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Vedolizumab for inflammatory bowel disease: From randomized controlled trials to real-life evidence

机译:维多珠单抗治疗炎症性肠病:从随机对照试验到现实生活中的证据

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摘要

The biologic antitumor necrosis factor alpha (anti-TNFα) agents have revolutionised the treatment of inflammatory bowel disease (IBD). However, some patients experience primary nonresponse, loss of response, or intolerance. Therefore, introducing a newer class of therapy with a mechanism of action that acts on different inflammatory pathways involved in IBD pathogenesis is appealing. Vedolizumab is a fully humanised monoclonal antibody that selectively targets α4β7 integrin. Based on the results of the pivotal clinical GEMINI trials, vedolizumab was approved for the treatment of adult patients with moderately to severely active ulcerative colitis (UC) and Crohn’s disease (CD) refractory or intolerant to either conventional therapy or TNFα inhibitors. This review describes the efficacy, safety, and tolerability of vedolizumab reported in both randomized, controlled, clinical trials and from real-world experience in patients with UC and CD in order to identify its place in treatment algorithms for IBD.
机译:生物抗肿瘤坏死因子α(抗TNFα)药物彻底改变了炎症性肠病(IBD)的治疗方法。但是,有些患者会出现原发性无反应,无反应或不耐受。因此,引入具有作用机制的新型治疗方法是有吸引力的,该作用机制作用于涉及IBD发病机理的不同炎症途径。 Vedolizumab是完全人源化的单克隆抗体,可选择性靶向α4β7整联蛋白。根据GEMINI关键临床试验的结果,维多珠单抗被批准用于治疗中度至重度溃疡性结肠炎(UC)和克罗恩病(CD)的成人患者,这些患者对常规疗法或TNFα抑制剂均难治或不耐受。这篇综述描述了在随机,对照,临床试验以及来自UC和CD患者的真实经验中报告的维多珠单抗的功效,安全性和耐受性,以便确定其在IBD治疗算法中的地位。

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