Overall Survival with Neoadjuvant Nivolumab plus Chemotherapy in Lung Cancer.

IF 96.2 1区 医学 Q1 MEDICINE, GENERAL & INTERNAL
Patrick M Forde, Jonathan D Spicer, Mariano Provencio, Tetsuya Mitsudomi, Mark M Awad, Changli Wang, Shun Lu, Enriqueta Felip, Scott J Swanson, Julie R Brahmer, Keith Kerr, Janis M Taube, Tudor-Eliade Ciuleanu, Fumihiro Tanaka, Gene B Saylors, Ke-Neng Chen, Hiroyuki Ito, Moishe Liberman, Claudio Martin, Stephen Broderick, Lily Wang, Junliang Cai, Quyen Duong, Stephanie Meadows-Shropshire, Joseph Fiore, Sumeena Bhatia, Nicolas Girard
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引用次数: 0

Abstract

Background: Neoadjuvant nivolumab plus chemotherapy significantly improved pathological complete response and event-free survival in patients with resectable non-small-cell lung cancer (NSCLC) in a phase 3 trial. Data are needed on overall survival.

Methods: In this open-label, phase 3 trial, patients with stage IB to IIIA resectable NSCLC were randomly assigned to receive nivolumab plus chemotherapy or chemotherapy alone for three cycles, followed by surgery. The primary end points were event-free survival and pathological complete response. Here, we report the results of the planned analysis of overall survival.

Results: A total of 358 patients were concurrently assigned to receive nivolumab plus chemotherapy (179 patients) or chemotherapy alone (179 patients). The final analysis of overall survival significantly favored neoadjuvant nivolumab plus chemotherapy over chemotherapy (hazard ratio for death, 0.72; 95% confidence interval [CI], 0.52 to 0.10; P = 0.048). At a median follow-up of 68.4 months, the 5-year overall survival was 65.4% with nivolumab plus chemotherapy and 55.0% with chemotherapy alone, with consistency across most subgroups. In exploratory analyses, the 5-year overall survival in the nivolumab-plus-chemotherapy group was 95.3% (95% CI, 82.7 to 98.8) among the patients with a pathological complete response and 55.7% (95% CI, 46.9 to 63.7) among those without such a response; survival was 75.0% among the patients with presurgery clearance of circulating tumor DNA (ctDNA) and 52.6% among those without such clearance. No new safety signals were observed.

Conclusions: Three cycles of neoadjuvant nivolumab plus chemotherapy significantly improved overall survival among patients with resectable NSCLC as compared with chemotherapy alone. (Funded by Bristol Myers Squibb; CheckMate 816 ClinicalTrials.gov number, NCT02998528.).

新辅助纳武单抗加化疗治疗肺癌的总生存率。
背景:在一项3期试验中,新辅助纳武单抗加化疗显著改善了可切除的非小细胞肺癌(NSCLC)患者的病理完全缓解和无事件生存期。需要总体生存数据。方法:在这项开放标签的3期试验中,IB至IIIA期可切除的非小细胞肺癌患者被随机分配接受纳武单抗加化疗或单独化疗3个周期,然后进行手术。主要终点为无事件生存期和病理完全缓解。在这里,我们报告了总生存期的计划分析结果。结果:共有358例患者同时被分配接受纳武单抗联合化疗(179例)或单独化疗(179例)。总生存期的最终分析明显支持新辅助纳武单抗加化疗优于化疗(死亡风险比,0.72;95%置信区间[CI], 0.52 ~ 0.10;p = 0.048)。在中位随访68.4个月时,纳武单抗联合化疗组的5年总生存率为65.4%,单独化疗组的5年总生存率为55.0%,在大多数亚组中是一致的。在探索性分析中,在有病理完全缓解的患者中,尼武单抗加化疗组的5年总生存率为95.3% (95% CI, 82.7至98.8),在无病理完全缓解的患者中,5年总生存率为55.7% (95% CI, 46.9至63.7);手术前循环肿瘤DNA (ctDNA)清除的患者生存率为75.0%,未清除的患者生存率为52.6%。没有观察到新的安全信号。结论:与单独化疗相比,新辅助纳武单抗加化疗3个周期显著提高了可切除NSCLC患者的总生存率。(资金来源:Bristol Myers Squibb;CheckMate 816 ClinicalTrials.gov号码,NCT02998528)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
New England Journal of Medicine
New England Journal of Medicine 医学-医学:内科
CiteScore
145.40
自引率
0.60%
发文量
1839
审稿时长
1 months
期刊介绍: The New England Journal of Medicine (NEJM) stands as the foremost medical journal and website worldwide. With an impressive history spanning over two centuries, NEJM boasts a consistent publication of superb, peer-reviewed research and engaging clinical content. Our primary objective revolves around delivering high-caliber information and findings at the juncture of biomedical science and clinical practice. We strive to present this knowledge in formats that are not only comprehensible but also hold practical value, effectively influencing healthcare practices and ultimately enhancing patient outcomes.
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