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Sipuleucel-T 联合雄激素受体靶向治疗去势抵抗性前列腺癌的Meta 分析。

Sipuleucel-T and Androgen Receptor-Directed Therapy for Castration-Resistant Prostate Cancer: A Meta-Analysis.

机构信息

Guangzhou Hospital of Guangzhou Military Region, Guangzhou, China.

School of Public Health, Guangzhou Medical University, Guangzhou, China.

出版信息

J Immunol Res. 2016;2016:4543861. doi: 10.1155/2016/4543861. Epub 2016 Dec 12.

Abstract

New treatments, such as sipuleucel-T and androgen receptor- (AR-) directed therapies (enzalutamide (Enz) and abiraterone acetate (AA)), have emerged and been approved for the management of castration-resistant prostate cancer (CRPC). There are still debates over their efficacy and clinical benefits. This meta-analysis aimed to investigate the efficacy and safety of sipuleucel-T and AR-directed therapies in patients with CRPC. RevMan 5.1 was used for pooled analysis and analysis of publication bias. Seven studies were included in the meta-analysis, with three studies in sipuleucel-T (totally 737 patients, 488 patients in treatment group, and 249 patients in placebo group) and four in AR-directed therapies (totally 5,199 patients, 3,015 patients in treatment group, and 2,184 patients in placebo group). Treatment with sipuleucel-T significantly improved overall survival in patients with CRPC and was not associated with increased risk of adverse event of grade ≥3 ( > 0.05). However, treatment with sipuleucel-T did not improve time-to-progression and reduction of prostate-specific antigen (PSA) level ≥50% was not significantly different from that with placebo. AR-directed therapies significantly improved overall survival in patients with CRPC and improved time-to-progression and reduction of PSA level ≥50%. AR-directed therapies did not increase risk of adverse event of grade ≥3 ( > 0.05).

摘要

新的治疗方法,如 sipuleucel-T 和雄激素受体(AR)靶向治疗(enzalutamide(Enz)和 abiraterone 醋酸盐(AA))已经出现并被批准用于治疗去势抵抗性前列腺癌(CRPC)。它们的疗效和临床获益仍存在争议。本荟萃分析旨在探讨 sipuleucel-T 和 AR 靶向治疗在 CRPC 患者中的疗效和安全性。RevMan 5.1 用于汇总分析和发表偏倚分析。荟萃分析共纳入 7 项研究,其中 3 项研究为 sipuleucel-T(共 737 例患者,治疗组 488 例,安慰剂组 249 例),4 项研究为 AR 靶向治疗(共 5199 例患者,治疗组 3015 例,安慰剂组 2184 例)。与安慰剂相比,sipuleucel-T 治疗可显著提高 CRPC 患者的总生存率,且与不良事件≥3 级(>0.05)风险增加无关。然而,sipuleucel-T 治疗并未改善进展时间,且 PSA 水平降低≥50%与安慰剂无显著差异。AR 靶向治疗可显著提高 CRPC 患者的总生存率,并改善进展时间和 PSA 水平降低≥50%。AR 靶向治疗未增加不良事件≥3 级的风险(>0.05)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2455/5183769/c5551eb732c8/JIR2016-4543861.001.jpg

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