We are a leading professional collective dedicated to advancing the understanding and clinical management of inherited gastrointestinal cancers. By bridging the gap between basic science and patient care, we serve as a primary authority for healthcare professionals and families navigating hereditary cancer syndromes.
Our Vision
Our vision is to eliminate the morbidity and early mortality associated with hereditary gastrointestinal cancers through proactive intervention and specialized expertise.
Our Mission
We aim to advance the science and clinical care of inherited conditions through rigorous research and comprehensive education. To achieve this, we provide:
- Professional Education: In-depth guidance on clinical management and molecular genetics for physicians, allied healthcare professionals, patients, and their families.
- Research & Collaboration: Exclusive access to collaborative trials and studies that push the boundaries of current medical knowledge.
- Registry Support: Specialized resources designed to help develop and maintain hereditary cancer registries.
- A Multidisciplinary Forum: A unique space for the exchange of ideas among experts in clinical care, healthcare policy, and gastrointestinal research.
Clinical & Research Focus
Our work encompasses a broad spectrum of hereditary gastrointestinal cancer syndromes, focusing on complex conditions such as:
- Lynch Syndrome and Hereditary Non-Polyposis Colorectal Cancer (HNPCC)
- Familial Adenomatous Polyposis (FAP) and MUTYH Associated Polyposis (MAP)
- Peutz-Jeghers and Juvenile Polyposis Syndromes
- PTEN Tumor Hamartoma and Hereditary Mixed Polyposis Syndromes
- Polymerase Proofreading-Associated Polyposis (PPAP)
- Serrated Polyposis and Familial Colorectal Cancer Type X
Through our multidisciplinary approach, we remain committed to transforming the landscape of hereditary cancer care and improving outcomes for affected families across the globe.