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Mednarodni projekti vir: SICRIS

Novel 99mTc-labeled somatostatin receptor antagonists in the diagnostic algorithm of neuroendocrine neoplasms – a feasibility study

Ključne besede
Medical Physics & Theranostics
Raziskovalci (1)
št. Evidenčna št. Ime in priimek Razisk. področje Vloga Obdobje Štev. publikacijŠtev. publikacij
1.  27760  dr. Urban Simončič  Fizika  Raziskovalec  2019 - 2023  120 
Organizacije (1)
št. Evidenčna št. Razisk. organizacija Kraj Matična številka Štev. publikacijŠtev. publikacij
1.  1554  Univerza v Ljubljani, Fakulteta za matematiko in fiziko  Ljubljana  1627007  34.130 
Povzetek
Neuroendocrine neoplasms (NEN) are a heterogeneous group of malignancies biologically characterized by overexpression of somatostatin receptors (SSTR) on cell membranes. Nuclear medicine is a molecular imaging method able to visualize NEN by means of radiopharmaceuticals that bind to SSTR, allowing prediction and evaluation of response to various therapies available. Recently, novel radiopharmaceuticals, based on SSTR antagonists, were shown to provide superior SSTR visualization than currently used agonists. The development of a widely available, quantitative imaging methodology in combination with improved single-photon emitting radiopharmaceuticals, presently not available, represents a significant advancement in NEN patient management. Hypothesis: SSTR antagonists are superior to agonists for visualization of NEN. A 99mTc-labelled SSTR antagonist imaged with a quantitative approach serves as an optimal molecular imaging tool for personalized management of NEN patients. Aim: (1) to select a 99mTc-labelled SSTR antagonist and establish a pharmaceutical formulation for NEN imaging; (2) to initiate a clinical feasibility study in NEN patients and (3) develop a robust, reproducible quantitative imaging method. Methods: From two promising new radiopharmaceuticals a superior candidate will be selected for clinical translation and a kit-formulation for radiolabelling developed. Ten NEN patients with proven SSTR expression on agonist imaging will be recruited. Patients will be imaged at predefined time points for assessment of pharmacodynamics, pharmacokinetics and dosimetry using a concurrently developed quantitative imaging protocol. Expected results and potential clinical impact: 99mTc-labelled SSTR antagonist is expected to be an effective, widely available method for quantitative assessment of SSTR status in NEN. As such, it will decisively influence management of patients with NEN, allowing a personalized therapeutic approach.
Zgodovina ogledov
Priljubljeno