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Real-World Analysis of the Efficacy of Rebiopsy and EGFR Mutation Test of Tissue and Plasma Samples in Drug-Resistant Non-Small Cell Lung Cancer

DC FieldValueLanguage
dc.contributor.author김지형-
dc.contributor.author김혜련-
dc.contributor.author안병철-
dc.contributor.author조병철-
dc.contributor.author허수진-
dc.contributor.author홍민희-
dc.date.accessioned2019-07-11T03:34:31Z-
dc.date.available2019-07-11T03:34:31Z-
dc.date.issued2019-
dc.identifier.issn0513-5796-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/170042-
dc.description.abstractPURPOSE: Standard treatment for cases of non-small cell lung cancer (NSCLC) exhibiting acquired drug resistance includes tumor rebiopsy, epidermal growth factor receptor (EGFR) mutation testing (e.g., for T790M mutations), and the subsequent administration of third-generation EGFR-tyrosine kinase inhibitors (EGFR-TKIs). However, rebiopsies are typically invasive, costly, and occasionally not feasible. Therefore, the present study aimed to assess rebiopsy procedures by analyzing real-world data collected by the ASTRIS study of patients with resistant NSCLC. MATERIALS AND METHODS: The present study used statistical models to evaluate data collected by the ASTRIS trial (NCT02474355) conducted at Yonsei Cancer Center, including the rebiopsy success rate, incidence of T790M mutations in collected tissue and plasma samples, and association of administered osimertinib treatment efficacy. RESULTS: In a total of 188 screened patients, 112 underwent rebiopsy. An adequate tumor specimen was obtained in 95 of these patients, the greatest majority of whom (43.8%) were subjected to bronchoscopy. T790M mutations were detected in 53.3% of successfully EGFR-tested rebiopsy samples. A total of 88 patients received osimertinib treatment, and the objective response rate and median progression-free survival time was 44.3% and 32.7 weeks, respectively, among the treated patients overall, but 57.8% and 45.0 weeks, and 35.2% and 20.4 weeks among patients who exhibited T790M-positive tissue (n=45) and plasma (n=54) samples, respectively. CONCLUSION: Approximately 60% of patients in the analyzed real-world cohort were eligible for tissue rebiopsy upon NSCLC progression. Osimertinib activity was higher in patients in whom T790M mutations were detected in tissues rather than in plasma samples.-
dc.description.statementOfResponsibilityopen-
dc.languageEnglish-
dc.publisherYonsei University-
dc.relation.isPartOfYONSEI MEDICAL JOURNAL-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rightshttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.titleReal-World Analysis of the Efficacy of Rebiopsy and EGFR Mutation Test of Tissue and Plasma Samples in Drug-Resistant Non-Small Cell Lung Cancer-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.googleauthorMin Hee Hong-
dc.contributor.googleauthorHye Ryun Kim-
dc.contributor.googleauthorBeung-Chul Ahn-
dc.contributor.googleauthorSu Jin Heo-
dc.contributor.googleauthorJee Hung Kim-
dc.contributor.googleauthorByoung Chul Cho-
dc.identifier.doi10.3349/ymj.2019.60.6.525-
dc.contributor.localIdA00999-
dc.contributor.localIdA01166-
dc.contributor.localIdA01166-
dc.contributor.localIdA05556-
dc.contributor.localIdA05556-
dc.contributor.localIdA03822-
dc.contributor.localIdA03822-
dc.contributor.localIdA04355-
dc.contributor.localIdA04355-
dc.contributor.localIdA04393-
dc.contributor.localIdA04393-
dc.relation.journalcodeJ02813-
dc.identifier.eissn1976-2437-
dc.identifier.pmid31124335-
dc.subject.keywordEGFR T790M-
dc.subject.keywordNon-small cell lung cancer-
dc.subject.keywordliquid biopsy-
dc.subject.keywordosimertinib-
dc.subject.keywordrebiopsy-
dc.contributor.alternativeNameKim, Jee Hung-
dc.contributor.affiliatedAuthor김지형-
dc.contributor.affiliatedAuthor김혜련-
dc.contributor.affiliatedAuthor김혜련-
dc.contributor.affiliatedAuthor안병철-
dc.contributor.affiliatedAuthor안병철-
dc.contributor.affiliatedAuthor조병철-
dc.contributor.affiliatedAuthor조병철-
dc.contributor.affiliatedAuthor허수진-
dc.contributor.affiliatedAuthor허수진-
dc.contributor.affiliatedAuthor홍민희-
dc.contributor.affiliatedAuthor홍민희-
dc.citation.volume60-
dc.citation.number6-
dc.citation.startPage525-
dc.citation.endPage534-
dc.identifier.bibliographicCitationYONSEI MEDICAL JOURNAL, Vol.60(6) : 525-534, 2019-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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