Neuroendocrine tumors (NETs) are a heterogeneous group of neoplasms characterized by their overexpression of somatostatin receptors (SSTRs), which can be utilized for peptide receptor radionuclide therapy. This review provides a comprehensive update on the clinical trials of radiolabeled SSTR-targeting radiopharmaceuticals since 2020, with a focus on somatostatin receptor agonists and antagonists radiolabeled with 68 Ga, 18 F, 99m Tc, 177 Lu, 161 Tb, 212 Pb, 67 Cu, and 225 Ac. Head-to-head clinical trials demonstrate that radiolabeled SSTR antagonists such as 68 GaGa-DOTA-JR11 and 68 GaGa-DOTA-LM3 offer improved lesion detection and tumor-to-background ratios (particularly in liver metastases) compared to radiolabeled agonists like 68 GaGa-DOTA-TOC and 64 CuCu-DOTA-TATE. Additionally, 18 F-labeled agents offer logistical and dosimetric advantages over 68 Ga, due to 18 F's longer half-life and cyclotron production, allowing for delayed imaging and increased availability to a wider range of patients. Emerging targeted alpha therapy agents, including 225 AcAc-DOTA-TATE, show promising results in treating disease resistant to conventional therapies due to the high linear energy transfer of alpha particles, which leads to improved localized cytotoxicity. Collectively, these developments support a shift toward more precise, receptor-specific theragnostics, emphasizing the need for further head-to-head clinical trials and integration of dosimetry-driven, personalized treatment planning in the management of NETs.
Haugh et al. (Thu,) studied this question.
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