Targeted Therapy in the Treatment of Castration-Resistant Prostate Cancer

被引:0
|
作者
Derleth, Christina L. [1 ]
Yu, Evan Y. [2 ,3 ]
机构
[1] Vanderbilt Univ, Dept Med, Div Hematol Oncol, Nashville, TN 37232 USA
[2] Univ Washington, Dept Med, Div Oncol, Seattle, WA 98195 USA
[3] Fred Hutchinson Canc Res Ctr, Seattle, WA 98104 USA
来源
ONCOLOGY-NEW YORK | 2013年 / 27卷 / 07期
关键词
ENDOTHELIAL GROWTH-FACTOR; PHASE-I; ANDROGEN ABLATION; POLY(ADP-RIBOSE) POLYMERASE; ANTISENSE OLIGONUCLEOTIDE; INCREASED SURVIVAL; MOLECULAR-CLONING; CLINICAL-TRIAL; DOUBLE-BLIND; HIGH-RISK;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In the field of metastatic castration-resistant prostate cancer, a bevy of novel therapeutics have recently been proven to extend survival via distinct mechanisms of action. Although revolutionary, these recent developments have not led to improved cure rates, and resistance eventually develops. Thus, further exploration into the biologic mechanisms of resistance to these new agents in prostate cancer has been necessary. This has opened the door to the development of agents designed to manipulate alternative biologic targets. In this review, we focus on the testosterone/androgen receptor pathway that is being targeted with potent new agents; we also discuss other important alternative biologic pathways that have given rise to new therapeutics that may attenuate prostate cancer growth, survival, and propagation.
引用
收藏
页码:620 / 628
页数:9
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