Johns Hopkins Kimmel Cancer Center, Baltimore, MD.
National University Bundang Hospital, Seongnam, Republic of Korea.
J Clin Oncol. 2023 Feb 20;41(6):1200-1212. doi: 10.1200/JCO.22.01503. Epub 2022 Oct 12.
We present 5-year results from CheckMate 227 Part 1, in which nivolumab plus ipilimumab improved overall survival (OS) versus chemotherapy in patients with metastatic non-small-cell lung cancer, regardless of tumor programmed death ligand 1 (PD-L1) status.
Adults with stage IV/recurrent non-small-cell lung cancer without mutations or alterations and with tumor PD-L1 ≥ 1% or < 1% (n = 1739) were randomly assigned. Patients with tumor PD-L1 ≥ 1% were randomly assigned to first-line nivolumab plus ipilimumab, nivolumab alone, or chemotherapy. Patients with tumor PD-L1 < 1% were randomly assigned to nivolumab plus ipilimumab, nivolumab plus chemotherapy, or chemotherapy. End points included exploratory 5-year results for efficacy, safety, and quality of life.
At a minimum follow-up of 61.3 months, 5-year OS rates were 24% versus 14% for nivolumab plus ipilimumab versus chemotherapy (PD-L1 ≥ 1%) and 19% versus 7% (PD-L1 < 1%). The median duration of response was 24.5 versus 6.7 months (PD-L1 ≥ 1%) and 19.4 versus 4.8 months (PD-L1 < 1%). Among patients surviving 5 years, 66% (PD-L1 ≥ 1%) and 64% (PD-L1 < 1%) were off nivolumab plus ipilimumab without initiating subsequent systemic anticancer treatment by the 5-year time point. Survival benefit continued after nivolumab plus ipilimumab discontinuation because of treatment-related adverse events, with a 5-year OS rate of 39% (combined PD-L1 ≥ 1% and < 1% populations). Quality of life in 5-year survivors treated with nivolumab plus ipilimumab was similar to that in the general US population through the 5-year follow-up. No new safety signals were observed.
With all patients off immunotherapy treatment for ≥ 3 years, nivolumab plus ipilimumab increased 5-year survivorship versus chemotherapy, including long-term, durable clinical benefit regardless of tumor PD-L1 expression. These data support nivolumab plus ipilimumab as an effective first-line treatment for patients with metastatic non-small-cell lung cancer.
我们展示了 CheckMate 227 第 1 部分的 5 年结果,纳武利尤单抗联合伊匹木单抗在转移性非小细胞肺癌患者中改善了总生存期(OS),与化疗相比,无论肿瘤程序性死亡配体 1(PD-L1)状态如何。
患有无 突变或 改变且肿瘤 PD-L1≥1%或<1%的 IV 期/复发性非小细胞肺癌成人(n=1739)被随机分配。肿瘤 PD-L1≥1%的患者被随机分配至一线纳武利尤单抗联合伊匹木单抗、纳武利尤单抗单药或化疗。肿瘤 PD-L1<1%的患者被随机分配至纳武利尤单抗联合伊匹木单抗、纳武利尤单抗联合化疗或化疗。终点包括疗效、安全性和生活质量的探索性 5 年结果。
在至少 61.3 个月的随访中,纳武利尤单抗联合伊匹木单抗组的 5 年 OS 率为 24%,化疗组为 14%(PD-L1≥1%),纳武利尤单抗联合伊匹木单抗组为 19%,化疗组为 7%(PD-L1<1%)。中位缓解持续时间为 24.5 个月 vs 6.7 个月(PD-L1≥1%)和 19.4 个月 vs 4.8 个月(PD-L1<1%)。在 5 年生存的患者中,66%(PD-L1≥1%)和 64%(PD-L1<1%)在 5 年时间点未接受纳武利尤单抗联合伊匹木单抗且未启动后续系统抗癌治疗。由于治疗相关不良事件停止纳武利尤单抗联合伊匹木单抗后,生存获益持续存在,联合 PD-L1≥1%和<1%人群的 5 年 OS 率为 39%。纳武利尤单抗联合伊匹木单抗治疗的 5 年生存者的生活质量在 5 年随访期间与一般美国人群相似。未观察到新的安全性信号。
所有患者免疫治疗治疗持续时间≥3 年,纳武利尤单抗联合伊匹木单抗与化疗相比提高了 5 年生存率,包括无论肿瘤 PD-L1 表达如何,长期、持久的临床获益。这些数据支持纳武利尤单抗联合伊匹木单抗作为转移性非小细胞肺癌患者的有效一线治疗。