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针对去势抵抗性前列腺癌中的分子抗性

Targeting molecular resistance in castration-resistant prostate cancer.

作者信息

Chandrasekar Thenappan, Yang Joy C, Gao Allen C, Evans Christopher P

机构信息

Department of Urology, University of California, Davis, USA.

, 4860 Y Street, Suite 3500, Sacramento, CA, 95817, USA.

出版信息

BMC Med. 2015 Sep 1;13:206. doi: 10.1186/s12916-015-0457-6.

Abstract

Multiple mechanisms of resistance contribute to the inevitable progression of hormone-sensitive prostate cancer to castration-resistant prostate cancer (CRPC). Currently approved therapies for CRPC include systemic chemotherapy (docetaxel and cabazitaxel) and agents targeting the resistance pathways leading to CRPC, including enzalutamide and abiraterone. While there is significant survival benefit, primary and secondary resistance to these therapies develops rapidly. Up to one-third of patients have primary resistance to enzalutamide and abiraterone; the remaining patients eventually progress on treatment. Understanding the mechanisms of resistance resulting in progression as well as identifying new targetable pathways remains the focus of current prostate cancer research. We review current knowledge of mechanisms of resistance to the currently approved treatments, development of adjunctive therapies, and identification of new pathways being targeted for therapeutic purposes.

摘要

多种耐药机制导致激素敏感性前列腺癌不可避免地进展为去势抵抗性前列腺癌(CRPC)。目前批准用于CRPC的疗法包括全身化疗(多西他赛和卡巴他赛)以及靶向导致CRPC的耐药途径的药物,包括恩杂鲁胺和阿比特龙。虽然有显著的生存获益,但这些疗法的原发性和继发性耐药迅速出现。高达三分之一的患者对恩杂鲁胺和阿比特龙有原发性耐药;其余患者最终会在治疗过程中病情进展。了解导致病情进展的耐药机制以及确定新的可靶向途径仍然是当前前列腺癌研究的重点。我们综述了目前关于对当前批准治疗的耐药机制、辅助疗法的开发以及为治疗目的而靶向的新途径的认识。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50e2/4556222/056760578f57/12916_2015_457_Fig1_HTML.jpg

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