Predictors of Response to Vedolizumab and Ustekinumab in Inflammatory Bowel Disease
A. Barré; J.-F. Colombel; R. Ungaro
DISCLOSURES Aliment Pharmacol Ther. 2018;47(7):896-905.
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IN THIS ARTICLE
Abstract and Introduction
Abstract
Background Increased knowledge of pathways involved in the pathogenesis of IBD has led to the development of new treatment options for Crohn's disease (CD) and ulcerative colitis (UC). Two new biological agents have been recently approved for IBD: vedolizumab and ustekinumab. They have different therapeutic targets (α4β7 integrin for vedolizumab and interleukin–12/23 pathways for ustekinumab) than the primary biological class, anti–tumour necrosis factor alpha (anti–TNF) agents. As the armamentarium for IBD increases in coming years, it will become important to understand factors associated with response in order to best position and personalise therapy.
Aim To summarise the current data on predictors of response to vedolizumab and ustekinumab in IBD patients.
Methods We conducted a comprehensive literature review. A PubMed search was performed using pre–defined key words and terms to identify relevant studies on predictors of response.
Results Patients with severe disease (by clinical activity and inflammatory biomarkers), or prior anti–TNF exposure are less likely to respond to vedolizumab. Ileocolonic disease, no prior surgery and uncomplicated phenotype were associated with better responses to ustekinumab in CD. Initial response seems to predict a better long–term maintenance in both therapies (P < 0.001). Contrary to anti–TNF therapies, immunogenicity appears to play less of a role in response.
Conclusion As the number of new biological therapies increase in IBD, identifying patients who are most likely to benefit from specific agents is of paramount importance to help best position IBD therapies.
