Systematic Hereditary Pancreatic Cancer Risk Assessment and Implications for Personalized Therapy
2 other identifiers
observational
271
1 country
1
Brief Summary
This research study is looking at people with cancer of the pancreas to find clinical factors that can explain the presence of genetic mutations
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Feb 2017
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
February 15, 2017
CompletedFirst Posted
Study publicly available on registry
February 23, 2017
CompletedStudy Start
First participant enrolled
February 24, 2017
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 7, 2019
CompletedStudy Completion
Last participant's last visit for all outcomes
February 1, 2028
ExpectedMarch 30, 2026
March 1, 2026
2.1 years
February 15, 2017
March 25, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
We will measure clinical factors (e.g. # of PDAC patients with a personal history of x,y,z; # of PDAC patients with a family history of x,y,z; # PDAC patients with a germline mutation in x,y,z) so as to develop a risk assessment tool
Up to 5 years
Secondary Outcomes (3)
Evaluate Patient Experience With Genetic Testing
up to 5 years
Summarize patient satisfaction with Genetic counseling
up to 5 years
Number of patients who disclose genetic testing results to relatives
up to 5 years
Eligibility Criteria
Patient seen at Dana Farber Cancer Institute with a diagnosis of pancreatic ductal adenocarcinoma
You may qualify if:
- Diagnosis of pancreatic ductal adenocarcinoma
- Signed initial informed consent
- Participant agrees to genetic counseling
You may not qualify if:
- Prospective participant unable to sign informed consent based on referring physician recommendation.
- Patient has neuroendocrine pancreatic tumor
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Dana-Farber Cancer Institutelead
- National Cancer Institute (NCI)collaborator
Study Sites (1)
Dana Farber Cancer Institute
Boston, Massachusetts, 02215, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Matthew B Yurgelun, MD
Dana-Farber Cancer Institute
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Matthew B. Yurgelun, MD
Study Record Dates
First Submitted
February 15, 2017
First Posted
February 23, 2017
Study Start
February 24, 2017
Primary Completion
April 7, 2019
Study Completion (Estimated)
February 1, 2028
Last Updated
March 30, 2026
Record last verified: 2026-03
Data Sharing
- IPD Sharing
- Will not share