Long-term survival with first-line nivolumab plus ipilimumab in patients with advanced non-small-cell lung cancer: a pooled analysis

医学 易普利姆玛 无容量 内科学 人口 养生 肺癌 肿瘤科 无进展生存期 癌症 化疗 免疫疗法 环境卫生
作者
Hossein Borghaei,Tudor Ciuleanu,J.-S. Lee,Adam Płużański,Reyes Bernabe Caro,Martin Gutierrez,Yuichiro Ohe,Makoto Nishio,Jonathan W. Goldman,Neal Ready,David R. Spigel,Sundhar Ramalingam,Luis Paz-Ares,Justin F. Gainor,Samreen Ahmed,Martin Reck,Michele Maio,Kenneth J. O'Byrne,Arteid Memaj,Faith E. Nathan,Phuong Tran,Matthew D. Hellmann,Julie R. Brahmer
出处
期刊:Annals of Oncology [Elsevier]
卷期号:34 (2): 173-185 被引量:3
标识
DOI:10.1016/j.annonc.2022.11.006
摘要

First-line nivolumab plus ipilimumab prolongs survival versus chemotherapy in advanced non-small-cell lung cancer (NSCLC). We further characterized clinical benefit with this regimen in a large pooled patient population and assessed the effect of response on survival.Data were pooled from four studies of first-line nivolumab plus ipilimumab in advanced NSCLC (CheckMate 227 Part 1, 817 cohort A, 568 Part 1, and 012). Overall survival (OS), progression-free survival (PFS), objective response rate, duration of response, and safety were assessed. Landmark analyses of OS by response status at 6 months and by tumor burden reduction in responders to nivolumab plus ipilimumab were also assessed.In the pooled population (N = 1332) with a minimum follow-up of 29.1-58.9 months, median OS was 18.6 months, with a 3-year OS rate of 35%; median PFS was 5.4 months (3-year PFS rate, 17%). Objective response rate was 36%; median duration of response was 23.7 months, with 38% of responders having an ongoing response at 3 years. In patients with tumor programmed death-ligand 1 (PD-L1) <1%, ≥1%, 1%-49%, or ≥50%, 3-year OS rates were 30%, 38%, 30%, and 48%. Three-year OS rates were 30% and 38% in patients with squamous or non-squamous histology. Efficacy outcomes in patients aged ≥75 years were similar to the overall pooled population (median OS, 20.1 months; 3-year OS rate, 34%). In the pooled population, responders to nivolumab plus ipilimumab at 6 months had longer post-landmark OS than those with stable or progressive disease; 3-year OS rates were 66%, 22%, and 14%, respectively. Greater depth of response was associated with prolonged survival; in patients with tumor burden reduction ≥80%, 50% to <80%, or 30% to <50%, 3-year OS rates were 85%, 72%, and 44%, respectively. No new safety signals were identified in the pooled population.Long-term survival benefit and durable response with nivolumab plus ipilimumab in this large patient population further support this first-line treatment option for advanced NSCLC.
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