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Characteristics and Clinical Outcomes of Non-small Cell Lung Cancer Patients in Korea With MET Exon 14 Skipping

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dc.contributor.authorHur, Joon Young-
dc.contributor.authorKu, Bo Mi-
dc.contributor.authorShim, Joon Ho-
dc.contributor.authorJung, Hyun Ae-
dc.contributor.authorSun, Jong-Mu-
dc.contributor.authorLee, Se-Hoon-
dc.contributor.authorAhn, Jin Seok-
dc.contributor.authorPark, Keunchil-
dc.contributor.authorAhn, Myung-Ju-
dc.date.accessioned2023-09-18T06:39:41Z-
dc.date.available2023-09-18T06:39:41Z-
dc.date.created2023-07-19-
dc.date.issued2020-05-
dc.identifier.issn0258-851X-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/190697-
dc.description.abstractBackground/Aim: MET exon 14 skipping occurs in 3-4% of patients with lung adenocarcinomas. In this study, we performed a comprehensive analysis of clinical data from Korean non-small cell lung cancer (NSCLC) patients with MET exon 14 skipping. Patients and Methods: Overall, 1,020 patients diagnosed with NSCLC between January 2015 and July 2017 were analyzed by next-generation sequencing. Results: MET exon 14 skipping was identified in 20 NSCLC patients (1.9%). The median age was 69 years (range=39-86 years), 60.0% were male, and most (55.0%) were ever-smokers. For first-line chemotherapy, the median overall survival was 9.5 months and progression free survival was 4.0 months, respectively. Twelve patients received pemetrexed-based chemotherapy and the overall response rate was 33.3% (4/12). Among four crizotinib-treated patients, one continued therapy for 8 months with the best response being disease stability. Conclusion: Given the poor clinical outcome and response to therapy for NSCLC, and the availability of promising anti-tumor MET inhibitors, screening for the MET exon 14 skip mutation should be incorporated into clinical practice.-
dc.language영어-
dc.language.isoen-
dc.publisherINT INST ANTICANCER RESEARCH-
dc.titleCharacteristics and Clinical Outcomes of Non-small Cell Lung Cancer Patients in Korea With MET Exon 14 Skipping-
dc.typeArticle-
dc.contributor.affiliatedAuthorHur, Joon Young-
dc.identifier.doi10.21873/invivo.11920-
dc.identifier.scopusid2-s2.0-85084898801-
dc.identifier.wosid000530682800058-
dc.identifier.bibliographicCitationIN VIVO, v.34, no.3, pp.1399 - 1406-
dc.relation.isPartOfIN VIVO-
dc.citation.titleIN VIVO-
dc.citation.volume34-
dc.citation.number3-
dc.citation.startPage1399-
dc.citation.endPage1406-
dc.type.rimsART-
dc.type.docType정기학술지(Article(Perspective Article포함))-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaResearch & Experimental Medicine-
dc.relation.journalWebOfScienceCategoryMedicine, Research & Experimental-
dc.subject.keywordAuthorCrizotinib-
dc.subject.keywordAuthorMET Exon 14 Skipping-
dc.subject.keywordAuthorNSCLC-
dc.identifier.urlhttps://iv.iiarjournals.org/content/34/3/1399-
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