Therapeutic Efficacy of a Bivalent Inhibitor of Prostate-Specific Membrane Antigen Labeled with (67)Cu

用 (67)Cu 标记的前列腺特异性膜抗原二价抑制剂的治疗效果

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Abstract

Radionuclide therapy targeting prostate-specific membrane antigen (PSMA) is promising for prostate cancer. We previously reported a ligand, (64)Cu-CuSarbisPSMA, featuring 2 lysine-ureido-glutamate groups. Here, we report the therapeutic potential of (67)Cu-CuSarbisPSMA. Methods: Growth of PSMA-positive xenografts was evaluated after treatment with (67)Cu-CuSarbisPSMA or (177)Lu-LuPSMA imaging and therapy (I&T). Results: At 13 d after injection, tumor growth was similarly inhibited by the 2 tracers in a dose-dependent manner. Survival was comparable after single (30 MBq) or fractionated (2 × 15 MBq, 2 wk apart) administrations. Conclusion:(67)Cu-CuSarbisPSMA is efficacious in a PSMA-expressing model of prostate cancer.

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