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.
J Immunother Cancer. 2020 Jun;8(1). doi: 10.1136/jitc-2019-000391.
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.
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.
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.
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.
NCT01515189.
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。
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。
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。
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。
NCT01515189。