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Prognostic and clinicopathological roles of programmed death-ligand 1 (PD-L1) expression in thymic epithelial tumors: A meta-analysis

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dc.contributor.authorKoh, Hyun Min-
dc.contributor.authorJang, Bo Gun-
dc.contributor.authorLee, Hyun Ju-
dc.contributor.authorHyun, Chang Lim-
dc.date.accessioned2024-12-02T22:00:44Z-
dc.date.available2024-12-02T22:00:44Z-
dc.date.issued2020-11-
dc.identifier.issn1759-7706-
dc.identifier.issn1759-7714-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/72144-
dc.description.abstractBackground Programmed death-ligand 1 (PD-L1) is one of the immune checkpoint proteins, and plays an important role in the progression and microenvironment of cancer. PD-L1 expression has been associated with poor survival in many cancers. Several studies have also shown an association between PD-L1 expression and the prognosis of patients with thymic epithelial tumors (TETs). In this study, we systematically evaluated the prognostic and clinicopathological roles of PD-L1 expression in TETs. Methods We searched the literature through PubMed, Embase and Cochrane library and chose the eligible studies, and subsequently performed a meta-analysis to evaluate the prognostic and clinicopathological roles of PD-L1 expression in TETs. Results Six of the 75 articles found in the literature were selected. PD-L1 expression was significantly related to unfavorable overall survival (hazard ratio 1.52, 95% confidence interval [CI]: 1.01-2.30,P= 0.046) in TETs. PD-L1 expression was significantly associated with male gender (odds ratio [OR] 1.55, 95% CI: 1.08-2.22,P= 0.017) and higher Masaoka stage (OR 3.93, 95% CI: 2.44-6.32,P< 0.001). Conclusions PD-L1 expression was correlated with unfavorable prognosis in TETs, indicating PD-L1 expression could help determine the prognosis of TET patients.-
dc.format.extent13-
dc.language영어-
dc.language.isoENG-
dc.publisherBlackwell Publishing Asia Pty Ltd-
dc.titlePrognostic and clinicopathological roles of programmed death-ligand 1 (PD-L1) expression in thymic epithelial tumors: A meta-analysis-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1111/1759-7714.13590-
dc.identifier.scopusid2-s2.0-85090970059-
dc.identifier.wosid000568870200001-
dc.identifier.bibliographicCitationThoracic Cancer, v.11, no.11, pp 3086 - 3098-
dc.citation.titleThoracic Cancer-
dc.citation.volume11-
dc.citation.number11-
dc.citation.startPage3086-
dc.citation.endPage3098-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaOncology-
dc.relation.journalResearchAreaRespiratory System-
dc.relation.journalWebOfScienceCategoryOncology-
dc.relation.journalWebOfScienceCategoryRespiratory System-
dc.subject.keywordAuthorMeta-analysis-
dc.subject.keywordAuthorprognosis-
dc.subject.keywordAuthorprogrammed death-ligand 1-
dc.subject.keywordAuthorthymic epithelial tumor-
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