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Comprehensive analysis of the characteristics and treatment outcomes of patients with non-small cell lung cancer treated with anti-PD-1 therapy in real-world practice

DC Field Value Language
dc.contributor.author김혜련-
dc.contributor.author박성용-
dc.contributor.author심효섭-
dc.contributor.author안병철-
dc.contributor.author윤홍인-
dc.contributor.author이창영-
dc.contributor.author조병철-
dc.contributor.author표경호-
dc.contributor.author홍민희-
dc.date.accessioned2019-07-23T06:46:19Z-
dc.date.available2019-07-23T06:46:19Z-
dc.date.issued2019-
dc.identifier.issn0171-5216-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/170301-
dc.description.abstractPURPOSE: Immune checkpoint inhibitors (ICI) have shown marked responses in patients with non-small cell lung cancer (NSCLC) in clinical trials. However, because such trials comprise cohorts selected based on specific criteria, it is unclear if their results represent routine clinical practice. METHODS: We examined 155 patients with advanced NSCLC who were administered either nivolumab or pembrolizumab at Yonsei Cancer Center, Korea between March 2014 and January 2019. Patient characteristics, EGFR/ALK mutation status, metastatic locations, response to ICIs, and adverse events were retrospectively analyzed. RESULTS: The median age was 64 years and 72.9% of patients were male; former or current smokers constituted 67.1% of the subjects. Adenocarcinoma was predominant (67.7%), and 50.3% of the patients underwent ≥ 2 previous treatments. Twenty-three patients (14.8%) were EGFR mutation- or ALK rearrangement-positive. The objective response rate (ORR) was 23.9% [95% confidence interval (CI) 17.4-31.4%]; the median progression-free survival (PFS) and overall survival (OS) were 3.06 (95% CI 1.893-4.21) and 10.25 (95% CI 5.39-15.11) months, respectively. Multivariate analysis identified ECOG performance status, EGFR mutation/ALK rearrangement status, liver metastasis and PD-L1 proportion as independent predictors of OS. Furthermore, 61.9% of the patients had adverse events of any grade; 38.1% had immune-related adverse events that were associated with PFS and OS on multivariate analysis. CONCLUSIONS: The real-world ORR, PFS, OS, and adverse event profiles were comparable to previous clinical trials despite the patients' different baseline characteristics. Our findings can aid in establishing effective immunotherapeutic management of NSCLC in routine clinical practice.-
dc.description.statementOfResponsibilityopen-
dc.languageEnglish, German-
dc.publisherSpringer-Verlag-
dc.relation.isPartOfJOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rightshttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAdult-
dc.subject.MESHAged-
dc.subject.MESHAged, 80 and over-
dc.subject.MESHAntibodies, Monoclonal, Humanized/administration & dosage-
dc.subject.MESHAntineoplastic Agents, Immunological/administration & dosage-
dc.subject.MESHCarcinoma, Non-Small-Cell Lung/drug therapy-
dc.subject.MESHCarcinoma, Non-Small-Cell Lung/immunology-
dc.subject.MESHCarcinoma, Non-Small-Cell Lung/pathology-
dc.subject.MESHFemale-
dc.subject.MESHHumans-
dc.subject.MESHLung Neoplasms/drug therapy-
dc.subject.MESHLung Neoplasms/immunology-
dc.subject.MESHLung Neoplasms/pathology-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHNivolumab/administration & dosage-
dc.subject.MESHProgrammed Cell Death 1 Receptor/antagonists & inhibitors-
dc.subject.MESHProgrammed Cell Death 1 Receptor/immunology-
dc.subject.MESHRetrospective Studies-
dc.subject.MESHTreatment Outcome-
dc.titleComprehensive analysis of the characteristics and treatment outcomes of patients with non-small cell lung cancer treated with anti-PD-1 therapy in real-world practice-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.googleauthorBeung-Chul Ahn-
dc.contributor.googleauthorKyoung-Ho Pyo-
dc.contributor.googleauthorChun-Feng Xin-
dc.contributor.googleauthorDongmin Jung-
dc.contributor.googleauthorHyo Sup Shim-
dc.contributor.googleauthorChang Young Lee-
dc.contributor.googleauthorSeong Yong Park-
dc.contributor.googleauthorHong In Yoon-
dc.contributor.googleauthorMin Hee Hong-
dc.contributor.googleauthorByoung Chul Cho-
dc.contributor.googleauthorHye Ryun Kim-
dc.identifier.doi10.1007/s00432-019-02899-y-
dc.contributor.localIdA01166-
dc.contributor.localIdA01508-
dc.contributor.localIdA02219-
dc.contributor.localIdA05556-
dc.contributor.localIdA04777-
dc.contributor.localIdA03245-
dc.contributor.localIdA03822-
dc.contributor.localIdA04809-
dc.contributor.localIdA04393-
dc.relation.journalcodeJ01283-
dc.identifier.eissn1432-1335-
dc.identifier.pmid30911841-
dc.subject.keywordImmunotherapy-
dc.subject.keywordNon-smallcelllungcancer-
dc.subject.keywordPD-1-
dc.subject.keywordReal-worldsetting-
dc.subject.keywordSurvival-
dc.contributor.alternativeNameKim, Hye Ryun-
dc.contributor.affiliatedAuthor김혜련-
dc.contributor.affiliatedAuthor박성용-
dc.contributor.affiliatedAuthor심효섭-
dc.contributor.affiliatedAuthor안병철-
dc.contributor.affiliatedAuthor윤홍인-
dc.contributor.affiliatedAuthor이창영-
dc.contributor.affiliatedAuthor조병철-
dc.contributor.affiliatedAuthor표경호-
dc.contributor.affiliatedAuthor홍민희-
dc.citation.volume145-
dc.citation.number6-
dc.citation.startPage1613-
dc.citation.endPage1623-
dc.identifier.bibliographicCitationJOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY, Vol.145(6) : 1613-1623, 2019-
dc.identifier.rimsid61927-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > BioMedical Science Institute (의생명과학부) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Pathology (병리학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Radiation Oncology (방사선종양학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Thoracic and Cardiovascular Surgery (흉부외과학교실) > 1. Journal Papers

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