Navigating familiar cancer risk

Genetic testing and familial cancer risk are becoming increasingly relevant in everyday general practice, yet many GPs report uncertainty in identifying high-risk patients, initiating appropriate investigations, and navigating referral pathways. This interactive eLearning module has been designed to build confidence and capability in managing patients with a family history suggestive of inherited cancer syndromes. 

Through a structured, case-based approach, participants will follow a realistic primary care scenario involving a patient concerned about her familial cancer risk. The course will guide learners through identifying key “red flags” in family history, including early-onset cancers, multi-generational patterns, and clustering of specific cancer types, and applying these findings to clinical decision-making. Participants will explore when genetic testing is appropriate, who in the family should be tested first, and how to effectively refer to familial cancer services or clinical genetics. 

The module also addresses interpretation of genetic test results, including complex concepts such as variants of uncertain significance, and supports GPs to communicate risk clearly while managing patient expectations and uncertainty. Emphasis is placed on shared decision-making and coordinating care within the broader healthcare system. 

Designed by experienced clinicians in genomics and primary care, this course uses interactive quizzes, decision points, and reflective questions to actively engage learners and reinforce application to practice. 

By the end of the activity, participants will be better equipped to identify patients at increased risk of hereditary cancer, make appropriate referrals, and support patients and families through informed, patient-centred care.