Journal Article

Genotypic and phenotypic analysis of familial male breast cancer shows under representation of the HER2 and basal subtypes in BRCA-associated carcinomas

Fox, Stephen B, Deb, Siddhartha, Jene, Nicholas, investigators, kConFab

2012

Overview

Background Male breast cancer (MBC) is an uncommon and relatively uncharacterised disease accounting for <1% of all breast cancers. A significant proportion occurs in families with a history of breast cancer and in particular those carrying BRCA2 mutations. Here we describe clinicopathological features and genomic BRCA1 and BRCA2 mutation status in a large cohort of familial MBCs. Methods Cases (n=60) included 3 BRCA1 and 25 BRCA2 mutation carries, and 32 non- BRCA1/2 (BRCAX) carriers with strong family histories of breast cancer. The cohort was examined with respect to mutation status, clinicopathological parameters including TNM staging, grade, histological subtype and intrinsic phenotype. Results Compared to the general population, MBC incidence was higher in all subgroups. In contrast to female breast cancer (FBC) there was greater representation of BRCA2 tumours (41.7% vs 8.3%, p=0.0008) and underrepresentation of BRCA1 tumours (5.0% vs 14.4%, p=0.0001). There was no correlation between mutation status and age of onset, disease specific survival (DSS) or other clincopathological factors. Comparison with sporadic MBC studies showed similar clinicopathological features. Prognostic variables affecting DSS included primary tumour size (p=0.003, HR:4.26 95%CI 1.63-11.11), age (p=0.002, HR:4.09 95%CI 1.65-10.12), lymphovascular (p=0.019, HR:3.25 95%CI 1.21-8.74) and perineural invasion (p=0.027, HR:2.82 95%CI 1.13-7.06). Unlike familial FBC, the histological subtypes seen in familial MBC were more similar to those seen in sporadic MBC with 46 (76.7%) pure invasive ductal carcinoma of no special type (IDC-NST), 2 (3.3%) invasive lobular carcinomas and 4 (6.7%) invasive papillary carcinoma. A further 8 (13.3%) IDC-NST had foci of micropapillary differentiation, with a strong trend for co-occurrence in BRCA2 carriers (p=0.058). Most tumours were of the luminal phenotype (89.7%), with infrequent HER2 (8.6%) and basal (1.7%) phenotype tumours seen. Conclusion MBC in BRCA1/2 carriers and BRCAX families is different to females. Unlike FBC, a clear BRCA1 phenotype is not seen but a possible BRCA2 phenotype of micropapillary histological subtype is suggested. Comparison with sporadic MBCs shows this to be a high-risk population making further recruitment and investigation of this cohort of value in further understanding these uncommon tumours.

• Publisher: BioMed Central,BioMed Central Ltd,Springer Nature B.V,BMC
• Subject: Adult / Aged / Aged, 80 and over / Analysis / Biomarkers, Tumor - metabolism / Biomedical and Life Sciences / Biomedicine / BRCA mutations / BRCA1 / BRCA1 Protein - metabolism / BRCA2 / BRCA2 Protein - metabolism / BRCAX / Breast cancer / Breast Neoplasms, Male - genetics / Breast Neoplasms, Male - metabolism / Breast Neoplasms, Male - pathology / Cancer Research / Cohort Studies / Familial / Family / Gene mutations / Genes, BRCA1 / Genes, BRCA2 / Genetic aspects / Genetic Association Studies / Genetic Predisposition to Disease / Genetics / genomics and epigenetics / Genotype / Health Promotion and Disease Prevention / Humans / Immunohistochemistry / Male / Male breast cancer / Medicine/Public Health / Microarray Analysis / Micropapillary / Middle Aged / Mutation / Oncology / Pathology / Phenotype / Physiological aspects / Receptor, ErbB-2 - genetics / Research Article / Risk factors / Studies / Surgical Oncology / Survival Rate / Tumor staging