University of Utah, Huntsman Cancer Institute, 2000 Circle of Hope, Ste 2123, Salt Lake City, UT 84112, USA.
Curr Urol Rep. 2013 Jun;14(3):174-83. doi: 10.1007/s11934-013-0322-0.
Until 2010, chemotherapy with docetaxel was the only approved agent for treatment of metastatic castrate resistant prostate cancer (mCRPC). Since then, the therapeutic landscape of mCRPC has changed rapidly. Multiple novel agents have received regulatory approval after demonstrating improved overall survival in separate randomized Phase 3 studies. These include immunotherapeutic agent sipuleucel-T, androgen axis inhibitors abiraterone and enzalutamide, and a novel microtubule inhibitor cabazitaxel. More recently, radium-223, a bone-targeting alpha emitting radiopharmaceutical, was reported to improve skeletal related events, as well as overall survival in a Phase 3 randomized study. Additionally, there are several promising agents in the advanced stages of clinical development. Here, we describe the agents recently shown to improve overall survival, and those that have reached the advanced stages of development in Phase 3 clinical trials. We will also propose a strategy for optimal sequencing of these agents in the treatment of mCRPC.
直到 2010 年,多西他赛化疗是治疗转移性去势抵抗性前列腺癌(mCRPC)的唯一批准药物。此后,mCRPC 的治疗格局迅速发生变化。多种新药物在单独的随机 3 期研究中显示出改善总生存期后获得了监管批准。其中包括免疫治疗药物 sipuleucel-T、雄激素轴抑制剂阿比特龙和恩杂鲁胺,以及一种新型微管抑制剂卡巴他赛。最近,一种针对骨骼的靶向α发射放射性药物镭-223在一项 3 期随机研究中报告称可改善骨骼相关事件和总生存期。此外,还有几种有前途的药物处于临床开发的后期阶段。在这里,我们描述了最近显示可改善总生存期的药物,以及那些在 3 期临床试验中已进入后期开发阶段的药物。我们还将提出一种策略,以优化这些药物在 mCRPC 治疗中的序贯使用。