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转移性前列腺癌的新药研发

New drug development in metastatic prostate cancer.

作者信息

Armstrong Andrew J, George Daniel J

机构信息

Division of Medical Oncology, Department of Medicine, Duke Comprehensive Cancer Center, DUMC, Durham, NC 27705, USA.

出版信息

Urol Oncol. 2008 Jul-Aug;26(4):430-7. doi: 10.1016/j.urolonc.2007.11.006.

Abstract

In 2007, drug development in castration-resistant metastatic prostate cancer (CRPC) remains challenging, due to the number of potentially viable molecular targets and clinical trials available, the lack of established surrogates for overall survival, and competing causes of mortality. This review will highlight the highest impact phase II and phase III trials of novel agents in the current CRPC landscape, and focus on both molecular targets and clinical trial designs that are more likely to demonstrate clinical benefit. The need for tissue correlative studies for target evaluation and drug mechanism is stressed to continue to advance the field and to define biomarkers that may identify patient populations that may derive a greater benefit from these molecular agents.

摘要

2007年,去势抵抗性转移性前列腺癌(CRPC)的药物研发仍然具有挑战性,这是由于潜在可行的分子靶点数量、可用的临床试验、缺乏已确立的总生存替代指标以及其他竞争性死亡原因。本综述将重点介绍当前CRPC领域新型药物的最具影响力的II期和III期试验,并聚焦于更有可能显示临床获益的分子靶点和临床试验设计。强调了进行组织相关性研究以评估靶点和药物机制的必要性,以持续推动该领域发展并确定可能识别出从这些分子药物中获益更大的患者群体的生物标志物。

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