4.3 Review

The safety of vedolizumab for the treatment of ulcerative colitis

Journal

EXPERT OPINION ON DRUG SAFETY
Volume 16, Issue 4, Pages 501-507

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1080/14740338.2017.1300251

Keywords

Inflammatory bowel disease; ulcerative colitis; anti-integrin; vedolizumab; safety; adverse events

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Introduction: Vedolizumab is a humanized monoclonal antibody to the 47-integrin that blocks lymphocyte trafficking to the gut and is approved for treatment of patients with moderate-to-severe ulcerative colitis (UC). The gut-selective mechanism of action has the potential to improve vedolizumab's safety profile compared to other approved biologic drugs.Areas covered: We review the mechanism of action, efficacy and safety of vedolizumab treatment for UC. The positioning of vedolizumab in management algorithms is also discussed.Expert opinion: The highly selective mechanism of action of vedolizumab restricts immunosuppressive effects to the gut. Vedolizumab is efficacious as induction and maintenance therapy in UC patients who are naive or refractory to tumor necrosis factor antagonists. No clinically important safety signals have been identified. Infusion reactions are reported in <5% of cases. The rates of adverse events (AE), serious AEs, and serious infections were not different between patients treated with placebo and those who received vedolizumab in a pooled analysis of six randomized controlled trials. Rates of malignancy and mortality in vedolizumab-exposed patients are similar to those of the general UC patient population. Progressive multifocal leukoencephalopathy has not been observed. Vedolizumab is a safe and effective therapy for UC with a unique mechanism of action.

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