Overall Survival with Amivantamab–Lazertinib in <i>EGFR</i> -Mutated Advanced NSCLC

James Chih‐Hsin Yang(National Taiwan University Hospital), Shun Lu(Shanghai Jiao Tong University), Hidetoshi Hayashi(Kindai University), Enriqueta Felip(Hebron University), Alexander I. Spira(Virginia Cancer Specialists), Nicolas Girard(Université de Versailles Saint-Quentin-en-Yvelines), Yu Jung Kim(Seoul National University Bundang Hospital), Se-Hoon Lee(Samsung Medical Center), Yurii Ostapenko(National Cancer Institute), Pongwut Danchaivijitr(Siriraj Hospital), Baogang Liu(Harbin Medical University), Adlinda Alip(University of Malaya), Ernesto Korbenfeld(Hospital Británico de Buenos Aires), Josiane Mourão Dias(Hospital de Câncer de Barretos), Benjamin Besse(Université Paris-Saclay), Antonio Passaro(European Institute of Oncology), Ki-Hyeong Lee(Chungbuk National University Hospital), Hailin Xiong(Huizhou Central People's Hospital), Soon-Hin How(International Islamic University Malaysia), Ying Cheng(Jilin Province Tumor Hospital), Gee-Chen Chang(Chung Shan Medical University Hospital), Hiroshige Yoshioka(Kansai Medical University), Michael Thomas(Heidelberg University), Danny T. Nguyen(City Of Hope National Medical Center), Sai‐Hong Ignatius Ou(University of California, Irvine), Sanjay Mukhedkar(St John of God Murdoch Hospital), Kumar Prabhash(Tata Memorial Hospital), M. D’Arcangelo(Ospedale "Santa Maria delle Croci" di Ravenna), Jorge Alatorre-Alexander(Bridge Pharma (United States)), Juan Carlos Vázquez Limón(Hospital Civil de Guadalajara), Sara Alves(IPO Porto), Daniil Stroyakovskiy(Moscow City Oncology Hospital №62), Marina Peregudova(Moscow State Regional Socio-Humanitarian Institute), Mehmet Alı Nahıt Şendur(Ankara Yıldırım Beyazıt University), Ozan Yazıcı(Gazi University), Raffaele Califano(The Christie NHS Foundation Trust), Vanesa Gutiérrez Calderón(Hospital Regional Universitario de Málaga), Filippo de Marinis(European Institute of Oncology), Sang‐We Kim(Ulsan College), Shirish M. Gadgeel(Henry Ford Health System), Scott Owen(McGill University Health Centre), John Xie(Johnson & Johnson (United States)), Tao Sun(Johnson & Johnson (United States)), Jaydeep Mehta(Johnson & Johnson (United States)), Raja Venkatasubramanian(Johnson & Johnson (United States)), Mariah Ennis(Johnson & Johnson (United States)), E. Fennema(Johnson & Johnson (United States)), Mahesh Daksh(Johnson & Johnson (United States)), Amy Roshak(Johnson & Johnson (United States)), Julie Man(Johnson & Johnson (United States)), Roland E. Knoblauch(Johnson & Johnson (United States)), Joshua Bauml(Johnson & Johnson (United States)), Mahadi Baig(Johnson & Johnson (United States)), Sujay Shah(Johnson & Johnson (United States)), Seema Sethi(Johnson & Johnson (United States)), Byoung Chul Cho(Yonsei University)
New England Journal of Medicine
September 7, 2025
Cited by 73

Abstract

BACKGROUND: (epidermal growth factor receptor)-mutated advanced non-small-cell lung cancer (NSCLC) was significantly improved with amivantamab-lazertinib as compared with osimertinib. Results of the protocol-specified final overall survival analysis in this trial have not been reported. METHODS: -mutated (exon 19 deletion or L858R substitution), locally advanced or metastatic NSCLC to receive amivantamab-lazertinib, osimertinib, or lazertinib. Overall survival (assessed in an analysis of the time from randomization to death from any cause) in the amivantamab-lazertinib group as compared with the osimertinib group was a key secondary end point. Additional end points included safety. RESULTS: A total of 429 participants each were assigned to receive amivantamab-lazertinib or osimertinib. Over a median follow-up of 37.8 months, amivantamab-lazertinib led to significantly longer overall survival than osimertinib (hazard ratio for death, 0.75; 95% confidence interval, 0.61 to 0.92; P = 0.005); 3-year overall survival was 60% and 51%, respectively. At the clinical cutoff date, 38% of participants in the amivantamab-lazertinib group and 28% in the osimertinib group were still receiving the assigned treatment. Adverse events of grade 3 or higher were more common with amivantamab-lazertinib (in 80% of participants) than with osimertinib (in 52%), particularly skin-related events, venous thromboembolism, and infusion-related events; these findings were consistent with the established safety profile of each treatment. No new safety signals were observed with additional follow-up. CONCLUSIONS: -mutated advanced NSCLC than osimertinib but was associated with an increased risk of adverse events of grade 3 or higher. (Funded by Janssen Research and Development; MARIPOSA ClinicalTrials.gov number, NCT04487080.).


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