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BackgroundTriple-negative (TN) tumours are the predominant breast cancer subtype in BRCA1 mutation carriers. Recently, it was proposed that all individuals below 50 years of age with TN breast cancer should be offered BRCA testing. We have evaluated the BRCA1 mutation frequency and the implications for clinical practice of undertaking genetic testing in women with TN breast cancer.MethodsWe undertook BRCA1 mutation analysis in 308 individuals with TN breast cancer, 159 individuals from unselected series of breast cancer and 149 individuals from series ascertained on the basis of young age and/or family history.ResultsBRCA1 mutations were present in 45 out of 308 individuals. Individuals with TN cancer <50 years had >10% likelihood of carrying a BRCA1 mutation in both the unselected (11 out of 58, 19%) and selected (26 out of 111, 23%) series. However, over a third would not have been offered testing using existing criteria. We estimate that testing all individuals with TN breast cancer <50 years would generate an extra 1200 tests annually in England.ConclusionWomen with TN breast cancer diagnosed below 50 years have >10% likelihood of carrying a BRCA1 mutation and are therefore eligible for testing in most centres. However, implementation may place short-term logistical and financial burdens on genetic services.

Original publication

DOI

10.1038/bjc.2012.31

Type

Journal article

Journal

British journal of cancer

Publication Date

03/2012

Volume

106

Pages

1234 - 1238

Addresses

Division of Genetics and Epidemiology, Institute of Cancer Research, 15 Cotswold Road, Sutton, Surrey SM2 5NG, UK.

Keywords

TNT Trial TMG, BCSC (UK), Humans, Breast Neoplasms, Receptor, erbB-2, BRCA1 Protein, Receptors, Estrogen, Receptors, Progesterone, Incidence, DNA Mutational Analysis, Age Factors, Mutation, Middle Aged, Female, Genetic Testing, Genetic Association Studies