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Overall Survival with Amivantamab-Lazertinib in EGFR-Mutated Advanced NSCLC

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dc.contributor.authorYang, James Chih-Hsin-
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.authorLee, Se-Hoon-
dc.contributor.authorOstapenko, Yurii-
dc.contributor.authorDanchaivijitr, Pongwut-
dc.contributor.authorLiu, Baogang-
dc.contributor.authorAlip, Adlinda-
dc.contributor.authorKorbenfeld, Ernesto-
dc.contributor.authorMourao Dias, Josiane-
dc.contributor.authorBesse, Benjamin-
dc.contributor.authorPassaro, Antonio-
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.authorYoshioka, Hiroshige-
dc.contributor.authorThomas, Michael-
dc.contributor.authorNguyen, Danny-
dc.contributor.authorOu, Sai-Hong Ignatius-
dc.contributor.authorMukhedkar, Sanjay-
dc.contributor.authorPrabhash, Kumar-
dc.contributor.authorD'Arcangelo, Manolo-
dc.contributor.authorAlatorre-Alexander, Jorge-
dc.contributor.authorVazquez Limon, Juan Carlos-
dc.contributor.authorAlves, Sara-
dc.contributor.authorStroyakovskiy, Daniil-
dc.contributor.authorPeregudova, Marina-
dc.contributor.authorSendur, Mehmet Ali Nahit-
dc.contributor.authorYazici, Ozan-
dc.contributor.authorCalifano, Raffaele-
dc.contributor.authorGutierrez Calderon, Vanesa-
dc.contributor.authorde Marinis, Filippo-
dc.contributor.authorKim, Sang-We-
dc.contributor.authorGadgeel, Shirish M.-
dc.contributor.authorOwen, Scott-
dc.contributor.authorXie, John-
dc.contributor.authorSun, Tao-
dc.contributor.authorMehta, Jaydeep-
dc.contributor.authorVenkatasubramanian, Raja-
dc.contributor.authorEnnis, Mariah-
dc.contributor.authorFennema, Elizabeth-
dc.contributor.authorDaksh, Mahesh-
dc.contributor.authorRoshak, Amy-
dc.contributor.authorMan, Julie-
dc.contributor.authorKnoblauch, Roland E.-
dc.contributor.authorBauml, Joshua M.-
dc.contributor.authorBaig, Mahadi-
dc.contributor.authorShah, Sujay-
dc.contributor.authorSethi, Seema-
dc.contributor.authorCho, Byoung Chul-
dc.date.accessioned2025-11-03T00:39:25Z-
dc.date.available2025-11-03T00:39:25Z-
dc.date.created2025-10-29-
dc.date.issued2025-10-
dc.identifier.issn0028-4793-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/208083-
dc.description.abstractBackground Previous results from this phase 3 trial showed that progression-free survival among participants with previously untreated EGFR (epidermal growth factor receptor)-mutated advanced non-small-cell lung cancer (NSCLC) was significantly improved with amivantamab-lazertinib as compared with osimertinib. Results of the protocol-specified final overall survival analysis in this trial have not been reported.Methods We randomly assigned, in a 2:2:1 ratio, participants with previously untreated EGFR-mutated (exon 19 deletion or L858R substitution), locally advanced or metastatic NSCLC to receive amivantamab-lazertinib, osimertinib, or lazertinib. Overall survival (assessed in an analysis of the time from randomization to death from any cause) in the amivantamab-lazertinib group as compared with the osimertinib group was a key secondary end point. Additional end points included safety.Results A total of 429 participants each were assigned to receive amivantamab-lazertinib or osimertinib. Over a median follow-up of 37.8 months, amivantamab-lazertinib led to significantly longer overall survival than osimertinib (hazard ratio for death, 0.75; 95% confidence interval, 0.61 to 0.92; P=0.005); 3-year overall survival was 60% and 51%, respectively. At the clinical cutoff date, 38% of participants in the amivantamab-lazertinib group and 28% in the osimertinib group were still receiving the assigned treatment. Adverse events of grade 3 or higher were more common with amivantamab-lazertinib (in 80% of participants) than with osimertinib (in 52%), particularly skin-related events, venous thromboembolism, and infusion-related events; these findings were consistent with the established safety profile of each treatment. No new safety signals were observed with additional follow-up.Conclusions Amivantamab-lazertinib led to significantly longer overall survival among participants with previously untreated EGFR-mutated advanced NSCLC than osimertinib but was associated with an increased risk of adverse events of grade 3 or higher. (Funded by Janssen Research and Development; MARIPOSA ClinicalTrials.gov number, NCT04487080.) In advanced non-small-cell lung cancer with EGFR mutations, amivantamab-lazertinib led to longer overall survival than osimertinib but was associated with an increased risk of adverse events of grade 3 or higher.-
dc.languageEnglish-
dc.publisherMassachusetts Medical Society-
dc.relation.isPartOfNEW ENGLAND JOURNAL OF MEDICINE-
dc.relation.isPartOfNEW ENGLAND JOURNAL OF MEDICINE-
dc.subject.MESHAcrylamides* / adverse effects-
dc.subject.MESHAcrylamides* / therapeutic use-
dc.subject.MESHAdult-
dc.subject.MESHAged-
dc.subject.MESHAniline Compounds* / adverse effects-
dc.subject.MESHAniline Compounds* / therapeutic use-
dc.subject.MESHAntibodies, Bispecific-
dc.subject.MESHAntineoplastic Combined Chemotherapy Protocols* / adverse effects-
dc.subject.MESHAntineoplastic Combined Chemotherapy Protocols* / therapeutic use-
dc.subject.MESHCarbazoles* / adverse effects-
dc.subject.MESHCarbazoles* / 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* / mortality-
dc.subject.MESHErbB Receptors / antagonists & inhibitors-
dc.subject.MESHErbB Receptors / genetics-
dc.subject.MESHFemale-
dc.subject.MESHHumans-
dc.subject.MESHIndoles-
dc.subject.MESHKaplan-Meier Estimate-
dc.subject.MESHLung Neoplasms* / drug therapy-
dc.subject.MESHLung Neoplasms* / genetics-
dc.subject.MESHLung Neoplasms* / mortality-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHMutation-
dc.subject.MESHProtein Kinase Inhibitors* / adverse effects-
dc.subject.MESHProtein Kinase Inhibitors* / therapeutic use-
dc.subject.MESHPyrimidines-
dc.titleOverall Survival with Amivantamab-Lazertinib in EGFR-Mutated Advanced NSCLC-
dc.typeArticle-
dc.contributor.googleauthorYang, James Chih-Hsin-
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.googleauthorLee, Se-Hoon-
dc.contributor.googleauthorOstapenko, Yurii-
dc.contributor.googleauthorDanchaivijitr, Pongwut-
dc.contributor.googleauthorLiu, Baogang-
dc.contributor.googleauthorAlip, Adlinda-
dc.contributor.googleauthorKorbenfeld, Ernesto-
dc.contributor.googleauthorMourao Dias, Josiane-
dc.contributor.googleauthorBesse, Benjamin-
dc.contributor.googleauthorPassaro, Antonio-
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.googleauthorYoshioka, Hiroshige-
dc.contributor.googleauthorThomas, Michael-
dc.contributor.googleauthorNguyen, Danny-
dc.contributor.googleauthorOu, Sai-Hong Ignatius-
dc.contributor.googleauthorMukhedkar, Sanjay-
dc.contributor.googleauthorPrabhash, Kumar-
dc.contributor.googleauthorD'Arcangelo, Manolo-
dc.contributor.googleauthorAlatorre-Alexander, Jorge-
dc.contributor.googleauthorVazquez Limon, Juan Carlos-
dc.contributor.googleauthorAlves, Sara-
dc.contributor.googleauthorStroyakovskiy, Daniil-
dc.contributor.googleauthorPeregudova, Marina-
dc.contributor.googleauthorSendur, Mehmet Ali Nahit-
dc.contributor.googleauthorYazici, Ozan-
dc.contributor.googleauthorCalifano, Raffaele-
dc.contributor.googleauthorGutierrez Calderon, Vanesa-
dc.contributor.googleauthorde Marinis, Filippo-
dc.contributor.googleauthorKim, Sang-We-
dc.contributor.googleauthorGadgeel, Shirish M.-
dc.contributor.googleauthorOwen, Scott-
dc.contributor.googleauthorXie, John-
dc.contributor.googleauthorSun, Tao-
dc.contributor.googleauthorMehta, Jaydeep-
dc.contributor.googleauthorVenkatasubramanian, Raja-
dc.contributor.googleauthorEnnis, Mariah-
dc.contributor.googleauthorFennema, Elizabeth-
dc.contributor.googleauthorDaksh, Mahesh-
dc.contributor.googleauthorRoshak, Amy-
dc.contributor.googleauthorMan, Julie-
dc.contributor.googleauthorKnoblauch, Roland E.-
dc.contributor.googleauthorBauml, Joshua M.-
dc.contributor.googleauthorBaig, Mahadi-
dc.contributor.googleauthorShah, Sujay-
dc.contributor.googleauthorSethi, Seema-
dc.contributor.googleauthorCho, Byoung Chul-
dc.identifier.doi10.1056/NEJMoa2503001-
dc.relation.journalcodeJ02371-
dc.identifier.eissn1533-4406-
dc.identifier.pmid40923797-
dc.identifier.urlhttps://www.nejm.org/doi/10.1056/NEJMoa2503001-
dc.contributor.affiliatedAuthorCho, Byoung Chul-
dc.identifier.wosid001564915100001-
dc.citation.volume393-
dc.citation.number17-
dc.citation.startPage1681-
dc.citation.endPage1693-
dc.identifier.bibliographicCitationNEW ENGLAND JOURNAL OF MEDICINE, Vol.393(17) : 1681-1693, 2025-10-
dc.identifier.rimsid89974-
dc.type.rimsART-
dc.description.journalClass1-
dc.description.journalClass1-
dc.subject.keywordPlusCELL LUNG-CANCER-
dc.subject.keywordPlusBRAIN METASTASES-
dc.subject.keywordPlusPLUS LAZERTINIB-
dc.subject.keywordPlusOSIMERTINIB-
dc.type.docTypeArticle; Early Access-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalWebOfScienceCategoryMedicine, General & Internal-
dc.relation.journalResearchAreaGeneral & Internal Medicine-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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