Moffitt Cancer Center's High-Risk Pancreatic Cancer Screening Clinic provides personalized risk assessment and surveillance for individuals who may have an increased likelihood of developing pancreatic cancer.
Routine pancreatic cancer screening is not recommended for the general population, making specialized evaluation important for identifying individuals who may benefit. Moffitt’s team reviews each person’s family history, genetic information, medical history and other relevant factors to determine whether pancreatic surveillance is appropriate.
The clinic is part of Moffitt's Pancreas Interception Center, which focuses on pancreatic cancer risk assessment, early detection and research.
If you have received test results indicative of pancreatic cancer, the experts at Moffitt can help. You can submit a new patient appointment request - no referral needed.
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Who Can Benefit from an Evaluation in the High-Risk Pancreatic Cancer Screening Clinic?

- Individuals with a strong family history of pancreatic cancer
- Individuals with multiple family members affected by pancreatic cancer
- People with an inherited genetic mutation or hereditary cancer syndrome associated with pancreatic cancer
- People with chronic or hereditary pancreatitis
- Individuals whose personal or family cancer history may suggest an inherited cancer syndrome
- People with new-onset diabetes or unexplained changes in blood sugar later in life
- Individuals with other qualifying medical or clinical risk factors
Having one or more risk factors does not mean a person will develop pancreatic cancer. Eligibility for surveillance is determined through an individualized clinical assessment.
Genetic Risk and Family History
Inherited changes in certain genes may increase pancreatic cancer risk. These can include genes associated with hereditary breast and ovarian cancer, Lynch syndrome, Peutz-Jeghers syndrome, familial atypical multiple mole melanoma syndrome and hereditary pancreatitis.
Genetic counseling can help patients understand their personal and family cancer history, determine whether genetic testing may be appropriate and interpret existing test results.