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

  • 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
  • Yonsei University College of Medicine
  • Kinki University
  • Seoul National University Bundang Hospital
  • Samsung Medical Center, Sungkyunkwan university
  • Jilin Cancer Hospital
  • The Fourth Affiliated Hospital of Harbin Medical University
  • University of Malaya
  • Huizhou Municipal Central Hospital of Guangdong Province
  • International Islamic University Malaysia
  • Chung Shan Medical University Hospital
  • National Taiwan University Hospital
  • Kansai Medical University Hospital
  • Ankara Yildirim Beyazit University
  • Tata Memorial Hospital
  • Kurume University School of Medicine
  • Kangbuk Samsung Hospital
  • National Cheng King University Hospital
  • National Cancer Center Hospital East
  • Faculty of Medicine, Prince of Songkla University
  • Johnson & Johnson
  • Shanghai Chest Hospital

Research output: Contribution to journalArticlepeer-review

4 Citations (Scopus)

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.

Original languageEnglish
Article number108496
JournalLung Cancer
Volume204
DOIs
Publication statusPublished - Jun 2025

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Amivantamab
  • Asian patient
  • EGFR TKI
  • EGFR-mutated NSCLC

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