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Cited 15 time in webofscience Cited 15 time in scopus
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Different relation between ERCC1 overexpression and treatment outcomes of two platinum agents in advanced biliary tract adenocarcinoma patients

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dc.contributor.authorHwang, I. G.-
dc.contributor.authorJang, J. S.-
dc.contributor.authorDo, J. H.-
dc.contributor.authorKang, J. H.-
dc.contributor.authorLee, G. W.-
dc.contributor.authorOh, S. Y.-
dc.contributor.authorKwon, H. C.-
dc.contributor.authorJun, H. J.-
dc.contributor.authorLim, H. Y.-
dc.contributor.authorLee, S.-
dc.contributor.authorChi, K. C.-
dc.contributor.authorLee, S. J.-
dc.date.available2019-05-29T11:35:17Z-
dc.date.issued2011-10-
dc.identifier.issn0344-5704-
dc.identifier.issn1432-0843-
dc.identifier.urihttps://scholarworks.bwise.kr/cau/handle/2019.sw.cau/21242-
dc.description.abstractPurpose The aim of this study is to evaluate the effect of excision repair cross-complementation group 1 (ERCC1) expression on treatment outcomes in advanced biliary tract adenocarcinoma (ABTA) patients treated with platinum-based chemotherapy. Methods One hundred and six patients with histologically confirmed adenocarcinoma of biliary tract were enrolled at 5 institutions in South Korea between January 2002 and September 2008. Of 106 patients, 93 were assessed by immunohistochemistry from tissue specimens. Sixty-five patients were treated with cisplatin-based regimens and the other 28 treated with oxaliplatin-based ones. Results For total study population, no significant differences were noted in progression-free survival (PFS) and overall survival (OS) between ERCC1-negative and ERCC1-positive patients, respectively (4.2 vs. 2.9 months, p = 0.116; 7.0 vs. 7.8 months, p = 0.143). In patients treated with cisplatin-based regimens, median PFS and OS were significantly longer in ERCC1-negative group than in ERCC1-positive group, respectively (4.6 vs. 1.9 months, p = 0.014; 9.1 vs. 7.9 months, p = 0.017). Disease control rate (DCR) was better in patients with ERCC1 negative than in patients with ERCC1 positive (p = 0.048). On the other hand, in patients treated with oxaliplatin-containing regimens, median PFS and OS tended to be longer in ERCC1-positive group, but these did not reach statistical significances. Response rate was better in patients with ERCC1 positive (p = 0.005). Conclusions ERCC1 shows a significant prognostic value in ABTA patients treated with cisplatin. A survival benefit was observed in ERCC1-negative patients from cisplatin-containing chemotherapy but not from oxaliplatin-containing ones. The action mechanism of ERCC1 on cisplatin may be different from that on oxaliplatin.-
dc.format.extent10-
dc.language영어-
dc.language.isoENG-
dc.publisherSPRINGER-
dc.titleDifferent relation between ERCC1 overexpression and treatment outcomes of two platinum agents in advanced biliary tract adenocarcinoma patients-
dc.typeArticle-
dc.identifier.doi10.1007/s00280-011-1558-3-
dc.identifier.bibliographicCitationCANCER CHEMOTHERAPY AND PHARMACOLOGY, v.68, no.4, pp 935 - 944-
dc.description.isOpenAccessN-
dc.identifier.wosid000297122300013-
dc.identifier.scopusid2-s2.0-80054768584-
dc.citation.endPage944-
dc.citation.number4-
dc.citation.startPage935-
dc.citation.titleCANCER CHEMOTHERAPY AND PHARMACOLOGY-
dc.citation.volume68-
dc.type.docTypeArticle-
dc.publisher.location미국-
dc.subject.keywordAuthorAdvanced biliary tract adenocarcinoma-
dc.subject.keywordAuthorERCC1-
dc.subject.keywordAuthorCisplatin-
dc.subject.keywordAuthorOxaliplatin-
dc.subject.keywordPlusMESSENGER-RNA LEVELS-
dc.subject.keywordPlusCELL LUNG-CANCER-
dc.subject.keywordPlusCISPLATIN PLUS GEMCITABINE-
dc.subject.keywordPlusADVANCED GASTRIC-CANCER-
dc.subject.keywordPlusTHYMIDYLATE SYNTHASE-
dc.subject.keywordPlusDNA-REPAIR-
dc.subject.keywordPlusFLUOROURACIL CHEMOTHERAPY-
dc.subject.keywordPlusCOLORECTAL-CANCER-
dc.subject.keywordPlusEXCISION-REPAIR-
dc.subject.keywordPlusOXALIPLATIN-
dc.relation.journalResearchAreaOncology-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryOncology-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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