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辅助伊匹单抗对比安慰剂用于 III 期黑色素瘤完全切除术后:欧洲癌症研究与治疗组织 18071 项双盲 III 期随机试验的长期随访结果。

Adjuvant ipilimumab versus placebo after complete resection of stage III melanoma: long-term follow-up results of the European Organisation for Research and Treatment of Cancer 18071 double-blind phase 3 randomised trial.

机构信息

Gustave Roussy Cancer Insitute and University Paris-Sud, France.

Veneto Institute of Oncology IOV-IRCCS, Padua, Italy.

出版信息

Eur J Cancer. 2019 Sep;119:1-10. doi: 10.1016/j.ejca.2019.07.001. Epub 2019 Aug 7.

DOI:10.1016/j.ejca.2019.07.001
PMID:31400634
Abstract

BACKGROUND

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.

CONCLUSIONS

Adjuvant therapy with ipilimumab prolongs RFS, DMFS and OS significantly. The benefit is sustained long term and consistent across subgroups.

摘要

背景

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。

患者和方法

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。

结论

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。

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