Chronic Pancreatitis, Healthy Control, Pancreatic Cancer, Pancreatic Cysts, Type II Diabetes
Conditions
Keywords
Pancreatic Cancer, Chronic Pancreatitis, Diseases of the pancreas
Brief summary
This proposed project is designed to collect data and specimens from patients/subjects presenting to the University of Michigan with a disease affecting the pancreas (or specific control populations). This protocol is focused on collecting data, blood samples, and tissue on subjects with pancreatic diseases, including pancreatic cancer, pancreatic cysts, pancreatitis, diabetic controls, jaundice/biliary obstruction controls, and otherwise healthy controls. We are collecting up to 50 mls of blood for research purposes only. Plasma, serum and buffy coat are collected and stored according to strict SOPs.
Detailed description
The recently funded GI SPORE, here at the University of Michigan, is focused on pancreatic and colon diseases. This protocol is focused on collecting data, blood samples, and tissue on subjects with pancreatic diseases, including pancreatic cancer, pancreatic cysts, pancreatitis, diabetic controls, jaundice/biliary obstruction controls, and otherwise healthy controls. A SPORE is an NCI-funded, Specialized Program in Research Excellence, with specific requirements. Those requirements include 4 projects with a clinical and a basic science Co-PI and several COREs, including a biospecimen core. Each project that has a human subjects component will require a separate protocol and IRB submission when those projects are to begin. The specific populations we are recruiting are determined by the aims of project 2 and by the need to create a repository as part of the biospecimen core (please see the grant for details on the aims of these 2 projects). A specially designed database is being built for this study to handle the data aspects. Our collaborators at Dartmouth College have significant experience in managing data as they have been our partners for our work in the EDRN (PI Brenner). Case report forms and other data collection tools have been developed and are being used to populate the database. All of the actual data will be completely deidentified per HIPAA regulations. We intend to model the data and specimen collection on the model used by our work with the NCI-EDRN. This includes a customized database, the use of kits with pre-labled, bar-coded aliquots, and standardized data collection forms (CRFs).
Interventions
PROCEDUREBlood Draw
Blood draw for research specimens only
Sponsors
University of Michigan
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes
Inclusion criteria
Overall Inclusion (all subjects must meet these criteria to be enrolled) * Adults 18 years of age or older * Able to physically tolerate removal of 50 ml of blood * Willing to sign informed consent.
Exclusion criteria
Overall Exclusion (for all subjects) * Pregnant or lactating * Known HIV/AIDS or Hepatitis C * Prepped for colonoscopy at the time of blood collection * Unable to understand English * Receiving chemotherapy or radiation at time of enrollment * Any cancer within 5 years of enrollment except any of the following: * Squamous cell carcinoma of the skin or Basal cell carcinoma of the skin * Carcinoma in situ of the cervix, Stages Ia or Ib invasive squamous cell carcinoma of the cervix treated by surgery only. (Excluded if had pelvic radiation) * Stage Ia Grade 1 adenocarcinoma of the endometrium treated with surgery
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Validation of glycoprotein panel as a pancreatic cancer biomarker | 5 years | To create a set of cases and controls to validate a novel glycoprotein panel for non-invasive or early detection of pancreatic cancer. |
Countries
United States
Outcome results
None listed