7 34

Cited 0 times in

Cited 0 times in

Amivantamab plus lazertinib versus osimertinib as first-line treatment in EGFR-mutated advanced non-small cell lung cancer: MARIPOSA Asian subset

Authors
 Byoung Chul Cho  ;  Hidetoshi Hayashi  ;  Jong-Seok Lee  ;  Se-Hoon Lee  ;  Pongwut Danchaivijitr  ;  Ying Cheng  ;  Baogang Liu  ;  Adlinda Alip  ;  Hailin Xiong  ;  Soon Hin How  ;  Gee-Chen Chang  ;  James Chih-Hsin Yang  ;  Hiroshige Yoshioka  ;  Mehmet Ali Nahit Şendur  ;  Kumar Prabhash  ;  Koichi Azuma  ;  Yun-Gyoo Lee  ;  Chien-Chung Lin  ;  Shingo Matsumoto  ;  Patrapim Sunpaweravong  ;  Yichuan Xia  ;  Melissa Martinez  ;  Joshua M Bauml  ;  Seema Sethi  ;  Shun Lu 
Citation
 LUNG CANCER, Vol.204 : 108496, 2025-06 
Journal Title
LUNG CANCER
ISSN
 0169-5002 
Issue Date
2025-06
MeSH
Acrylamides* / administration & dosage ; Acrylamides* / therapeutic use ; Adult ; Aged ; 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
Amivantamab ; Asian patient ; EGFR TKI ; EGFR-mutated NSCLC
Abstract
Introduction: The incidence of epidermal growth factor receptor (EGFR) mutations is higher among Asian patients with advanced non-small cell lung cancer than the general advanced non-small cell lung cancer population. We evaluated the efficacy and safety of amivantamab in combination with lazertinib versus osimertinib in Asian participants from the phase 3 MARIPOSA study who had treatment-naïve advanced non-small cell lung cancer with common EGFR mutations.

Methods: Participants were randomized 2:2:1 to receive amivantamab-lazertinib, osimertinib alone, or lazertinib alone. The primary endpoint was progression-free survival based on blinded independent central review per RECIST v1.1. Secondary endpoints included overall survival, objective response rate, duration of response, and safety. Exploratory endpoints included extracranial progression-free survival and post-progression outcomes.

Results: Of 1074 randomized participants, 629 were Asian, with 250 and 251 randomized to the amivantamab-lazertinib and osimertinib arms, respectively. Among Asian participants, at a median follow-up of 22.5 months, amivantamab-lazertinib showed a 35 % reduction in the risk of disease progression or death versus osimertinib (hazard ratio, 0.65; P < 0.001). Consistent with the overall population, median progression-free survival was 27.5 and 18.3 months in the amivantamab-lazertinib and osimertinib arms, respectively. The objective response rate was 88 % for amivantamab-lazertinib versus 85 % for osimertinib. The median duration of response among confirmed responders improved by 8.6 months for amivantamab-lazertinib versus osimertinib. Favorable trends were also seen for overall survival, extracranial progression-free survival, and post-progression outcomes for amivantamab-lazertinib over osimertinib. Adverse events in Asian participants were similar to those in the overall population.

Conclusions: Amivantamab-lazertinib demonstrated superior progression-free survival versus osimertinib in Asian participants, with a tolerable safety profile. These results were consistent with those in the overall population.
Files in This Item:
T202505564.pdf Download
DOI
10.1016/j.lungcan.2025.108496
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/22282913/207240
사서에게 알리기
  feedback

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

Browse

Links