Introduction: Prostate specific membrane antigen (PSMA), highly expressed in metastatic castration-resistant prostate cancer (mCRPC), is an established therapeutic target. Theranostic PSMA-targeting agents are widely used in patient management and has shown improved outcomes for mCRPC patients. Earlier, we optimized a urea-based probe for radionuclide visualization of PSMA-expression using computer modeling. With the purpose to develop a targeting agent equally suitable for radionuclide imaging and therapy, the agent containing DOTA chelator was designed (BQ7876). The aim of the study was to test the hypothesis that Lu-labeled BQ7876 possesses target binding and biodistribution properties potentially enabling its use for radiotherapy.

Methods: BQ7876 was synthesized and labeled with Lu-177. Specificity and affinity of [Lu]Lu-BQ7876 to PSMA-expressing PC3-pip cells was evaluated and its processing after binding to cells was studied. Animal studies in mice were performed to assess its biodistribution , target specificity and dosimetry. [Lu]Lu-PSMA-617 was simultaneously evaluated for comparison.

Results: BQ7876 was labeled with Lu-177 with radiochemical yield >99%. Its binding to PSMA was specific and when tested in antigen saturation conditions as well as in PSMA-negative PC-3 tumors. The binding of [Lu]Lu-BQ7876 to living cells was characterized by rapid association, while the dissociation included a rapid and a slow phase with affinities K = 3.8 nM and K = 25 nM. The half-maximal inhibitory concentration for Lu-BQ7876 was 59 nM that is equal to 61 nM for Lu-PSMA-617. Cellular processing of [Lu]Lu-BQ7876 was accompanied by slow internalization. [Lu]Lu-BQ7876 was cleared from blood and normal tissues rapidly. Initial elevated uptake in kidneys decreased rapidly, and by 3 h post injection, the renal uptake (13 ± 3%ID/g) did not differ significantly from tumor uptake (9 ± 3%ID/g). Tumor uptake was stable between 1 and 3 h followed by a slow decline. The highest absorbed dose was in kidneys, followed by organs and tissues in abdomen.

Discussion: Biodistribution studies in mice demonstrated that targeting properties of [Lu]Lu-BQ7876 are not inferior to properties of [Lu]Lu-PSMA-617, but do not offer any decisive advantages.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10565663PMC
http://dx.doi.org/10.3389/fonc.2023.1221103DOI Listing

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