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首页> 外文期刊>Critical reviews in oncology/hematology >Metastatic castration resistant prostate cancer: current strategies of management in the Middle East.
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Metastatic castration resistant prostate cancer: current strategies of management in the Middle East.

机译:转移去势抵抗性前列腺癌:中东地区当前的治疗策略。

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摘要

Although most patients with prostate cancer respond to initial androgen-deprivation therapy, progression to castration-resistant prostate cancer (CRPC) is almost inevitable. In 2004, the docetaxel/prednisone regimen was approved for the management of patients with metastatic CRPC, becoming the standard first-line therapy. Recent advances have also led to an unprecedented number of approved new drugs; thus, providing several treatment options for patients with metastatic CRPC. Five new drugs have received US Food and Drug Administration-approval between 2010 and 2012: sipuleucel-T, an immunotherapeutic agent; cabazitaxel, a novel microtubule inhibitor; abiraterone acetate, a new androgen biosynthesis inhibitor; enzalutamide, a novel androgen receptor inhibitor; and denosumab, a bone-targeting agent. Such drugs are either already marketed or about to be marketed in the Middle East. Data supporting the approval of each of these agents are described in this review, as are recent approaches to the treatment of metastatic CRPC.
机译:尽管大多数前列腺癌患者对最初的雄激素剥夺疗法有反应,但几乎不可避免地会发展为去势抵抗性前列腺癌(CRPC)。 2004年,多西他赛/泼尼松方案被批准用于转移性CRPC患者的治疗,成为标准的一线治疗药物。最近的进展也导致了前所未有的批准新药数量。因此,为转移性CRPC患者提供了几种治疗选择。 2010年至2012年间,五种新药已获得美国食品药品监督管理局的批准:sipuleucel-T,一种免疫治疗剂;卡巴他赛,一种新型的微管抑制剂;醋酸阿比特龙酯,一种新的雄激素生物合成抑制剂; enzalutamide,一种新型的雄激素受体抑制剂;和denosumab,一种骨靶向剂。这类药物已经在中东销售,或即将在中东销售。这篇综述描述了支持这些药物中每一种药物批准的数据,以及治疗转移性CRPC的最新方法。

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