Vedolizumab as Induction and Maintenance Therapy for Ulcerative Colitis

Brian G. Feagan(Western University), Paul Rutgeerts, Bruce E. Sands(Icahn School of Medicine at Mount Sinai), Stephen B. Hanauer(University of Chicago), Jean‐Frédéric Colombel(Centre Hospitalier Universitaire de Lille), William J. Sandborn(University of California San Diego), Gert Van Assche, Jeffrey Axler(Sinai Hospital), Hyo Jong Kim(Kyung Hee University Dental Hospital), Silvio Danese, Irving H. Fox(Millennium Engineering and Integration (United States)), Catherine Milch(Millennium Engineering and Integration (United States)), Serap Sankoh(Millennium Engineering and Integration (United States)), Tim Wyant(Millennium Engineering and Integration (United States)), Jing Xu(Millennium Engineering and Integration (United States)), Asit Parikh(Millennium Engineering and Integration (United States))
New England Journal of Medicine
August 21, 2013
Cited by 2,836Open Access
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Abstract

BACKGROUND: Gut-selective blockade of lymphocyte trafficking by vedolizumab may constitute effective treatment for ulcerative colitis. METHODS: We conducted two integrated randomized, double-blind, placebo-controlled trials of vedolizumab in patients with active disease. In the trial of induction therapy, 374 patients (cohort 1) received vedolizumab (at a dose of 300 mg) or placebo intravenously at weeks 0 and 2, and 521 patients (cohort 2) received open-label vedolizumab at weeks 0 and 2, with disease evaluation at week 6. In the trial of maintenance therapy, patients in either cohort who had a response to vedolizumab at week 6 were randomly assigned to continue receiving vedolizumab every 8 or 4 weeks or to switch to placebo for up to 52 weeks. A response was defined as a reduction in the Mayo Clinic score (range, 0 to 12, with higher scores indicating more active disease) of at least 3 points and a decrease of at least 30% from baseline, with an accompanying decrease in the rectal bleeding subscore of at least 1 point or an absolute rectal bleeding subscore of 0 or 1. RESULTS: Response rates at week 6 were 47.1% and 25.5% among patients in the vedolizumab group and placebo group, respectively (difference with adjustment for stratification factors, 21.7 percentage points; 95% confidence interval [CI], 11.6 to 31.7; P<0.001). At week 52, 41.8% of patients who continued to receive vedolizumab every 8 weeks and 44.8% of patients who continued to receive vedolizumab every 4 weeks were in clinical remission (Mayo Clinic score ≤2 and no subscore >1), as compared with 15.9% of patients who switched to placebo (adjusted difference, 26.1 percentage points for vedolizumab every 8 weeks vs. placebo [95% CI, 14.9 to 37.2; P<0.001] and 29.1 percentage points for vedolizumab every 4 weeks vs. placebo [95% CI, 17.9 to 40.4; P<0.001]). The frequency of adverse events was similar in the vedolizumab and placebo groups. CONCLUSIONS: Vedolizumab was more effective than placebo as induction and maintenance therapy for ulcerative colitis. (Funded by Millennium Pharmaceuticals; GEMINI 1 ClinicalTrials.gov number, NCT00783718.).


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