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Overall survival for amivantamab plus lazertinib versus osimertinib as first-line treatment in Asian participants with EGFR-mutant advanced NSCLC: A MARIPOSA subset analysis

Authors
 Hayashi, Hidetoshi  ;  Cho, Byoung Chul  ;  Kim, Yu Jung  ;  Lee, Se-Hoon  ;  Danchaivijitr, Pongwut  ;  Alip, Adlinda  ;  Xiong, Hailin  ;  How, Soon-Hin  ;  Chang, Gee-Chen  ;  Yang, James Chih-Hsin  ;  Yamanaka, Yuta  ;  Sendur, Mehmet Ali Nahit  ;  Prabhash, Kumar  ;  Azuma, Koichi  ;  Akawung, Alianu  ;  Fennema, Elizabeth  ;  Tang, Xiaodan  ;  Shah, Sujay  ;  Sethi, Seema  ;  Lu, Shun 
Citation
 LUNG CANCER, Vol.214, 2026-04 
Article Number
 109305 
Journal Title
LUNG CANCER
ISSN
 0169-5002 
Issue Date
2026-04
MeSH
Acrylamides* / administration & dosage ; Acrylamides* / therapeutic use ; Adult ; Aged ; Aged, 80 and over ; Aniline Compounds* / administration & dosage ; Aniline Compounds* / therapeutic use ; Antineoplastic Combined Chemotherapy Protocols* / therapeutic use ; Asian People / genetics ; Carcinoma, Non-Small-Cell Lung* / drug therapy ; Carcinoma, Non-Small-Cell Lung* / genetics ; Carcinoma, Non-Small-Cell Lung* / mortality ; Carcinoma, Non-Small-Cell Lung* / pathology ; ErbB Receptors / genetics ; Female ; Humans ; Indoles ; Lung Neoplasms* / drug therapy ; Lung Neoplasms* / genetics ; Lung Neoplasms* / mortality ; Lung Neoplasms* / pathology ; Male ; Middle Aged ; Mutation* ; Pyrimidines ; Treatment Outcome
Keywords
Asian ; Amivantamab plus lazertinib ; Overall survival ; EGFR-mutated NSCLC ; EGFR TKI
Abstract
Background: Approximately 60 % of lung cancer cases occur in Asia, indicating an epidemiological disparity and need for effective therapies. Amivantamab-lazertinib is approved for first-line EGFR-mutated advanced non-small cell lung cancer (NSCLC) in many countries. In the protocol-specified final overall survival (OS) analysis of MARIPOSA (NCT04487080), amivantamab-lazertinib showed a statistically significant and clinically meaningful improvement in OS versus osimertinib (HR, 0.75; P = 0.005) among all participants. We evaluated OS for amivantamab-lazertinib versus osimertinib in Asian participants. Patients and methods: Participants with previously untreated EGFR-mutated, locally advanced/metastatic NSCLC were randomized 2:2:1 to receive amivantamab-lazertinib, osimertinib, or lazertinib (for evaluating contribution of components). Self-identified Asian race was a stratification factor. OS was a key secondary endpoint. Results: Of 1074 randomized participants, 629 self-identified as Asian (amivantamab-lazertinib:250; osimertinib:251; lazertinib:128). At a median follow-up of 38.7 months, amivantamab-lazertinib significantly prolonged OS versus osimertinib among Asian participants. Median OS was not reached (NR; 95 % CI, NR-NR) for amivantamab-lazertinib versus 38.4 months (95 % CI, 35.1-NR) for osimertinib (HR, 0.74; 95 % CI, 0.56-0.97; nominal P = 0.026). Assuming exponential distribution of OS in both arms, amivantamab-lazertinib is projected to prolong median OS among Asian participants by > 12 months versus osimertinib. At 36 months, 61 % and 53 % were alive in the amivantamab-lazertinib and osimertinib arms. Safety profile was consistent with the overall population. Conclusions: Consistent with the overall population, amivantamab-lazertinib significantly improved OS versus osimertinib among Asian participants with previously untreated EGFR-mutated advanced NSCLC, making it the first regimen to improve survival among Asian patients.
Files in This Item:
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DOI
10.1016/j.lungcan.2026.109305
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/22282913/211536
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