Expert care, clear answers and support you can trust
Pancreatic cancer is often diagnosed at a late stage, when treatment options are limited. For people with certain genetic factors or family history, screening can help detect abnormalities earlier, when they may be more treatable.
Our high-risk pancreatic cancer screening program provides personalized guidance, advanced screening tools and specialty-trained experts to help you understand your risk and take proactive steps toward protecting your health.
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Call: (800) 367-0982 Monday-Friday 8 a.m. - 5 p.m.
Why screening matters for high-risk patients
Pancreatic cancer can be a devastating disease, and many people do not experience symptoms until it has progressed. New research shows that individuals with specific genetic mutations or strong family history may benefit from early and ongoing screening.
Screening offers the chance to identify concerning changes sooner and to connect with experts who can support prevention, monitoring and early intervention.
What the high-risk program includes
Risk evaluation and education
Your first visit includes a detailed discussion about your personal and family history, your level of risk, as well as the role and limitations of available screening tools.
Our team will help you understand your options and guide you through next steps, including whether genetic counseling or testing may be appropriate.
Ongoing monitoring
Once enrolled, you’ll receive ongoing care based on national guidelines. This includes follow-up with recommended imaging tests and regular risk assessments to ensure your screening plan stays up-to-date.
Care close to home
You can receive screening support through in-person or telehealth visits, bringing expert care to you wherever you are.
Our multidisciplinary team includes specialists in:
- Surgical oncology
- Medical oncology
- Gastroenterology
- Medical genetics
- Radiology
Who should consider high-risk pancreatic screening
You may benefit from screening if you meet one of the following criteria. If you’re unsure whether you meet these criteria, your primary care provider can help you review your history and guide your next steps.
Family history–based risk
- Two or more relatives on the same side of your family with pancreatic cancer
- One relative with pancreatic cancer and one of these gene mutations:
- ATM
- BRCA1 or BRCA2
- MLH1, MSH2, MSH6, EPCAM (Lynch Syndrome)
- PALB2 TP53 (Li-Fraumeni Syndrome)
Genetic mutation–based risk (even without family history)
- STK11 (Peutz-Jeghers Syndrome)
- CDKN2A (Familial Atypical Multiple Mole Melanoma)
Genetic mutation–based risk (even without family history)
- STK11 (Peutz-Jeghers Syndrome)
- CDKN2A (Familial Atypical Multiple Mole Melanoma)
Other high-risk conditions
- Diagnosis of hereditary pancreatitis
Screening tests that may be recommended
Your screening plan may include advanced imaging such as:
- MRI
- Endoscopic ultrasound (EUS)
These techniques can help detect early abnormalities in the pancreas, even before symptoms appear.
Benefits of participating in the program
- Annual screening with the goal of early detection
- Collaborative care from experts in oncology, genetics, gastroenterology and radiology
- Lifestyle guidance to help you manage risk factors
- Opportunities to participate in research studies focused on pancreatic cancer