Five-year survival outcomes with nivolumab plus ipilimumab versus chemotherapy as first-line treatment for metastatic non-small-cell lung cancer in CheckMate 227 Journal Article


Authors: Brahmer, J. R.; Lee, J. S.; Ciuleanu, T. E.; Bernabe Caro, R.; Nishio, M.; Urban, L.; Audigier-Valette, C.; Lupinacci, L.; Sangha, R.; Pluzanski, A.; Burgers, J.; Mahave, M.; Ahmed, S.; Schoenfeld, A. J.; Paz-Ares, L. G.; Reck, M.; Borghaei, H.; O'Byrne, K. J.; Gupta, R. G.; Bushong, J.; Li, L.; Blum, S. I.; Eccles, L. J.; Ramalingam, S. S.
Article Title: Five-year survival outcomes with nivolumab plus ipilimumab versus chemotherapy as first-line treatment for metastatic non-small-cell lung cancer in CheckMate 227
Abstract: PURPOSEWe 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.METHODSAdults with stage IV/recurrent non-small-cell lung cancer without EGFR mutations or ALK 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.RESULTSAt 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.CONCLUSIONWith 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. © American Society of Clinical Oncology.
Keywords: adult; controlled study; genetics; antineoplastic agent; metabolism; ipilimumab; quality of life; neoplasm recurrence, local; randomized controlled trial; antineoplastic combined chemotherapy protocols; carcinoma, non-small-cell lung; lung neoplasms; lung tumor; tumor recurrence; drug therapy; programmed death 1 ligand 1; non small cell lung cancer; nivolumab; humans; human; b7-h1 antigen
Journal Title: Journal of Clinical Oncology
Volume: 41
Issue: 6
ISSN: 0732-183X
Publisher: American Society of Clinical Oncology  
Date Published: 2023-02-20
Start Page: 1200
End Page: 1212
Language: English
DOI: 10.1200/jco.22.01503
PUBMED: 36223558
PROVIDER: scopus
PMCID: PMC9937094
DOI/URL:
Notes: Article -- Export Date: 1 March 2023 -- Source: Scopus
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