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Updated: Aug 13, 2026

A Whole Body Dosimetry Protocol for Peptide-Receptor Radionuclide Therapy (PRRT): 2D Planar Image and Hybrid 2D+3D SPECT/CT Image Methods
Published on: April 24, 2020
Peptide receptor radionuclide therapy (PRRT) and the pituitary: safety and efficacy
Francesco Ferraù1,2, Elena Sofia Blanca1, Carla Paola Costa1
1Endocrinology Unit, University Hospital "G. Martino" , Messina, Italy.
Abstract:
Peptide receptor radionuclide therapy (PRRT) is an emerging and promising targeted treatment for aggressive pituitary neuroendocrine tumours (PitNETs) and pituitary carcinomas refractory to conventional therapies. Its use is supported by the frequent expression of somatostatin receptors (SSTRs), predominantly SSTR2, in pituitary tumour cells, enabling selective delivery of β-emitting radionuclides, such as 177Lu-DOTATATE and 90Y-DOTATOC, resulting in targeted antitumour and antisecretory effects. This narrative review summarises current limited evidence on PRRT efficacy and safety in aggressive pituitary tumours. Successful outcomes have been reported in some cases in terms of tumour growth reduction and/or hormonal reduction or relief of mass-effect-related symptoms. PRRT-related adverse events are mostly mild and transient, predominantly haematological, with clinically significant renal toxicity uncommon when amino acid nephroprotection is used. Preserved pituitary function and no clinically significant PRRT-induced hypopituitarism have been reported. Overall, PRRT represents a biologically rational and potentially effective option for selected patients with SSTR-positive aggressive PitNETs after failure of previous therapies.
Insights
Peptide receptor radionuclide therapy (PRRT) shows promise for aggressive pituitary tumors. This treatment targets somatostatin receptors, offering potential tumor control and symptom relief with manageable side effects.
Area of Science:
- Endocrinology
- Nuclear Medicine
- Oncology
Background:
- Aggressive pituitary neuroendocrine tumors (PitNETs) and carcinomas often resist conventional treatments.
- Somatostatin receptors (SSTR), particularly SSTR2, are frequently overexpressed on these tumor cells.
- This overexpression allows for targeted delivery of radiolabeled somatostatin analogs.
Purpose of the Study:
- To review the current evidence on the efficacy and safety of Peptide Receptor Radionuclide Therapy (PRRT) for aggressive pituitary tumors.
- To assess PRRT's potential as a targeted treatment option for refractory PitNETs.
Main Methods:
- Narrative review of existing literature on PRRT in aggressive pituitary tumors.
- Analysis of reported outcomes regarding tumor response, hormonal control, and symptom relief.
- Evaluation of PRRT-related adverse events and toxicity, including nephroprotection strategies.
Main Results:
- PRRT demonstrated successful outcomes in some cases, including reduced tumor growth and hormonal secretion.
- Symptomatic relief from mass effects was also reported.
- Adverse events were generally mild and transient, primarily hematologic; renal toxicity was uncommon with amino-acid nephroprotection.
- Pituitary function was largely preserved, with no significant PRRT-induced hypopituitarism.
Conclusions:
- PRRT is a biologically rational and potentially effective therapeutic option for selected patients with SSTR-positive aggressive pituitary tumors.
- It offers a targeted approach for patients who have failed previous therapies.
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