首页> 外文期刊>Comparative Effectiveness Research >Comparison of infliximab and ustekinumab for the treatment of moderate-to-severe psoriasis: an indirect comparison meta-analysis
【24h】

Comparison of infliximab and ustekinumab for the treatment of moderate-to-severe psoriasis: an indirect comparison meta-analysis

机译:英夫利昔单抗和乌斯他单抗治疗中度至重度银屑病的比较:间接比较荟萃分析

获取原文
       

摘要

Objectives: As no direct comparisons have been made between infliximab and ustekinumab, the present study's aim was to estimate these drugs' relative efficacy in the treatment of moderate-to-severe psoriasis.Methods: Eleven randomized controlled trials of infliximab 5 mg/kg and ustekinumab 45 mg or 90 mg, reporting Psoriasis Area and Severity Index (PASI) 75 and PASI 90 end points, were identified from a systematic literature review. Of these, five were excluded because they had inappropriate intervention (n = 1), inappropriate patient population (n = 3), or a small sample size (n = 1). Ultimately, six studies were included in the networks. Log odds ratio (OR) of achieving PASI 75 or PASI 90 was used as the treatment effect in fixed- and random-effects mixed treatment comparison meta-analysis.Results: Based on the results of the random-effects model, when compared to infliximab 5 mg/kg, the OR of ustekinumab 90 mg and ustekinumab 45 mg achieving a PASI 75 following 12 weeks of treatment was 0.57 CrI (0.19, 1.29) and 0.44 (0.15, 0.99), respectively. Similarly, the odds of achieving PASI 90 was 0.77 (0.09, 2.70) for ustekinumab 90 mg and 0.63 (0.07, 2.20) for ustekinumab 45 mg. Infliximab 5 mg/kg had the highest probability of being the most effective of all treatments considered, in attaining a PASI 75 (92%) and PASI 90 response (76%). Ustekinumab 90 mg had the highest probability of being ranked second in attaining a PASI 75 (84%) and PASI 90 response (62%). Results from the random- and fixed-effects models were consistent.Conclusion: A greater proportion of patients with plaque psoriasis are expected to achieve a PASI 75 or PASI 90 response when treated with infliximab 5 mg/kg than with ustekinumab 90 mg or 45 mg.
机译:目的:由于尚未在英夫利昔单抗和乌斯替尼单抗之间进行直接比较,因此本研究的目的是评估这些药物在中重度牛皮癣治疗中的相对疗效。方法:11项5 mg / kg英夫利昔单抗随机对照试验和从系统的文献回顾中鉴定出报告了牛皮癣面积和严重程度指数(PASI)75和PASI 90终点的ustekinumab 45 mg或90 mg。其中有5例被排除在外,因为他们进行了不适当的干预(n = 1),患者群体不适当(n = 3)或样本量较小(n = 1)。最终,网络中包含了六项研究。在固定和随机效应混合治疗比较荟萃分析中,将达到PASI 75或PASI 90的对数比值比(OR)用作治疗效果。结果:与英夫利昔单抗相比,基于随机效应模型的结果在5 mg / kg的剂量下,治疗12周后达到PASI 75的ustekinumab 90 mg和ustekinumab 45 mg的OR分别为0.57 CrI(0.19,1.29)和0.44(0.15,0.99)。同样,ustekinumab 90 mg达到PASI 90的几率是0.77(0.09,2.70),ustekinumab 45 mg达到0.63(0.07,2.20)。在获得考虑的PASI 75(92%)和PASI 90反应(76%)的情况下,英夫利昔单抗5 mg / kg成为所有治疗中最有效的可能性最高。 Ustekinumab 90 mg在获得PASI 75(84%)和PASI 90反应(62%)方面排名第二的可能性最高。结论:与5 mg / kg英夫利昔单抗相比,预期有90%的乌斯替单抗治疗的斑块状银屑病患者可实现PASI 75或PASI 90反应。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号