Controversies in <scp>NEN</scp> : An <scp>ENETS</scp> position statement on the interchangeability of somatostatin receptor <scp>PET</scp> tracers

Molecular imaging of the somatostatin receptor (SSTR) plays a key role in the management of patients with neuroendocrine neoplasms in general, and neuroendocrine tumours in particular. Over the last 2 decades, gallium-68 labelled somatostatin analogues have revolutionised SSTR imaging through the advent of SSTR positron emission tomography (PET), leading to better staging and theranostic imaging. Recent advances in the development of PET SSTR tracers continue to change the field, with novel tracers labelled with different radionuclides such as fluorine-18 and copper-64, or based on new antagonist vector molecules. The advent of these innovations generates questions, such as which tracers can be used in clinical practice, how to compare scans performed with different tracers, or can antagonists be used to select patients for peptide receptor radionuclide therapy? This 'controversy paper' from the European Neuroendocrine Tumor Society provides an overview of the relevant evidence to answer these questions, and provides guidance to clinicians and nuclear medicine physicians for contemporary use of SSTR PET.

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Publication Details

Journal
Journal of Neuroendocrinology
Published
2026-06-30
DOI
https://doi.org/10.1111/jne.70220
Primary Topic
Neuroendocrine Tumor Research Advances
Type
article
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article

Controversies in NEN : An ENETS position statement on the interchangeability of somatostatin receptor PET tracers

Valentina Ambrosini, Nicola Fazio, Gregory Kaltsas, Christophe M. Deroose et al.
Journal of Neuroendocrinology
Neuroendocrine Tumor Research Advances
article

Controversies in NEN : An ENETS position statement on the interchangeability of somatostatin receptor PET tracers

Valentina Ambrosini, Nicola Fazio, Gregory Kaltsas, Christophe M. Deroose, Andreas Kjær, Eva Tiensuu Janson, Johannes Hofland, Ángela Lamarca, Anna Sowa-Staszczak
article en

Abstract

Molecular imaging of the somatostatin receptor (SSTR) plays a key role in the management of patients with neuroendocrine neoplasms in general, and neuroendocrine tumours in particular. Over the last 2 decades, gallium-68 labelled somatostatin analogues have revolutionised SSTR imaging through the advent of SSTR positron emission tomography (PET), leading to better staging and theranostic imaging. Recent advances in the development of PET SSTR tracers continue to change the field, with novel tracers labelled with different radionuclides such as fluorine-18 and copper-64, or based on new antagonist vector molecules. The advent of these innovations generates questions, such as which tracers can be used in clinical practice, how to compare scans performed with different tracers, or can antagonists be used to select patients for peptide receptor radionuclide therapy? This 'controversy paper' from the European Neuroendocrine Tumor Society provides an overview of the relevant evidence to answer these questions, and provides guidance to clinicians and nuclear medicine physicians for contemporary use of SSTR PET.

Journal of NeuroendocrinologyVol. 38(7)
Jagiellonian University (PL), National and Kapodistrian University of Athens (GR), Science for Life Laboratory (SE), Copenhagen University Hospital (DK), Rigshospitalet (DK), Azienda USL di Bologna (IT), Hospital Universitario Fundación Jiménez Díaz (ES), Erasmus MC Cancer Institute (NL), European Institute of Oncology (IT), Universidad Autónoma de Madrid (ES), University of Bologna (IT), KU Leuven (BE)
Openalex Percentile: Top 8%
Neuroendocrine Tumor Research Advances
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