Pancreatic Cancer Detection Consortium (PCDC) Prospective Cohorts
Purpose
This study evaluates individuals without pancreatic cancer, but who have been determined to be at higher-than-average lifetime risk of developing pancreatic cancer to help detect pancreatic cancer or other cancers at an earlier time when they might be more easily treated and cured.
Condition
- Pancreatic Carcinoma
Eligibility
- Eligible Ages
- Over 18 Years
- Eligible Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- PDAC FAMILY HISTORY OR PDAC RELATED GENETIC MUTATIONS: - Age: 50 or older, plus at least one of the following: - Mutation unknown or absent: - 2+ relatives with PDAC on same side of family where 2 affected are first degree related to each other and at least 1 affected is first degree related to subject; - OR 2+ affected first degree relatives [(FDR), defined as blood related parents, siblings, or children] - Known pathogenic/likely pathogenic (P/LP) mutation in at least one of the following: - CDKN2A/p16, Peutz-Jeghers syndrome (PJS) serine/threonine kinase 11 (STK11), Hereditary pancreatitis with confirmed protease serine 1 (PRSS1) - OR 1+ or second degree relative (SDR) with PDAC and a known P/LP mutation in one or more of: - ATM, BRCA1, BRCA2, PALB2, Lynch syndrome (MLH1, MSH2, MSH6, PMS2, EPCAM), TP53 - HIGH-RISK OR WORRISOME PANCREATIC CYSTS: - 18 years of age or greater and meeting Fukuoka worrisome (FW) or Fukuoka high-risk (FHR) criteria - High risk stigmata: - Obstructive Jaundice in a patient with cystic lesion of the head of the pancreas - Enhancing mural nodule ≥ 5 mm - Main pancreatic duct ≥ 10 mm - Worrisome features: - Presence of pancreatic duct stricture, defined as focal pancreatic duct narrowing with upstream duct => 6 mm - Cyst ≥ 3 cm - Enhancing mural nodule < 5 mm - Thickened/Enhancing cyst wall - Main duct size 5-9 mm - Pancreatitis - Lymphadenopathy - Increased CA 19-9 - Cyst growth rate ≥ 5 mm /2 years
Exclusion Criteria
- Is unable to provide informed consent - Has received a non-autologous bone marrow transplant or has an active hematologic malignancy (i.e., leukemia or lymphoma) - Current or prior history of PDAC or total pancreatectomy - Is currently a prison inmate - Is not able to speak or read English
Study Design
- Phase
- Study Type
- Observational
- Observational Model
- Cohort
- Time Perspective
- Prospective
Arm Groups
| Arm | Description | Assigned Intervention |
|---|---|---|
| Observational | Participants undergo blood sample collection, complete questionnaires, have their medical records reviewed and undergo pancreatic cyst fluid collection during standard of care endoscopic ultrasounds fine needle aspiration. |
|
Recruiting Locations
San Francisco, California 94158
Peoria, Illinois 61615
Baltimore, Maryland 21231
Boston, Massachusetts 02215
Rochester, Minnesota 55905
Omaha, Nebraska 68198-6805
Portland, Oregon 97201
Pittsburgh, Pennsylvania 15232
Randall Brand, MD
412-864-7516
More Details
- Status
- Recruiting
- Sponsor
- Mayo Clinic
Detailed Description
PRIMARY OBJECTIVES: I. To develop a cohort (biobank of biospecimens and data) of subjects without pancreatic cancer who are at highrisk for pancreatic cancer due to: a strong family history, a mutation in a known pancreatic cancer predisposition gene, or fukuoka worrisome or high-risk pancreatic cysts. II. To follow the cohort subjects longitudinally and collect biospecimens and follow-up data and record medical outcomes. III. To make biospecimen available to PCDC-approved projects to validate potential biomarkers for performance using nested case-control prospective designs. OUTLINE: This is an observational study. Participants undergo blood sample collection, complete questionnaires, have their medical records reviewed and undergo pancreatic cyst fluid collection during standard of care endoscopic ultrasounds fine needle aspiration.