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类风湿关节炎患者起始使用阿巴西普的机会性感染风险:累积临床试验数据。

Risk of opportunistic infections in patients with rheumatoid arthritis initiating abatacept: cumulative clinical trial data.

机构信息

Bristol Myers Squibb, Princeton, NJ, 08543, USA.

Current affiliation: Physicians Research Center, LLC, Toms River, NJ, 08753, USA.

出版信息

Arthritis Res Ther. 2021 Jan 11;23(1):17. doi: 10.1186/s13075-020-02399-2.

Abstract

BACKGROUND

To evaluate incidence of opportunistic infections (OIs) in patients with rheumatoid arthritis (RA) treated with abatacept in clinical trials.

METHODS

This pooled analysis of 16 randomized, double-blind/open-label trials, with ≥ 1 abatacept (intravenous or subcutaneous) arm, and with/without placebo control covered cumulative (controlled short-term and open-label long-term) abatacept exposure periods. OIs were analyzed separately in controlled (abatacept and placebo individually) and cumulative periods. OIs were identified using a prespecified list; events were independently adjudicated. Unadjusted incidence rates (IRs; per 100 patient-years) with 95% confidence intervals (CIs) were calculated.

RESULTS

In cumulative periods, 7044 patients received abatacept, with a mean (standard deviation) duration of exposure of 36.9 (26.2) months (21,274 patient-years of exposure). IRs (95% CIs) of OIs were 0.17 (0.05-0.43) for abatacept and 0.56 (0.22-1.15) for placebo during the controlled periods and 0.21 (0.15-0.28) for abatacept during the cumulative periods. There was 1 case of tuberculosis in both the abatacept (IR [95% CI] 0.04 [0.00-0.24]) and placebo (IR [95% CI] 0.08 [0.00-0.44]) groups during the controlled periods; 13 verified tuberculosis cases (IR [95% CI] 0.06 [0.03-0.10]) were reported in the cumulative period. Herpes zoster was reported numerically more often with abatacept (IR 1.9 [1.4-2.5]), versus placebo (1.7 [1.1-2.6]) in the controlled periods; within the cumulative period, herpes zoster IR (95% CI) was 1.53 (1.36-1.71) for abatacept-treated patients.

CONCLUSION

In controlled periods of the clinical trials, abatacept-treated patients had similarly low rates of OIs compared with placebo-treated patients. Overall, OI rates were similar among abatacept-treated patients in the controlled and cumulative periods and consistent with the ranges reported in the literature.

摘要

背景

评估临床试验中接受阿巴西普治疗的类风湿关节炎(RA)患者的机会性感染(OIs)发生率。

方法

这是一项对 16 项随机、双盲/开放标签试验的汇总分析,这些试验均有阿巴西普(静脉或皮下)治疗组,并且有/没有安慰剂对照,涵盖了累积(对照短期和开放标签长期)阿巴西普暴露期。在对照期(阿巴西普和安慰剂分别对照)和累积期分别分析 OIs。使用预先指定的清单识别 OIs;事件由独立裁决。计算未经调整的发病率(IR;每 100 患者年)及其 95%置信区间(CI)。

结果

在累积期,7044 名患者接受了阿巴西普治疗,平均(标准差)暴露时间为 36.9(26.2)个月(21274 患者年暴露)。对照期阿巴西普的 OIs 发生率为 0.17(0.05-0.43),安慰剂为 0.56(0.22-1.15);累积期阿巴西普的 OIs 发生率为 0.21(0.15-0.28)。对照期,阿巴西普组和安慰剂组各有 1 例结核病(IR[95%CI]0.04[0.00-0.24]和 IR[95%CI]0.08[0.00-0.44]);累积期报告了 13 例确诊结核病病例(IR[95%CI]0.06[0.03-0.10])。对照期,阿巴西普组报告的带状疱疹发生率高于安慰剂组(IR 1.9[1.4-2.5],安慰剂组为 1.7[1.1-2.6]);在累积期,阿巴西普治疗患者的带状疱疹发病率(95%CI)为 1.53(1.36-1.71)。

结论

在临床试验的对照期,与安慰剂组相比,接受阿巴西普治疗的患者 OIs 发生率同样较低。总体而言,在对照期和累积期,接受阿巴西普治疗的患者的 OI 发生率相似,与文献报道的范围一致。

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