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Breast cancer in high-risk Afrikaner families: Is BRCA founder mutation testing sufficient?

Overview of attention for article published in South African Medical Journal, February 2016
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Title
Breast cancer in high-risk Afrikaner families: Is BRCA founder mutation testing sufficient?
Published in
South African Medical Journal, February 2016
DOI 10.7196/samj.2016.v106i3.10285
Pubmed ID
Authors

Heather Jessica Seymour, Tasha Wainstein, Shelley Macaulay, Tabitha Haw, Amanda Krause

Abstract

Germline pathogenic mutations in cancer susceptibility genes result in inherited cancer syndromes. In the Afrikaner population of South Africa (SA), three founder mutations in the BRCA genes that lead to hereditary breast and ovarian cancer syndrome (HBOCS) have been identified. To investigate the uptake and type of molecular testing performed on patients for HBOCS, to determine the prevalence of the three Afrikaner founder BRCA mutations as well as non-founder BRCA mutations in the study population, and to analyse the utility of two mutation prediction models (Breast and Ovarian Analysis of Disease Incidence and Carrier Estimation Algorithm (BOADICEA) and Manchester scoring method) in assisting with the decision for the most cost-effective testing option. A retrospective file review was performed on counsellees of self-reported Afrikaner ancestry from Johannesburg, SA (2001 - 2014), with a personal or family history of breast and/or ovarian cancer. Demographic and family history information was recorded and Manchester and BOADICEA scores were calculated for each patient. Of 86 unrelated counsellees whose files were reviewed, 54 (62.8%) underwent BRCA genetic testing; 18 (33.3%) tested positive for a mutation, and 14 of these (77.8%) for an Afrikaner founder mutation. Twelve counsellees had the BRCA2 c.7934delG mutation. Four non-founder mutations were identified. BOADICEA scores were significantly higher in counsellees who tested positive for a mutation than in those who tested negative. Founder mutation testing should be performed as a first-line option. BOADICEA is very useful in identifying counsellees at high risk for a BRCA mutation and also assists with the decision to pursue further testing following a negative founder mutation result. These findings assist in guiding an informed genetic counselling service for at-risk individuals with an Afrikaner background.

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Geographical breakdown

Country Count As %
Unknown 40 100%

Demographic breakdown

Readers by professional status Count As %
Student > Postgraduate 7 18%
Student > Master 7 18%
Student > Bachelor 4 10%
Student > Ph. D. Student 3 8%
Researcher 3 8%
Other 6 15%
Unknown 10 25%
Readers by discipline Count As %
Medicine and Dentistry 11 28%
Biochemistry, Genetics and Molecular Biology 10 25%
Agricultural and Biological Sciences 3 8%
Immunology and Microbiology 2 5%
Psychology 1 3%
Other 1 3%
Unknown 12 30%