The Pancreatic Cancer Early Detection Program provides a comprehensive, personalized consultation tailored to the needs of the individual patient. Many patients will meet first with a genetic counselor who will review family history and other risk factors for cancer, explain the role of genetic testing for hereditary cancer syndromes, offer testing (if appropriate), and provide an overall cancer risk assessment. Those patients considered to be at increased risk of pancreas cancer can then choose to consult our Pancreatic Cancer Early Detection Program clinicians. We arrange for appropriate high-risk pancreas cancer screening, either clinically or as a part of a prospective research study [CAPS5 and PanFAM1, PRECEDE, and Pancreatic Cyst Study EA2185]. If needed, we can also assist with arranging consultations with other specialists for a multidisciplinary approach to cancer prevention and surveillance.
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