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

ArmDescriptionAssigned 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.
  • Other: Non-Interventional Study
    Non-interventional study

Recruiting Locations

University of California, San Francisco
San Francisco, California 94158
Contact:
Kimberly S. Kirkwood, MD
415-502-0427
kim.kirkwood@ucsf.edu

Piedmont Healthcare
Atlanta, Georgia 30309
Contact:
Meiri Eyal
404-425-1777
eyal.meiri@piedmont.org

OSF Saint Francis Medical Center
Peoria, Illinois 61615
Contact:
Chandler Wilfong, MD
309-691-4005
chandler.d.wilfong@osfhealthcare.org

The Johns Hopkins University School of Medicine
Baltimore, Maryland 21231
Contact:
Michael Goggins, MD
410-955-3511
mgoggins@jhmi.edu

Dana-Farber Cancer Institute
Boston, Massachusetts 02215
Contact:
Brian Wolpin, MD, MPH
617-632-6942
brian_wolpin@dfci.harvard.edu

Mayo Clinic in Rochester
Rochester, Minnesota 55905
Contact:
Clinical Trials Referral Office
855-776-0015
mayocliniccancerstudies@mayo.edu

University of Nebraska Medical Center
Omaha, Nebraska 68198-6805
Contact:
Kelsey Klute, MD
402-559-1880
Kelsey.klute@unmc.edu

Oregon Health & Science University
Portland, Oregon 97201
Contact:
Rosalie Sears, PhD
503-494-6885
searsr@ohsu.edu

University of Pittsburgh
Pittsburgh, Pennsylvania 15232
Contact:
Randall Brand, MD
412-864-7516

More Details

Status
Recruiting
Sponsor
Mayo Clinic

Study Contact

Clinical Trials Referral Office
855-776-0015
mayocliniccancerstudies@mayo.edu

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.