Navigating familial cancer risk in general practice

This 60-minute interactive webinar equips GPs and primary care clinicians with the practical skills and confidence to recognise hereditary cancer risk in everyday practice. Through real-world clinical cases and guided discussion, participants will learn how to identify key “red-flag” features in a family history that suggest an inherited cancer syndrome, determine which patients warrant referral to a Familial Cancer Service (FCS), and apply the CanRisk assessment tool to support evidence-based risk evaluation.

The session will also explore how to interpret genetic test results,  including variants of uncertain significance and reinforce the critical principle that not all cancers are linked to a single gene. Participants will discover the most appropriate investigations and assessments to initiate prior to or alongside referral, and gain a clear understanding of both public and private referral pathways to ensure timely and coordinated care.

Throughout the session, an expert genetics specialist and experienced GP educator will share practical insights, answer questions, and provide actionable tips for integrating genetic risk assessment into routine consultations. A strong focus on shared decision-making will help clinicians tailor recommendations to patients’ values, preferences, and family circumstances, supporting them through the genetic testing journey.

By the end of this webinar, attendees will be able to confidently assess familial cancer risk, initiate appropriate next steps, and empower patients and families with accurate, personalised information.

Key features:

• Real-world case discussions and interactive Q&A

• Practical guidance on using the CanRisk tool

• Interpreting complex genetic results and communicating uncertainty

• Navigating public and private FCS referral pathways
  CPD hours: Category 2 (RACGP) / Educational Activity (ACRRM)

This is a Medcast Continuing Medical Education (CME) course.