Comparing the Efficacy and Safety of Adalimumab and Vedolizumab in Treating Moderate to Severe Crohn's Disease and Ulcerative Colitis.

Adalimumab Crohn’s disease Inflammatory bowel disease PRISMA Ulcerative colitis Vedolizumab

Journal

Gastroenterology research
ISSN: 1918-2805
Titre abrégé: Gastroenterology Res
Pays: Canada
ID NLM: 101519422

Informations de publication

Date de publication:
Dec 2023
Historique:
received: 19 08 2023
accepted: 14 10 2023
medline: 8 1 2024
pubmed: 8 1 2024
entrez: 8 1 2024
Statut: ppublish

Résumé

Numerous patients with inflammatory bowel disease (IBD) do not respond to conventional or biological therapy. Adalimumab (ADA) and vedolizumab (VDZ), according to certain research, may be a useful alternative treatment for these people. The purpose of this study was to assess the effectiveness and safety of using ADA and VDZ to treat moderate to severe IBD: Crohn's disease (CD) and ulcerative colitis (UC). We searched PubMed, Medline, Web of Science, Scopus, the Cochrane Library, Embase, Google Scholar, CINAHL, Clinicaltrials.gov, and WHO trials registry (ICTRP). Randomized controlled trials (RCTs) comparing ADA or VDZ with placebo in participants with active CD or UC were included. The primary outcomes were the clinical response and remission at induction and maintenance phases and mucosal healing. The secondary outcome was the incidence of profound negative events. The research used Comprehensive Meta-Analysis version 3 (Biostat Inc., USA). Eighteen RCTs were incorporated, in which 11 studies described the usefulness and safeness of ADA or VDZ in CD patients, and seven studies investigated the efficacy and safety of ADA or VDZ in UC patients. The meta-analysis revealed that both ADA and VDZ treatments were superior to placebo for producing clinical remission and eliciting clinical response at induction and maintenance phases in individuals with moderately to severely active CD or UC. Interestingly, we found that ADA was superior to VDZ as first-line treatment for patients with CD, but not UC. ADA and VDZ are effective and safe in CD and UC patients. However, RCTs of a larger number of patients are still required for better assessing the safety profile of ADA and VDZ.

Sections du résumé

Background UNASSIGNED
Numerous patients with inflammatory bowel disease (IBD) do not respond to conventional or biological therapy. Adalimumab (ADA) and vedolizumab (VDZ), according to certain research, may be a useful alternative treatment for these people. The purpose of this study was to assess the effectiveness and safety of using ADA and VDZ to treat moderate to severe IBD: Crohn's disease (CD) and ulcerative colitis (UC).
Methods UNASSIGNED
We searched PubMed, Medline, Web of Science, Scopus, the Cochrane Library, Embase, Google Scholar, CINAHL, Clinicaltrials.gov, and WHO trials registry (ICTRP). Randomized controlled trials (RCTs) comparing ADA or VDZ with placebo in participants with active CD or UC were included. The primary outcomes were the clinical response and remission at induction and maintenance phases and mucosal healing. The secondary outcome was the incidence of profound negative events. The research used Comprehensive Meta-Analysis version 3 (Biostat Inc., USA).
Results UNASSIGNED
Eighteen RCTs were incorporated, in which 11 studies described the usefulness and safeness of ADA or VDZ in CD patients, and seven studies investigated the efficacy and safety of ADA or VDZ in UC patients. The meta-analysis revealed that both ADA and VDZ treatments were superior to placebo for producing clinical remission and eliciting clinical response at induction and maintenance phases in individuals with moderately to severely active CD or UC. Interestingly, we found that ADA was superior to VDZ as first-line treatment for patients with CD, but not UC.
Conclusion UNASSIGNED
ADA and VDZ are effective and safe in CD and UC patients. However, RCTs of a larger number of patients are still required for better assessing the safety profile of ADA and VDZ.

Identifiants

pubmed: 38186583
doi: 10.14740/gr1664
pmc: PMC10769610
doi:

Types de publication

Journal Article

Langues

eng

Pagination

289-306

Informations de copyright

Copyright 2023, Merza et al.

Déclaration de conflit d'intérêts

None to declare.

Auteurs

Nooraldin Merza (N)

Department of Internal Medicine, University of Toledo, Toledo, OH, USA.

Yusuf Nawras (Y)

University of Toledo College of Medicine and Life Sciences, Toledo, OH, USA.

Omar Saab (O)

Department of Internal Medicine, Cleavland Clinic, Cleavland, OH, USA.

Dushyant Singh Dahiya (DS)

Department of Gastroenterology, University of Kansas Medical Center, Kansas City, KS, USA.

Zohaib Ahmed (Z)

Department of Gastroenterology, University of Toledo, Toledo, OH, USA.

Meghana Ranabothu (M)

University of Toledo College of Medicine and Life Sciences, Toledo, OH, USA.

Safa Boujemaa (S)

Biotechnology Development, Institute Pasteur De Tunis, University De Tunis El Manar, Tunis, Tunisia.

Mona Hassan (M)

Department of Gastroenterology, University of Toledo, Toledo, OH, USA.

Abdallah Kobeissy (A)

Department of Gastroenterology, University of Toledo, Toledo, OH, USA.

Kirthi Lilley (K)

Department of Gastroenterology, Wayne State University, Detroit, MI, USA.

Classifications MeSH