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Gastroenteropancreatic neuroendocrine tumours (GEP-NET) - Imaging and staging
Tobias Baumann1, Christof Rottenburger2, Guillaume Nicolas3
1Clinic of Radiology and Nuclear Medicine, University of Basel Hospital, Basel, Switzerland.
Abstract:
Detection of gastroenteropancreatic neuroendocrine tumours (GEP-NETs) and monitoring of treatment response relies mainly on morphological imaging such as computed tomography (CT) and magnetic resonance imaging (MRI). Molecular imaging techniques also in combination with CT (hybrid imaging) greatly benefit patient management, including better localization of occult tumours and better staging. Somatostatin receptor scintigraphy (SRS) and somatostatin receptor (SSTR) positron emission tomography (PET) play a central role in the diagnostic work-up of patients with well-differentiated GEP-NETs. SSTR PET/CT is superior to SRS and should be used whenever available. (18)F-DOPA and (18)F-FDG PET/CT is inferior to SSTR PET/CT at least in patients with well-differentiated GEP-NETs. Both SSTR PET/CT and SRS have limitations, such as relatively low detection rate of benign insulinomas, poorly differentiated GEP-NETs and liver metastases. New innovations such as SSTR PET/MRI, radiolabelled SSTR antagonists and glucagon-like peptide-1 receptor (GLP-1R) agonists might further improve imaging of GEP-NETs.
Insights
Somatostatin receptor positron emission tomography/computed tomography (SSTR PET/CT) is the preferred molecular imaging for gastroenteropancreatic neuroendocrine tumours (GEP-NETs). While effective, SSTR PET/CT and scintigraphy have limitations, with new innovations showing promise for improved GEP-NET detection.
Area of Science:
- Nuclear Medicine
- Oncology
- Radiology
Background:
- Morphological imaging (CT, MRI) is standard for gastroenteropancreatic neuroendocrine tumour (GEP-NET) detection and treatment monitoring.
- Molecular imaging, especially hybrid imaging (PET/CT), enhances patient management through improved tumor localization and staging.
- Somatostatin receptor scintigraphy (SRS) and somatostatin receptor (SSTR) positron emission tomography (PET) are crucial for diagnosing well-differentiated GEP-NETs.
Purpose of the Study:
- To evaluate the role and limitations of current molecular imaging techniques in GEP-NET diagnosis.
- To compare the efficacy of SSTR PET/CT with SRS and other PET tracers.
- To highlight emerging innovations for improved GEP-NET imaging.
Main Methods:
- Review of current literature on molecular imaging for GEP-NETs.
- Comparison of SSTR PET/CT, SRS, (18)F-DOPA PET/CT, and (18)F-FDG PET/CT.
- Discussion of limitations and potential of novel imaging agents and techniques.
Main Results:
- SSTR PET/CT is superior to SRS for well-differentiated GEP-NETs and should be prioritized.
- (18)F-DOPA and (18)F-FDG PET/CT are less effective than SSTR PET/CT in well-differentiated GEP-NETs.
- SSTR PET/CT and SRS show limitations in detecting benign insulinomas, poorly differentiated GEP-NETs, and liver metastases.
Conclusions:
- SSTR PET/CT is the leading molecular imaging modality for GEP-NETs, offering advantages over SRS.
- Current techniques have limitations, necessitating further research and development.
- Emerging technologies like SSTR PET/MRI and GLP-1R agonists hold potential for advancing GEP-NET imaging.
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