Novel targeted therapeutics for metastatic castration-resistant prostate cancer

被引:74
作者
Antonarakis, Emmanuel S. [1 ]
Carducci, Michael A. [1 ]
Eisenberger, Mario A. [1 ]
机构
[1] Sidney Kimmel Comprehens Canc Ctr Johns Hopkins, Baltimore, MD 21231 USA
关键词
Metastatic castration-resistant prostate cancer; Targeted therapies; Immune therapies; Molecular targets; Clinical trials; Drug development; GROWTH-FACTOR RECEPTOR; RANDOMIZED PHASE-II; ANDROGEN-INDEPENDENT PROGRESSION; MITOXANTRONE PLUS PREDNISONE; IGF BINDING PROTEIN-3; ENDOTHELIN-A RECEPTOR; HIGH-DOSE CALCITRIOL; CELLULAR IMMUNOTHERAPY; CONTROLLED-TRIAL; IMATINIB MESYLATE;
D O I
10.1016/j.canlet.2009.08.012
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Virtually all patients that succumb to prostate cancer die of metastatic castration-resistant disease. Although docetaxel is the standard of care for these patients and is associated with a modest prolongation of survival, there is an urgent need for novel treatment strategies for metastatic prostate cancer. In the last several years, great strides have been made in our understanding of the biological and molecular mechanisms driving prostate cancer growth and progression, and this has resulted in widespread clinical testing of numerous new targeted therapies. This review discusses some of the key therapeutic agents that have emerged for the treatment of metastatic castration-resistant prostate cancer in the last 5 years, with an emphasis on both molecular targets and clinical trial design. These agents include mammalian target of rapamycin (mTOR) pathway inhibitors, anti-angiogenic drugs, epidermal growth factor receptor (EGFR) inhibitors, insulin-like growth factor (IGF) pathway inhibitors, apoptosis-inducing drugs, endothelin receptor antagonists, receptor activator of nuclear factor kappa B (RANK) ligand inhibitors, vitamin D analogues, cytochrome P17 enzyme inhibitors, androgen receptor modulators, epigenetic therapies, vaccine therapies, and cytotoxic T lymphocyte-associated antigen (CTLA)-4 blocking agents. (C) 2009 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:1 / 13
页数:13
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