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一线治疗化疗初治转移性去势抵抗性前列腺癌的安全性和疗效:系统评价和间接比较。

Safety and Efficacy of First-Line Treatments for Chemotherapy-Naive Metastatic Castration-Resistant Prostate Cancer: A Systematic Review and Indirect Comparison.

机构信息

Department of Urology, The Third Affiliated Hospital of Sun Yat-Sen University, Guangzhou 510630, China.

出版信息

Biomed Res Int. 2017 Dec 7;2017:3941217. doi: 10.1155/2017/3941217. eCollection 2017.

Abstract

Recently, several drugs have been introduced for the first-line treatment of chemotherapy-naive metastatic castration-resistant prostate cancer (mCRPC), but few studies have compared treatment outcomes directly. This indirect comparison among 10 clinical trials ( = 4870 patients) retrieved from PubMed, Web of Science, Cochrane Collaboration, and ClinicalTrails.gov was performed to assess the safety and efficacy of docetaxel, cabazitaxel, abiraterone, enzalutamide, and sipuleucel-T for the initial treatment of mCRPC. No significant differences in primary outcome (overall survival) were found among initial treatments. However, docetaxel had the highest probability (37.53%) of being the most effective, but at the cost of more adverse events, while enzalutamide was associated with the best secondary outcomes (prostate-specific antigen response, progression-free survival, quality of life, and adverse event profile). Thus, docetaxel is recommended as the first agent used for the chemotherapy of mCRPC, while enzalutamide is recommended as the first nonchemotherapy treatment. Additional clinical trials are needed to confirm these findings and establish the optimal order for multidrug treatment of mCRPC.

摘要

最近,有几种药物被引入用于化疗初治转移性去势抵抗性前列腺癌(mCRPC)的一线治疗,但很少有研究直接比较治疗结果。本研究通过间接比较从 PubMed、Web of Science、Cochrane 协作和 ClinicalTrials.gov 检索到的 10 项临床试验(=4870 例患者),评估多西他赛、卡巴他赛、阿比特龙、恩扎鲁胺和 sipuleucel-T 用于 mCRPC 初始治疗的安全性和有效性。初始治疗的主要结局(总生存期)无显著差异。然而,多西他赛最有可能(37.53%)是最有效的,但代价是更多的不良事件,而恩扎鲁胺与最佳次要结局(前列腺特异性抗原反应、无进展生存期、生活质量和不良事件谱)相关。因此,建议将多西他赛作为 mCRPC 化疗的首选药物,而恩扎鲁胺则推荐作为首选的非化疗治疗药物。需要进一步的临床试验来证实这些发现,并确定 mCRPC 多药治疗的最佳顺序。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/901d/5989298/e668e3303c9e/BMRI2017-3941217.001.jpg

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