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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

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dc.contributor.author조병철-
dc.date.accessioned2025-09-02T08:16:38Z-
dc.date.available2025-09-02T08:16:38Z-
dc.date.issued2025-06-
dc.identifier.issn0169-5002-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/207240-
dc.description.abstractIntroduction: 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.description.statementOfResponsibilityopen-
dc.languageEnglish-
dc.publisherElsevier Scientific Publishers-
dc.relation.isPartOfLUNG CANCER-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.subject.MESHAcrylamides* / administration & dosage-
dc.subject.MESHAcrylamides* / therapeutic use-
dc.subject.MESHAdult-
dc.subject.MESHAged-
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.titleAmivantamab plus lazertinib versus osimertinib as first-line treatment in EGFR-mutated advanced non-small cell lung cancer: MARIPOSA Asian subset-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.googleauthorByoung Chul Cho-
dc.contributor.googleauthorHidetoshi Hayashi-
dc.contributor.googleauthorJong-Seok Lee-
dc.contributor.googleauthorSe-Hoon Lee-
dc.contributor.googleauthorPongwut Danchaivijitr-
dc.contributor.googleauthorYing Cheng-
dc.contributor.googleauthorBaogang Liu-
dc.contributor.googleauthorAdlinda Alip-
dc.contributor.googleauthorHailin Xiong-
dc.contributor.googleauthorSoon Hin How-
dc.contributor.googleauthorGee-Chen Chang-
dc.contributor.googleauthorJames Chih-Hsin Yang-
dc.contributor.googleauthorHiroshige Yoshioka-
dc.contributor.googleauthorMehmet Ali Nahit Şendur-
dc.contributor.googleauthorKumar Prabhash-
dc.contributor.googleauthorKoichi Azuma-
dc.contributor.googleauthorYun-Gyoo Lee-
dc.contributor.googleauthorChien-Chung Lin-
dc.contributor.googleauthorShingo Matsumoto-
dc.contributor.googleauthorPatrapim Sunpaweravong-
dc.contributor.googleauthorYichuan Xia-
dc.contributor.googleauthorMelissa Martinez-
dc.contributor.googleauthorJoshua M Bauml-
dc.contributor.googleauthorSeema Sethi-
dc.contributor.googleauthorShun Lu-
dc.identifier.doi10.1016/j.lungcan.2025.108496-
dc.contributor.localIdA03822-
dc.relation.journalcodeJ02174-
dc.identifier.eissn1872-8332-
dc.identifier.pmid40300278-
dc.subject.keywordAmivantamab-
dc.subject.keywordAsian patient-
dc.subject.keywordEGFR TKI-
dc.subject.keywordEGFR-mutated NSCLC-
dc.contributor.alternativeNameCho, Byoung Chul-
dc.contributor.affiliatedAuthor조병철-
dc.citation.volume204-
dc.citation.startPage108496-
dc.identifier.bibliographicCitationLUNG CANCER, Vol.204 : 108496, 2025-06-
dc.identifier.rimsid88874-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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