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阿那白滞素(一种重组人白细胞介素-1受体拮抗剂[r-metHuIL-1ra])用于类风湿关节炎患者:一项大型国际多中心安慰剂对照试验。

Anakinra, a recombinant human interleukin-1 receptor antagonist (r-metHuIL-1ra), in patients with rheumatoid arthritis: A large, international, multicenter, placebo-controlled trial.

作者信息

Fleischmann Roy M, Schechtman Joy, Bennett Ralph, Handel Malcolm L, Burmester Gerd-Rudiger, Tesser John, Modafferi Dennis, Poulakos Jennifer, Sun Gordon

机构信息

St. Paul University Hospital, Dallas, Texas 75235, USA.

出版信息

Arthritis Rheum. 2003 Apr;48(4):927-34. doi: 10.1002/art.10870.

Abstract

OBJECTIVE

To evaluate the safety of anakinra (a recombinant human interleukin-1 receptor antagonist) in a large population of patients with rheumatoid arthritis (RA), typical of those seen in clinical practice.

METHODS

A total of 1,414 patients were randomly assigned to treatment with 100 mg of anakinra or placebo, administered daily by subcutaneous injection. Background medications included disease-modifying antirheumatic drugs, corticosteroids, and nonsteroidal antiinflammatory drugs, alone or in combination. The primary end point was safety, which was evaluated by adverse events (including infections), discontinuation from study due to adverse events, and death.

RESULTS

Safety was evaluated in 1,399 patients (1,116 in the anakinra group and 283 in the placebo group; 15 patients were randomized but did not receive any study drug) during the initial 6-month, double-blind, placebo-controlled phase of this long-term safety study. Baseline demographics, disease characteristics, and concomitant medications were similar between the 2 groups. The study group included patients with numerous comorbid conditions and a wide range of RA disease activity. Serious adverse events occurred at a similar rate in the anakinra group and the placebo group (7.7% and 7.8%, respectively). Serious infectious episodes were observed more frequently in the anakinra group (2.1% versus 0.4% in the placebo group). The rate of withdrawal due to adverse events was 13.4% in the anakinra group and 9.2% in the placebo group.

CONCLUSION

Results from this large, placebo-controlled safety study demonstrate that anakinra is safe and well tolerated in a diverse population of patients with RA, including those with comorbid conditions and those using multiple combinations of concomitant therapies. Although the frequency of serious infection was slightly higher in the anakinra group, no infection was attributed to opportunistic microorganisms or resulted in death.

摘要

目的

在大量类风湿关节炎(RA)患者中评估阿那白滞素(一种重组人白细胞介素-1受体拮抗剂)的安全性,这些患者具有临床实践中常见的典型特征。

方法

总共1414例患者被随机分配接受100mg阿那白滞素或安慰剂治疗,通过皮下注射每日给药。背景用药包括改善病情抗风湿药、皮质类固醇和非甾体抗炎药,单独或联合使用。主要终点是安全性,通过不良事件(包括感染)、因不良事件退出研究和死亡来评估。

结果

在这项长期安全性研究的初始6个月双盲安慰剂对照阶段,对1399例患者(阿那白滞素组1116例,安慰剂组283例;15例患者随机分组但未接受任何研究药物)进行了安全性评估。两组的基线人口统计学、疾病特征和合并用药情况相似。研究组包括患有多种合并症和广泛RA疾病活动度的患者。阿那白滞素组和安慰剂组严重不良事件的发生率相似(分别为7.7%和7.8%)。阿那白滞素组更频繁地观察到严重感染发作(2.1%,而安慰剂组为0.4%)。因不良事件导致的退出率在阿那白滞素组为13.4%,在安慰剂组为9.2%。

结论

这项大型安慰剂对照安全性研究的结果表明,阿那白滞素在包括合并症患者和使用多种联合治疗的不同RA患者群体中是安全且耐受性良好的。尽管阿那白滞素组严重感染的频率略高,但没有感染归因于机会性微生物或导致死亡。

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