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在一项 III 期临床试验中,比较了晚期黑色素瘤患者使用伊匹单抗 10mg/kg 和 3mg/kg 的疗效,随访 5 年后的总生存率。

Overall survival at 5 years of follow-up in a phase III trial comparing ipilimumab 10 mg/kg with 3 mg/kg in patients with advanced melanoma.

机构信息

Melanoma, Cancer Immunotherapy and Innovative Therapy Unit, Istituto Nazionale Tumori IRCCS Fondazione Pascale, Napoli, Italy

Unit of Melanoma Medical Oncology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milano, Lombardia, Italy.

出版信息

J Immunother Cancer. 2020 Jun;8(1). doi: 10.1136/jitc-2019-000391.

Abstract

BACKGROUND

We have previously reported significantly longer overall survival (OS) with ipilimumab 10 mg/kg versus ipilimumab 3 mg/kg in patients with advanced melanoma, with higher incidences of adverse events (AEs) at 10 mg/kg. This follow-up analysis reports a 5-year update of OS and safety.

METHODS

This randomized, multicenter, double-blind, phase III trial included patients with untreated or previously treated unresectable stage III or IV melanoma. Patients were randomly assigned (1:1) to ipilimumab 10 mg/kg or 3 mg/kg every 3 weeks for 4 doses. The primary end point was OS.

RESULTS

At a minimum follow-up of 61 months, median OS was 15.7 months (95% CI 11.6 to 17.8) at 10 mg/kg and 11.5 months (95% CI 9.9 to 13.3) at 3 mg/kg (HR 0.84, 95% CI 0.71 to 0.99; p=0.04). In a subgroup analysis, median OS of patients with asymptomatic brain metastasis was 7.0 months (95% CI 4.0 to 12.8) in the 10 mg/kg group and 5.7 months (95% CI 4.2 to 7.0) in the 3 mg/kg group. In patients with wild-type or mutant tumors, median OS was 13.8 months (95% CI 10.2 to 17.0) and 33.2 months (95% CI 19.4 to 45.2) in the 10 mg/kg group, and 11.2 months (95% CI 9.2 to 13.8) and 19.7 months (95% CI 11.6 to 25.3) in the 3 mg/kg group, respectively. The incidence of grade 3/4 treatment-related AEs was 36% in the 10 mg/kg group vs 20% in the 3 mg/kg group, and deaths due to treatment-related AEs occurred in four (1%) and two patients (1%), respectively.

CONCLUSIONS

This 61-month follow-up of a phase III trial showed sustained long-term survival in patients with advanced melanoma who started metastatic treatment with ipilimumab monotherapy, and confirmed the significant benefit for those who received ipilimumab 10 mg/kg vs 3 mg/kg. These results suggest the emergence of a plateau in the OS curve, consistent with previous ipilimumab studies.

TRIAL REGISTRATION NUMBER

NCT01515189.

摘要

背景

我们之前报道过,与伊匹单抗 3mg/kg 相比,晚期黑色素瘤患者使用伊匹单抗 10mg/kg 治疗的总生存期(OS)显著延长,10mg/kg 组不良反应(AE)发生率更高。本随访分析报告了 OS 和安全性的 5 年更新结果。

方法

这是一项随机、多中心、双盲、III 期临床试验,纳入了未经治疗或先前治疗无法切除的 III 期或 IV 期黑色素瘤患者。患者以 1:1 的比例随机分配(1:1)接受伊匹单抗 10mg/kg 或 3mg/kg,每 3 周一次,共 4 次。主要终点是 OS。

结果

在至少 61 个月的随访中,10mg/kg 组的中位 OS 为 15.7 个月(95%CI 11.6 至 17.8),3mg/kg 组为 11.5 个月(95%CI 9.9 至 13.3)(HR 0.84,95%CI 0.71 至 0.99;p=0.04)。在亚组分析中,无症状脑转移患者 10mg/kg 组的中位 OS 为 7.0 个月(95%CI 4.0 至 12.8),3mg/kg 组为 5.7 个月(95%CI 4.2 至 7.0)。在野生型或突变型肿瘤患者中,10mg/kg 组的中位 OS 为 13.8 个月(95%CI 10.2 至 17.0)和 33.2 个月(95%CI 19.4 至 45.2),3mg/kg 组分别为 11.2 个月(95%CI 9.2 至 13.8)和 19.7 个月(95%CI 11.6 至 25.3)。10mg/kg 组 3/4 级治疗相关 AE 的发生率为 36%,3mg/kg 组为 20%,与治疗相关的 AE 导致的死亡分别发生在 4 例(1%)和 2 例(1%)患者中。

结论

这项 III 期试验的 61 个月随访显示,接受伊匹单抗单药治疗的晚期黑色素瘤患者的长期生存持续延长,并且证实了接受伊匹单抗 10mg/kg 治疗的患者比接受 3mg/kg 治疗的患者获益显著。这些结果表明 OS 曲线出现平台期,与之前的伊匹单抗研究一致。

试验注册号

NCT01515189。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75c2/7279645/f1377d4c52d7/jitc-2019-000391f01.jpg

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