Biomarker Study in Pancreatic Neuroendocrine Tumours
NCT03130205 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 30
Last updated 2017-08-25
Summary
The biology of pancreatic neuroendocrine tumors can change during the disease course. This evolution of disease can manifest through increases in tumor proliferation rate, resistance to medical therapy and/or a change in tumor hormone secretion. This study aims to characterize how the biology of pancreatic neuroendocrine tumors change over time, measured by; patient symptoms, biochemistry, contrast enhanced computed tomography, FDG-PET and core needle biopsy with histopathological analysis (Ki67 index and tumor cell differentiation). Uptake on 18F-FDG-PET will be correlated directly to tumor cell proliferation rate. Fraction of patients with spatial heterogeneity in FDG uptake as well as metachronous changes in all collected data will be documented. Biomaterial from whole blood and core needle biopsies will be characterized on the molecular level, and those findings will be integrated to the above specified clinical parameters.
Conditions
Interventions
- PROCEDURE
-
Core Needle Biopsy
Core Needle Biopsy is performed from liver metastasis.
- RADIATION
-
Computed Tomography
Computed Tomography
- RADIATION
-
18F-FDG-PET
18F Fluorodeoxyglucose Positron emission tomography
- PROCEDURE
-
Phlebotomy
3 EDTA tubes drawn from peripheral vein
- GENETIC
-
Molecular genetic analysis
Performed on biomaterial from peripheral vein and core needle biopsy
Sponsors & Collaborators
-
Uppsala University
lead OTHER
Principal Investigators
-
Barbro Eriksson, MD PhD · Akademiska Sjukhuset, Uppsala
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2017-05-01
- Primary Completion
- 2021-01-01
- Completion
- 2022-01-01
Countries
- Sweden
Study Locations
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