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Discordant human epidermal growth factor receptor 2 and hormone receptor status in primary and metastatic breast cancer and response to trastuzumab

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dc.contributor.authorChang, Hye Jung-
dc.contributor.authorHan, Sae-Won-
dc.contributor.authorOh, Do-Youn-
dc.contributor.authorIm, Seock-Ah-
dc.contributor.authorJeon, Yoon Kyung-
dc.contributor.authorPark, In Ae-
dc.contributor.authorHan, Wonshick-
dc.contributor.authorNoh, Dong-Young-
dc.contributor.authorBang, Yung-Jue-
dc.contributor.authorKim, Tae-You-
dc.date.accessioned2021-01-31T11:56:11Z-
dc.date.available2021-01-31T11:56:11Z-
dc.date.created2020-12-23-
dc.date.created2020-12-23-
dc.date.issued2011-05-
dc.identifier.citationJapanese Journal of Clinical Oncology, Vol.41 No.5, pp.593-599-
dc.identifier.issn0368-2811-
dc.identifier.other119687-
dc.identifier.urihttps://hdl.handle.net/10371/173150-
dc.description.abstractBackground: Recent studies have shown that the human epidermal growth factor receptor 2 status of a metastatic site may differ from that of the primary site. This difference may influence patient prognosis and response to therapy. Methods: We conducted a retrospective study using immunohistochemistry and/or fluorescent in situ hybridization to compare human epidermal growth factor receptor 2 and hormone receptor status in primary and metastatic breast cancers. Results: Fifty-six patients were included in this study. Conversion from hormone receptor positive in the primary tumor to hormone receptor negative in the metastasis occurred in 12 patients (21.4%), and hormone receptor negative to hormone receptor positive conversion occurred in two patients (3.6%). Human epidermal growth factor receptor 2 status was discordant between primary and metastatic lesions in seven patients (12.5%). All of the five patients who converted from human epidermal growth factor receptor 2 negative status to human epidermal growth factor receptor positive received trastuzumab-based chemotherapy. Overall response rate and median progression-free survival for concordant human epidermal growth factor receptor 2 positive patients were 69.2% and 16.9 months, whereas that of patients with positive conversion of human epidermal growth factor receptor 2 were 40.0% and 7.6 months, respectively (overall response rate; P = 0.169 and progression-free survival; P = 0.004). Conclusion: Discordance in human epidermal growth factor receptor 2 and hormone receptor status between primary and metastatic tumors was observed, which led to altered treatment decisions. Evaluation of human epidermal growth factor receptor 2 and hormone receptor in metastatic tumors should be considered in patients with breast cancer.-
dc.language영어-
dc.publisherOxford University Press-
dc.titleDiscordant human epidermal growth factor receptor 2 and hormone receptor status in primary and metastatic breast cancer and response to trastuzumab-
dc.typeArticle-
dc.contributor.AlternativeAuthor임석아-
dc.identifier.doi10.1093/jjco/hyr020-
dc.citation.journaltitleJapanese Journal of Clinical Oncology-
dc.identifier.wosid000290316700001-
dc.identifier.scopusid2-s2.0-79955833377-
dc.citation.endpage599-
dc.citation.number5-
dc.citation.startpage593-
dc.citation.volume41-
dc.identifier.sci000290316700001-
dc.description.isOpenAccessY-
dc.contributor.affiliatedAuthorOh, Do-Youn-
dc.contributor.affiliatedAuthorIm, Seock-Ah-
dc.contributor.affiliatedAuthorJeon, Yoon Kyung-
dc.contributor.affiliatedAuthorPark, In Ae-
dc.contributor.affiliatedAuthorHan, Wonshick-
dc.contributor.affiliatedAuthorNoh, Dong-Young-
dc.contributor.affiliatedAuthorBang, Yung-Jue-
dc.contributor.affiliatedAuthorKim, Tae-You-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusIN-SITU HYBRIDIZATION-
dc.subject.keywordPlusOF-AMERICAN-PATHOLOGISTS-
dc.subject.keywordPlusESTROGEN-RECEPTOR-
dc.subject.keywordPlusADJUVANT CHEMOTHERAPY-
dc.subject.keywordPlusHER-2/NEU EXPRESSION-
dc.subject.keywordPlusTISSUE MICROARRAY-
dc.subject.keywordPlusHETEROGENEITY-
dc.subject.keywordPlusHER2-
dc.subject.keywordPlusONCOGENE-
dc.subject.keywordPlusSOCIETY-
dc.subject.keywordAuthorHER2-
dc.subject.keywordAuthorhormone receptor-
dc.subject.keywordAuthortrastuzumab-
dc.subject.keywordAuthorbreast cancer-
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  • Department of Medicine
Research Area Clinical Medicine

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