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dc.contributor.authorEngstrøm, Monica J
dc.contributor.authorValla, Marit
dc.contributor.authorBofin, Anna M.
dc.date.accessioned2018-04-30T07:47:42Z
dc.date.available2018-04-30T07:47:42Z
dc.date.created2017-03-16T14:21:34Z
dc.date.issued2017
dc.identifier.citationBreast Cancer Research and Treatment. 2017, 163 (2), 207-217.nb_NO
dc.identifier.issn0167-6806
dc.identifier.urihttp://hdl.handle.net/11250/2496463
dc.description.abstractPurpose Basal marker expression in triple-negative breast cancers identifies basal-like tumours, and thus separates the TN group into two prognostic groups. However, the expression and prognostic significance of basal markers in luminal breast cancers are poorly described. The aim of this study was to investigate the expression and prognostic value of basal markers (CK5, CK14 and EGFR) in luminal breast cancer. Methods A total of 1423 formalin-fixed, paraffin-embedded breast cancer tumours from a well-characterized cohort of Norwegian women, previously reclassified into molecular subtypes using IHC and ISH, were included in the study. For the present study, tumours expressing at least one of the basal markers CK5, CK14 or EGFR were defined as basal marker positive. Cumulative incidence of death from breast cancer and hazard ratio analyses were used to assess prognosis according to basal marker expression. Results and conclusion In total, 470 cases (33.0%) were basal marker positive. A higher proportion of the basal marker-positive tumours were of histopathological grade 3 compared to basal marker negative. For hormone receptor-positive, HER2-negative cases, we found better prognosis for basal marker-positive breast cancer compared to basal marker negative. For all subtypes combined, poorer prognosis for basal marker-negative cases was found in histopathological grade 2 tumours but not among grade 1 and 3.nb_NO
dc.language.isoengnb_NO
dc.publisherSpringer Verlagnb_NO
dc.titleBasal markers and prognosis in luminal breast cancernb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionacceptedVersionnb_NO
dc.source.pagenumber207-217nb_NO
dc.source.volume163nb_NO
dc.source.journalBreast Cancer Research and Treatmentnb_NO
dc.source.issue2nb_NO
dc.identifier.doi10.1007/s10549-017-4182-z
dc.identifier.cristin1458809
dc.description.localcodeThis is a post-peer-review, pre-copyedit version of an article published in [Breast Cancer Research and Treatment]. The final authenticated version is available online at: https://link.springer.com/article/10.1007%2Fs10549-017-4182-znb_NO
cristin.unitcode194,65,20,0
cristin.unitcode194,65,15,0
cristin.unitnameInstitutt for samfunnsmedisin og sykepleie
cristin.unitnameInstitutt for klinisk og molekylær medisin
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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