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Switching from originator adalimumab to biosimilar SB5 in a rheumatology cohort: persistence on treatment, predictors of drug interruption and safety analysis

AIMS: Medical and non-medical switching strategies have been adopted in Europe in the last few years. We aimed to investigate persistence on treatment with a SB5 Adalimumab (SB5) biosimilar after switching from Adalimumab (ADA) originator among patients with inflammatory rheumatic musculoskeletal di...

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Autores principales: Bruni, Cosimo, Gentileschi, Stefano, Pacini, Giovanni, Bardelli, Marco, Tofani, Lorenzo, Bartoli, Francesca, Baldi, Caterina, Cometi, Laura, Fiori, Ginevra, Nacci, Francesca, Cantarini, Luca, Guiducci, Serena, Moggi-Pignone, Alberto, Frediani, Bruno, Matucci-Cerinic, Marco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8804457/
https://www.ncbi.nlm.nih.gov/pubmed/35116080
http://dx.doi.org/10.1177/1759720X211033679
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author Bruni, Cosimo
Gentileschi, Stefano
Pacini, Giovanni
Bardelli, Marco
Tofani, Lorenzo
Bartoli, Francesca
Baldi, Caterina
Cometi, Laura
Fiori, Ginevra
Nacci, Francesca
Cantarini, Luca
Guiducci, Serena
Moggi-Pignone, Alberto
Frediani, Bruno
Matucci-Cerinic, Marco
author_facet Bruni, Cosimo
Gentileschi, Stefano
Pacini, Giovanni
Bardelli, Marco
Tofani, Lorenzo
Bartoli, Francesca
Baldi, Caterina
Cometi, Laura
Fiori, Ginevra
Nacci, Francesca
Cantarini, Luca
Guiducci, Serena
Moggi-Pignone, Alberto
Frediani, Bruno
Matucci-Cerinic, Marco
author_sort Bruni, Cosimo
collection PubMed
description AIMS: Medical and non-medical switching strategies have been adopted in Europe in the last few years. We aimed to investigate persistence on treatment with a SB5 Adalimumab (SB5) biosimilar after switching from Adalimumab (ADA) originator among patients with inflammatory rheumatic musculoskeletal diseases (iRMD), identifying possible predictors of drug interruption and describing adverse events. METHOD: iRMD patients previously switched to SB5 after at least 6 months of ADA were enrolled. Data on concomitant medications, disease flares, and persistence on SB5 up to the last available follow up were collected retrospectively. Kaplan–Meier and Cox regression models were used. RESULT: A total of 172 patients (106 females, ADA duration 5.8 ± 3.8 years) were enrolled, including 34 rheumatoid arthritis, 59 psoriatic arthritis, and 61 axial spondyloarthritis patients. In a 10 ± 3 months follow up, 65 (37.8%) patients presented with adverse events, with 46 (26.7%) showing a clinically defined disease flare (no disease activity and patient reported outcomes assessment were available); 24 patients interrupted SB5 permanently (among them, 11 back-switched to ADA and 8 were prescribed a different biological therapy). Probability of persistence on SB5 was 94.7% at 6 months and 85.1% at 12 months. Baseline corticosteroid [hazard ratio (HR) 3.209, 95% confidence interval (CI) 1.193–8.635, p = 0.021] and therapy with nonsteroidal anti-inflammatory drugs (NSAIDs) (HR 2.876, 95% CI 1.229–6.727, p = 0.015), as well as the baseline corticosteroid dose (HR 1.200, 95%CI 1.026–1.403, p = 0.022) were predictors of drug interruption. CONCLUSION: Our data on persistence of treatment and adverse events are in line with previous reports. Further large cohort studies may confirm baseline corticosteroid and NSAIDs use as predictors of SB5 interruption, helping to identify patients at higher risk of failure after switching.
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spelling pubmed-88044572022-02-02 Switching from originator adalimumab to biosimilar SB5 in a rheumatology cohort: persistence on treatment, predictors of drug interruption and safety analysis Bruni, Cosimo Gentileschi, Stefano Pacini, Giovanni Bardelli, Marco Tofani, Lorenzo Bartoli, Francesca Baldi, Caterina Cometi, Laura Fiori, Ginevra Nacci, Francesca Cantarini, Luca Guiducci, Serena Moggi-Pignone, Alberto Frediani, Bruno Matucci-Cerinic, Marco Ther Adv Musculoskelet Dis The Role of Biosimilars in the Management of Rheumatic Diseases AIMS: Medical and non-medical switching strategies have been adopted in Europe in the last few years. We aimed to investigate persistence on treatment with a SB5 Adalimumab (SB5) biosimilar after switching from Adalimumab (ADA) originator among patients with inflammatory rheumatic musculoskeletal diseases (iRMD), identifying possible predictors of drug interruption and describing adverse events. METHOD: iRMD patients previously switched to SB5 after at least 6 months of ADA were enrolled. Data on concomitant medications, disease flares, and persistence on SB5 up to the last available follow up were collected retrospectively. Kaplan–Meier and Cox regression models were used. RESULT: A total of 172 patients (106 females, ADA duration 5.8 ± 3.8 years) were enrolled, including 34 rheumatoid arthritis, 59 psoriatic arthritis, and 61 axial spondyloarthritis patients. In a 10 ± 3 months follow up, 65 (37.8%) patients presented with adverse events, with 46 (26.7%) showing a clinically defined disease flare (no disease activity and patient reported outcomes assessment were available); 24 patients interrupted SB5 permanently (among them, 11 back-switched to ADA and 8 were prescribed a different biological therapy). Probability of persistence on SB5 was 94.7% at 6 months and 85.1% at 12 months. Baseline corticosteroid [hazard ratio (HR) 3.209, 95% confidence interval (CI) 1.193–8.635, p = 0.021] and therapy with nonsteroidal anti-inflammatory drugs (NSAIDs) (HR 2.876, 95% CI 1.229–6.727, p = 0.015), as well as the baseline corticosteroid dose (HR 1.200, 95%CI 1.026–1.403, p = 0.022) were predictors of drug interruption. CONCLUSION: Our data on persistence of treatment and adverse events are in line with previous reports. Further large cohort studies may confirm baseline corticosteroid and NSAIDs use as predictors of SB5 interruption, helping to identify patients at higher risk of failure after switching. SAGE Publications 2021-07-23 /pmc/articles/PMC8804457/ /pubmed/35116080 http://dx.doi.org/10.1177/1759720X211033679 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 The Role of Biosimilars in the Management of Rheumatic Diseases
Bruni, Cosimo
Gentileschi, Stefano
Pacini, Giovanni
Bardelli, Marco
Tofani, Lorenzo
Bartoli, Francesca
Baldi, Caterina
Cometi, Laura
Fiori, Ginevra
Nacci, Francesca
Cantarini, Luca
Guiducci, Serena
Moggi-Pignone, Alberto
Frediani, Bruno
Matucci-Cerinic, Marco
Switching from originator adalimumab to biosimilar SB5 in a rheumatology cohort: persistence on treatment, predictors of drug interruption and safety analysis
title Switching from originator adalimumab to biosimilar SB5 in a rheumatology cohort: persistence on treatment, predictors of drug interruption and safety analysis
title_full Switching from originator adalimumab to biosimilar SB5 in a rheumatology cohort: persistence on treatment, predictors of drug interruption and safety analysis
title_fullStr Switching from originator adalimumab to biosimilar SB5 in a rheumatology cohort: persistence on treatment, predictors of drug interruption and safety analysis
title_full_unstemmed Switching from originator adalimumab to biosimilar SB5 in a rheumatology cohort: persistence on treatment, predictors of drug interruption and safety analysis
title_short Switching from originator adalimumab to biosimilar SB5 in a rheumatology cohort: persistence on treatment, predictors of drug interruption and safety analysis
title_sort switching from originator adalimumab to biosimilar sb5 in a rheumatology cohort: persistence on treatment, predictors of drug interruption and safety analysis
topic The Role of Biosimilars in the Management of Rheumatic Diseases
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8804457/
https://www.ncbi.nlm.nih.gov/pubmed/35116080
http://dx.doi.org/10.1177/1759720X211033679
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