Vedolizumab versus ustekinumab in Crohn’s disease with prior anti-tumor necrosis factor failure: an updated meta-analysis

Author:

Milioli Natália Junkes1,Fernandes Matheus Vanzin2,Correa Tulio L.3,Antunes Vanio2,Martins Otávio Cosendey4,Florêncio de Mesquita Cynthia5,Baraldo Stefano6,Furfaro Federica7

Affiliation:

1. Department of Gastroenterology and Gastrointestinal Endoscopy, Pontifical Catholic University of Rio Grande do Sul

2. Department of Gastroenterology and Gastrointestinal Endoscopy, Porto Alegre Health Science’s Federal University, Porto Alegre, Brazil

3. Department of Gastroenterology, Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA

4. Department of Gastroenterology, Federal University of Juiz de Fora, Juiz de Fora

5. Department of Gastroenterology, Federal University of Pernambuco, Recife

6. Department of Endoscopy, Barretos Cancer Hospital, Barretos, Brazil

7. Department of Gastroenterology and Gastrointestinal Endoscopy, IRCCS San Raffaele Scientific Institute, Milan, Italy

Abstract

Ustekinumab and vedolizumab are key treatment options for Crohn’s disease patients who fail anti-tumor necrosis factor (TNF) therapy. This updated meta-analysis aims to compare the efficacy and safety of these two drugs. We performed a systematic review in PubMed, Embase, and Cochrane databases searching for randomized and nonrandomized studies comparing vedolizumab versus ustekinumab in patients with Crohn’s disease with previous anti-TNF failure or intolerance. The primary outcome was steroid-free clinical remission (SFR) at the pos-induction (12–16 weeks) and maintenance period (48–52 weeks). The odds ratio (OR) was used for binary outcomes with their respective 95% confidence interval (CI). Heterogeneity was assessed using the Cochran Q test and I 2 statistics. This meta-analysis included 11 studies and 2724 patients. There was a significant difference favoring ustekinumab in SFR at pos-induction (OR, 1.44; 95% CI, 1.11–1.88; P = 0.006; I 2 = 27%) and maintenance periods (OR, 1.86; 95% CI, 1.23–2.82; P = 0.003; I 2 = 80%), in clinical remission at pos-induction period (OR, 2.04; 95% CI, 1.58–2.63; P < 0.001; I 2 = 3%), and in treatment discontinuation due to adverse events (OR, 0.31; 95% CI, 0.16–0.60; P < 0.001; I 2 = 0%). In patients with Crohn’s disease with prior anti-TNF failure, ustekinumab showed higher SFR during both the pos-induction and maintenance period and a lower rate of treatment discontinuation due to adverse events.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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