Lazertinib Versus Gefitinib Tyrosine Kinase Inhibitors in Treatment-Naíve Patients With EGFR-Mutated Advanced NSCLC: Analysis of the Asian Subpopulation in LASER301

dc.contributor.authorReungwetwattana T.
dc.contributor.authorCho B.C.
dc.contributor.authorLee K.H.
dc.contributor.authorPang Y.K.
dc.contributor.authorFong C.H.
dc.contributor.authorKang J.H.
dc.contributor.authorLee Y.G.
dc.contributor.authorLim C.S.
dc.contributor.authorDanchaivijitr P.
dc.contributor.authorLim Y.N.
dc.contributor.authorLee Y.
dc.contributor.authorHow S.H.
dc.contributor.authorGeater S.
dc.contributor.authorLee S.S.
dc.contributor.authorMin Y.J.
dc.contributor.authorKim J.H.
dc.contributor.authorLee J.S.
dc.contributor.authorLee G.W.
dc.contributor.authorSoo R.A.
dc.contributor.authorLee S.Y.
dc.contributor.authorChoi S.Y.
dc.contributor.authorAhn M.J.
dc.contributor.otherMahidol University
dc.date.accessioned2023-10-04T18:01:59Z
dc.date.available2023-10-04T18:01:59Z
dc.date.issued2023-10-01
dc.description.abstractIntroduction: Lazertinib is a third-generation central nervous system–penetrant tyrosine kinase inhibitor targeting mutant EGFR in NSCLC. Lazertinib exhibited improved efficacy versus gefitinib in the LASER301 study; this subset analysis compared lazertinib with gefitinib among Asian patients. Methods: The phase 3 LASER301 study evaluated lazertinib efficacy and safety in treatment-naive patients with EGFR-mutated (exon 19 deletion or L858R) locally advanced or metastatic NSCLC. Patients were randomized one-to-one and received either lazertinib or gefitinib. The primary end point was investigator-assessed progression-free survival using Response Evaluation Criteria in Solid Tumors version 1.1. Secondary end points included overall survival, objective response rate, duration of response, and safety. Results: Between February 13, 2020, and July 29, 2022, among 258 patients of Asian descent, the median progression-free survival was significantly longer with lazertinib than gefitinib (20.6 versus 9.7 mo; hazard ratio: 0.46; 95% confidence interval [CI]: 0.34–0.63, p < 0.001), and the benefit was consistent across predefined subgroups (exon 19 deletion, L858R, baseline central nervous system metastases). Objective response rate and disease control rates were similar between treatment groups. The median duration of response was 19.4 months (95% CI: 16.6–24.9) versus 9.6 months (95% CI: 6.9–12.4) in the lazertinib versus gefitinib group. Adverse event rates in Asian patients were comparable with the overall LASER301 population. Adverse events leading to discontinuation in the lazertinib and gefitinib groups were 13% and 12%, respectively. Conclusions: In LASER301, efficacy and safety results in Asian patients were consistent with the overall population. Lazertinib exhibited better efficacy than gefitinib in Asian patients with a tolerable safety profile.
dc.identifier.citationJournal of Thoracic Oncology Vol.18 No.10 (2023) , 1351-1361
dc.identifier.doi10.1016/j.jtho.2023.06.016
dc.identifier.eissn15561380
dc.identifier.issn15560864
dc.identifier.pmid37702629
dc.identifier.scopus2-s2.0-85171987980
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/90299
dc.rights.holderSCOPUS
dc.subjectMedicine
dc.titleLazertinib Versus Gefitinib Tyrosine Kinase Inhibitors in Treatment-Naíve Patients With EGFR-Mutated Advanced NSCLC: Analysis of the Asian Subpopulation in LASER301
dc.typeConference Paper
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85171987980&origin=inward
oaire.citation.endPage1361
oaire.citation.issue10
oaire.citation.startPage1351
oaire.citation.titleJournal of Thoracic Oncology
oaire.citation.volume18
oairecerif.author.affiliationThe Catholic University of Korea Seoul St. Mary's Hospital
oairecerif.author.affiliationUlsan University Hospital
oairecerif.author.affiliationSiriraj Hospital
oairecerif.author.affiliationYonsei Cancer Hospital
oairecerif.author.affiliationChungbuk National University Hospital
oairecerif.author.affiliationHospital Pulau Pinang
oairecerif.author.affiliationSeoul National University Bundang Hospital
oairecerif.author.affiliationHospital Umum Sarawak
oairecerif.author.affiliationYuhan Corporation
oairecerif.author.affiliationNational Cancer Center, Gyeonggi
oairecerif.author.affiliationInje University, College of Medicine
oairecerif.author.affiliationSamsung Medical Center, Sungkyunkwan university
oairecerif.author.affiliationSKKU School of Medicine
oairecerif.author.affiliationFaculty of Medicine Ramathibodi Hospital, Mahidol University
oairecerif.author.affiliationUniversity of Malaya Medical Centre
oairecerif.author.affiliationGyeongsang National University (GSNU), College of Medicine
oairecerif.author.affiliationPrince of Songkla University
oairecerif.author.affiliationCollege of Medicine, Pochon CHA University
oairecerif.author.affiliationNational University Cancer Institute
oairecerif.author.affiliationHospital Tengku Ampuan Afzan
oairecerif.author.affiliationHospital Sultan Ismail

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