Breast cancer specialists’ experiences and attitudes towards mainstream genetic testing for patients with breast cancer
Abstract
BACKGROUND: Germline genetic testing is an increasingly important component of treatment decision-making for clinicians and patients with breast cancer. To address increased demand and expedite access to genetic testing for these patients, the Parkville Familial Cancer Centre (PFCC) in Victoria, Australia, implemented a breast mainstream genetic testing program. The program educates and supports breast cancer specialists to provide eligible patients with pre-test information, gain consent, and arrange genetic testing during their routine cancer appointments. This study aimed to explore breast cancer specialists’ experiences and opinions of the education program and of facilitating mainstream genetic testing for their patients. METHODS: Specialists who had attended the mainstream genetic testing education were invited to complete an online survey about the training provided through the education program and their experience of deploying mainstream genetic testing in their practice. Descriptive statistics were compiled, and content analysis used for open text responses. RESULTS: Forty-five breast cancer specialists (breast surgeons, medical oncologists, radiation oncologists and breast care nurses) responded (45% response rate). Most respondents had discussed (87%) and consented (80%) patients for mainstream genetic testing. Most specialists (81%) rated their confidence levels as high or very high for consenting patients to mainstream genetic testing. The majority (89%) indicated that they believed mainstream genetic testing should be part of their role and felt well supported by the PFCC (90%). CONCLUSION: Breast cancer specialists used the education they received in the mainstream education program and were supported to deliver mainstream breast cancer genetic testing to their patients.
Fields of Study & Subjects
BRCA gene mutations in cancer
PARP inhibition in cancer therapy
Prenatal Screening and Diagnostics
Publication details
- Journal / source
- Hereditary Cancer in Clinical Practice
- Publisher
- Springer Science and Business Media LLC
- Volume
- 24
- Issue
- 1
- Publication date
- 24 April 2026
- Language
- EN