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

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          Abstract

          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.

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          Most cited references45

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          A simple index of Crohn's-disease activity.

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            Review article: loss of response to anti-TNF treatments in Crohn's disease.

            Loss of response to anti-TNF agents in Crohn's disease is an emerging clinical problem.
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              Efficacy of biological therapies in inflammatory bowel disease: systematic review and meta-analysis.

              Crohn's disease (CD) and ulcerative colitis (UC) are inflammatory disorders of the gastrointestinal tract of unknown etiology. Evidence for treatment of the condition with biological therapies exists, but no systematic review and meta-analysis has examined this issue in its entirety. MEDLINE, EMBASE, and the Cochrane central register of controlled trials were searched (through to December 2010). Trials recruiting adults with active or quiescent CD or UC and comparing biological therapies (anti-tumor necrosis factor-α (TNFα) antibodies or natalizumab) with placebo were eligible. Dichotomous symptom data were pooled to obtain relative risk (RR) of failure to achieve remission in active disease and RR of relapse of activity in quiescent disease once remission had occurred, with a 95% confidence interval (CI). The search strategy identified 3,061 citations, 27 of which were eligible. Anti-TNFα antibodies and natalizumab were both superior to placebo in inducing remission of luminal CD (RR of no remission=0.87; 95% CI 0.80-0.94 and RR=0.88; 95% CI 0.83-0.94, respectively). Anti-TNFα antibodies were also superior to placebo in preventing relapse of luminal CD (RR of relapse=0.71; 95% CI 0.65-0.76). Infliximab was superior to placebo in inducing remission of moderate to severely active UC (RR=0.72; 95% CI 0.57-0.91). Biological therapies were superior to placebo in inducing remission of active CD and UC, and in preventing relapse of quiescent CD.
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                Author and article information

                Contributors
                Journal
                World J Gastroenterol
                World J. Gastroenterol
                WJG
                World Journal of Gastroenterology
                Baishideng Publishing Group Inc
                1007-9327
                2219-2840
                21 June 2018
                21 June 2018
                : 24
                : 23
                : 2457-2467
                Affiliations
                IBD Unit, Azienda Ospedaliera San Camillo-Forlanini, Rome 00152, Italy. marialiascribano@ 123456virgilio.it
                Author notes

                Author contributions: Scribano ML solely contributed to this paper.

                Correspondence to: Maria Lia Scribano, MD, IBD Unit, Azienda Ospedaliera San Camillo-Forlanini, Circonvallazione Gianicolense, 87, Rome 00152, Italy. marialiascribano@ 123456virgilio.it

                Telephone: +39-6-58703308 Fax: +39-6-58704328

                Article
                jWJG.v24.i23.pg2457
                10.3748/wjg.v24.i23.2457
                6010939
                29930467
                5c97abf5-6b5f-4af7-8d4f-e6c0ca39616d
                ©The Author(s) 2018. Published by Baishideng Publishing Group Inc. All rights reserved.

                This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial.

                History
                : 16 April 2018
                : 6 May 2018
                : 18 May 2018
                Categories
                Minireviews

                vedolizumab,crohn’s disease,real-world,efficacy,ulcerative colitis,controlled trial,effectiveness,safety

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