Radiotherapy Department, Léon Bérard Center, Lyon, France; CNRS UMR 5220, INSERM U1044, INSA, University of Lyon, Lyon, France.
Cellular and Molecular Radiobiology, Lucien Neuwirth Cancer Institute, and Institute of Nuclear Physics of Lyon, Lyon-Sud Faculty of Medicine, Lyon, France.
Lancet Oncol. 2019 Dec;20(12):1740-1749. doi: 10.1016/S1470-2045(19)30486-3. Epub 2019 Oct 16.
Radiotherapy is the standard salvage treatment after radical prostatectomy. To date, the role of androgen deprivation therapy has not been formally shown. In this follow-up study, we aimed to update the results of the GETUG-AFU 16 trial, which assessed the efficacy of radiotherapy plus androgen suppression versus radiotherapy alone.
GETUG-AFU 16 was an open-label, multicentre, phase 3, randomised, controlled trial that enrolled men (aged ≥18 years) with Eastern Cooperative Oncology Group performance status of 0 or 1, with histologically confirmed adenocarcinoma of the prostate (but no previous androgen suppression or pelvic radiotherapy), stage pT2, T3, or T4a (bladder neck involvement only) and pN0 or pNx according to the tumour, node, metastasis (TNM) staging system, whose prostate-specific antigen (PSA) concentration increased from 0·1 ng/mL to between 0·2 ng/mL and 2·0 ng/mL after radical prostatectomy, without evidence of clinical disease. Patients were assigned through central randomisation (1:1) to short-term androgen suppression (subcutaneous injection of 10·8 mg goserelin on the first day of irradiation and 3 months later) plus radiotherapy (3D conformal radiotherapy or intensity modulated radiotherapy of 66 Gy in 33 fractions, 5 days a week for 7 weeks) or radiotherapy alone. Randomisation was stratified using a permuted block method (block sizes of two and four) according to investigational site, radiotherapy modality, and prognosis. The primary endpoint was progression-free survival in the intention-to-treat population. This post-hoc one-shot data collection done 4 years after last data cutoff included patients who were alive at the time of the primary analysis and updated long-term patient status by including dates for first local progression, metastatic disease diagnosis, or death (if any of these had occurred) or the date of the last tumour evaluation or last PSA measurement. Survival at 120 months was reported. Late serious adverse effects were assessed. This trial is registered on ClinicalTrials.gov, NCT00423475.
Between Oct 19, 2006, and March 30, 2010, 743 patients were randomly assigned, 374 to radiotherapy alone and 369 to radiotherapy plus goserelin. At the time of data cutoff (March 12, 2019), the median follow-up was 112 months (IQR 102-123). The 120-month progression-free survival was 64% (95% CI 58-69) for patients treated with radiotherapy plus goserelin and 49% (43-54) for patients treated with radiotherapy alone (hazard ratio 0·54, 0·43-0·68; stratified log-rank test p<0·0001). Two cases of secondary cancer occurred since the primary analysis, but were not considered to be treatment related. No treatment-related deaths occurred.
The 120-month progression-free survival confirmed the results from the primary analysis. Salvage radiotherapy combined with short-term androgen suppression significantly reduced risk of biochemical or clinical progression and death compared with salvage radiotherapy alone. The results of the GETUG-AFU 16 trial confirm the efficacy of androgen suppression plus radiotherapy as salvage treatment in patients with increasing PSA concentration after radical prostatectomy for prostate cancer.
The French Health ministry, AstraZeneca, la Ligue Contre le Cancer, and La Ligue de Haute-Savoie.
放疗是根治性前列腺切除术后的标准挽救治疗。迄今为止,雄激素剥夺疗法的作用尚未得到正式证实。在这项随访研究中,我们旨在更新 GETUG-AFU 16 试验的结果,该试验评估了放疗联合雄激素抑制与单纯放疗的疗效。
GETUG-AFU 16 是一项开放标签、多中心、III 期、随机对照试验,纳入了年龄≥18 岁、东部合作肿瘤学组体能状态为 0 或 1、组织学证实为前列腺腺癌(但无先前的雄激素抑制或盆腔放疗)、pT2、T3 或 T4a(仅累及膀胱颈)和 pN0 或 pNx(根据肿瘤、淋巴结、转移(TNM)分期系统)、前列腺特异性抗原(PSA)浓度在根治性前列腺切除术后从 0·1ng/mL 增加到 0·2ng/mL 至 2·0ng/mL 之间、且无临床疾病的患者。患者通过中央随机化(1:1)分配至短期雄激素抑制(在照射的第一天和 3 个月后皮下注射 10·8mg 戈舍瑞林)加放疗(3D 适形放疗或强度调制放疗 66Gy,33 个分次,每周 5 天,共 7 周)或单纯放疗。随机化采用按研究地点、放疗方式和预后分层的交替块方法(块大小为 2 和 4)。主要终点是意向治疗人群中的无进展生存期。这是在最后一次数据截止日期后 4 年进行的一次一次性数据收集,包括在主要分析时存活的患者,并通过包括首次局部进展、转移性疾病诊断或死亡(如果发生任何这些情况)或最后一次肿瘤评估或最后一次 PSA 测量的日期,更新长期患者状态。报告了 120 个月的生存率。评估了晚期严重不良事件。这项试验在 ClinicalTrials.gov 上注册,NCT00423475。
在 2006 年 10 月 19 日至 2010 年 3 月 30 日期间,共随机分配了 743 名患者,374 名患者接受单纯放疗,369 名患者接受放疗加戈舍瑞林。在数据截止日期(2019 年 3 月 12 日)时,中位随访时间为 112 个月(IQR 102-123)。放疗加戈舍瑞林组的 120 个月无进展生存率为 64%(95%CI 58-69),单纯放疗组为 49%(43-54)(风险比 0·54,0·43-0·68;分层对数秩检验 p<0·0001)。自主要分析以来,发生了两例继发性癌症,但被认为与治疗无关。无治疗相关死亡。
120 个月的无进展生存率证实了主要分析的结果。挽救性放疗联合短期雄激素抑制与单纯挽救性放疗相比,显著降低了生化或临床进展和死亡的风险。GETUG-AFU 16 试验的结果证实了雄激素抑制联合放疗作为根治性前列腺切除术后 PSA 浓度升高的前列腺癌患者的挽救性治疗的疗效。
法国卫生部、阿斯利康、法国抗癌联盟和上萨瓦省联盟。