Abstract | BACKGROUND AND AIMS: METHODS: We conducted a systematic literature search in PubMed and the Cochrane Library, up to October 2018. Interventional and non-interventional studies as well as case-series studying vedolizumab and EIMs in adult patients with IBD were considered eligible. RESULTS: Three interventional studies [one randomized trial, n = 1032; and two open-label trials, n = 347], five non-interventional studies [n = 1496] and three case-series [n = 17] were included. Vedolizumab did not show any effectiveness in primary sclerosing cholangitis [PSC]. While no effect was seen in pre-existing manifestations regarding arthralgia and arthritis, the occurrence of new rheumatic symptoms was lower among vedolizumab users compared to placebo; occurrence was higher, however, with vedolizumab than with tumour necrosis factor inhibitors. Finally, vedolizumab appears not to be efficacious for the treatment of cutaneous manifestations. CONCLUSIONS: There is no strong evidence to suggest that vedolizumab may be efficacious for the treatment of pre-existing EIMs [especially PSC, rheumatic and cutaneous manifestations], although it may reduce the occurrence of new EIMs.
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Authors | Thomas Chateau, Stefanos Bonovas, Catherine Le Berre, Nicolas Mathieu, Silvio Danese, Laurent Peyrin-Biroulet |
Journal | Journal of Crohn's & colitis
(J Crohns Colitis)
Vol. 13
Issue 12
Pg. 1569-1577
(Dec 10 2019)
ISSN: 1876-4479 [Electronic] England |
PMID | 31076751
(Publication Type: Journal Article, Systematic Review)
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Copyright | Copyright © 2019 European Crohn’s and Colitis Organisation (ECCO). Published by Oxford University Press. All rights reserved. For permissions, please email: [email protected]. |
Chemical References |
- Antibodies, Monoclonal, Humanized
- Gastrointestinal Agents
- Integrins
- vedolizumab
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Topics |
- Antibodies, Monoclonal, Humanized
(pharmacology)
- Arthritis
(drug therapy, etiology)
- Cholangitis, Sclerosing
(drug therapy, etiology)
- Gastrointestinal Agents
(pharmacology)
- Humans
- Inflammatory Bowel Diseases
(complications)
- Integrins
(antagonists & inhibitors)
- Skin Diseases
(drug therapy, etiology)
- Treatment Outcome
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