Overall Survival with Osimertinib in Resected <i>EGFR</i> -Mutated NSCLC

Masahiro Tsuboi(Chinese Academy of Medical Sciences & Peking Union Medical College), Roy S. Herbst(Chinese Academy of Medical Sciences & Peking Union Medical College), Thomas John(The University of Melbourne), Terufumi Kato(Chinese Academy of Medical Sciences & Peking Union Medical College), Margarita Majem(Chinese Academy of Medical Sciences & Peking Union Medical College), Christian Grohé(Chinese Academy of Medical Sciences & Peking Union Medical College), Jie Wang(Chinese Academy of Medical Sciences & Peking Union Medical College), Jonathan W. Goldman(University of California, Los Angeles), Shun Lü(Shanghai Jiao Tong University), Wu‐Chou Su(Chinese Academy of Medical Sciences & Peking Union Medical College), Filippo de Marinis(Chinese Academy of Medical Sciences & Peking Union Medical College), Frances A. Shepherd(University Health Network), Ki Hyeong Lee(Chinese Academy of Medical Sciences & Peking Union Medical College), Nhieu Thi Le(Chinese Academy of Medical Sciences & Peking Union Medical College), Arunee Dechaphunkul(Prince of Songkla University), Dariusz M. Kowalski(Chinese Academy of Medical Sciences & Peking Union Medical College), Lynne Poole(AstraZeneca (United Kingdom)), Ana Bolanos(Chinese Academy of Medical Sciences & Peking Union Medical College), Yuri Rukazenkov(AstraZeneca (United Kingdom)), Yi‐Long Wu(Chinese Academy of Medical Sciences & Peking Union Medical College)
New England Journal of Medicine
June 4, 2023
Cited by 599

Abstract

BACKGROUND: )-mutated, stage IB to IIIA non-small-cell lung cancer (NSCLC), adjuvant osimertinib therapy, with or without previous adjuvant chemotherapy, resulted in significantly longer disease-free survival than placebo in the ADAURA trial. We report the results of the planned final analysis of overall survival. METHODS: In this phase 3, double-blind trial, we randomly assigned eligible patients in a 1:1 ratio to receive osimertinib (80 mg once daily) or placebo until disease recurrence was observed, the trial regimen was completed (3 years), or a discontinuation criterion was met. The primary end point was investigator-assessed disease-free survival among patients with stage II to IIIA disease. Secondary end points included disease-free survival among patients with stage IB to IIIA disease, overall survival, and safety. RESULTS: Of 682 patients who underwent randomization, 339 received osimertinib and 343 received placebo. Among patients with stage II to IIIA disease, the 5-year overall survival was 85% in the osimertinib group and 73% in the placebo group (overall hazard ratio for death, 0.49; 95.03% confidence interval [CI], 0.33 to 0.73; P<0.001). In the overall population (patients with stage IB to IIIA disease), the 5-year overall survival was 88% in the osimertinib group and 78% in the placebo group (overall hazard ratio for death, 0.49; 95.03% CI, 0.34 to 0.70; P<0.001). One new serious adverse event, pneumonia related to coronavirus disease 2019, was reported after the previously published data-cutoff date (the event was not considered by the investigator to be related to the trial regimen, and the patient fully recovered). Adjuvant osimertinib had a safety profile consistent with that in the primary analysis. CONCLUSIONS: -mutated, stage IB to IIIA NSCLC. (Funded by AstraZeneca; ADAURA ClinicalTrials.gov number, NCT02511106.).


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