International Doctoral School, University of Seville, Faculty of Medicine, Seville, Spain.
Department of Diagnostic Radiology, The Fifth Clinical Medical College of Henan University of Chinese Medicine (Zhengzhou People's Hospital), Zhengzhou, China.
Medicine (Baltimore). 2022 Oct 7;101(40):e30590. doi: 10.1097/MD.0000000000030590.
Vedolizumab is a humanized monoclonal antibody that inhibits gut-selective α4β7 integrins on the surface of leukocytes, preventing their trafficking into the gastrointestinal tract, and ultimately achieves the effect of suppressing intestinal inflammation. This study aimed to evaluate the efficacy and safety of vedolizumab in the treatment of inflammatory bowel disease.
After a systematic review of relevant studies, the pooled relative risk (RR) and 95% confidence intervals (CIs) were calculated to evaluate the effect. Heterogeneity was explored using sensitivity analysis, univariate meta-regression, and subgroup analysis. Potential publication bias was evaluated using Egger test and trim-and-fill method.
Nine randomized controlled trials involving 4268 participants were included in the meta-analysis. During induction therapy, vedolizumab was more effective than placebo in treating active ulcerative colitis and Crohn disease in terms of clinical response (RR = 1.55, 95%CI: 1.35-1.78), clinical remission (RR = 1.90, 95%CI: 1.50-2.41), and mucosal healing (RR = 1.53, 95%CI: 1.21-1.95). A superior effect in terms of durable Clinical or Crohn disease Activity Index-100 response (RR = 1.65, 95%CI: 1.20-2.26), clinical remission (RR = 1.92, 95%CI: 1.48-2.50), and glucocorticoid-free remission (RR = 2.22, 95%CI: 1.71-2.90) was found during maintenance treatment. Vedolizumab was not associated with any adverse events and was as safe as placebo in terms of the risk of serious adverse reactions.
Vedolizumab may be safe and effective as an induction and maintenance therapy for the treatment of inflammatory bowel disease; however, further studies are needed to validate this conclusion.
维得利珠单抗是一种人源化单克隆抗体,可抑制白细胞表面的肠道选择性 α4β7 整合素,阻止其向胃肠道迁移,从而达到抑制肠道炎症的效果。本研究旨在评估维得利珠单抗治疗炎症性肠病的疗效和安全性。
系统检索相关研究后,计算汇总相对风险(RR)及其 95%置信区间(CI)以评估疗效。采用敏感性分析、单变量 meta 回归和亚组分析探索异质性。采用 Egger 检验和剪补法评估潜在发表偏倚。
纳入的 9 项随机对照试验共纳入 4268 例患者。在诱导治疗中,与安慰剂相比,维得利珠单抗在治疗活动期溃疡性结肠炎和克罗恩病方面更有效,表现在临床缓解(RR=1.55,95%CI:1.35-1.78)、临床缓解(RR=1.90,95%CI:1.50-2.41)和黏膜愈合(RR=1.53,95%CI:1.21-1.95)方面。在维持治疗中,维得利珠单抗在持续临床或克罗恩病活动指数-100 缓解(RR=1.65,95%CI:1.20-2.26)、临床缓解(RR=1.92,95%CI:1.48-2.50)和无糖皮质激素缓解(RR=2.22,95%CI:1.71-2.90)方面的效果更优。维得利珠单抗与安慰剂相比,不良反应发生率无差异,且严重不良反应风险更低。
维得利珠单抗作为诱导和维持治疗炎症性肠病的药物可能安全且有效,但还需要进一步研究来验证这一结论。