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Central Nervous System Outcomes of Lazertinib Treatment in EGFR-Mutated Advanced NSCLC: Pooled Analysis From LASER201 and LASER301

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dc.contributor.authorYang, James CH-
dc.contributor.authorAhn, Myung-Ju-
dc.contributor.authorKim, Joo-Hang-
dc.contributor.authorLee, Yun-Gyoo-
dc.contributor.authorHan, Ji-Youn-
dc.contributor.authorLee, Ki Hyeong-
dc.contributor.authorZimina, Anastasia-
dc.contributor.authorKim, Dong-Wan-
dc.contributor.authorLee, Kyung-Hee-
dc.contributor.authorLee, Sung Sook-
dc.contributor.authorLim, Chun Sen-
dc.contributor.authorLim, Yueh Ni-
dc.contributor.authorMin, Young Joo-
dc.contributor.authorOrlov, Sergey-
dc.contributor.authorLee, Youngjoo-
dc.contributor.authorKim, YuKyung-
dc.contributor.authorKwon, Mi-Jung-
dc.contributor.authorLee, Hana-
dc.contributor.authorCho, Hyeonchae-
dc.contributor.authorCho, Byoung Chul-
dc.date.accessioned2026-03-25T02:16:53Z-
dc.date.available2026-03-25T02:16:53Z-
dc.date.created2026-03-25-
dc.date.issued2025-12-
dc.identifier.issn1525-7304-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/211439-
dc.description.abstractBackground Lazertinib, a brain-penetrant, third-generation epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (TKI), significantly improved efficacy in patients with treatment-naïve, EGFR -mutated advanced non-small cell lung cancer (NSCLC) in the clinical trials, LASER201 and LASER301. This analysis evaluated the efficacy and safety of lazertinib in patients with EGFR -mutated NSCLC and CNS metastases using pooled data from LASER201 and LASER301. Patients and Methods Patients with treatment-naïve, EGFR -mutated advanced NSCLC and stable CNS metastases who were treated with lazertinib in a cohort of LASER201 and LASER301 were included. Intracranial progression-free survival (iPFS), intracranial objective response rate (iORR), intracranial disease control rate (iDCR), intracranial duration of response (iDoR), and treatment-emergent adverse events (TEAEs) were assessed. Results A total of 64 patients were included in the intracranial full analysis set (iFAS); 24 patients had at least 1 measurable CNS lesion at baseline. The median iPFS was 27.7 months (95% CI: 15.7-32.8) in the iFAS population. For patients with at least 1 measurable CNS lesion at baseline, iORR was 92% and iDCR was 96%. The median iDoR was 26.5 months (95% CI: 8.3-30.1). TEAEs were reported in 98% of patients in the iFAS population, with grade ≥3 TEAEs occurring in 55% of patients. The most common TEAEs were paresthesia (47%), rash (41%), and pruritus (36%). Conclusion In this pooled analysis of LASER201 and LASER301, lazertinib demonstrated a clinically meaningful treatment benefit and consistent safety profile in patients with EGFR -mutated advanced NSCLC and CNS metastases. © 2025 The Authors.-
dc.language영어-
dc.publisherElsevier Inc.-
dc.relation.isPartOfClinical Lung Cancer-
dc.subject.MESHAdult-
dc.subject.MESHAged-
dc.subject.MESHAged, 80 and over-
dc.subject.MESHBrain Neoplasms* / drug therapy-
dc.subject.MESHBrain Neoplasms* / secondary-
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.MESHCentral Nervous System Neoplasms* / drug therapy-
dc.subject.MESHCentral Nervous System Neoplasms* / secondary-
dc.subject.MESHErbB Receptors / genetics-
dc.subject.MESHFemale-
dc.subject.MESHHumans-
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.MESHPrognosis-
dc.subject.MESHProtein Kinase Inhibitors* / therapeutic use-
dc.subject.MESHTreatment Outcome-
dc.titleCentral Nervous System Outcomes of Lazertinib Treatment in EGFR-Mutated Advanced NSCLC: Pooled Analysis From LASER201 and LASER301-
dc.typeArticle-
dc.contributor.googleauthorYang, James CH-
dc.contributor.googleauthorAhn, Myung-Ju-
dc.contributor.googleauthorKim, Joo-Hang-
dc.contributor.googleauthorLee, Yun-Gyoo-
dc.contributor.googleauthorHan, Ji-Youn-
dc.contributor.googleauthorLee, Ki Hyeong-
dc.contributor.googleauthorZimina, Anastasia-
dc.contributor.googleauthorKim, Dong-Wan-
dc.contributor.googleauthorLee, Kyung-Hee-
dc.contributor.googleauthorLee, Sung Sook-
dc.contributor.googleauthorLim, Chun Sen-
dc.contributor.googleauthorLim, Yueh Ni-
dc.contributor.googleauthorMin, Young Joo-
dc.contributor.googleauthorOrlov, Sergey-
dc.contributor.googleauthorLee, Youngjoo-
dc.contributor.googleauthorKim, YuKyung-
dc.contributor.googleauthorKwon, Mi-Jung-
dc.contributor.googleauthorLee, Hana-
dc.contributor.googleauthorCho, Hyeonchae-
dc.contributor.googleauthorCho, Byoung Chul-
dc.identifier.doi10.1016/j.cllc.2025.08.007-
dc.identifier.pmid41067998-
dc.subject.keywordBrain metastases-
dc.subject.keywordCNS-
dc.subject.keywordLazertinib-
dc.subject.keywordNSCLC-
dc.subject.keywordTKI-
dc.contributor.affiliatedAuthorCho, Byoung Chul-
dc.identifier.scopusid2-s2.0-105018064137-
dc.citation.volume26-
dc.citation.number8-
dc.citation.startPage642-
dc.citation.endPage650.e6-
dc.identifier.bibliographicCitationClinical Lung Cancer, Vol.26(8) : 642-650.e6, 2025-12-
dc.identifier.rimsid92262-
dc.type.rimsART-
dc.description.journalClass1-
dc.description.journalClass1-
dc.subject.keywordAuthorBrain metastases-
dc.subject.keywordAuthorCNS-
dc.subject.keywordAuthorLazertinib-
dc.subject.keywordAuthorNSCLC-
dc.subject.keywordAuthorTKI-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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