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Multiple switches from the originator infliximab to biosimilars is effective and safe in inflammatory bowel disease : a prospective multicenter cohort study
ID Hanžel, Jurij (Author), ID Jansen, Jeroen M. (Author), ID ter Steege, Rinze W. F. (Author), ID Gecse, Krisztina B. (Author), ID D'Haens, Geert R. (Author)

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Abstract
Background: Though a single nonmedical switch from the originator infliximab (IFX) to a biosimilar is considered effective and safe for most patients with inflammatory bowel disease (IBD), very limited data are available on multiple successive switches. Methods: We performed a prospective multicenter cohort study of adult IBD patients who underwent 2 switches from the originator IFX to CT-P13 to SB2 (group 1), 1 switch from CT-P13 to SB2 (group 2), and 1 switch from the originator IFX to CT-P13 (group 3). Patients were assessed at 4 and 12 months since the most recent switch for remission using clinical (physician’s assessment) and biochemical (C-reactive protein [CRP], and fecal calprotectin [FC]) measures. Patients discontinuing treatment for ineffectiveness or adverse events before month 12 were imputed as nonremitters. Results: One hundred seventy-six patients (Crohn’s disease 71%, ulcerative colitis 27.8%, IBD unclassified 1.2%; group 1, 69; group 2, 80; group 3, 27) were included. At 12 months after the most recent switch 76.9% (40 of 52, group 1), 65.7% (46 of 70, group 2) and 76.9% (20 of 26, group 3) of patients were in clinical remission. Treatment persistence at 12 months was 85.0%, 87.0%, and 70.1%, respectively. There were no significant differences in the rate of clinical, CRP, FC remission, or treatment persistence at 12 months between the 3 groups. Infusion reactions occurred in 1.7% of patients (3/176), all in patients with antidrug antibodies from group 2. Conclusions: Multiple successive switching and switching between biosimilars of IFX seemed to be effective and safe.

Language:English
Keywords:SB2, CT-P13, multiple switches, Crohn's disease, inflammatory bowel disease, ulcerative colitis, adults, feces, c-reactive protein, infliximab, adverse event, leukocyte l1 antigen complex, infusion procedures, biosimilar pharmaceuticals, disease remission, imputation, antidrug antibody, infliximab-dyyb
Work type:Article
Typology:1.01 - Original Scientific Article
Organization:MF - Faculty of Medicine
Publication status:Published
Publication version:Version of Record
Year:2022
Number of pages:Str. 495-501
Numbering:Vol. 28, iss. 4
PID:20.500.12556/RUL-141896 This link opens in a new window
UDC:616.3
ISSN on article:1536-4844
DOI:10.1093/ibd/izab099 This link opens in a new window
COBISS.SI-ID:65359363 This link opens in a new window
Publication date in RUL:11.10.2022
Views:409
Downloads:77
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Record is a part of a journal

Title:Inflammatory bowel diseases
Shortened title:Inflamm. bowel dis.
Publisher:Oxford University Press, Crohn’s & Colitis Foundation
ISSN:1536-4844
COBISS.SI-ID:519035417 This link opens in a new window

Licences

License:CC BY-NC 4.0, Creative Commons Attribution-NonCommercial 4.0 International
Link:http://creativecommons.org/licenses/by-nc/4.0/
Description:A creative commons license that bans commercial use, but the users don’t have to license their derivative works on the same terms.

Secondary language

Language:Slovenian
Keywords:Chronova bolezen, infliksimab, biološka zdravila, gastroenterologija

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