PET / CT
+3
Study of the Diagnostic Value of Hybrid PET/MR and PET/CT in Neuroendocrine Diseases and Tumor Induced Osteomalacia
Sponsored by Wuhan Union Hospital, China
About this trial
Last updated 2 years ago
Study ID
XLan-S1002
Status
Recruiting
Type
Observational
Placebo
No
Accepting
20 to 80 Years
All
Trial Timing
Ended 2 years ago
What is this trial about?
Neuroendocrine tumors (NETs) are rare neoplasms arising from the diffuse endocrine system
and spreading throughout the different organs and tissues of the body. Tumor-induced
osteomalacia (TIO) , is a rare, serious paraneoplastic syndrome primarily derived from a
benign tumor of mesenchymal tissue. NETs and mesenchymal tumors are often insidious and
are undetectable by conventional imaging techniques including ultrasound, computed
tomography and magnetic resonance, while a permanent cure will rely on exact localization
and completely removal of the tumor.
Positron emission tomography (PET) provides a valuable tool for the diagnosis and
differential diagnosis, staging, efficacy evaluation and recurrence monitoring of various
tumors. NETs and mesenchymal tumors overexpress somatostatin receptors (SSTRs), so
molecular imaging using radiolabeled somatostatin analogues may be one of the best ways
to detect the occult tumors. Recently, somatostatin analogue labelled with gallium-68
(68Ga-DOTA-TATE) as a novel positron tracer has shown to be effective for the detection
of NETs and mesenchymal tumors. In this prospective study, the investigators will use the
most advanced imaging equipment, integrated PET/MR,and PET / CT with specific imaging
agent 68Ga-DOTA-TATE and conventional imaging agent [F-18]fluorodeoxyglucose to image
patients suspected or confirmed NETs and TIO, the aim is to explore the value of hybrid
PET/MR and PET/CT in neuroendocrine diseases and TIO.
What are the participation requirements?
Inclusion Criteria
- Patients with suspected or confirmed NETs or patients with suspected TIO
Exclusion Criteria
- Acute systemic diseases and electrolyte disorders.
- Pregnant or lactating women.
- Participated in other clinical trials within 4 weeks before the start of the study.
Locations
Location
Status
Recruiting