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Colorectal cancer (CRC) is common, affecting approximately 140,000 individuals annually in the United States. The average person has a 5% lifetime risk to develop CRC. As with all cancers, CRC develops due to a combination of genetic, biologic, and environment factors interacting together. Approximately 5-10% cases of CRC are due to a hereditary syndrome, where a single gene alteration conveys a high risk of CRC and sometimes other cancers. The resources below provide opportunities to learn about hereditary colorectal cancer syndromes, how to use family history to assess risk level, genetic testing, using genetic information to inform management, and communicating with patients about genetic risk.
Lynch Syndrome Factsheet. Describes the clinical features, diagnosis, testing and genetics of Lynch syndrome (hereditary nonpolyposis colorectal cancer).
Familial Adenomatous Polyposis Factsheet. Describes the clinical features, diagnosis, testing and genetics of familial adenomatous polyopsis (FAP) and attenuated FAP.
MUTYH-Associated Adenomatous Polyposis Factsheet. Describes the clinical features, diagnosis, testing and genetics ofMUTYH-associated polyposis (MAP).
Genetically Related Cancers Tool.Lists the associated cancers and unique characteristics of common cancer susceptibility genes.
Cancer Risk Assessment Tool.Helps identify red flags and stratify cancer risk based on family history.
Family History Collection Tips & Tools.Provides tips, resources, and tools for family history collection in clinical practice.
Family History Questionnaire. A collection form for medical family history data that can be printed and used in clinical practice.
Pedigree Tool. A template to record a pedigree with standard pedigree nomenclature.
Hereditary Cancer Management Guidelines Factsheet. Lists and links to evidence-based guidelines and professional society publications that address management of hereditary and familial cancer.
Hereditary Cancer Panels. Provides considerations when evaluating different multi-gene panels for hereditary cancer testing.
Genetic Testing Methods eBook. Provides information about different genetic testing methods currently used in testing for hereditary cancer syndromes (enhanced e-book available for download).
Communicating Risk Factsheet.Outlines key points to consider when communicating risk to patients.
Pretest Counseling Key Points Factsheet.Outlines key points to address during pretest counseling.
Components of a Cancer Genetic Counseling Session Factsheet.Discusses the core components of a cancer genetic counseling session.
GINA Discussion Guide. Provides talking points and key information about genetic discrimination and the Genetic Information Nondiscrimination Act (GINA), which protects individuals from the misuse of genetic information in health insurance and employment.
Free, self-directed programs for continuing education credit.
Collecting Family History with Sufficient Detail. Practice asking the right questions to elicit enough information to assess family history disease risk and get tools to implement your skills.
Categorizing Cancer Risk. Analyze family histories and classify patients' risk into average, increased (moderate), or high risk for cancer.
Using Family History to Inform Management. Practice determining appropriate management based on family history risk stratification.
Identifying Red Flags and Patterns That Increase Cancer Risk. Practice identifying risk factors in case scenarios and receive tools to help make this task easy to implement in your practice.
Cancer Pretest Decisions and Counseling. Practice deciding when and if genetic testing is appropriate given a patient's clinical and personal context.
Interpreting Cancer Genetic Testing Results. Practice interpreting genetic testing results within a patient's specific context.