Abstract PD7-06: Multi-gene testing in a male breast cancer cohort: Insights and unexpected results

Abstract

Abstract INTRODUCTION: The role of BRCA2 and BRCA1 in male breast cancer is well established, however, there is limited data regarding the role of other genes in male breast cancer. The aim of this study was to assess the clinical characteristics and genetic testing outcomes in men diagnosed with breast cancer undergoing multi-gene testing. METHODS: Test results were reviewed for male breast cancer patients who underwent analysis of breast cancer-associated genes via multi-gene testing from March 2012 to March 2015. Panels consisted of 5-49 genes, depending on the test ordered. Clinical histories provided on test requisition forms were assessed. Statistical analysis was performed using the Wilcoxon Rank Test and the Fisher's exact test. RESULTS: Approximately 12% (33/280) of men diagnosed with breast cancer were identified to carry a pathogenic mutation/likely pathogenic variant, ∼2% (5/280) were identified to carry a moderate risk mutation (APC p.I1307K or CHEK2 p.I157T), ∼1% (2/280) were identified to carry a monoallelic MUTYH mutation, ∼18% (51/280) had a variant of unknown significance but were otherwise negative, and ∼67% (189/280) tested negative. The mutation rate was highest for BRCA2, at 7.3% (18/247 tested), followed by CHEK2, at 5.1% (10/196 tested). Of note, 3 men tested positive for multiple mutations: one man had BRCA2 and ATM mutations, one man had BRCA2 and TP53 mutations, and one man, with a clinical diagnosis of ataxia-telangiectasia, had two ATM mutations. The average age at diagnosis for mutation-positive men (62.5 years) was not significantly different from negative men (59.6 years) (p=0.269). However, the average age of diagnosis for men with CHEK2 1100delC mutations (46.0 years) was significantly lower than the average age of diagnosis for men who were otherwise positive (p=0.012). Fourteen of the mutation-positive men were found to have multiple cancers; colon polyps, melanoma, and cancers of the bladder, prostate and pancreas were reported in more than one individual. Based on the family history provided, two men who tested positive for BRCA2 mutations would not otherwise have met NCCN criteria for testing. The majority of men in this cohort with a family history of male breast cancer (10/19) tested negative for a mutation. Five mutation-positive patients were found to have a family history of male breast cancer: three with CHEK2 mutations; one with a BRCA2 and a TP53 mutation; and one with two ATM mutations. Men with CHEK2 mutations were significantly more likely to have a family history of male breast cancer compared to other positive men (p=0.020) as were men with multiple mutations (p=0.008). CONCLUSION: In this cohort of male breast cancer patients, multi-gene testing identified mutations in patients that would not previously have been identified with a single gene testing approach and allowed for identification of families with multiple mutations. Age at diagnosis and family history were not predictive of positive test results in general, although men with CHEK2 100delC mutations were diagnosed at a significantly younger age. Although 30% of this cohort was not tested for CHEK2, the CHEK2 mutation rate in the men tested was second in frequency to BRCA2, suggesting a role for CHEK2 testing in male breast cancer patients. Citation Format: Pritzlaff M, Summerour P, McFarland R, Li S, Laduca H. Multi-gene testing in a male breast cancer cohort: Insights and unexpected results. [abstract]. In: Proceedings of the Thirty-Eighth Annual CTRC-AACR San Antonio Breast Cancer Symposium: 2015 Dec 8-12; San Antonio, TX. Philadelphia (PA): AACR; Cancer Res 2016;76(4 Suppl):Abstract nr PD7-06.