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雄激素剥夺治疗(ADT)联合阿比特龙、多西他赛、双膦酸盐、塞来昔布或联合方案治疗转移性去势敏感性前列腺癌(mHSPC)的网状 Meta 分析。

Addition of abiraterone, docetaxel, bisphosphonate, celecoxib or combinations to androgen-deprivation therapy (ADT) for metastatic hormone-sensitive prostate cancer (mHSPC): a network meta-analysis.

机构信息

Nuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, UK.

Clinical Oncology Sector, Faculdade de Medicina do ABC, Santo André, Brazil.

出版信息

Prostate Cancer Prostatic Dis. 2018 Nov;21(4):516-523. doi: 10.1038/s41391-018-0055-8. Epub 2018 Jun 6.

Abstract

BACKGROUND

Patients with metastatic prostate cancer have poor prognosis. In this study, we compared the addition of abiraterone, docetaxel, bisphosphonate, celecoxib or combinations to standard ADT vs. ADT alone for patients with mHSPC in terms of overall survival (OS), failure-free survival (FFS), and adverse events.

METHODS

We searched PubMed and performed a network meta-analysis to generate probabilistic inferences and provide efficacy rankings in terms of posterior hazard ratios with 95% credible intervals (CrI), surface under the cumulative ranking curve (SUCRA), probability better than competing treatments, and probability best.

RESULTS

Seven trials were included (LATITUTE, STAMPEDE, CHAARTED, GETUG-AFU15, ZAPCA, CALGB 90202, and MRC PR05). Compared to ADT alone, evidence suggests abiraterone + ADT (OS HR: 0.60; 95% CrI: 0.50-0.71, FFS HR: 0.31; 95% CrI: 0.25-0.38) could be superior in terms of OS and FFS compared to docetaxel + ADT (OS 0.74; 95% CrI: 0.63-0.86, FFS 0.62; 95% CrI: 0.53-0.74), bisphosphonate + ADT (OS: 0.87; 95% CrI: 0.75-1.00, FFS 0.87; 95% CrI: 0.75-1.00), celecoxib + ADT (OS: 0.91; 95% CrI: 0.71-1.17, FFS: 0.86; 95% CrI: 0.68-1.08), or triple combinations. Abiraterone + ADT suggests improved survival with 97% certainty for a 19% reduction in risk of death compared to docetaxel + ADT (HR: 0.81; 95% CrI: 0.66-1.00).

DISCUSSION

Addition of abiraterone to standard ADT may possibly outperform the addition of docetaxel, bisphosphonates, celecoxib, or combinations to standard ADT in terms of OS and FFS.

摘要

背景

转移性前列腺癌患者预后较差。在这项研究中,我们比较了在 mHSPC 患者中,与单独 ADT 相比,阿比特龙、多西他赛、双膦酸盐、塞来昔布或联合用药对总生存期(OS)、无失败生存期(FFS)和不良事件的影响。

方法

我们检索了 PubMed 并进行了网络荟萃分析,以生成概率推断,并提供后验危险比(95%可信区间 [CrI])、累积排序曲线下面积(SUCRA)、优于竞争治疗的概率和最佳概率的疗效排名。

结果

共纳入 7 项试验(LATITUTE、STAMPEDE、CHAARTED、GETUG-AFU15、ZAPCA、CALGB 90202 和 MRC PR05)。与单独 ADT 相比,阿比特龙联合 ADT(OS HR:0.60;95% CrI:0.50-0.71,FFS HR:0.31;95% CrI:0.25-0.38)在 OS 和 FFS 方面可能优于多西他赛联合 ADT(OS 0.74;95% CrI:0.63-0.86,FFS 0.62;95% CrI:0.53-0.74)、双膦酸盐联合 ADT(OS:0.87;95% CrI:0.75-1.00,FFS:0.87;95% CrI:0.75-1.00)、塞来昔布联合 ADT(OS:0.91;95% CrI:0.71-1.17,FFS:0.86;95% CrI:0.68-1.08)或三联治疗。阿比特龙联合 ADT 可能优于多西他赛联合 ADT,可使死亡风险降低 19%,97%确定度下的生存率提高(HR:0.81;95% CrI:0.66-1.00)。

讨论

与单独 ADT 相比,阿比特龙联合 ADT 可能在 OS 和 FFS 方面优于多西他赛、双膦酸盐、塞来昔布或联合用药。

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