3.8 Article

Clinical Trials of Cancer Therapies Targeting Prostate-Specific Membrane Antigen

Journal

REVIEWS ON RECENT CLINICAL TRIALS
Volume 2, Issue 3, Pages 182-190

Publisher

BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/157488707781662724

Keywords

Prostate-specific membrane antigen; prostate cancer; immunotherapy; antibody-drug conjugate

Funding

  1. National Institutes of Health [CA107653, CA095928, CA091746, CA101069]
  2. DOD [PC060746, W81XWH-04-1-0113]
  3. NATIONAL CANCER INSTITUTE [R43CA095928, R44CA091746, R43CA107653, R01CA101069, R43CA091746, R44CA095928, R44CA107653] Funding Source: NIH RePORTER

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Prostate cancer is the most common non-cutaneous cancer of men in the United States and represents their second-leading cause of cancer-related death. Metastatic disease is largely resistant to conventional chemotherapies, and targeted therapies are urgently needed. Prostate-specific membrane antigen (PSMA) is a prototypical cell-surface marker of prostate cancer. PSMA is an integral, non-shed, type 2 membrane protein with abundant and nearly universal expression in prostate carcinoma, but has limited extra-prostatic expression. In addition, PSMA is expressed in the neovasculature of other solid tumors. These findings have spurred development of PSMA-targeted therapies for cancer, and first-generation products have entered clinical testing. Vaccine approaches have included recombinant protein, nucleic acid and cell-based strategies, and anti-PSMA immune responses have been demonstrated in the absence of significant toxicity. Therapy with drug-conjugated and radiolabeled antibodies has yielded objective clinical responses as measured by reductions in serum prostate-specific antigen and/or imageable tumor volume. However, responses were observed in a minor fraction of patients and at doses near the maximum tolerated dose. Overall, these initial studies have provided measured proof of concept for PSMA-based therapies, and second-generation antibody and vaccine products may hold the key to exploit PSMA for molecularly targeted therapy of prostate and other cancers.

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