Vedolizumab as Induction and Maintenance Therapy for Crohn's Disease in Patients Naive to or Who Have Failed Tumor Necrosis Factor Antagonist Therapy
Abstract
Background: Vedolizumab is a gut-selective alpha(4)beta(7) integrin antagonist for the treatment of moderately to severely active Crohn's disease (CD). Aims of this study were to characterize the efficacy and safety of vedolizumab induction and maintenance therapy in patients who were naive to tumor necrosis factor-alpha (TNF-alpha) antagonist therapy (TNF-naive) or who had discontinued TNF-a antagonist therapy because of inadequate response (i.e., primary nonresponse), loss of response, or intolerance (collectively classified as the TNF-failure population).
Methods: Post hoc analyses of the efficacy data for 516 TNF-naive and 960 TNF-failure patients from the GEMINI 2 and GEMINI 3 trials were evaluated at weeks 6, 10, and 52 and included clinical remission (CD Activity Index [CDAI] score = 100-point decrease from baseline in CDAI score), durable clinical remission (remission at >= 80% of visits), and corticosteroid-free remission. Adverse events were summarized for the TNF-naive and TNF-failure subgroups by treatment received.
Results: Among patients who responded to vedolizumab induction at week 6, 48.9% of TNF-naive and 27.7% of TNF-failure patients were in remission with vedolizumab at week 52 (versus 26.8% and 12.8% with placebo). Clinical efficacy was similar between the different types of TNF-alpha antagonist failure or the number of prior TNF-alpha antagonists failed.
Safety profiles were similar in both subpopulations. Conclusions: Vedolizumab had increased efficacy over placebo in CD patients irrespective of TNF-a antagonist treatment history.
Overall, rates of response and remission were numerically higher in patients receiving vedolizumab as a first biologic than in patients who had experienced TNF failure.