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dc.contributor.authorLund-Iversen, Marius
dc.contributor.authorScott, Helge
dc.contributor.authorStrøm, Erik Heyerdahl
dc.contributor.authorTheiss, Noah
dc.contributor.authorBrustugun, Odd Terje
dc.contributor.authorGrønberg, Bjørn Henning
dc.date.accessioned2018-09-10T14:13:12Z
dc.date.available2018-09-10T14:13:12Z
dc.date.created2018-07-05T14:56:51Z
dc.date.issued2018
dc.identifier.citationAnticancer Research. 2018, 38 (4), 2261-2269.nb_NO
dc.identifier.issn0250-7005
dc.identifier.urihttp://hdl.handle.net/11250/2561844
dc.description.abstractBackground/Aim: The favorable prognosis of women with non-small-cell lung cancer (NSCLC) compared to men might be explained by sex hormone-related mechanisms. We investigated whether this observation could be explained by the expression of estrogen receptor-alpha (ER-α) in tumor tissue. Materials and Methods: Archived, formalin fixed, paraffin embedded tumor tissue samples were retrospectively analyzed for nuclear expression of ER-α with immunohistochemistry. Results: Biopsies from 222 patients were analyzed. Twenty-three percent were ER-α positive. Fifty-four percent of the patients were men and 46% of the tumors were adenocarcinomas. One hundred-nine (49%) patients received pemetrexed and carboplatin and 113 (51%) received gemcitabine and carboplatin. Females with ER-α positive tumors who received PC had a substantial survival benefit over all other groups (20 vs. 4.6 months; p=0.003). Conclusion: ER-α is an independent prognostic factor in advanced NSCLC and might also be a predictive factor for response to pemetrexed/carboplatin in women.nb_NO
dc.language.isoengnb_NO
dc.publisherInternational Institute of Anticancer Research (IIAR)nb_NO
dc.titleExpression of estrogen receptor-α and survival in advanced-stage non-small cell lung cancernb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionpublishedVersionnb_NO
dc.source.pagenumber2261-2269nb_NO
dc.source.volume38nb_NO
dc.source.journalAnticancer Researchnb_NO
dc.source.issue4nb_NO
dc.identifier.doi10.21873/anticanres.12470
dc.identifier.cristin1595958
dc.description.localcodeThis article will not be available due to copyright restrictions (c) 2018 by International Institute of Anticancer Research (IIAR)nb_NO
cristin.unitcode194,65,15,0
cristin.unitnameInstitutt for klinisk og molekylær medisin
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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