The programme was developed to present to both clinicians and researchers the most up-to-date information on hereditary breast and ovarian cancer.
Upon completion of the programme the learner will be able to:
- Better and more efficiently identify individuals who are at high risk for hereditary cancer;
- Review the latest developments in the genetics and molecular science of hereditary breast and ovarian cancer;
- Be able to discriminate between clinically useful and less clinically useful breast cancer susceptibility gene tests;
- Be aware of how somatic (tumour) molecular genetics can inform findings from germline genetic testing;
- Describe state of the art approaches to the management of individuals with inherited mutations;
- Apply cutting edge science to treat breast and/or ovarian cancer patients who have inherited mutations;
- Identify and understand prevention and early diagnostic strategies for individuals at risk for hereditary breast cancer;
- Compare and contrast BRCA management models in countries with different health resources and priorities;
- Identify issues and elaborate priorities for hereditary breast and ovarian cancer basic science and clinical research;
- Fully consider ethical issues surrounding population testing for breast and ovarian cancer risk;
- Better understand the factors influencing risk communication among families carrying a BRCA mutation.