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Somatostatin receptor scintigraphy

(SRS, octreotide scan, nuclear imaging of neuroendocrine tumors, NET detection)

Somatostatin receptor scintigraphy (SRS) is a nuclear imaging technique used to locate and stage neuroendocrine tumors (NETs), as well as detect metastases and/or early tumor recurrence.
SRS is currently a standard imaging modality indicated for NET staging, invaluable both in terms of choice of the best treatment option (surgery, hormonal treatment, chemotherapy, radionuclide therapy) and treatment follow-up. This study is particularly recommended in patients with NETs, who will later undergo radionuclide therapy with labelled somatostatin analogues.
The study makes use of Tc-99m radiopharmaceutical (isotopic tracer). This isotope has low gamma radiation energy and a short half-life (about 6 h), and thus is absolutely safe. Radiation load received by the patient due to SRS is lower than the one received due to many conventional radiological imaging procedures, e.g. CT of the abdomen. Somatostatin receptor scintigraphy can be offered to patients of any age and be repeated multiple times, as clinically indicated.
Different somatostatin receptor subtypes are present on the surface of the neuroendocrine tumor cells. All in all, there are five subtypes: SST1, SST2, SST3, SST4 and SST5, the most common among them being SST2 and SST5. Particles of theTc-99m based somatostatin analogue radiopharmaceuticals (e.g. Tektrotide, HYNIC-TATE, Neo-SPECT) attach themselves to these receptors, due to which even small primary tumors and metastases can be visualized in the whole-body and SPECT scintigraphic images. Somatostatin receptor scintigraphy is also a valuable diagnostic tool for detection of early tumor recurrence.

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