Linker modifications in radiolabeled RM26-based antagonists to gastrin-releasing peptide receptor (GRPR) improved tracers' pharmacokinetics.

Radionuclide targeting of gastrin-releasing peptide receptor (GRPR) holds significant diagnostic and therapeutic potential, particularly in PSMA-negative/low-grade prostate cancer, estrogen receptor-positive breast cancer, and other malignancies. Recently, our group reported the development and results of the Phase I clinical evaluation of [Tc]Tc-maSSS-PEG2-RM26, an antagonist GRPR-targeting SPECT imaging agent. This study focuses on developing the next generation of RM-26-based GRPR antagonists with enhanced metabolic stability and improved pharmacokinetics. Four new RM-26-based agents containing sarcosine (Sar) at position 11 to improve the in vivo stability and with more hydrophilic linkers were designed: Pep1 - maSSS-PEG2-[Sar]RM26, Pep2 - maSSS-PEG6-[Sar]RM26, Pep3 - maSSS-PEG2-Pip-[Sar]RM26, and Pep4 - maSSS-EEE-[Sar]RM26. These analogs were compared both in vitro and in vivo with [Tc]Tc-maSSS-PEG2-RM26 as a reference. In PC-3 cells, [Tc]Tc-Pep1, [Tc]Tc-Pep2 and [Tc]Tc-Pep3, but not [Tc]Tc-Pep4, specifically bound to GRPR and exhibited low nanomolar affinity. When compared in vivo, [Tc]Tc-Pep1, [Tc]Tc-Pep2, and [Tc]Tc-Pep3 demonstrated rapid blood clearance with different degrees of hepatobiliary excretion, particularly [Tc]Tc-Pep2 and [Tc]Tc-Pep3 had significantly lower activity uptake in the liver and gastrointestinal tract compared to [Tc]Tc-maSSS-PEG2-RM26. Both [Tc]Tc-Pep2 and [Tc]Tc-Pep3 showed improved metabolic stability, bound specifically to GRPR in vivo, and demonstrated a tendency (not statistically significant) for higher tumor activity uptake compared to the reference peptide. Biodistribution data were confirmed by SPECT/CT imaging. In conclusion, the analogs with an elongation of the PEG2-linker either up to PEG6 (Pep2) or with the addition of a basic piperidine-containing moiety (Pep3) demonstrated an improvement of the pharmacokinetic properties of these agents and justify further investigations.