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合并用药对系统性红斑狼疮患者贝利尤单抗疗效和安全性的影响。

Impact of concomitant medication use on belimumab efficacy and safety in patients with systemic lupus erythematosus.

作者信息

Schwarting A, Dooley M A, Roth D A, Edwards L, Thompson A, Wilson B

机构信息

University Hospital Mainz, ACURA Rheumatology Center, Bad Kreuznach, Germany

University of North Carolina, Chapel Hill, NC, USA.

出版信息

Lupus. 2016 Dec;25(14):1587-1596. doi: 10.1177/0961203316655215. Epub 2016 Aug 3.

Abstract

Practicing physicians have requested efficacy and safety data for belimumab, when used with specific systemic lupus erythematosus (SLE) medications. This was a post hoc analysis of pooled efficacy and safety data from patients who received belimumab 10 mg/kg plus standard of care (SoC) or placebo (SoC) in two Phase III, randomized trials, BLISS-52 and BLISS-76. Patients were categorized into four groups based on baseline concomitant medication usage: steroids only; antimalarials (AM) only; steroids + AM; or steroids + AM + immunosuppressants (IS). The primary endpoint was the SLE Responder Index (SRI) at Week 52. SRI over time and individual SRI components were secondary endpoints. Time to first flare and changes in concomitant medications were exploratory endpoints. Safety was assessed using adverse event (AE) reporting. Across 834 patients, steroids + AM was the largest group (n = 346, 41.5%) and AM only was the smallest (n = 77, 9.2%). Disease duration was shortest in the steroids + AM group (5.7 years vs 6.4-7.1 years); SELENA-SLEDAI scores were similar across groups. At Week 52, the percentage of SRI responders was greatest in the steroids + AM group for belimumab 10 mg/kg (59%) compared with placebo (44%); treatment response and SRI component improvements were also observed across other groups. The probability of experiencing an SLE flare was reduced in the steroids-only group for patients who received belimumab 10 mg/kg compared with placebo (64.3% vs 78.1%; hazard ratio 0.64; 95% confidence interval: 0.42-0.96). There was little or no change in daily AM or IS dose in any group. For all groups, there was a general decrease in steroid dose over time; a quarter to a third of patients experienced decreased steroid doses at Week 52. The overall safety profile was similar across treatment arms and concomitant medication groups, with the exception of serious AEs in the steroids + AM group (belimumab 10 mg/kg 16%, placebo 8%). The efficacy and safety of belimumab in combination with SoC was demonstrated for various groupings of steroids, AM and IS. These findings may improve the understanding of the safety and efficacy of adding belimumab to different treatments.

摘要

执业医师要求提供贝利尤单抗与特定系统性红斑狼疮(SLE)药物联用时的疗效和安全性数据。这是一项对两项III期随机试验BLISS - 52和BLISS - 76中接受10mg/kg贝利尤单抗加标准治疗(SoC)或安慰剂(SoC)的患者的汇总疗效和安全性数据进行的事后分析。根据基线合并用药情况,将患者分为四组:仅用类固醇;仅用抗疟药(AM);类固醇 + AM;或类固醇 + AM + 免疫抑制剂(IS)。主要终点是第52周时的SLE缓解指数(SRI)。SRI随时间变化情况以及各个SRI组成部分为次要终点。首次发作时间和合并用药的变化为探索性终点。通过不良事件(AE)报告评估安全性。在834例患者中,类固醇 + AM组人数最多(n = 346,41.5%),仅用AM组人数最少(n = 77,9.2%)。类固醇 + AM组的疾病持续时间最短(5.7年,而其他组为6.4 - 7.1年);各组的SELENA - SLEDAI评分相似。在第52周时,对于10mg/kg贝利尤单抗,类固醇 + AM组的SRI缓解者百分比最高(59%),高于安慰剂组(44%);在其他组中也观察到了治疗反应和SRI组成部分的改善。与安慰剂相比,接受10mg/kg贝利尤单抗的仅用类固醇组患者发生SLE发作的概率降低(64.3%对78.1%;风险比0.64;95%置信区间:0.42 - 0.96)。任何组的每日AM或IS剂量几乎没有变化。对于所有组,随着时间推移类固醇剂量总体上有所降低;在第52周时,四分之一至三分之一的患者类固醇剂量降低。除了类固醇 + AM组的严重不良事件(10mg/kg贝利尤单抗组为16%,安慰剂组为8%)外,各治疗组和合并用药组的总体安全性概况相似。贝利尤单抗与SoC联合使用时,在类固醇、AM和IS的各种组合情况下均显示出疗效和安全性。这些发现可能有助于更好地理解在不同治疗中添加贝利尤单抗的安全性和疗效。

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