Overall Survival with Neoadjuvant Nivolumab plus Chemotherapy in Lung Cancer

Patrick M. Forde(Trinity College Dublin), Jonathan Spicer(McGill University Health Centre), Mariano Provencio(Hospital Universitario Puerta de Hierro Majadahonda), Tetsuya Mitsudomi(Kindai University), Mark M. Awad(Memorial Sloan Kettering Cancer Center), Changli Wang(Tianjin Medical University Cancer Institute and Hospital), Shun Lu(Shanghai Jiao Tong University), Enriqueta Felip(Hebron University), Steven Swanson(Brigham and Women's Hospital), Julie R. Brahmer(Bloomberg (United States)), Keith M. Kerr(Aberdeen Royal Infirmary), Janis M. Taube(Bloomberg (United States)), Tudor–Eliade Ciuleanu(Institute of Oncology Prof. Dr. Ion Chiricuta), Fumihiro Tanaka(University of Occupational and Environmental Health Japan), Gene B. Saylors, Ke-Neng Chen(Peking University), Hiroyuki Ito(Kanagawa Prefectural Hospital Organization), Moïshe Liberman(Centre Hospitalier de l’Université de Montréal), Claudio Martín(Instituto Alexander Fleming), Stephen Broderick(Bloomberg (United States)), Lily Wang(Bristol-Myers Squibb (United States)), Junliang Cai(Bristol-Myers Squibb (United States)), Quyen Duong(Bristol-Myers Squibb (United States)), S. Meadows–Shropshire(Bristol-Myers Squibb (United States)), Joseph Fiore(Bristol-Myers Squibb (United States)), Simi Bhatia(Bristol-Myers Squibb (United States)), Nicolas Girard(Institut du Thorax)
New England Journal of Medicine
June 2, 2025
Cited by 135

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], 0.523 to 0.998; 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.).


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