Related Experiment Video
Updated: Jun 16, 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
Imaging of neuroendocrine tumours with gamma-emitting radiopharmaceuticals
E Bombardieri1, A Coliva, M Maccauro
1Division of Nuclear Medicine, Fondazione IRCCS "Istituto Nazionale dei Tumori", Milan, Italy. emilio.bombardieri@istitutotumori.mi.it
Abstract:
Nuclear medicine can image some tumors by means of receptor specific radiopharmaceuticals, and offers the possibility to characterize cancer through the detection of its receptor expression. This is the case of neuroendocrine tumours (NETs), that are visualized by different radiolabelled somatostatin analogues that bind 5 distinct somatostatin receptor types (named sstr1-5) that show different tissue distribution. The subtypes sstr2 and sstr5 are the most commonly expressed in NETs. Until now the most widely used radiolabelled somatostatin analogue for planar and single photon emission computed tomography (SPECT) has been [(111)In]pentetreotide, because of its commercial availability. Other analogues labelled with gamma emitting radionuclides are [(99m)Tc]EDDA/HYNIC-TOC, [(99m)Tc]P829, [(111)In]DOTA-lanreotide, [(111)In]DOTA-NOC-ATE, [(111)In]DOTA-BOC-ATE. However, these compounds have not been successful for the routine use. Moreover, NETs express various receptors that can be depicted by different radiopharmaceuticals, such as [(123)I]VIP and [(111)In]GLP-1. Besides this, some precursors of the catecholamines metabolism, as meta-iodo-benzyl-guanidine (MIBG), labelled with (123)I or (131)I, accumulates in neuroendocrine tissues, in particular those of sympathoadrenal lineage. MIBG scintigraphy is currently indicated for neuroblastoma, paraganglioma and phaeocromocitoma. An impressive technological progress has been achieved recently with PET and, in particular, with the development of hybrid instrumentations (PET/CT) combining nuclear imaging with radiological imaging providing both functional and morphologic information. Among positron emitting tracers, the [(18)F]FDG is the most diffuse in oncology, but other more effective tracers are available for NETs, such as the analogues labelled with 68Ga. The diagnostic sensitivity and accuracy of these technology is superior to that of gamma emitting radiopharmaceuticals, but the fact that they are not still registered limits their use in the clinical practice. This overview summarizes the state of art of NETs imaging, focusing the attention mainly on gamma-emitting tracers.
Insights
Nuclear medicine imaging for neuroendocrine tumors (NETs) utilizes receptor-specific radiopharmaceuticals. While gamma-emitting tracers like [(111)In]pentetreotide are common, newer positron emission tomography (PET) tracers offer superior diagnostic accuracy for NETs.
Area of Science:
- Nuclear Medicine
- Oncology
- Radiopharmacology
Background:
- Neuroendocrine tumors (NETs) express somatostatin receptors (sstr1-5), particularly sstr2 and sstr5.
- Traditional imaging relies on gamma-emitting radiopharmaceuticals like [(111)In]pentetreotide, with limited routine success for other analogues.
- Other NETs receptors can be targeted by tracers like [(123)I]VIP and [(111)In]GLP-1, and MIBG is used for sympathoadrenal tumors.
Purpose of the Study:
- To review the current state of nuclear medicine imaging for neuroendocrine tumors (NETs).
- To highlight the role of various radiopharmaceuticals, focusing on gamma-emitting tracers.
- To discuss advancements in PET imaging for NETs.
Main Methods:
- Review of radiolabelled somatostatin analogues for SPECT imaging.
- Discussion of other radiopharmaceuticals targeting different NETs receptors.
- Overview of MIBG scintigraphy for specific neuroendocrine tissues.
- Exploration of positron emission tomography (PET) tracers, including 68Ga-labelled analogues and [(18)F]FDG.
Main Results:
- [(111)In]pentetreotide is the most established gamma-emitting tracer for NETs, despite limitations of other analogues.
- PET tracers, especially 68Ga-labelled analogues, demonstrate superior diagnostic sensitivity and accuracy compared to gamma emitters.
- The clinical adoption of advanced PET tracers is hindered by their lack of registration.
Conclusions:
- Gamma-emitting tracers remain a focus for NETs imaging, with ongoing use of established agents.
- PET/CT technology offers significant advantages in functional and morphological information for NETs.
- Further clinical integration of advanced PET tracers is needed to fully leverage their diagnostic potential in NETs.
Related Concept Videos
Imaging Studies II: Positron Emission Tomography and Scintigraphy
Fundamental Principles of PET
Positron Emission Tomography
One of the main requirements of a PET scan is a positron-emitting radioisotope, which is produced in a cyclotron and then attached to a substance used by the part of the body being...
Radiological Investigation III: Pulmonary Angiogram and PET Scan
Pulmonary Angiogram
A Pulmonary Angiogram is an invasive procedure involving injecting a contrast medium through a catheter threaded into the pulmonary artery or the right side of the heart to visualize the pulmonary vasculature. Computed Tomography (CT) scans have mainly replaced this...
