Gustave Roussy Cancer Insitute and University Paris-Sud, France.
Veneto Institute of Oncology IOV-IRCCS, Padua, Italy.
Eur J Cancer. 2019 Sep;119:1-10. doi: 10.1016/j.ejca.2019.07.001. Epub 2019 Aug 7.
Since 2015, adjuvant therapy with ipilimumab is an approved treatment for stage III melanoma based on a significantly prolonged recurrence-free survival (RFS). At a median follow-up of 5.3 years, RFS, distant metastasis-free survival (DMFS) and overall survival (OS) were each significantly prolonged in the ipilimumab group compared with the placebo group, despite a 53.3% (ipilimumab) versus 4.6% (placebo) treatment discontinuation rate due to adverse events. We present now long-term follow-up results of this European Organisation for Research and Treatment of Cancer 18071 trial.
PATIENTS, METHODS AND RESULTS: A total of 99 sites randomised 951 patients with stage III cutaneous melanoma (excluding lymph node metastasis ≤1 mm or in-transit metastasis) with adequate resection of lymph nodes to receive intravenous infusions of ipilimumab 10 mg/kg or placebo, every 3 weeks for 4 doses, then every 3 months for up to 3 years. The RFS, DMFS and OS, as reported by the local investigators, were assessed by the intention-to-treat analysis. Among 431 patients randomised at 63 sites and who were still alive at the analysis reported in 2016, recent follow-up information could be obtained for 264 patients. The median OS follow-up was 6.9 years. The RFS (hazard ratio [HR] 0.75, 95% confidence interval 0.63-0.88; P < 0.001), DMFS (HR 0.76, 0.64-0.90; P = 0.002) and OS (HR 0.73, 0.60-0.89; P = 0.002) benefit observed in the ipilimumab group was durable with an 8.7% absolute difference at 7 years for OS. The benefit was consistent across subgroups.
Adjuvant therapy with ipilimumab prolongs RFS, DMFS and OS significantly. The benefit is sustained long term and consistent across subgroups.
自 2015 年以来,基于显著延长无复发生存期(RFS),伊匹单抗辅助治疗被批准用于 III 期黑色素瘤。在中位随访 5.3 年时,与安慰剂组相比,伊匹单抗组的 RFS、无远处转移生存(DMFS)和总生存(OS)均显著延长,尽管由于不良反应,伊匹单抗组的治疗中断率为 53.3%(伊匹单抗),而安慰剂组为 4.6%。我们现在报告这项欧洲癌症研究与治疗组织 18071 试验的长期随访结果。
共有 99 个中心随机分配了 991 例 III 期皮肤黑色素瘤(不包括淋巴结转移≤1mm 或转移灶)患者,这些患者均接受了淋巴结清扫术,然后接受静脉注射伊匹单抗 10mg/kg 或安慰剂,每 3 周 1 次,共 4 次,然后每 3 个月 1 次,最长 3 年。局部研究者报告的 RFS、DMFS 和 OS 通过意向治疗分析进行评估。在 2016 年报告的分析中,63 个中心随机分配的 431 例患者仍存活,其中 264 例患者获得了最新随访信息。中位 OS 随访时间为 6.9 年。伊匹单抗组的 RFS(风险比[HR]0.75,95%置信区间 0.63-0.88;P<0.001)、DMFS(HR 0.76,0.64-0.90;P=0.002)和 OS(HR 0.73,0.60-0.89;P=0.002)获益是持久的,OS 获益在 7 年时的绝对差异为 8.7%。该获益在各亚组中是一致的。
伊匹单抗辅助治疗显著延长 RFS、DMFS 和 OS。获益是长期持续的,并且在各亚组中是一致的。