首页> 外文期刊>Tropical Journal of Pharmaceutical Research >Efficacy and safety of guselkumab for the treatment of patients with moderate-to-severe plaque psoriasis: A meta-analysis of randomized clinical trials
【24h】

Efficacy and safety of guselkumab for the treatment of patients with moderate-to-severe plaque psoriasis: A meta-analysis of randomized clinical trials

机译:Guselkumab治疗中度至重度斑块牛皮癣患者的疗效和安全性:随机临床试验的META分析

获取原文
           

摘要

Purpose: To conduct a systematic analysis on data from randomized controlled trials (RCTs) on different doses of guselkumab, and provide high-quality evidence for its use in the treatment of patients with moderate-to-severe plaque psoriasis (PsO). Methods: Related studies were searched using online search engines including MEDLINE, PubMed, and central registry of Cochrane controlled trials from January 2001 to October 2017. Only randomized, placebo-controlled, double-blind clinical trials involving guselkumab- and placebo-treated PsO subjects were included. Results: Five eligible double-blind, randomized, and placebo-controlled trials involving patients with moderate-to-severe PsO subjects treated with guselkumab were included. Compared with the placebo groups, the proportion of patients with improvements in Psoriasis Area and Severity Index (PASI) 75 (RR= 12.14; 95% CI= 9.11-16.16; p 0.05); severe adverse events (SAEs) (RR = 1.32; 95% CI =0.69-2.54; p 0.05) and study discontinuations (RR = 0.79; 95% CI = 0.42-1.48; p 0.05) between the two groups. Conclusion: This meta-analysis summarizes available evidence for the use of guselkumab in psoriasis. The results suggest that guselkumab is superior to placebo in moderate-to-severe psoriasis, and is well-tolerated, effective, and safe in improving the severity of disease and quality of life.
机译:目的:对来自不同剂量的Guselkumab的随机对照试验(RCT)进行系统分析,并为其用于治疗中度至重度斑块牛皮癣(PSO)的患者提供高质量证据。方法:使用在线搜索引擎搜查相关研究,包括从2001年1月至2017年1月到10月的Cochrane对照试验的Medline,Pubmed和Central Registry。只有随机,安慰剂控制,双盲临床试验,包括Guselkumab-和安慰剂治疗的PSO受试者包括在内。结果:涉及涉及用Guselkumab治疗的中度至严重的PSO受试者的5个符合条件的双盲,随机和安慰剂对照试验。与安慰剂组相比,牛皮癣面积和严重程度指数(PASI)75改善患者的比例(RR = 12.14; 95%CI = 9.11-16.16; p 0.05);严重不良事件(SAES)(RR = 1.32; 95%CI = 0.69-2.54; P> 0.05),两组之间的研究中断(RR = 0.79; 95%CI = 0.42-1.48; p> 0.05)。结论:这种荟萃分析总结了在牛皮癣中使用Guselkumab的可用证据。结果表明,Guselkumab优于安慰剂中度至严重的牛皮癣,并且具有良好的耐受性,有效和安全,提高疾病的严重程度和生活质量。

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