The Cancer Genetics Program is designed to increase knowledge in the area of hereditary cancer genetics. This slide-based, expert-led course provides a comprehensive collection on an array of topics related to the genetic cancer risk assessment process. The course addresses ways to improve the taking and documenting of family history, as well as interpreting those results. The program is composed of site-specific sections on core concepts that include recognition of hereditary cancer syndromes, quantitative risk assessment, establishing a cancer risk assessment service, and special counseling and ethical, legal, and social issues in cancer genetics.
- Apply basic concepts of cancer genetics, risk assessment and currently available testing into patient care practices.
- Recognize genetic testing for common cancer syndromes and how to interpret Variants of Unknown Significance (VUS)
- Consider the emergent strategies and the latest advances in early detection cancers (breast, GI, etc.)
- Analyze genome wide association studies (GWAS) and principles of next generation technology in tumor/germline DNA and gene panels.
- Summarize key learnings from each core section and utilize approaches to improve the process of recognition and referral of hereditary cancer syndromes within physician practices.
CME credit is available for this course.
ACGME Competencies addressed: Medical Knowledge
Note: This course is accessible through mobile devices as well as personal computers