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Clinical factors associated with discontinuation of ts/bDMARDs in rheumatic patients from the BIOBADASER III registry

Biologic and targeted synthetic disease-modifying antirheumatic drugs (ts/bDMARDs) play a pivotal role in the treatment of rheumatoid arthritis (RA), psoriatic arthritis (PsA), and ankylosing spondylitis (AS). Persistence of therapy provides an index of a drug’s overall effectiveness. The objective...

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Autores principales: Prior-Español, A., Sánchez-Piedra, C., Campos, J., Manero, F. J., Pérez-García, C., Bohórquez, C., Busquets-Pérez, N., Blanco-Madrigal, J. M., Díaz-Torne, C., Sánchez-Alonso, F., Mateo, L., Holgado-Pérez, S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8159943/
https://www.ncbi.nlm.nih.gov/pubmed/34045525
http://dx.doi.org/10.1038/s41598-021-90442-w
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author Prior-Español, A.
Sánchez-Piedra, C.
Campos, J.
Manero, F. J.
Pérez-García, C.
Bohórquez, C.
Busquets-Pérez, N.
Blanco-Madrigal, J. M.
Díaz-Torne, C.
Sánchez-Alonso, F.
Mateo, L.
Holgado-Pérez, S.
author_facet Prior-Español, A.
Sánchez-Piedra, C.
Campos, J.
Manero, F. J.
Pérez-García, C.
Bohórquez, C.
Busquets-Pérez, N.
Blanco-Madrigal, J. M.
Díaz-Torne, C.
Sánchez-Alonso, F.
Mateo, L.
Holgado-Pérez, S.
author_sort Prior-Español, A.
collection PubMed
description Biologic and targeted synthetic disease-modifying antirheumatic drugs (ts/bDMARDs) play a pivotal role in the treatment of rheumatoid arthritis (RA), psoriatic arthritis (PsA), and ankylosing spondylitis (AS). Persistence of therapy provides an index of a drug’s overall effectiveness. The objective of the study was to identify factors associated with discontinuation of ts/bDMARDs in a real-world dataset. The study population comprised patients diagnosed with RA, PsA, and AS included in the BIOBADASER registry for whom follow-up data were available until November 2019. Patient features and treatment data were included in the analysis. The Kaplan–Meier method was used to study survival of the different drugs according to the reason for discontinuation. Factors associated with discontinuation were studied using Cox regression models and bivariate and multivariate analyses. P values of less than 0.05 were regarded as statistically significant. The study population comprised 4,752 patients who received a total of 8,377 drugs, of which 4,411 (52.65%) were discontinued. The Kaplan–Meier curves showed that survival for first-line treatment was greater in all 3 groups (p < 0.001). Patients with RA had a greater risk of discontinuation if they were younger (HR, 0.99; 95% CI 0.99–1.00), if they were receiving anti-TNFα agents (HR, 0.61; 95% CI 0.54–0.70), and if they had more comorbid conditions (HR, 1.09; 95% CI 1.00–1.17). Patients with PsA had a higher risk if they were women (HR, 1.36; 95% CI 1.15–1.62) and if they were receiving other ts/bDMARDs (HR, 1.29; 95% CI 1.05–1.59). In patients with AS, risk increased with age (HR, 1.01; 95% CI 1.00–1.02), as did the number of comorbid conditions (HR, 1.27; 95% CI 1.12–1.45). The factors that most affected discontinuation of ts/bDMARDs were line of treatment, age, type of drug, sex, comorbidity and the year of initiation of treatment. The association with these factors differed with each disease, except for first-line treatment, which was associated with a lower risk of discontinuation in all 3 diseases.
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spelling pubmed-81599432021-05-28 Clinical factors associated with discontinuation of ts/bDMARDs in rheumatic patients from the BIOBADASER III registry Prior-Español, A. Sánchez-Piedra, C. Campos, J. Manero, F. J. Pérez-García, C. Bohórquez, C. Busquets-Pérez, N. Blanco-Madrigal, J. M. Díaz-Torne, C. Sánchez-Alonso, F. Mateo, L. Holgado-Pérez, S. Sci Rep Article Biologic and targeted synthetic disease-modifying antirheumatic drugs (ts/bDMARDs) play a pivotal role in the treatment of rheumatoid arthritis (RA), psoriatic arthritis (PsA), and ankylosing spondylitis (AS). Persistence of therapy provides an index of a drug’s overall effectiveness. The objective of the study was to identify factors associated with discontinuation of ts/bDMARDs in a real-world dataset. The study population comprised patients diagnosed with RA, PsA, and AS included in the BIOBADASER registry for whom follow-up data were available until November 2019. Patient features and treatment data were included in the analysis. The Kaplan–Meier method was used to study survival of the different drugs according to the reason for discontinuation. Factors associated with discontinuation were studied using Cox regression models and bivariate and multivariate analyses. P values of less than 0.05 were regarded as statistically significant. The study population comprised 4,752 patients who received a total of 8,377 drugs, of which 4,411 (52.65%) were discontinued. The Kaplan–Meier curves showed that survival for first-line treatment was greater in all 3 groups (p < 0.001). Patients with RA had a greater risk of discontinuation if they were younger (HR, 0.99; 95% CI 0.99–1.00), if they were receiving anti-TNFα agents (HR, 0.61; 95% CI 0.54–0.70), and if they had more comorbid conditions (HR, 1.09; 95% CI 1.00–1.17). Patients with PsA had a higher risk if they were women (HR, 1.36; 95% CI 1.15–1.62) and if they were receiving other ts/bDMARDs (HR, 1.29; 95% CI 1.05–1.59). In patients with AS, risk increased with age (HR, 1.01; 95% CI 1.00–1.02), as did the number of comorbid conditions (HR, 1.27; 95% CI 1.12–1.45). The factors that most affected discontinuation of ts/bDMARDs were line of treatment, age, type of drug, sex, comorbidity and the year of initiation of treatment. The association with these factors differed with each disease, except for first-line treatment, which was associated with a lower risk of discontinuation in all 3 diseases. Nature Publishing Group UK 2021-05-27 /pmc/articles/PMC8159943/ /pubmed/34045525 http://dx.doi.org/10.1038/s41598-021-90442-w Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Prior-Español, A.
Sánchez-Piedra, C.
Campos, J.
Manero, F. J.
Pérez-García, C.
Bohórquez, C.
Busquets-Pérez, N.
Blanco-Madrigal, J. M.
Díaz-Torne, C.
Sánchez-Alonso, F.
Mateo, L.
Holgado-Pérez, S.
Clinical factors associated with discontinuation of ts/bDMARDs in rheumatic patients from the BIOBADASER III registry
title Clinical factors associated with discontinuation of ts/bDMARDs in rheumatic patients from the BIOBADASER III registry
title_full Clinical factors associated with discontinuation of ts/bDMARDs in rheumatic patients from the BIOBADASER III registry
title_fullStr Clinical factors associated with discontinuation of ts/bDMARDs in rheumatic patients from the BIOBADASER III registry
title_full_unstemmed Clinical factors associated with discontinuation of ts/bDMARDs in rheumatic patients from the BIOBADASER III registry
title_short Clinical factors associated with discontinuation of ts/bDMARDs in rheumatic patients from the BIOBADASER III registry
title_sort clinical factors associated with discontinuation of ts/bdmards in rheumatic patients from the biobadaser iii registry
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8159943/
https://www.ncbi.nlm.nih.gov/pubmed/34045525
http://dx.doi.org/10.1038/s41598-021-90442-w
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