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Systematic Hereditary Pancreatic Cancer Risk Assessment and Implications for Personalized Therapy

Dana-Farber Cancer Institute logo

Dana-Farber Cancer Institute

Status

Active, not recruiting

Conditions

Pancreatic Cancer

Study type

Observational

Funder types

Other
NIH

Identifiers

NCT03060720
16-448
P50CA127003 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

This research study is looking at people with cancer of the pancreas to find clinical factors that can explain the presence of genetic mutations

Full description

This research is being done to identify which pancreatic cancer patients should undergo genetic evaluation. A patient's personal and family history of cancer is the information typically used to make this decision, but there are currently no accurate, evidence-based guidelines that exist to help doctors use this information to make a decision.

The investigators hope that by testing all new pancreatic cancer patients, they can determine which clinical factors predict for genetic mutations in order to create a risk assessment tool.

The investigators want to determine which patients with pancreatic cancer will benefit from genetic testing. To do so, the investigators will offer all patients with pancreatic cancer in the Dana-Farber Gastrointestinal Oncology clinic referral for genetic evaluation. At the Cancer Genetics and Prevention clinic appointment, the provider will review the patient's personal and familial history of cancer and offer genetic testing.

Enrollment

271 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Diagnosis of pancreatic ductal adenocarcinoma
  • Signed initial informed consent
  • Participant agrees to genetic counseling

Exclusion criteria

  • Prospective participant unable to sign informed consent based on referring physician recommendation.
  • Patient has neuroendocrine pancreatic tumor

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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