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Updated: Jun 21, 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
Targeted radionuclide therapy for neuroendocrine tumours: principles and application
Maralyn R Druce1, Val Lewington, Ashley B Grossman
1Centre for Endocrinology, Barts and the London School of Medicine, London, UK.
Abstract:
Neuroendocrine tumours comprise a group of neoplasms with variable clinical behaviour. Their growth and spread is often very slow and initially asymptomatic, and thus they are often metastatic at the time of diagnosis and incurable by surgery. An exciting therapeutic strategy for cytoreduction, both for stabilisation of tumour growth and inhibition of hormone production, is the use of targeted radionuclide therapy. Evidence from large-scale, randomised, placebo-controlled trials is very difficult to obtain in these rare diseases, but current data appear promising. It is timely to review the principles underlying the use of these therapies, together with the clinical outcomes to date and potential directions for future research.
Insights
Targeted radionuclide therapy shows promise for managing neuroendocrine tumors (NETs), offering a strategy to control tumor growth and hormone production when surgery is not an option. Further research is needed due to the rarity of these neoplasms.
Area of Science:
- Oncology
- Nuclear Medicine
- Endocrinology
Background:
- Neuroendocrine tumors (NETs) are rare neoplasms with variable behavior, often diagnosed at a metastatic stage and incurable by surgery.
- Slow growth and initial asymptomatic presentation contribute to late-stage diagnosis.
Purpose of the Study:
- To review the principles of targeted radionuclide therapy for NETs.
- To summarize current clinical outcomes and discuss future research directions for this therapeutic strategy.
Main Methods:
- Review of existing literature and clinical data on targeted radionuclide therapy in neuroendocrine tumors.
- Analysis of evidence from randomized controlled trials, acknowledging limitations due to disease rarity.
Main Results:
- Targeted radionuclide therapy is an emerging strategy for cytoreduction in NETs.
- This therapy aims to stabilize tumor growth and inhibit hormone production.
- Current data, though limited by trial size, appear promising for managing NETs.
Conclusions:
- Targeted radionuclide therapy presents a viable and promising approach for managing advanced or metastatic neuroendocrine tumors.
- Despite challenges in conducting large-scale trials for rare diseases, the evidence supports its role in cytoreduction and symptom management.
- Future research should focus on refining techniques and expanding evidence for this innovative treatment modality.
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