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Incidence comparison of adverse events in patients with inflammatory bowel disease receiving different biologic agents: retrospective long-term evaluation

Barberio, Brigida; Savarino, Edoardo Vincenzo; Card, Timothy; Canova, Cristina; Baldisser, Francesco; Gubbiotti, Alessandro; Massimi, Davide; Ghisa, Matteo; Zingone, Fabiana

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Authors

Brigida Barberio

Edoardo Vincenzo Savarino

Dr TIM CARD tim.card@nottingham.ac.uk
CLINICAL ASSOCIATE PROFESSOR

Cristina Canova

Francesco Baldisser

Alessandro Gubbiotti

Davide Massimi

Matteo Ghisa

Fabiana Zingone



Abstract

Background/Aims Current literature is lacking in studies comparing the incidence of adverse events (AEs) in patients with inflammatory bowel diseases (IBD) treated with adalimumab (ADA) or vedolizumab (VDZ) in a real-life scenario. Therefore, our primary aim was to compare the AEs occurring in patients taking ADA to those of patients taking VDZ.

Methods In this single center study, data on AEs from IBD patients who underwent treatment with ADA and VDZ were retrospectively collected. AE rates per 100 person-years were calculated. A Cox regression model was used to estimate the hazard ratios of the AEs between the 2 drugs.

Results A total of 16 ADA patients (17.2%) and 11 VDZ patients (7.6%) had AEs causing drug interruption during the study period (P=0.02). Most of the AEs were noninfectious extraintestinal events (50% in ADA and 54.5% in VDZ) while infections accounted for 31.2% of the AEs in patients treated with ADA and 27.3% in those treated with VDZ. The incidence rate of AEs causing withdrawal of therapy was 13.2 per 100 person-years for ADA and 5.3 per 100 person-years for VDZ, corresponding to a 76% lower risk in patients in VDZ. Considering the first year of treatment, we observed 34 subjects treated with ADA (36.5%) having at least 1 AEs and 57 (39.3%) among those taking VDZ (P=0.67).

Conclusions VDZ has a lower incidence rate of AEs causing withdrawal of treatment compared to ADA but a similar risk of AEs not causing drug interruption. Real-life head-to-head studies are still necessary to further explore the safety profile of these drugs.

Citation

Barberio, B., Savarino, E. V., Card, T., Canova, C., Baldisser, F., Gubbiotti, A., Massimi, D., Ghisa, M., & Zingone, F. (2022). Incidence comparison of adverse events in patients with inflammatory bowel disease receiving different biologic agents: retrospective long-term evaluation. Intestinal Research, 20(1), 114-123. https://doi.org/10.5217/ir.2021.00037

Journal Article Type Article
Acceptance Date Jun 16, 2021
Online Publication Date Aug 4, 2021
Publication Date Jan 30, 2022
Deposit Date Feb 3, 2025
Publicly Available Date Feb 3, 2025
Journal Intestinal Research
Print ISSN 1598-9100
Electronic ISSN 2288-1956
Publisher Korean Association for the Study of Intestinal Diseases
Peer Reviewed Peer Reviewed
Volume 20
Issue 1
Pages 114-123
DOI https://doi.org/10.5217/ir.2021.00037
Keywords Inflammatory bowel disease; Biological therapy; Adalimumab; Vedolizumab; Adverse events
Public URL https://nottingham-repository.worktribe.com/output/7355838
Publisher URL https://irjournal.org/journal/view.php?doi=10.5217/ir.2021.00037
Additional Information Received: 2021-02-27; Accepted: 2021-06-16; Published online: 2021-08-04; Print publication: 2022-01-30

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Publisher Licence URL
https://creativecommons.org/licenses/by/4.0/

Copyright Statement
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.





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