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使用或不使用雌莫司汀化疗治疗去势抵抗性前列腺癌:一项系统评价和荟萃分析。

Chemotherapy with or without estramustine for treatment of castration-resistant prostate cancer: A systematic review and meta-analysis.

作者信息

Qin Zhiqiang, Li Xiao, Zhang Jianzhong, Tang Jingyuan, Han Peng, Xu Zhen, Yu Yajie, Yang Chengdi, Wang Chengming, Xu Ting, Xu Zicheng, Zou Qing

机构信息

aDepartment of Urologic Surgery, The Affiliated Cancer Hospital of Jiangsu Province of Nanjing Medical University bDepartment of Urology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.

出版信息

Medicine (Baltimore). 2016 Sep;95(39):e4801. doi: 10.1097/MD.0000000000004801.

Abstract

BACKGROUND

Recently, increasing relevant studies researched the efficacy of castration resistant prostate cancer (CRPC) patients using chemotherapy with or without estramustine, in order to assess the efficacy and toxicity of combining estramustine with chemotherapy for the treatment of CRPC.

METHODS

Relevant randomized clinical trials were systematically searched from the databases Pubmed, Embase, and Web of science up to April 1, 2016. Data were centrally extracted and analyzed from the previous studies by 2 independent reviewers. The primary endpoint was overall survival (OS) with pooled hazard ratios. Secondary endpoints were prostate-specific antigen (PSA) response and grade 3 or 4 toxicity using pooled odds ratios. Stata version 12.0 software was used for statistical analysis.

RESULTS

Overall, this meta-analysis identified 9 eligible articles, including a total of 956 patients, who had been accrued between January 1, 1993 and December 1, 2010 and randomly divided into chemotherapy with estramustine and without estramustine. Chemotherapy (with or without estramustine) consisted of docetaxel, paclitaxel, ixabepilone, epirubicin, and vinblastine. Patients who received chemotherapy with estramustine had a better improvement in PSA response rate, comparing those without estramustine (OR = 1.84, 95% CI = 1.20-2.80). However, OS between the 2 groups indicated no significant differences (HR = 0.90, 95% CI = 0.77-1.05). Besides, these results of meta-analysis showed no obvious differences between these 2 groups in grade 3 or 4 adverse effects, including anemia (OR = 0.78, 95% CI = 0.38-1.57), neutropenia (OR = 0.91, 95% CI = 0.59-1.43), thrombocytopenia (OR = 0.68, 95% CI = 0.19-2.42), nausea (OR = 2.34, 95% CI = 0.81-6.72), vomiting (OR = 2.43, 95% CI = 0.69-8.51), diarrhea (OR = 3.45, 95% CI = 0.93-12.76), fatigue (OR = 0.67, 95% CI = 0.32-1.41), neuropathy (OR = 0.54, 95% CI = 0.21-1.44), allergic reaction (OR = 1.60, 95% CI = 0.37-6.84), thromboembolic event (OR = 2.18, 95% CI = 0.86-5.51), and edema (OR = 1.02, 95% CI = 0.18-5.95).

CONCLUSIONS

This meta-analysis indicated chemotherapy with additional estramustine increased the PSA response rate. However, OS and grade 3 or 4 toxicity were not improved for these patients with CRPC.

摘要

背景

最近,越来越多的相关研究探讨了去势抵抗性前列腺癌(CRPC)患者使用化疗联合或不联合雌莫司汀的疗效,以评估雌莫司汀联合化疗治疗CRPC的疗效和毒性。

方法

截至2016年4月1日,从PubMed、Embase和科学网数据库中系统检索相关随机临床试验。由2名独立审阅者对先前研究的数据进行集中提取和分析。主要终点是总生存期(OS),采用合并风险比。次要终点是前列腺特异性抗原(PSA)反应以及3级或4级毒性,采用合并比值比。使用Stata 12.0软件进行统计分析。

结果

总体而言,这项荟萃分析确定了9篇符合条件的文章,共纳入956例患者,这些患者于1993年1月1日至2010年12月1日期间入组,并随机分为接受含雌莫司汀化疗组和不含雌莫司汀化疗组。化疗(联合或不联合雌莫司汀)包括多西他赛、紫杉醇、伊沙匹隆、表柔比星和长春碱。与未接受含雌莫司汀化疗的患者相比,接受含雌莫司汀化疗的患者PSA反应率改善更好(OR = 1.84,95%CI = 1.20 - 2.80)。然而,两组之间的总生存期无显著差异(HR = 0.90,95%CI = 0.77 - 1.05)。此外,荟萃分析结果显示,两组在3级或4级不良反应方面无明显差异,包括贫血(OR = 0.78,95%CI = 0.38 - 1.57)、中性粒细胞减少(OR = 0.91,95%CI = 0.59 - 1.43)、血小板减少(OR = 0.68,95%CI = 0.19 - 2.42)、恶心(OR = 2.34,95%CI = 0.81 - 6.72)、呕吐(OR = 2.43,95%CI = 0.69 - 8.51)、腹泻(OR = 3.45,95%CI = 0.93 - 12.76)、疲劳(OR = 0.67,95%CI = 0.32 - 1.41)、神经病变(OR = 0.54,95%CI = 0.21 - 1.44)、过敏反应(OR = 1.60,95%CI = 0.37 - 6.84)、血栓栓塞事件(OR = 2.18,95%CI = 0.86 - 5.51)和水肿(OR = 1.02,95%CI = 0.18 - 5.95)。

结论

这项荟萃分析表明,联合雌莫司汀的化疗可提高PSA反应率。然而,对于这些CRPC患者,总生存期和3级或4级毒性并未得到改善。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4909/5265899/1bd686b94040/medi-95-e4801-g002.jpg

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