%0 Journal Article
%T Male breast cancer risk associated with pathogenic variants in genes other than BRCA1/2: an Italian case-control study.
%A Bucalo A
%A Conti G
%A Valentini V
%A Capalbo C
%A Bruselles A
%A Tartaglia M
%A Bonanni B
%A Calistri D
%A Coppa A
%A Cortesi L
%A Giannini G
%A Gismondi V
%A Manoukian S
%A Manzella L
%A Montagna M
%A Peterlongo P
%A Radice P
%A Russo A
%A Tibiletti MG
%A Turchetti D
%A Viel A
%A Zanna I
%A Palli D
%A Silvestri V
%A Ottini L
%J Eur J Cancer
%V 188
%N 0
%D 2023 07 2
%M 37262986
%F 10.002
%R 10.1016/j.ejca.2023.04.022
%X Germline pathogenic variants (PVs) in BRCA1/2 genes are associated with breast cancer (BC) risk in both women and men. Multigene panel testing is being increasingly used for BC risk assessment, allowing the identification of PVs in genes other than BRCA1/2. While data on actionable PVs in other cancer susceptibility genes are now available in female BC, reliable data are still lacking in male BC (MBC). This study aimed to provide the patterns, prevalence and risk estimates associated with PVs in non-BRCA1/2 genes for MBC in order to improve BC prevention for male patients.
We performed a large case-control study in the Italian population, including 767 BRCA1/2-negative MBCs and 1349 male controls, all screened using a custom 50 cancer gene panel.
PVs in genes other than BRCA1/2 were significantly more frequent in MBCs compared with controls (4.8% vs 1.8%, respectively) and associated with a threefold increased MBC risk (OR: 3.48, 95% CI: 1.88-6.44; p < 0.0001). PV carriers were more likely to have personal (p = 0.03) and family (p = 0.02) history of cancers, not limited to BC. PALB2 PVs were associated with a sevenfold increased MBC risk (OR: 7.28, 95% CI: 1.17-45.52; p = 0.034), and ATM PVs with a fivefold increased MBC risk (OR: 4.79, 95% CI: 1.12-20.56; p = 0.035).
This study highlights the role of PALB2 and ATM PVs in MBC susceptibility and provides risk estimates at population level. These data may help in the implementation of multigene panel testing in MBC patients and inform gender-specific BC risk management and decision making for patients and their families.