Abstract
An important role is reserved for nuclear imaging techniques in the imaging of neuroendocrine tumors (NETs). Somatostatin receptor scintigraphy (SRS) with In-111-DTPA-octreotide is currently the most important tracer in the diagnosis, staging and selection for peptide receptor radionuclide therapy (PRRT). In the past decade, different positron-emitting tomography (PET) tracers have been developed. The largest group is the 68 Gallium-labeled somatostatin analogs (Ga-68-SSA). Several studies have demonstrated their superiority compared to SRS in sensitivity and specificity. Furthermore, patient comfort and effective dose are favorable for Ga-68-SSA. Other PET targets like (F-18-[C-11]-5-hydroxy- L-tryptophan (C-11-5-HTP) and 6-F-18-L-3,4-dihydroxyphenylalanine (F-18-DOPA) were developed recently. For insulinomas, glucagon-like peptide-1 receptor imaging is a promising new technique. The evaluation of response after PRRT and other therapies is a challenge. Currently, the official follow-up is performed with radiological imaging techniques. The role of nuclear medicine may increase with the newest tracers for PET. In this review, the different nuclear imaging techniques and tracers for the imaging of NETs will be discussed. (C) 2015 S. Karger AG, Basel
Original language | Undefined/Unknown |
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Pages (from-to) | 73-87 |
Number of pages | 15 |
Journal | Frontiers of Hormone Research |
Volume | 44 |
DOIs | |
Publication status | Published - 2015 |
Research programs
- EMC MM-01-39-01
- EMC MM-01-40-01