inclusion criteria were histologically proven biochemical recurrence, clinical stage T1-T2 upon relapse, multiparametric magnetic resonance imaging data, prostate-specific antigen (PSA) level ≤10 ng/ml prior to salvage SBRT, PSA doubling time >10 mo, and an International Prostate Symptom Score of ≤12.
Five or six fractions of 6 Gy were delivered using focal SBRT.
Dose-limiting toxicity (DLT) was defined as grade ≥3 gastrointestinal or genitourinary tract toxicity, or any grade 4 toxicity (according to the National Cancer Institute Common Terminology Criteria for Adverse Events version 4.03) occurring in the first 18 wk following treatment initiation. A time-to-event continual reassessment method was used to select the dose regimen.
Twenty-one patients were treated (median [interquartile range] age: 76.8 yr [72.2-80.8]), including 12 at 6 × 6 dose level. No DLT was observed. The acute grade 2 genitourinary tract toxicity rate was 19%. With a median follow-up of 12.3 mo, the estimated cumulative incidence of late grade 2 genitourinary toxicity was 41.2% (95% confidence interval: 18.1-63.1%). No grade >2 genitourinary toxicity and no grade ≥2 gastrointestinal toxicity were reported. All treated patients were alive and relapse free at the last follow-up.
A 6 × 6 Gy dose regimen was selected for our phase 2 study of salvage SBRT. With a short follow-up period, the level of toxicity appears to be acceptable.
There is no consensus on the best local treatment for patients with local relapse after radiotherapy for prostate cancer. Prospective data are very scarce. Our early phase trial allowed us to recommend six fractions of 6 Gy using high-precision radiotherapy for further studies.
对于原发性外照射放疗后前列腺癌复发的最佳局部挽救治疗,目前尚无共识。立体定向体部放疗(SBRT)的前瞻性数据非常有限。
确定挽救性 SBRT 的最佳剂量方案。
设计、地点和参与者:本报告涉及 GETUG-AFU31 多中心开放性研究的 1 期部分。主要纳入标准为组织学证实的生化复发、复发时临床分期为 T1-T2、多参数磁共振成像数据、挽救性 SBRT 前 PSA 水平≤10ng/ml、PSA 倍增时间>10 个月和国际前列腺症状评分≤12。
采用焦点 SBRT 给予 5 或 6 个 6Gy 的分次剂量。
剂量限制毒性(DLT)定义为治疗开始后 18 周内发生的任何等级≥3 的胃肠道或泌尿生殖系统毒性,或任何等级 4 毒性(根据国家癌症研究所不良事件通用术语标准 4.03 版)。采用时间事件连续再评估方法选择剂量方案。
共治疗 21 例患者(中位[四分位间距]年龄:76.8 岁[72.2-80.8]),其中 12 例接受 6×6 剂量水平治疗。未观察到 DLT。急性 2 级泌尿生殖系统毒性发生率为 19%。中位随访 12.3 个月时,晚期 2 级泌尿生殖系统毒性累积发生率估计为 41.2%(95%置信区间:18.1-63.1%)。未报告任何>2 级泌尿生殖系统毒性和任何≥2 级胃肠道毒性。所有治疗患者在最后一次随访时均存活且无复发。
我们选择了 6×6Gy 的剂量方案用于挽救性 SBRT 的 2 期研究。在随访时间较短的情况下,毒性水平似乎可以接受。
对于接受前列腺癌放疗后局部复发的患者,目前尚无最佳局部治疗方法。前瞻性数据非常有限。我们的早期试验允许我们推荐使用高精度放疗进行 6 个 6Gy 的分次剂量,以进行进一步研究。