Radioimmunotherapy of prostate cancer in human xenografts using monoclonal antibodies specific to prostate specific membrane antigen (PSMA): Studies in nude mice

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Abstract
BACKGROUND Prostate specific membrane antigen (PSMA), expressed by virtually all prostate cancers is an ideal target for targeted therapy of prostate cancer. Radiolabeled J591 monoclonal antibody (MAb) binds with high affinity to an extracellular epitope of PSMA and localizes specifically in PSMA positive LNCaP tumors in vivo. METHODS Pre‐clinical radioimmunotherapy (RIT) studies using 131I‐huJ591 and 90Y‐1,4,7,10‐tetraazacyclododecane‐N,N′,N′′,N′′′‐tetraacetic acid (DOTA)‐huJ591 MAbs were studied in nude mice bearing LNCaP xenografts. RESULTS A 15–90% reduction in mean tumor volume was observed after a single dose of 131I‐huJ591 (3.7–11.1 MBq) or 90Y‐DOTA‐huJ591 (3.7–7.4 MBq). The median survival time increased 2–3 times relative to untreated controls. Multiple administrations of fractionated doses of 90Y‐DOTA‐huJ591 were even more effective with minimal toxicity. Radiation dose to blood and tumor was higher with 90Y than with 131I. The maximum tolerated dose (MTD) is 5.55 MBq for 90Y‐DOTA‐huJ591 and more than 11.1 MBq for 131I‐huJ591. For 90Y‐DOTA‐huJ591 at MTD, dose to the tumor was 2,753 cGy. CONCLUSIONS In nude mice bearing PSMA positive tumors, radiation dose to the tumor with 90Y‐DOTA‐J591 is greater for large tumors than with 131I‐J591. The theoretical and practical considerations strongly suggest that 90Y‐DOTA‐huJ591 may be a suitable radiopharmaceutical for the treatment of prostate cancer.