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Overall Survival with Amivantamab-Lazertinib in EGFR-Mutated Advanced NSCLC

Authors
 Yang, James Chih-Hsin  ;  Lu, Shun  ;  Hayashi, Hidetoshi  ;  Felip, Enriqueta  ;  Spira, Alexander I.  ;  Girard, Nicolas  ;  Kim, Yu Jung  ;  Lee, Se-Hoon  ;  Ostapenko, Yurii  ;  Danchaivijitr, Pongwut  ;  Liu, Baogang  ;  Alip, Adlinda  ;  Korbenfeld, Ernesto  ;  Mourao Dias, Josiane  ;  Besse, Benjamin  ;  Passaro, Antonio  ;  Lee, Ki-Hyeong  ;  Xiong, Hailin  ;  How, Soon-Hin  ;  Cheng, Ying  ;  Chang, Gee-Chen  ;  Yoshioka, Hiroshige  ;  Thomas, Michael  ;  Nguyen, Danny  ;  Ou, Sai-Hong Ignatius  ;  Mukhedkar, Sanjay  ;  Prabhash, Kumar  ;  D'Arcangelo, Manolo  ;  Alatorre-Alexander, Jorge  ;  Vazquez Limon, Juan Carlos  ;  Alves, Sara  ;  Stroyakovskiy, Daniil  ;  Peregudova, Marina  ;  Sendur, Mehmet Ali Nahit  ;  Yazici, Ozan  ;  Califano, Raffaele  ;  Gutierrez Calderon, Vanesa  ;  de Marinis, Filippo  ;  Kim, Sang-We  ;  Gadgeel, Shirish M.  ;  Owen, Scott  ;  Xie, John  ;  Sun, Tao  ;  Mehta, Jaydeep  ;  Venkatasubramanian, Raja  ;  Ennis, Mariah  ;  Fennema, Elizabeth  ;  Daksh, Mahesh  ;  Roshak, Amy  ;  Man, Julie  ;  Knoblauch, Roland E.  ;  Bauml, Joshua M.  ;  Baig, Mahadi  ;  Shah, Sujay  ;  Sethi, Seema  ;  Cho, Byoung Chul 
Citation
 NEW ENGLAND JOURNAL OF MEDICINE, Vol.393(17) : 1681-1693, 2025-10 
Journal Title
NEW ENGLAND JOURNAL OF MEDICINE
ISSN
 0028-4793 
Issue Date
2025-10
MeSH
Acrylamides* / adverse effects ; Acrylamides* / therapeutic use ; Adult ; Aged ; Aniline Compounds* / adverse effects ; Aniline Compounds* / therapeutic use ; Antibodies, Bispecific ; Antineoplastic Combined Chemotherapy Protocols* / adverse effects ; Antineoplastic Combined Chemotherapy Protocols* / therapeutic use ; Carbazoles* / adverse effects ; Carbazoles* / therapeutic use ; Carcinoma, Non-Small-Cell Lung* / drug therapy ; Carcinoma, Non-Small-Cell Lung* / genetics ; Carcinoma, Non-Small-Cell Lung* / mortality ; ErbB Receptors / antagonists & inhibitors ; ErbB Receptors / genetics ; Female ; Humans ; Indoles ; Kaplan-Meier Estimate ; Lung Neoplasms* / drug therapy ; Lung Neoplasms* / genetics ; Lung Neoplasms* / mortality ; Male ; Middle Aged ; Mutation ; Protein Kinase Inhibitors* / adverse effects ; Protein Kinase Inhibitors* / therapeutic use ; Pyrimidines
Abstract
Background Previous results from this phase 3 trial showed that progression-free survival among participants with previously untreated EGFR (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 We randomly assigned, in a 2:2:1 ratio, participants with previously untreated EGFR-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 Amivantamab-lazertinib led to significantly longer overall survival among participants with previously untreated EGFR-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.) In advanced non-small-cell lung cancer with EGFR mutations, amivantamab-lazertinib led to longer overall survival than osimertinib but was associated with an increased risk of adverse events of grade 3 or higher.
Full Text
https://www.nejm.org/doi/10.1056/NEJMoa2503001
DOI
10.1056/NEJMoa2503001
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
Yonsei Authors
Cho, Byoung Chul(조병철) ORCID logo https://orcid.org/0000-0002-5562-270X
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/208083
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