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A propensity score-weighted comparison between adalimumab originator and its biosimilars, ABP501 and SB5, in inflammatory bowel disease: a multicenter Italian study

BACKGROUND: Adalimumab is an effective and safe biological drug for the treatment of inflammatory bowel disease (IBD). Nowadays, several biosimilar agents are available, but data regarding their efficacy and safety in patients with IBD are still lacking. We aimed to compare the effectiveness and tol...

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Autores principales: Barberio, Brigida, Cingolani, Linda, Canova, Cristina, Barbieri, Giulia, Sablich, Renato, Urbano, Maria Teresa, Bertani, Lorenzo, Costa, Francesco, Bodini, Giorgia, Demarzo, Maria Giulia, Ferronato, Antonio, Buda, Andrea, Melatti, Piera, Massimi, Davide, Savarino, Edoardo Vincenzo, Zingone, Fabiana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8295962/
https://www.ncbi.nlm.nih.gov/pubmed/34349836
http://dx.doi.org/10.1177/17562848211031420
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author Barberio, Brigida
Cingolani, Linda
Canova, Cristina
Barbieri, Giulia
Sablich, Renato
Urbano, Maria Teresa
Bertani, Lorenzo
Costa, Francesco
Bodini, Giorgia
Demarzo, Maria Giulia
Ferronato, Antonio
Buda, Andrea
Melatti, Piera
Massimi, Davide
Savarino, Edoardo Vincenzo
Zingone, Fabiana
author_facet Barberio, Brigida
Cingolani, Linda
Canova, Cristina
Barbieri, Giulia
Sablich, Renato
Urbano, Maria Teresa
Bertani, Lorenzo
Costa, Francesco
Bodini, Giorgia
Demarzo, Maria Giulia
Ferronato, Antonio
Buda, Andrea
Melatti, Piera
Massimi, Davide
Savarino, Edoardo Vincenzo
Zingone, Fabiana
author_sort Barberio, Brigida
collection PubMed
description BACKGROUND: Adalimumab is an effective and safe biological drug for the treatment of inflammatory bowel disease (IBD). Nowadays, several biosimilar agents are available, but data regarding their efficacy and safety in patients with IBD are still lacking. We aimed to compare the effectiveness and tolerability between adalimumab originator, ABP501 and SB5 biosimilars in patients with IBD in the short term (after induction and after 6 months of treatment) through a propensity score-weighted multicenter cohort study. METHODS: We included 156 patients with IBD, 69 patients with ulcerative colitis and 87 patients with Crohn’s disease (CD) receiving ABP501 or SB5 biosimilars from January 2019 to April 2020 for moderate-to-severe disease. For comparison, a group of age- and sex-matched patients treated with adalimumab originator was used. We collected clinical and biochemical data after induction and at 6 months of treatment. Endoscopic data were recorded only at baseline. RESULTS: Overall, clinical benefit was achieved by 86.4% and 85.3% after induction and at 6 months, respectively, without a statistically significant difference between the three treatment groups (p = 0.68 and p = 0.46). However, after induction, we found significant differences between the two types of the disease (ulcerative colitis or CD, p = 0.004), with a greater clinical benefit achieved by patients with CD. Also, the therapeutic optimization rate between the three drugs was not statistically significant different (p = 0.30). All treatments showed a good safety profile, with only 10 patients who needed to stop therapy because of adverse events. CONCLUSION: Adalimumab biosimilars seem to be as effective and safe as the originator in patients with IBD. Surely, they represent a great opportunity to reduce the costs of biological therapies, however larger and longer real-life studies are necessary.
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spelling pubmed-82959622021-08-03 A propensity score-weighted comparison between adalimumab originator and its biosimilars, ABP501 and SB5, in inflammatory bowel disease: a multicenter Italian study Barberio, Brigida Cingolani, Linda Canova, Cristina Barbieri, Giulia Sablich, Renato Urbano, Maria Teresa Bertani, Lorenzo Costa, Francesco Bodini, Giorgia Demarzo, Maria Giulia Ferronato, Antonio Buda, Andrea Melatti, Piera Massimi, Davide Savarino, Edoardo Vincenzo Zingone, Fabiana Therap Adv Gastroenterol Original Research BACKGROUND: Adalimumab is an effective and safe biological drug for the treatment of inflammatory bowel disease (IBD). Nowadays, several biosimilar agents are available, but data regarding their efficacy and safety in patients with IBD are still lacking. We aimed to compare the effectiveness and tolerability between adalimumab originator, ABP501 and SB5 biosimilars in patients with IBD in the short term (after induction and after 6 months of treatment) through a propensity score-weighted multicenter cohort study. METHODS: We included 156 patients with IBD, 69 patients with ulcerative colitis and 87 patients with Crohn’s disease (CD) receiving ABP501 or SB5 biosimilars from January 2019 to April 2020 for moderate-to-severe disease. For comparison, a group of age- and sex-matched patients treated with adalimumab originator was used. We collected clinical and biochemical data after induction and at 6 months of treatment. Endoscopic data were recorded only at baseline. RESULTS: Overall, clinical benefit was achieved by 86.4% and 85.3% after induction and at 6 months, respectively, without a statistically significant difference between the three treatment groups (p = 0.68 and p = 0.46). However, after induction, we found significant differences between the two types of the disease (ulcerative colitis or CD, p = 0.004), with a greater clinical benefit achieved by patients with CD. Also, the therapeutic optimization rate between the three drugs was not statistically significant different (p = 0.30). All treatments showed a good safety profile, with only 10 patients who needed to stop therapy because of adverse events. CONCLUSION: Adalimumab biosimilars seem to be as effective and safe as the originator in patients with IBD. Surely, they represent a great opportunity to reduce the costs of biological therapies, however larger and longer real-life studies are necessary. SAGE Publications 2021-07-20 /pmc/articles/PMC8295962/ /pubmed/34349836 http://dx.doi.org/10.1177/17562848211031420 Text en © The Author(s), 2021 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Research
Barberio, Brigida
Cingolani, Linda
Canova, Cristina
Barbieri, Giulia
Sablich, Renato
Urbano, Maria Teresa
Bertani, Lorenzo
Costa, Francesco
Bodini, Giorgia
Demarzo, Maria Giulia
Ferronato, Antonio
Buda, Andrea
Melatti, Piera
Massimi, Davide
Savarino, Edoardo Vincenzo
Zingone, Fabiana
A propensity score-weighted comparison between adalimumab originator and its biosimilars, ABP501 and SB5, in inflammatory bowel disease: a multicenter Italian study
title A propensity score-weighted comparison between adalimumab originator and its biosimilars, ABP501 and SB5, in inflammatory bowel disease: a multicenter Italian study
title_full A propensity score-weighted comparison between adalimumab originator and its biosimilars, ABP501 and SB5, in inflammatory bowel disease: a multicenter Italian study
title_fullStr A propensity score-weighted comparison between adalimumab originator and its biosimilars, ABP501 and SB5, in inflammatory bowel disease: a multicenter Italian study
title_full_unstemmed A propensity score-weighted comparison between adalimumab originator and its biosimilars, ABP501 and SB5, in inflammatory bowel disease: a multicenter Italian study
title_short A propensity score-weighted comparison between adalimumab originator and its biosimilars, ABP501 and SB5, in inflammatory bowel disease: a multicenter Italian study
title_sort propensity score-weighted comparison between adalimumab originator and its biosimilars, abp501 and sb5, in inflammatory bowel disease: a multicenter italian study
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8295962/
https://www.ncbi.nlm.nih.gov/pubmed/34349836
http://dx.doi.org/10.1177/17562848211031420
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