🇮🇪Ireland
16°C Partly Cloudy · Dublin
Live Updates
--:--:-- IST
Contributor sign in
Latest
Clinical Trials in Canada / NCT04970056
Recruiting Observational

Pancreatic Cancer Early Detection Consortium

NCT04970056 · tracked via the Priya Life Science Canada tracker
Phase
Observational
Started
2020-09-18
Last updated
2026-07-22

Condition(s) studied

Pancreas CancerPancreas CystPancreatic Ductal AdenocarcinomaGenetic Predisposition

Study summary

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)

Trial sites (60)

FacilityCityRegionStatus
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

Other trials for the same condition

Official registry record

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.

View NCT04970056 on ClinicalTrials.gov ↗ ← All trials in Canada