The purpose of the Pancreatic Cancer Early Detection (PRECEDE) Consortium is to conduct research on multiple aspects of early detection and prevention of pancreatic ductal adenocarcinoma (PDAC) by establishing a multisite cohort of individuals with family history of PDAC and/or individuals carrying pathogenic/likely pathogenic germline variants (PGVs) in genes linked to PDAC risk for longitudinal follow up.
Eligibility
Sex
ALL
Min age
18 Years
Max age
90 Years
Healthy volunteers
Accepted
Inclusion Criteria:
Individuals from the following groups who present for clinical evaluation and assessment of PDAC risk at any of the participating sites can be offered participation in the PRECEDE database:
Cohort 1
Individuals without history of PDAC meeting any of the following criteria:
1. 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; age 50+ or ≤10 years younger than earliest PDAC in family at time of diagnosis.
2. 2 affected first degree relatives with PDAC; age 50+ or 10 years younger than earliest PDAC in family
3. BRCA1, BRCA2, PALB2, ATM, MLH1, MSH2, MSH6, PMS2, EPCAM pathogenic or likely pathogenic variant AND 1 first or second degree relative with PDAC; age 50+ or 10 years younger than earliest PDAC in family
4. Familial Atypical Moles and Malignant Melanoma (FAMMM) with pathogenic or likely pathogenic CDKN2A variant; age 40+
5. Peutz-Jegher syndrome with STK11 pathogenic or likely pathogenic variant; age 35+
6. Hereditary pancreatitis with PRSS1 pathogenic or likely pathogenic variant and history of pancreatitis; age 40+
Cohort 2
Individuals without history of PDAC meeting any of the following criteria:
1. ATM, BRCA1, BRCA2, or PALB2 pathogenic or likely pathogenic variant regardless of family history, age 50+
2. 2+ relatives with PDAC on the same side of family, any degree of relation, not meeting other criteria above; age 50+ or 10 years younger than earliest PDAC in family
3. 1 first degree relative with PDAC ≤ age 45; age up to 10 years younger than PDAC diagnosis in family member
Cohort 3 Individual meeting criteria for Cohorts 1 or 2 EXCEPT age (i.e. too young to qualify for Cohorts 1 or 2)
Cohort 4 Individuals without history of PDAC presenting for evaluation who do not meet any criteria for 1-3, 6, or the Cyst Cohort.
Cohort 5 Individuals without history of PDAC who are not otherwise engaged in pancreas surveillance at a participating site may be invited to participate in the PRECEDE database and to donate a biosample (e.g. blood, saliva, and/or buccal swab) for discovery studies. This may include relatives of individuals in Cohorts 1-4,6, and the Cyst Cohort.
Cohort 6a
Individuals diagnosed with PDAC or pancreatic high-grade dysplasia after enrollment in PRECEDE meeting any of the following criteria:
1. Family history includes at least one first degree relative with PDAC, or 2 relatives with PDAC who are first degree related to each other
2. Personal or family history of a pathogenic or likely pathogenic germline variant in ATM, BRCA1, BRCA2, CDKN2A, EPCAM, MLH1, MSH2, MSH6, PALB2,PMS2, PRSS1, STK11
Cohort 6b
Individuals with a personal history of PDAC or pancreatic high-grade dysplasia meeting any of the following criteria:
1. Family history includes at least one first degree relative with PDAC, or 2 relatives with PDAC who are first degree related to each other
2. Personal or family history of a pathogenic or likely pathogenic germline variant in ATM, BRCA1, BRCA2, CDKN2A, EPCAM, MLH1, MSH2, MSH6, PALB2,PMS2, PRSS1, STK11
3. Diagnosed ≤ age 45
Cohort 6c Individuals with newly diagnosed early stage (stage I or stage II) PDAC seen at a PRECEDE site that do not meet the criteria for 6a or 6b.
Cohort 6d Individuals with PDAC seen at a PRECEDE site that do not meet the criteria for 6a, 6b, or 6c.
Cyst Cohort Individuals with a personal history of a pancreatic cystic neoplasm not meeting any criteria for Cohorts 1-3 or 6 (no known family history of PDAC, no known pathogenic germline variants linked to PDAC risk)
Exclusion Criteria:
* Individuals not meeting the criteria above.
Primary outcome measure(s)
Development of PDAC — Through study completion, an average of 6 years Diagnosis of PDAC
Trial sites (60)
Facility
City
Region
Status
Mayo Clinic Arizona
Phoenix
Arizona
Not Yet Recruiting
Honor Health Research Institute
Scottsdale
Arizona
Recruiting
Providence Health and Services
Burbank
California
Recruiting
City of Hope
Duarte
California
Recruiting
UC San Diego Moores Cancer Center
La Jolla
California
Recruiting
Cedars-Sinai Medical Center
Los Angeles
California
Recruiting
UCLA Health
Los Angeles
California
Recruiting
Hoag
Newport Beach
California
Recruiting
UC Irvine Health
Orange
California
Recruiting
UC Davis
Sacramento
California
Recruiting
University of California, San Francisco (UCSF)
San Francisco
California
Recruiting
Yale University
New Haven
Connecticut
Recruiting
Mayo Clinic Jacksonville
Jacksonville
Florida
Recruiting
University of Miami
Miami
Florida
Recruiting
Moffitt Cancer Center
Tampa
Florida
Recruiting
Emory University Hospital
Atlanta
Georgia
Recruiting
Illinois CancerCare
Bloomington
Illinois
Recruiting
University of Chicago Medicine
Chicago
Illinois
Recruiting
NorthShore University HealthSystem
Evanston
Illinois
Recruiting
University of Kansas Medical Center
Kansas City
Kansas
Recruiting
Massachusetts General Hospital
Boston
Massachusetts
Recruiting
Umass Memorial Medical Center
Worcester
Massachusetts
Recruiting
University of Michigan
Ann Arbor
Michigan
Recruiting
Beaumont/Corewell Health
Royal Oak
Michigan
Recruiting
University of Nebraska Medical Center
Omaha
Nebraska
Recruiting
Hackensack Meridian Health
Hackensack
New Jersey
Recruiting
Memorial Sloan Kettering Cancer Center
New York
New York
Not Yet Recruiting
Icahn School of Medicine At Mount Sinai
New York
New York
Recruiting
Columbia University Irving Medical Center
New York
New York
Recruiting
University of Rochester Medical Center
Rochester
New York
Recruiting
White Plains Hospital
White Plains
New York
Recruiting
The Ohio State University
Columbus
Ohio
Recruiting
Oregon Health & Science University
Portland
Oregon
Recruiting
University of Pennsylvania
Philadelphia
Pennsylvania
Recruiting
Fox Chase Cancer Center
Philadelphia
Pennsylvania
Recruiting
University of Pittsburgh Medical Center (Upmc)
Pittsburgh
Pennsylvania
Recruiting
University of Tennessee Graduate School of Medicine
Knoxville
Tennessee
Recruiting
The University of Texas Southwestern Medical Center
Dallas
Texas
Terminated
MD Anderson Center
Houston
Texas
Withdrawn
Huntsman Cancer Institute
Salt Lake City
Utah
Recruiting
+ 20 more sites — see the full list on the official registry below.
More Arbor Research Collaborative for Health trials in Canada
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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