Peptide receptor radionuclide therapy (PRRT) involves administration of a radioactive particulate emitter (lutetium-177) linked to a ligand of somatostatin receptor (DOTATATE) in an attempt to selectively kill neuroendocrine carcinoma cells.
For a brief introduction of neuroendocrine tumours (NETs), neuroendocrine carcinomas (NECs) and somatostatin receptors (SSTR), please visit the page on SSTR PET.
The beta emitter lutetium-177 (or 177Lu) complexed with DOTATATE is used as the radiopharmaceutical (RP) at SSNI for PRRT. It has a physical half-life of 162 h. Apart from beta particles, it also emits gamma photons that allow for its imaging (performing scan) following administration of PRRT.
It is mandatory for patients to undergo SSTR PET to determine suitability for PRRT. PRRT is best suited for those with well-differentiated and moderately differentiated NECs. Those with poorly differentiated NECs tend to show high FDG uptake, and hence, some of the PRRT candidates may have to also undergo a whole-body FDG PET-CT.
Lutetium-177 is avidly reabsorbed by kidney cells, hence, steps are taken to reduce radiation dose to the kidneys (including lowering the amount of drug administered), and in some cases, rejecting patients with severely impaired kidney function.
Likewise, particular caution is exercised in those with history and/or tendency of bone marrow suppression because of recent chemotherapy and/or extensive radiotherapy.
For additional information, please visit the following links.