Program:
09:00-09:20 General introduction Frederik Hes
09:20-10:30 Breast Cancer (HBOC), diagnosis, guidelines for surveillance Jenneke van den Ende
10:30-10:45 Break
10:45-12:45 Colorectal Cancer Kathleen Claes, Karin Dahan (small break included)
Lynch syndrome, diagnosis, guidelines for surveillance, and cases
Polyposis syndromes, diagnosis, guidelines for surveillance and cases
12:45-13:30 Lunch break
13:30-14:30 Cases: Jenneke van den Ende, Frederik Hes
in 2 groups of students, cases are discussed with choice of genetic tests, results, follow-up plan and counseling
14:30-15:30 Tumor genetics and implications for treatment Philippe Giron
15:30-15:45 Break
15:45-17:00 Rare cancers Frederik Hes
Endocrine tumor syndromes, rare gastro-intestinal syndromes, geno-onco-dermatoses
Preparatory literature:
10 rare tumors that warrant a genetics referral , Belgian guidelines for Managing Hereditary Breast and Ovarian Cancer , National consensus and clinical guidance for diagnosis and management of Lynch Syndrome and NCCN Guidelines: Genetic/ Familial High‐ Risk Assessment.