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Real-World Study of Osimertinib in Korean Patients with Epidermal Growth Factor Receptor T790M Mutation-Positive Non-Small Cell Lung Cancer

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dc.contributor.author김은영-
dc.contributor.author이상훈-
dc.date.accessioned2023-03-22T02:39:07Z-
dc.date.available2023-03-22T02:39:07Z-
dc.date.issued2023-01-
dc.identifier.issn1598-2998-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/193643-
dc.description.abstractPurpose: Although osimertinib is the standard-of-care treatment of epidermal growth factor receptor (EGFR) T790M mutation-positive non-small cell lung cancer, real-world evidence on the efficacy of osimertinib is not enough to reflect the complexity of the entire course of treatment. Herein, we report on the use of osimertinib in patients with EGFR T790M mutation-positive non-small cell lung cancer who had previously received EGFR tyrosine kinase inhibitor (TKI) treatment in Korea. Materials and methods: Patients with confirmed EGFR T790M after disease progression of prior EGFR-TKI were enrolled and administered osimertinib 80 mg daily. The primary effectiveness outcome was progression-free survival, with time-to-treatment discontinuation, treatment and adverse effects leading to treatment discontinuation, and overall survival being the secondary endpoints. Results: A total of 558 individuals were enrolled, and 55.2% had investigator-assessed responses. The median progression-free survival was 14.2 months (95% confidence interval [CI], 13.0 to 16.4), and the median time-to-treatment discontinuation was 15.0 months (95% CI, 14.1 to 15.9). The median overall survival was 36.7 months (95% CI, 30.9 to not reached). The benefit with osimertinib was consistent regardless of the age, sex, smoking history, and primary EGFR mutation subtype. However, hepatic metastases at the time of diagnosis, the presence of plasma EGFR T790M, and the shorter duration of prior EGFR-TKI treatment were poor predictors of osimertinib treatment. Ten patients (1.8%), including three with pneumonitis, had to discontinue osimertinib due to severe adverse effects. Conclusion: Osimertinib demonstrated its clinical effectiveness and survival benefit for EGFR T790M mutation-positive in Korean patients with no new safety signals.-
dc.description.statementOfResponsibilityopen-
dc.languageEnglish, Korean-
dc.publisherOfficial journal of Korean Cancer Association-
dc.relation.isPartOfCANCER RESEARCH AND TREATMENT-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.subject.MESHAntineoplastic Agents* / adverse effects-
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.MESHErbB Receptors / genetics-
dc.subject.MESHHumans-
dc.subject.MESHLung Neoplasms* / drug therapy-
dc.subject.MESHLung Neoplasms* / genetics-
dc.subject.MESHLung Neoplasms* / pathology-
dc.subject.MESHMutation-
dc.subject.MESHProtein Kinase Inhibitors / adverse effects-
dc.subject.MESHRepublic of Korea-
dc.titleReal-World Study of Osimertinib in Korean Patients with Epidermal Growth Factor Receptor T790M Mutation-Positive Non-Small Cell Lung Cancer-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.googleauthorJang Ho Lee -
dc.contributor.googleauthor Eun Young Kim-
dc.contributor.googleauthor Cheol-Kyu Park-
dc.contributor.googleauthor Shin Yup Lee-
dc.contributor.googleauthor Min Ki Lee-
dc.contributor.googleauthor Seong-Hoon Yoon-
dc.contributor.googleauthor Jeong Eun Lee-
dc.contributor.googleauthor Sang Hoon Lee-
dc.contributor.googleauthor Seung Joon Kim-
dc.contributor.googleauthor Sung Yong Lee-
dc.contributor.googleauthor Jun Hyeok Lim-
dc.contributor.googleauthor Tae-Won Jang-
dc.contributor.googleauthor Seung Hun Jang-
dc.contributor.googleauthor Kye Young Lee-
dc.contributor.googleauthor Seung Hyeun Lee-
dc.contributor.googleauthor Sei Hoon Yang -
dc.contributor.googleauthor Dong Won Park-
dc.contributor.googleauthor Chan Kwon Park-
dc.contributor.googleauthor Hye Seon Kang -
dc.contributor.googleauthor Chang Dong Yeo-
dc.contributor.googleauthor Chang-Min Choi-
dc.contributor.googleauthor Jae Cheol Lee-
dc.identifier.doi10.4143/crt.2022.381-
dc.contributor.localIdA00811-
dc.contributor.localIdA02836-
dc.relation.journalcodeJ00453-
dc.identifier.eissn2005-9256-
dc.identifier.pmid36049499-
dc.subject.keywordEGFR T790M-
dc.subject.keywordNon–small cell lung cancer-
dc.subject.keywordOsimertinib-
dc.subject.keywordReal-world efficacy-
dc.contributor.alternativeNameKim, Eun Young-
dc.contributor.affiliatedAuthor김은영-
dc.contributor.affiliatedAuthor이상훈-
dc.citation.volume55-
dc.citation.number1-
dc.citation.startPage112-
dc.citation.endPage122-
dc.identifier.bibliographicCitationCANCER RESEARCH AND TREATMENT, Vol.55(1) : 112-122, 2023-01-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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