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Medical strategies for treatment of castration resistant prostate cancer (CRPC) docetaxel resistant

机译:治疗去势抵抗性前列腺癌(CRPC)多西他赛的医学策略

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摘要

The current landscape of treatment of castration-resistant prostate cancer (CRPC) has recently changed. Cabazitaxel, a new taxane with potential antineoplastic activity, has been approved by Food and Drug Administration (FDA) after docetaxel failure. In a phase III trial, cabazitaxel showed increased overall survival (OS) compared with mitoxantrone (15.1 vs. 12.7 mo, HR 0.70, 95% CI 0.59-0.83, p < 0.0001). Furthermore, chemotherapy is not the only strategy available: several studies have shown as CRPC remains dependent on androgen receptor function for growth. Abiraterone acetate, an irreversible inhibitor of CYP17, has also been approved by the FDA after docetaxel failure. In a phase III trial comparing abiraterone acetate to placebo, abiraterone showed improvement in OS (14.8 vs. 10.4 mo, HR 0.65, 95% CI 0.54-0.77; p < 0.0001). This review will discuss current options and the ongoing trials for second-line treatment of CRPC including chemotherapy, hormonal therapies, antiangiogenetic and immune strategies.
机译:最近,去势抵抗性前列腺癌(CRPC)的治疗现状发生了变化。紫杉醇是一种具有潜在抗肿瘤活性的新型紫杉烷,多西紫杉醇治疗失败后已被食品药品监督管理局(FDA)批准。在一项III期试验中,卡巴他赛与米托蒽醌相比具有更高的总生存期(OS)(15.1 vs. 12.7 mo,HR 0.70,95%CI 0.59-0.83,p <0.0001)。此外,化学疗法不是唯一可用的策略:多项研究表明,CRPC仍依赖雄激素受体的生长。 CYP17的不可逆抑制剂乙酸阿比特龙在多西紫杉醇失败后也被FDA批准。在一项比较乙酸阿比特龙酯和安慰剂的III期试验中,阿比特龙显示OS改善(14.8 vs. 10.4 mo,HR 0.65,95%CI 0.54-0.77; p <0.0001)。这篇综述将讨论CRPC的二线治疗的当前选择和正在进行的试验,包括化学疗法,激素疗法,抗血管生成和免疫策略。

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