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采用贝叶斯方法评估肿瘤坏死因子-α(TNF-α)抑制剂循环治疗与转换为非 TNF 生物制剂治疗对 TNF-α抑制剂应答不足的类风湿关节炎患者的疗效比较。

Comparative effectiveness of cycling of tumor necrosis factor-α (TNF-α) inhibitors versus switching to non-TNF biologics in rheumatoid arthritis patients with inadequate response to TNF-α inhibitor using a Bayesian approach.

机构信息

School of Pharmacy, Sungkyunkwan University, 300 Cheonchoen-dong, Jangan-gu, Suwon, Gyeonggi-do, 440-746, South Korea.

出版信息

Arch Pharm Res. 2014 May;37(5):662-70. doi: 10.1007/s12272-014-0337-1. Epub 2014 Jan 28.

DOI:10.1007/s12272-014-0337-1
PMID:24469604
Abstract

Alternative tumor necrosis factor-α (TNF-α) inhibitors and non-TNF biologics are available as treatment options for rheumatoid arthritis patients who exhibit inadequate response to TNF-α inhibitor (TNF-IR patients). These agents have considerable efficacy compared with placebo, but head-to-head comparisons among these agents have not been performed. The objective of this study was to use Bayesian approach to compare the effectiveness of cycling TNF-α inhibitors versus switching to non-TNF biologics in TNF-IR patients. A systematic review was conducted using MEDLINE and Cochrane library. Key endpoints were the American College of Rheumatology (ACR) responses of 20/50/70 and the health assessment questionnaire (HAQ) score change at six months. Bayesian outcomes were calculated as the probability that OR is greater than one and HAQ score change difference is less than zero. Compared with TNF-α inhibitors, non-TNF biologics were associated with higher ACR response rates; in ACR20, the OR was 1.639 for abatacept [P(OR > 1) = 90.7 %], 1.871 for rituximab [P(OR > 1) = 96.2 %] and 3.52 for tocilizumab [P(OR > 1) = 99.9 %]. Similar trends were shown in the HAQ change comparison; the median differences (MD) were -0.259 for abatacept [P(MD < 0) = 100 %], -0.160 for rituximab [P(MD < 0) = 98.2 %], and -0.200 for tocilizumab [P(MD < 0) = 99.3 %]. In conclusion, switching to non-TNF biologics was more effective than cycling TNF-α inhibitor in TNF-IR patients.

摘要

在对肿瘤坏死因子-α(TNF-α)抑制剂反应不足的类风湿关节炎(RA)患者中,可选择使用其他 TNF-α抑制剂和非 TNF 类生物制剂进行治疗。与安慰剂相比,这些药物具有显著的疗效,但尚未对这些药物进行直接比较。本研究旨在采用贝叶斯方法比较在 TNF-α抑制剂反应不足的患者中,交替使用 TNF-α抑制剂与转换使用非 TNF 类生物制剂的疗效。检索 MEDLINE 和 Cochrane 图书馆,进行系统评价。主要终点为美国风湿病学会(ACR)20/50/70 反应和 6 个月时健康评估问卷(HAQ)评分变化。贝叶斯结果计算为比值比(OR)大于 1 和 HAQ 评分变化差值小于 0 的概率。与 TNF-α抑制剂相比,非 TNF 类生物制剂与更高的 ACR 反应率相关;在 ACR20 中,阿巴西普的 OR 为 1.639[P(OR > 1) = 90.7%],利妥昔单抗为 1.871[P(OR > 1) = 96.2%],托珠单抗为 3.52[P(OR > 1) = 99.9%]。HAQ 变化比较也显示出相似的趋势;阿巴西普的中位数差值(MD)为-0.259[P(MD < 0) = 100%],利妥昔单抗为-0.160[P(MD < 0) = 98.2%],托珠单抗为-0.200[P(MD < 0) = 99.3%]。结论:与交替使用 TNF-α抑制剂相比,转换使用非 TNF 类生物制剂在 TNF-α抑制剂反应不足的患者中更有效。

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