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Lazertinib Versus Osimertinib in Previously Untreated EGFR-Mutant Advanced NSCLC: A Randomized, Double-Blind, Exploratory Analysis From MARIPOSA

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dc.contributor.authorLee, Se-Hoon-
dc.contributor.authorLu, Shun-
dc.contributor.authorHayashi, Hidetoshi-
dc.contributor.authorFelip, Enriqueta-
dc.contributor.authorSpira, Alexander I.-
dc.contributor.authorGirard, Nicolas-
dc.contributor.authorKim, Yu Jung-
dc.contributor.authorOstapenko, Yurii-
dc.contributor.authorDanchaivijitr, Pongwut-
dc.contributor.authorLiu, Baogang-
dc.contributor.authorAlip, Adlinda-
dc.contributor.authorKorbenfeld, Ernesto-
dc.contributor.authorDias, Josiane Mourao-
dc.contributor.authorLee, Ki Hyeong-
dc.contributor.authorXiong, Hailin-
dc.contributor.authorHow, Soon Hin-
dc.contributor.authorCheng, Ying-
dc.contributor.authorChang, Gee-Chen-
dc.contributor.authorYang, James Chih-Hsin-
dc.contributor.authorBesse, Benjamin-
dc.contributor.authorThomas, Michael-
dc.contributor.authorShah, Sujay-
dc.contributor.authorBaig, Mahadi-
dc.contributor.authorCurtin, Joshua C.-
dc.contributor.authorZhang, Jiarui-
dc.contributor.authorXie, John-
dc.contributor.authorSun, Tao-
dc.contributor.authorSethi, Seema-
dc.contributor.authorWang, Miao-
dc.contributor.authorFennema, Elizabeth-
dc.contributor.authorDaksh, Mahesh-
dc.contributor.authorEnnis, Mariah-
dc.contributor.authorBauml, Joshua M.-
dc.contributor.authorCho, Byoung Chul-
dc.date.accessioned2025-12-23T01:22:13Z-
dc.date.available2025-12-23T01:22:13Z-
dc.date.created2025-12-11-
dc.date.issued2025-11-
dc.identifier.issn1556-0864-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/209506-
dc.description.abstractIntroduction: Lazertinib is a central nervous system-penetrant, third-generation EGFR tyrosine kinase inhibitor (TKI) that was selected for combination with amivantamab due to its relatively low rates of wild-type EGFR toxicities. In the phase 3 MARIPOSA study, amivantamab plus lazertinib (amivantamab-lazertinib) significantly improved progression-free survival (PFS; p < 0.001) versus osimertinib in participants with treatment-naive EGFR-mutant advanced NSCLC. A lazertinib monotherapy arm was included to assess the contribution of components in the combination. This is the first randomized, double-blind comparison of two third-generation EGFR TKIs, lazertinib and osimertinib. Methods: In MARIPOSA, 1074 participants were randomized 2:2:1 to receive amivantamab-lazertinib (n = 429), osimertinib monotherapy (n = 429), or lazertinib mono-therapy (n = 216). This exploratory analysis compared the efficacy and safety of lazertinib and osimertinib Results: At a median follow-up of 22.0 months, median PFS was 18.5 months for lazertinib versus 16.6 months for osimertinib (hazard ratio = 0.98, 95% confidence interval: 0.79-1.22; p = 0.86). PFS results were comparable between arms among predefined subgroups. Among participants with measurable disease at baseline, objective response rate was 83% for lazertinib versus 85% for osimertinib, with a median duration of response among confirmed responders of 16.6 months versus 16.8 months, respectively. Median overall survival was not reached for both arms (hazard ratio = 1.00, 95% confidence interval: 0.73-1.38) at the interim analysis. Adverse events for both arms were mostly grades 1 to 2 and frequently related to EGFR inhibition. Lazertinib was associated with lower rates of QT interval prolongation versus osimertinib. Conclusions: Lazertinib demonstrated comparable efficacy and safety to osimertinib, including in predefined subgroups.-
dc.languageEnglish-
dc.publisherElsevier-
dc.relation.isPartOfJOURNAL OF THORACIC ONCOLOGY-
dc.relation.isPartOfJOURNAL OF THORACIC ONCOLOGY-
dc.subject.MESHAcrylamides* / pharmacology-
dc.subject.MESHAcrylamides* / therapeutic use-
dc.subject.MESHAdult-
dc.subject.MESHAged-
dc.subject.MESHAniline Compounds* / pharmacology-
dc.subject.MESHAniline Compounds* / therapeutic use-
dc.subject.MESHCarcinoma, Non-Small-Cell Lung* / drug therapy-
dc.subject.MESHCarcinoma, Non-Small-Cell Lung* / genetics-
dc.subject.MESHCarcinoma, Non-Small-Cell Lung* / pathology-
dc.subject.MESHDouble-Blind Method-
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* / pathology-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHMutation-
dc.subject.MESHProtein Kinase Inhibitors* / therapeutic use-
dc.subject.MESHPyrimidines-
dc.subject.MESHSurvival Rate-
dc.titleLazertinib Versus Osimertinib in Previously Untreated EGFR-Mutant Advanced NSCLC: A Randomized, Double-Blind, Exploratory Analysis From MARIPOSA-
dc.typeArticle-
dc.contributor.googleauthorLee, Se-Hoon-
dc.contributor.googleauthorLu, Shun-
dc.contributor.googleauthorHayashi, Hidetoshi-
dc.contributor.googleauthorFelip, Enriqueta-
dc.contributor.googleauthorSpira, Alexander I.-
dc.contributor.googleauthorGirard, Nicolas-
dc.contributor.googleauthorKim, Yu Jung-
dc.contributor.googleauthorOstapenko, Yurii-
dc.contributor.googleauthorDanchaivijitr, Pongwut-
dc.contributor.googleauthorLiu, Baogang-
dc.contributor.googleauthorAlip, Adlinda-
dc.contributor.googleauthorKorbenfeld, Ernesto-
dc.contributor.googleauthorDias, Josiane Mourao-
dc.contributor.googleauthorLee, Ki Hyeong-
dc.contributor.googleauthorXiong, Hailin-
dc.contributor.googleauthorHow, Soon Hin-
dc.contributor.googleauthorCheng, Ying-
dc.contributor.googleauthorChang, Gee-Chen-
dc.contributor.googleauthorYang, James Chih-Hsin-
dc.contributor.googleauthorBesse, Benjamin-
dc.contributor.googleauthorThomas, Michael-
dc.contributor.googleauthorShah, Sujay-
dc.contributor.googleauthorBaig, Mahadi-
dc.contributor.googleauthorCurtin, Joshua C.-
dc.contributor.googleauthorZhang, Jiarui-
dc.contributor.googleauthorXie, John-
dc.contributor.googleauthorSun, Tao-
dc.contributor.googleauthorSethi, Seema-
dc.contributor.googleauthorWang, Miao-
dc.contributor.googleauthorFennema, Elizabeth-
dc.contributor.googleauthorDaksh, Mahesh-
dc.contributor.googleauthorEnnis, Mariah-
dc.contributor.googleauthorBauml, Joshua M.-
dc.contributor.googleauthorCho, Byoung Chul-
dc.identifier.doi10.1016/j.jtho.2025.06.030-
dc.relation.journalcodeJ01909-
dc.identifier.eissn1556-1380-
dc.identifier.pmid40617394-
dc.subject.keywordEGFR-mutant NSCLC-
dc.subject.keywordFirst-line treatment-
dc.subject.keywordLaz-ertinib-
dc.subject.keywordOsimertinib-
dc.subject.keywordTyrosine kinase inhibitor-
dc.contributor.affiliatedAuthorCho, Byoung Chul-
dc.identifier.scopusid2-s2.0-105012856780-
dc.identifier.wosid001616611700012-
dc.citation.volume20-
dc.citation.number11-
dc.citation.startPage1655-
dc.citation.endPage1668-
dc.identifier.bibliographicCitationJOURNAL OF THORACIC ONCOLOGY, Vol.20(11) : 1655-1668, 2025-11-
dc.identifier.rimsid90341-
dc.type.rimsART-
dc.description.journalClass1-
dc.description.journalClass1-
dc.subject.keywordAuthorEGFR-mutant NSCLC-
dc.subject.keywordAuthorFirst-line treatment-
dc.subject.keywordAuthorLaz-ertinib-
dc.subject.keywordAuthorOsimertinib-
dc.subject.keywordAuthorTyrosine kinase inhibitor-
dc.subject.keywordPlus1ST-LINE OSIMERTINIB-
dc.subject.keywordPlusRESISTANCE-
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-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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