Cancer Centre, Mount Vernon Hospital, Northwood, UK; University of Manchester, UK.
Cancer Centre, Mount Vernon Hospital, Northwood, UK.
Radiother Oncol. 2021 Jan;154:214-219. doi: 10.1016/j.radonc.2020.09.047. Epub 2020 Oct 2.
A randomised phase-III trial compared external beam radiotherapy (EBRT) alone with EBRT combined with high-dose-rate brachytherapy boost (HDR-BTb) in localised prostate adenocarcinoma. Previous analysis, at median follow up of 85 months, demonstrated improved relapse free survival (RFS) with EBRT + HDR-BTb. This data has now been updated with a median follow up of 131 months.
From December 1997 to August 2005, patients were assigned either to EBRT alone delivering 55 Gy in 20 fractions over 4 weeks or EBRT followed by a temporary high-dose-rate implant delivering 2 × 8·5 Gy over 24 h. The primary endpoint was RFS defined by a PSA rise ≥2.0 µg/l above nadir, clinical progression or death. Actuarial survival rates and Hazard Ratios (HRs) were calculated using the Kaplan-Meier method and Cox's Proportional Hazard Model, respectively. Secondary endpoints were overall survival (OS), urinary and bowel toxicity.
One hundred and six patients received EBRT alone and 110 EBRT + HDR-BTb. Median time to relapse was 137 months in the HDR-BTb arm compared to 82 months for EBRT alone (p = 0·01). A 27% risk of recurrence with EBRT alone was observed (p = 0·001), resulting in a 21% improvement in RFS at 12 years with EBRT + HDR-BTb. In multivariate analysis treatment arm, risk category and no androgen deprivation therapy were significant covariates for risk of relapse. Differences in overall survival were not significant.
At 12 years there remains a significant improvement in RFS after EBRT + HDR-BTb; both treatments were equitoxic for severe late urinary and bowel events and urethral strictures.
一项随机 III 期试验比较了单纯外照射放疗(EBRT)与 EBRT 联合高剂量率近距离放疗(HDR-BTb)治疗局限性前列腺腺癌。前期分析中位随访 85 个月时,EBRT+HDR-BTb 治疗组无复发生存率(RFS)改善。现在已经更新了中位随访 131 个月的数据。
1997 年 12 月至 2005 年 8 月,患者被随机分为单纯 EBRT 组,给予 55Gy/20 次/4 周;或 EBRT 后行临时高剂量率植入术,24 小时内给予 2×8.5Gy。主要终点为 PSA 升高≥2.0μg/l 超过最低点、临床进展或死亡定义的 RFS。采用 Kaplan-Meier 法和 Cox 比例风险模型计算生存率和风险比(HR)。次要终点为总生存(OS)、尿便毒性。
106 例患者接受单纯 EBRT,110 例患者接受 EBRT+HDR-BTb。HDR-BTb 组中位复发时间为 137 个月,单纯 EBRT 组为 82 个月(p=0.01)。单纯 EBRT 组复发风险为 27%(p=0.001),EBRT+HDR-BTb 组 12 年时 RFS 提高 21%。多因素分析中,治疗组、危险分层和无雄激素剥夺治疗是复发风险的显著协变量。OS 差异无统计学意义。
EBRT+HDR-BTb 治疗后 12 年 RFS 仍显著改善;两种治疗方法对严重晚期尿便事件和尿道狭窄的毒性相当。