Clinical Trials of Cancer Therapies Targeting Prostate-Specific Membrane Antigen

被引:60
|
作者
Olson, William C. [1 ]
Heston, Warren D. W. [2 ]
Rajasekaran, Ayyappan K. [3 ]
机构
[1] PSMA Dev Co LLC, Tarrytown, NY USA
[2] Cleveland Clin Fdn, Res Program Prostate Canc, Cleveland, OH 44195 USA
[3] Univ Calif Los Angeles, David Geffen Sch Med, Dept Pathol & Lab Med, Los Angeles, CA 90095 USA
基金
美国国家卫生研究院;
关键词
Prostate-specific membrane antigen; prostate cancer; immunotherapy; antibody-drug conjugate;
D O I
10.2174/157488707781662724
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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.
引用
收藏
页码:182 / 190
页数:9
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