This clinical trial studies using the addition of blood-based tests and symptom review to standard-of-care pancreatic cancer screening procedures for the detection of pancreatic ductal adenocarcinoma in high-risk individuals. Current pancreatic cancer screening guidelines recommend annual contrast-enhanced magnetic resonance imaging (MRI)/magnetic resonance cholangiopancreatography (MRCP) alternating with endoscopic ultrasound (EUS). Adding blood-based tests and symptom review to standard-of-care procedures may better detect PDAC in high-risk individuals.
Study sponsor and potential other locations can be found on ClinicalTrials.gov for NCT06122896.
Locations matching your search criteria
United States
Massachusetts
Boston
Brigham and Women's HospitalStatus: Active
Contact: Matthew Boland Yurgelun
Phone: 617-632-6835
Dana-Farber Cancer InstituteStatus: Active
Contact: Matthew Boland Yurgelun
Phone: 617-632-6835
PRIMARY OBJECTIVES:
I. To establish a prospective cohort of individuals at high-risk for PDAC with biobanked blood, symptom data, and clinical data for use in the development and validation of novel PDAC early detection biomarkers and screening strategies.
II. To validate novel screening strategies that integrate established PDAC risk biomarkers with standard-of-care surveillance imaging in high-risk individuals.
III. To conduct exploratory analyses of microbiome, protease, and other stool related research.
SECONDARY OBJECTIVES:
I. To explore commercial collaborations for the early detection of pancreatic cancer using blood-based assays.
II. To investigate effectiveness of novel biomarkers derived from incidental clinical imaging studies and electronic medical records.
OUTLINE:
Patients undergo blood, stool and/or saliva sample collection throughout the study. Patients also undergo MRI, MRCP and EUS throughout the study.
After completion of study intervention, patients are followed up for 20 years.
Lead OrganizationDana-Farber Harvard Cancer Center
Principal InvestigatorMatthew Boland Yurgelun