Breast cancer survival in Nordic BRCA2 mutation carriers—unconventional association with oestrogen receptor status

dc.contributor.authorOlafsdottir, Elinborg J.
dc.contributor.authorBorg, Ake
dc.contributor.authorJensen, Maj Britt
dc.contributor.authorGerdes, Anne Marie
dc.contributor.authorJohansson, Anna L.V.
dc.contributor.authorBarkardottir, Rosa B.
dc.contributor.authorJohannsson, Oskar T.
dc.contributor.authorEjlertsen, Bent
dc.contributor.authorSønderstrup, Ida Marie Heeholm
dc.contributor.authorHovig, Eivind
dc.contributor.authorLænkholm, Anne Vibeke
dc.contributor.authorHansen, Thomas van Overeem
dc.contributor.authorOlafsdottir, Gudridur H.
dc.contributor.authorRossing, Maria
dc.contributor.authorJonasson, Jon G.
dc.contributor.authorSigurdsson, Stefan
dc.contributor.authorLoman, Niklas
dc.contributor.authorNilsson, Martin P.
dc.contributor.authorNarod, Steven A.
dc.contributor.authorTryggvadottir, Laufey
dc.contributor.departmentFaculty of Medicine
dc.date.accessioned2025-11-20T08:21:13Z
dc.date.available2025-11-20T08:21:13Z
dc.date.issued2020-11-24
dc.descriptionPublisher Copyright: © 2020, The Author(s), under exclusive licence to Cancer Research UK.en
dc.description.abstractBackground: The natural history of breast cancer among BRCA2 carriers has not been clearly established. In a previous study from Iceland, positive ER status was a negative prognostic factor. We sought to identify factors that predicted survival after invasive breast cancer in an expanded cohort of BRCA2 carriers. Methods: We studied 608 women with invasive breast cancer and a pathogenic BRCA2 mutation (variant) from four Nordic countries. Information on prognostic factors and treatment was retrieved from health records and by analysis of archived tissue specimens. Hazard ratios (HR) were estimated for breast cancer-specific survival using Cox regression. Results: About 77% of cancers were ER-positive, with the highest proportion (83%) in patients under 40 years. ER-positive breast cancers were more likely to be node-positive (59%) than ER-negative cancers (34%) (P < 0.001). The survival analysis included 584 patients. Positive ER status was protective in the first 5 years from diagnosis (multivariate HR = 0.49; 95% CI 0.26–0.93, P = 0.03); thereafter, the effect was adverse (HR = 1.91; 95% CI 1.07–3.39, P = 0.03). The adverse effect of positive ER status was limited to women who did not undergo endocrine treatment (HR = 2.36; 95% CI 1.26–4.44, P = 0.01) and patients with intact ovaries (HR = 1.99; 95% CI 1.11–3.59, P = 0.02). Conclusions: The adverse effect of a positive ER status in BRCA2 carriers with breast cancer may be contingent on exposure to ovarian hormones.en
dc.description.versionPeer revieweden
dc.format.extent8
dc.format.extent698568
dc.format.extent1608-1615
dc.identifier.citationOlafsdottir, E J, Borg, A, Jensen, M B, Gerdes, A M, Johansson, A L V, Barkardottir, R B, Johannsson, O T, Ejlertsen, B, Sønderstrup, I M H, Hovig, E, Lænkholm, A V, Hansen, T V O, Olafsdottir, G H, Rossing, M, Jonasson, J G, Sigurdsson, S, Loman, N, Nilsson, M P, Narod, S A & Tryggvadottir, L 2020, 'Breast cancer survival in Nordic BRCA2 mutation carriers—unconventional association with oestrogen receptor status', British Journal of Cancer, vol. 123, no. 11, pp. 1608-1615. https://doi.org/10.1038/s41416-020-01056-4en
dc.identifier.doi10.1038/s41416-020-01056-4
dc.identifier.issn0007-0920
dc.identifier.other37679177
dc.identifier.otherae63b436-4d74-458f-97d6-f5361fe55bc2
dc.identifier.other85091156088
dc.identifier.other32939053
dc.identifier.urihttps://hdl.handle.net/20.500.11815/6304
dc.language.isoen
dc.relation.ispartofseriesBritish Journal of Cancer; 123(11)en
dc.relation.urlhttps://www.scopus.com/pages/publications/85091156088en
dc.rightsinfo:eu-repo/semantics/openAccessen
dc.subjectOncologyen
dc.subjectCancer Researchen
dc.subjectSDG 3 - Good Health and Well-beingen
dc.titleBreast cancer survival in Nordic BRCA2 mutation carriers—unconventional association with oestrogen receptor statusen
dc.type/dk/atira/pure/researchoutput/researchoutputtypes/contributiontojournal/articleen

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