Biomarker Study of Pancreatic Neuroendocrine Tumours
NCT03741517 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 40
Last updated 2022-05-18
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, DOTATOC-PET, FDG-PET and core needle biopsy with histopathological analysis (Ki67 index and tumor cell differentiation). Uptake on 68Ga-DOTATOC and 18F-FDG-PET will be correlated directly to tumor cell proliferation rate. Fraction of patients with spatial heterogeneity in DOTATOC as well as 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
- Pancreatic Neuroendocrine Tumor
Interventions
- RADIATION
-
18F-FDG-PET
Fludeoxyglucose F18
- RADIATION
-
68Ga-DOTATOC-PET
DOTA-tyr3-Octreotide Ga68
- RADIATION
-
Computed tomography
Computed tomography of thorax and abdomen with 3-phase contrast
- OTHER
-
Core needle biopsy
Core needle biopsy of metastatic lesions
- OTHER
-
Phlebotomy
Phlebotomy from peripheral vein
Sponsors & Collaborators
-
Uppsala University
lead OTHER
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2019-01-30
- Primary Completion
- 2024-12-31
- Completion
- 2024-12-31
Countries
- Sweden
Study Locations
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