Inhibition of angiogenesis: Treatment options for patients with metastatic prostate cancer

被引:69
作者
Figg, WD [1 ]
Kruger, EA [1 ]
Price, DK [1 ]
Kim, S [1 ]
Dahut, WD [1 ]
机构
[1] NCI, Med Branch, Div Clin Sci, NIH, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
antiangiogenesis; cancer therapy; clinical trials; prostate carcinoma;
D O I
10.1023/A:1015626410273
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Prostate cancer is the most frequently diagnosed malignancy and the second most common cause of cancer-related death in men in the United States. Unfortunately, at the current time, no curative treatments are available for metastatic prostate cancer. As is the case for most solid tumors, the recruitment of blood vessels (angiogenesis) is key for the progression and metastasis of prostate cancer. Inhibition of this process is an attractive approach to treatment. Many antiangiogenic agents are currently in clinical development. The following discussion will outline the importance of angiogenesis in the metastasis and progression of prostate cancer, summarize the current surrogate markers of angiogenesis available for the drug development of antiangiogenic agents, and review examples of investigational agents that target tumor angiogenesis (e.g., TNP-470, Thalidomide, CC5013, Carboxyamido-triazole (CAI), Endostatin, SU5416 , SU6668, Bevacizumab (Anti-VEGF rhuMAb), and 2-Methoxyestradiol).
引用
收藏
页码:183 / 194
页数:12
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