A product review of vedolizumab in inflammatory bowel disease

被引:19
|
作者
Battat, Robert [1 ,2 ]
Dulai, Parambir S. [1 ,2 ]
Jairath, Vipul [2 ,3 ,4 ]
Vande Casteele, Niels [1 ,2 ]
机构
[1] Univ Calif San Diego, Dept Med, Div Gastroenterol, Inflammatory Bowel Dis Ctr, La Jolla, CA 92093 USA
[2] Robarts Clin Trials Inc, London, ON, Canada
[3] Univ Western Ontario, Dept Med, London, ON, Canada
[4] Univ Western Ontario, Dept Epidemiol & Biostat, London, ON, Canada
关键词
Anti-integrin therapy; Crohn's disease; gut-selective; inflammatory bowel disease; ulcerative colitis; vedolizumab; MUCOSAL VASCULAR ADDRESSIN; ACTIVE ULCERATIVE-COLITIS; COTTON-TOP TAMARIN; CROHNS-DISEASE; INDUCTION THERAPY; MAINTENANCE THERAPY; POSTOPERATIVE COMPLICATIONS; HUMANIZED ANTIBODY; TREATED PATIENTS; TROUGH LEVELS;
D O I
10.1080/21645515.2019.1591139
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Vedolizumab is a monoclonal antibody to the alpha 4 beta 7 integrin that selectively reduces intestinal lymphocyte trafficking, thereby providing a safe and effective treatment option for patients with inflammatory bowel disease (IBD). This product review outlines the unique mechanism of vedolizumab in addition to efficacy, safety, pharmacokinetic and pharmacodynamic data from clinical trials, observational studies and meta-analyses. Vedolizumab has been shown to be effective as a first- or second-line induction and maintenance therapy in both ulcerative colitis (UC) and Crohn's disease (CD). Prolonged induction therapy may increase efficacy, particularly in tumor necrosis factor-alpha-exposed CD patients. To date, no drug-specific safety signals have been identified. In addition to the presence of an apparent exposure-response relationship, vedolizumab has demonstrated consistent pharmacodynamic effects on alpha 4 beta 7, mucosal vascular addressin cell adhesion molecule 1 and other cell adhesion molecules. Future efforts should focus on identifying predictive biomarkers capable of guiding personalized IBD treatment with vedolizumab.
引用
收藏
页码:2482 / 2490
页数:9
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