Amivantamab plus lazertinib versus osimertinib as first-line treatment in EGFR-mutated advanced non-small cell lung cancer: MARIPOSA Asian subset
| dc.contributor.author | Cho B.C. | |
| dc.contributor.author | Hayashi H. | |
| dc.contributor.author | Lee J.S. | |
| dc.contributor.author | Lee S.H. | |
| dc.contributor.author | Danchaivijitr P. | |
| dc.contributor.author | Cheng Y. | |
| dc.contributor.author | Liu B. | |
| dc.contributor.author | Alip A. | |
| dc.contributor.author | Xiong H. | |
| dc.contributor.author | How S.H. | |
| dc.contributor.author | Chang G.C. | |
| dc.contributor.author | Yang J.C.H. | |
| dc.contributor.author | Yoshioka H. | |
| dc.contributor.author | Nahit Şendur M.A. | |
| dc.contributor.author | Prabhash K. | |
| dc.contributor.author | Azuma K. | |
| dc.contributor.author | Lee Y.G. | |
| dc.contributor.author | Lin C.C. | |
| dc.contributor.author | Matsumoto S. | |
| dc.contributor.author | Sunpaweravong P. | |
| dc.contributor.author | Xia Y. | |
| dc.contributor.author | Martinez M. | |
| dc.contributor.author | Bauml J.M. | |
| dc.contributor.author | Sethi S. | |
| dc.contributor.author | Lu S. | |
| dc.contributor.correspondence | Cho B.C. | |
| dc.contributor.other | Mahidol University | |
| dc.date.accessioned | 2025-05-09T18:36:25Z | |
| dc.date.available | 2025-05-09T18:36:25Z | |
| dc.date.issued | 2025-06-01 | |
| dc.description.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. | |
| dc.identifier.citation | Lung Cancer Vol.204 (2025) | |
| dc.identifier.doi | 10.1016/j.lungcan.2025.108496 | |
| dc.identifier.eissn | 18728332 | |
| dc.identifier.issn | 01695002 | |
| dc.identifier.scopus | 2-s2.0-105003847308 | |
| dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/123456789/110000 | |
| dc.rights.holder | SCOPUS | |
| dc.subject | Biochemistry, Genetics and Molecular Biology | |
| dc.subject | Medicine | |
| dc.title | Amivantamab plus lazertinib versus osimertinib as first-line treatment in EGFR-mutated advanced non-small cell lung cancer: MARIPOSA Asian subset | |
| dc.type | Article | |
| mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=105003847308&origin=inward | |
| oaire.citation.title | Lung Cancer | |
| oaire.citation.volume | 204 | |
| oairecerif.author.affiliation | Siriraj Hospital | |
| oairecerif.author.affiliation | Kansai Medical University Hospital | |
| oairecerif.author.affiliation | Ankara Yildirim Beyazit University | |
| oairecerif.author.affiliation | Seoul National University Bundang Hospital | |
| oairecerif.author.affiliation | Kindai University | |
| oairecerif.author.affiliation | Shanghai Chest Hospital | |
| oairecerif.author.affiliation | National Cheng Kung University Hospital | |
| oairecerif.author.affiliation | National Taiwan University Hospital | |
| oairecerif.author.affiliation | Universiti Malaya | |
| oairecerif.author.affiliation | Chung Shan Medical University | |
| oairecerif.author.affiliation | Faculty of Medicine, Prince of Songkla University | |
| oairecerif.author.affiliation | Harbin Medical University | |
| oairecerif.author.affiliation | Tata Memorial Hospital | |
| oairecerif.author.affiliation | Yonsei University | |
| oairecerif.author.affiliation | International Islamic University Malaysia | |
| oairecerif.author.affiliation | National Cancer Center Hospital East | |
| oairecerif.author.affiliation | Johnson & Johnson | |
| oairecerif.author.affiliation | Kurume University School of Medicine | |
| oairecerif.author.affiliation | Sungkyunkwan University School of Medicine | |
| oairecerif.author.affiliation | Jilin Cancer Hospital | |
| oairecerif.author.affiliation | Huizhou Municipal Central Hospital of Guangdong Province |
