dc.contributor.author
Pujana Genestar, M. Ángel
dc.contributor.author
KConFab Investigators
dc.contributor.author
Hereditary Breast and Ovarian Cancer Research Group Netherlands (HEBON)
dc.contributor.author
Epidemiological study of BRCA1 & BRCA2 Mutation Carriers (EMBRACE)
dc.date.issued
2018-12-11T11:24:32Z
dc.date.issued
2018-12-11T11:24:32Z
dc.date.issued
2016-02-09
dc.date.issued
2018-07-25T07:52:23Z
dc.identifier
https://hdl.handle.net/2445/126883
dc.description.abstract
Background: BRCA1 and, more commonly, BRCA2 mutations are associated with increased risk of male breast cancer (MBC). However, only a paucity of data exists on the pathology of breast cancers (BCs) in men with BRCA1/2 mutations. Using the largest available dataset, we determined whether MBCs arising in BRCA1/2 mutation carriers display specific pathologic features and whether these features differ from those of BRCA1/2 female BCs (FBCs). Methods: We characterised the pathologic features of 419 BRCA1/2 MBCs and, using logistic regression analysis, contrasted those with data from 9675 BRCA1/2 FBCs and with population-based data from 6351 MBCs in the Surveillance, Epidemiology, and End Results (SEER) database. Results: Among BRCA2 MBCs, grade significantly decreased with increasing age at diagnosis (P = 0.005). Compared with BRCA2 FBCs, BRCA2 MBCs were of significantly higher stage (P for trend = 2 x 10(-5)) and higher grade (P for trend = 0.005) and were more likely to be oestrogen receptor-positive [odds ratio (OR) 10.59; 95 % confidence interval (CI) 5.15-21.80] and progesterone receptor-positive (OR 5.04; 95 % CI 3.17-8.04). With the exception of grade, similar patterns of associations emerged when we compared BRCA1 MBCs and FBCs. BRCA2 MBCs also presented with higher grade than MBCs from the SEER database (P for trend = 4 x 10(-12)). Conclusions: On the basis of the largest series analysed to date, our results show that BRCA1/2 MBCs display distinct pathologic characteristics compared with BRCA1/2 FBCs, and we identified a specific BRCA2-associated MBC phenotype characterised by a variable suggesting greater biological aggressiveness (i.e., high histologic grade). These findings could lead to the development of gender-specific risk prediction models and guide clinical strategies appropriate for MBC management.
dc.format
application/pdf
dc.publisher
BioMed Central
dc.relation
Reproducció del document publicat a: https://doi.org/10.1186/s13058-016-0671-y
dc.relation
Breast Cancer Research, 2016, vol. 18, num. 15
dc.relation
https://doi.org/10.1186/s13058-016-0671-y
dc.relation
info:eu-repo/grantAgreement/EC/FP7/223175/EU//COGS
dc.rights
cc by (c) Silvestri et al., 2016
dc.rights
http://creativecommons.org/licenses/by/3.0/es/
dc.rights
info:eu-repo/semantics/openAccess
dc.source
Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))
dc.subject
Càncer de mama
dc.title
Male breast cancer in BRCA1 and BRCA2 mutation carriers: pathology data from the Consortium of Investigators of Modifiers of BRCA1/2
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/publishedVersion