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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

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dc.contributor.authorHayashi, Hidetoshi-
dc.contributor.authorCho, Byoung Chul-
dc.contributor.authorKim, Yu Jung-
dc.contributor.authorLee, Se-Hoon-
dc.contributor.authorDanchaivijitr, Pongwut-
dc.contributor.authorAlip, Adlinda-
dc.contributor.authorXiong, Hailin-
dc.contributor.authorHow, Soon-Hin-
dc.contributor.authorChang, Gee-Chen-
dc.contributor.authorYang, James Chih-Hsin-
dc.contributor.authorYamanaka, Yuta-
dc.contributor.authorSendur, Mehmet Ali Nahit-
dc.contributor.authorPrabhash, Kumar-
dc.contributor.authorAzuma, Koichi-
dc.contributor.authorAkawung, Alianu-
dc.contributor.authorFennema, Elizabeth-
dc.contributor.authorTang, Xiaodan-
dc.contributor.authorShah, Sujay-
dc.contributor.authorSethi, Seema-
dc.contributor.authorLu, Shun-
dc.date.accessioned2026-03-27T02:13:13Z-
dc.date.available2026-03-27T02:13:13Z-
dc.date.created2026-03-20-
dc.date.issued2026-04-
dc.identifier.issn0169-5002-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/211536-
dc.description.abstractBackground: 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.-
dc.languageEnglish-
dc.publisherElsevier Scientific Publishers-
dc.relation.isPartOfLUNG CANCER-
dc.relation.isPartOfLUNG CANCER-
dc.subject.MESHAcrylamides* / administration & dosage-
dc.subject.MESHAcrylamides* / therapeutic use-
dc.subject.MESHAdult-
dc.subject.MESHAged-
dc.subject.MESHAged, 80 and over-
dc.subject.MESHAniline Compounds* / administration & dosage-
dc.subject.MESHAniline Compounds* / therapeutic use-
dc.subject.MESHAntineoplastic Combined Chemotherapy Protocols* / therapeutic use-
dc.subject.MESHAsian People / genetics-
dc.subject.MESHCarcinoma, Non-Small-Cell Lung* / drug therapy-
dc.subject.MESHCarcinoma, Non-Small-Cell Lung* / genetics-
dc.subject.MESHCarcinoma, Non-Small-Cell Lung* / mortality-
dc.subject.MESHCarcinoma, Non-Small-Cell Lung* / pathology-
dc.subject.MESHErbB Receptors / genetics-
dc.subject.MESHFemale-
dc.subject.MESHHumans-
dc.subject.MESHIndoles-
dc.subject.MESHLung Neoplasms* / drug therapy-
dc.subject.MESHLung Neoplasms* / genetics-
dc.subject.MESHLung Neoplasms* / mortality-
dc.subject.MESHLung Neoplasms* / pathology-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHMutation*-
dc.subject.MESHPyrimidines-
dc.subject.MESHTreatment Outcome-
dc.titleOverall survival for amivantamab plus lazertinib versus osimertinib as first-line treatment in Asian participants with EGFR-mutant advanced NSCLC: A MARIPOSA subset analysis-
dc.typeArticle-
dc.contributor.googleauthorHayashi, Hidetoshi-
dc.contributor.googleauthorCho, Byoung Chul-
dc.contributor.googleauthorKim, Yu Jung-
dc.contributor.googleauthorLee, Se-Hoon-
dc.contributor.googleauthorDanchaivijitr, Pongwut-
dc.contributor.googleauthorAlip, Adlinda-
dc.contributor.googleauthorXiong, Hailin-
dc.contributor.googleauthorHow, Soon-Hin-
dc.contributor.googleauthorChang, Gee-Chen-
dc.contributor.googleauthorYang, James Chih-Hsin-
dc.contributor.googleauthorYamanaka, Yuta-
dc.contributor.googleauthorSendur, Mehmet Ali Nahit-
dc.contributor.googleauthorPrabhash, Kumar-
dc.contributor.googleauthorAzuma, Koichi-
dc.contributor.googleauthorAkawung, Alianu-
dc.contributor.googleauthorFennema, Elizabeth-
dc.contributor.googleauthorTang, Xiaodan-
dc.contributor.googleauthorShah, Sujay-
dc.contributor.googleauthorSethi, Seema-
dc.contributor.googleauthorLu, Shun-
dc.identifier.doi10.1016/j.lungcan.2026.109305-
dc.relation.journalcodeJ02174-
dc.identifier.eissn1872-8332-
dc.identifier.pmid41689889-
dc.subject.keywordAsian-
dc.subject.keywordAmivantamab plus lazertinib-
dc.subject.keywordOverall survival-
dc.subject.keywordEGFR-mutated NSCLC-
dc.subject.keywordEGFR TKI-
dc.contributor.affiliatedAuthorCho, Byoung Chul-
dc.identifier.scopusid2-s2.0-105030134618-
dc.identifier.wosid001694682300001-
dc.citation.volume214-
dc.identifier.bibliographicCitationLUNG CANCER, Vol.214, 2026-04-
dc.identifier.rimsid92077-
dc.type.rimsART-
dc.description.journalClass1-
dc.description.journalClass1-
dc.subject.keywordAuthorAsian-
dc.subject.keywordAuthorAmivantamab plus lazertinib-
dc.subject.keywordAuthorOverall survival-
dc.subject.keywordAuthorEGFR-mutated NSCLC-
dc.subject.keywordAuthorEGFR TKI-
dc.subject.keywordPlusCELL LUNG-CANCER-
dc.subject.keywordPlusBRAIN METASTASES-
dc.subject.keywordPlusMUTATION-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalWebOfScienceCategoryOncology-
dc.relation.journalWebOfScienceCategoryRespiratory System-
dc.relation.journalResearchAreaOncology-
dc.relation.journalResearchAreaRespiratory System-
dc.identifier.articleno109305-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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