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Updated: Aug 9, 2026

A Practical Guide for the Production and PET/CT Imaging of 68Ga-DOTATATE for Neuroendocrine Tumors in Daily Clinical Practice
Published on: April 17, 2019
Neuroendocrine tumors and somatostatin: imaging techniques
W W de Herder1, D J Kwekkeboom, R Valkema
1Section of Endocrinology, Department of Internal Medicine, Erasmus Rotterdam, the Netherlands. w.w.deherder@erasmusmc.nl
Abstract:
Tumors and metastases bearing the somatostatin receptor subtypes 2 (SSTR2) or SSTR5 can be visualized in vivo after injection of radiolabeled octapeptide somatostatin analogs like 111In-pentetreotide. The sensitivity of 111In-pentetreotide scintigraphy for the detection of carcinoid tumors is 86-95%. The sensitivity of 111In-pentetreotide scintigraphy for the detection of gastrinomas, vasoactive intestinal polypeptide-secreting tumors, and glucagonomas as well as clinically non-functioning lesions is 75-100%. However, for insulinoma this is 50-60%. 111In-pentetreotide scintigraphy generally has a lower detection rate for benign pheochromocytomas than 123I-MIBG scintigraphy, but it can have a complementary role for the staging of malignant pheochromocytomas. It can also be used for the detection of extra-adrenal pheochromocytomas and paragangliomas. Most GH- and TSH-secreting pituitary adenomas can be visualized using 111In-pentetreotide. 111In-pentetreotide scintigraphy is negative in microprolactinomas and ACTH-secreting pituitary microadenomas. 111In-pentetreotide scintigraphy has been successful for the localization of extra-pituitary ACTH-secreting tumors and their metastases, and especially for occult tumors. A large variety of lesions in and around the pituitary region express somatostatin receptors and, therefore, can be visualized by 111In-pentetreotide scintigraphy.
Insights
111In-pentetreotide scintigraphy effectively detects various neuroendocrine tumors, including carcinoids and pituitary adenomas, by targeting somatostatin receptors. However, its sensitivity varies for specific tumors like insulinomas and benign pheochromocytomas.
Area of Science:
- Nuclear Medicine
- Oncology
- Endocrinology
Background:
- Somatostatin receptor subtypes 2 (SSTR2) and SSTR5 are expressed in various tumors and metastases.
- Radiolabeled somatostatin analogs, such as 111In-pentetreotide, can visualize these SSTR-expressing lesions in vivo.
Purpose of the Study:
- To evaluate the diagnostic utility and sensitivity of 111In-pentetreotide scintigraphy for detecting a range of neuroendocrine tumors and other lesions.
- To compare its efficacy with other imaging modalities like 123I-MIBG scintigraphy for specific tumor types.
Main Methods:
- Administration of 111In-pentetreotide, a radiolabeled octapeptide somatostatin analog.
- Scintigraphic imaging to visualize tumors and metastases expressing SSTR2 or SSTR5.
Main Results:
- High sensitivity (86-95%) for carcinoid tumors.
- Variable sensitivity for other neuroendocrine tumors (75-100% for gastrinomas, VIPomas, glucagonomas; 50-60% for insulinomas).
- Complementary role in staging malignant pheochromocytomas and detecting extra-adrenal tumors; effective for pituitary adenomas but not microprolactinomas or some ACTH-secreting microadenomas.
Conclusions:
- 111In-pentetreotide scintigraphy is a valuable tool for visualizing SSTR-expressing tumors, with varying sensitivity depending on tumor type.
- It plays a crucial role in diagnosing and staging neuroendocrine tumors, including carcinoids, pituitary adenomas, and pheochromocytomas.
- Its utility is particularly noted for extra-pituitary ACTH-secreting tumors and occult lesions.
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