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Long-term remission and biologic persistence rates: 12-year real-world data

BACKGROUND: Biologic therapies have greatly improved outcomes in rheumatoid arthritis (RA) and psoriatic arthritis (PsA). Yet, our ability to predict long-term remission and persistence or continuation of therapy remains limited. This study explores predictors of remission and persistence of the ini...

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Autores principales: Murray, Kieran, Turk, Matthew, Alammari, Yousef, Young, Francis, Gallagher, Phil, Saber, Tajvur, Fearon, Ursula, Veale, Douglas J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7807520/
https://www.ncbi.nlm.nih.gov/pubmed/33441191
http://dx.doi.org/10.1186/s13075-020-02380-z
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author Murray, Kieran
Turk, Matthew
Alammari, Yousef
Young, Francis
Gallagher, Phil
Saber, Tajvur
Fearon, Ursula
Veale, Douglas J.
author_facet Murray, Kieran
Turk, Matthew
Alammari, Yousef
Young, Francis
Gallagher, Phil
Saber, Tajvur
Fearon, Ursula
Veale, Douglas J.
author_sort Murray, Kieran
collection PubMed
description BACKGROUND: Biologic therapies have greatly improved outcomes in rheumatoid arthritis (RA) and psoriatic arthritis (PsA). Yet, our ability to predict long-term remission and persistence or continuation of therapy remains limited. This study explores predictors of remission and persistence of the initial biologic therapy in patients after 12 years. Furthermore, outcomes with adalimumab and etanercept are compared. PATIENTS AND METHODS: RA and PsA patients were prospectively recruited from a biologic clinic. Outcomes on commencing therapy, at 1 year and 12 years were reviewed. Demographics, medications, morning stiffness, patient global health score, tender and swollen joint counts, antibody status, CRP and HAQ were collected. Outcomes at 1 year and 12 years are reported and predictors of biologic persistence and EULAR-defined remission (DAS28-CRP < 2.6) are examined with univariate and multivariate analysis. RESULTS: A total of 403 patients (274 RA and 129 PsA) were analysed. PsA patients were more likely to be male, in full-time employment and have completed higher education. PsA had higher remission rates than RA at both 1 year (60.3% versus 34.5%, p < 0.001) and 12 years (91.3% versus 60.6%, p < 0.001). This difference persisted when patients were matched for baseline disease activity (p < 0.001). Biologic continuation rates were high for RA and PsA at 1 year (49.6% versus 58.9%) and 12 years (38.2% versus 52.3%). In PsA, patients starting on etanercept had lower CRP at 12 years (p = 0.041). Multivariate analysis showed 1-year continuation [OR 4.28 (1.28–14.38)] and 1-year low-disease activity [OR 3.90 (95% CI 1.05–14.53)] was predictive of a 12-year persistence. Persistence with initial biologic at 12 years [OR 4.98 (95% CI 1.83–13.56)] and male gender [OR 4.48 (95% CI 1.25–16.01)] predicted 12 year remission. CONCLUSIONS: This is the first study to show better response to biologic therapy in PsA compared to RA at 12 years. Long-term persistence with initial biologic agent was high and was predicted by biologic persistence and low-disease activity at 1 year. Interestingly, PsA patients had higher levels of employment, educational attainment, and long-term remission rates compared to RA patients.
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spelling pubmed-78075202021-01-14 Long-term remission and biologic persistence rates: 12-year real-world data Murray, Kieran Turk, Matthew Alammari, Yousef Young, Francis Gallagher, Phil Saber, Tajvur Fearon, Ursula Veale, Douglas J. Arthritis Res Ther Research Article BACKGROUND: Biologic therapies have greatly improved outcomes in rheumatoid arthritis (RA) and psoriatic arthritis (PsA). Yet, our ability to predict long-term remission and persistence or continuation of therapy remains limited. This study explores predictors of remission and persistence of the initial biologic therapy in patients after 12 years. Furthermore, outcomes with adalimumab and etanercept are compared. PATIENTS AND METHODS: RA and PsA patients were prospectively recruited from a biologic clinic. Outcomes on commencing therapy, at 1 year and 12 years were reviewed. Demographics, medications, morning stiffness, patient global health score, tender and swollen joint counts, antibody status, CRP and HAQ were collected. Outcomes at 1 year and 12 years are reported and predictors of biologic persistence and EULAR-defined remission (DAS28-CRP < 2.6) are examined with univariate and multivariate analysis. RESULTS: A total of 403 patients (274 RA and 129 PsA) were analysed. PsA patients were more likely to be male, in full-time employment and have completed higher education. PsA had higher remission rates than RA at both 1 year (60.3% versus 34.5%, p < 0.001) and 12 years (91.3% versus 60.6%, p < 0.001). This difference persisted when patients were matched for baseline disease activity (p < 0.001). Biologic continuation rates were high for RA and PsA at 1 year (49.6% versus 58.9%) and 12 years (38.2% versus 52.3%). In PsA, patients starting on etanercept had lower CRP at 12 years (p = 0.041). Multivariate analysis showed 1-year continuation [OR 4.28 (1.28–14.38)] and 1-year low-disease activity [OR 3.90 (95% CI 1.05–14.53)] was predictive of a 12-year persistence. Persistence with initial biologic at 12 years [OR 4.98 (95% CI 1.83–13.56)] and male gender [OR 4.48 (95% CI 1.25–16.01)] predicted 12 year remission. CONCLUSIONS: This is the first study to show better response to biologic therapy in PsA compared to RA at 12 years. Long-term persistence with initial biologic agent was high and was predicted by biologic persistence and low-disease activity at 1 year. Interestingly, PsA patients had higher levels of employment, educational attainment, and long-term remission rates compared to RA patients. BioMed Central 2021-01-13 2021 /pmc/articles/PMC7807520/ /pubmed/33441191 http://dx.doi.org/10.1186/s13075-020-02380-z Text en © The Author(s) 2021 Open AccessThis 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/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Murray, Kieran
Turk, Matthew
Alammari, Yousef
Young, Francis
Gallagher, Phil
Saber, Tajvur
Fearon, Ursula
Veale, Douglas J.
Long-term remission and biologic persistence rates: 12-year real-world data
title Long-term remission and biologic persistence rates: 12-year real-world data
title_full Long-term remission and biologic persistence rates: 12-year real-world data
title_fullStr Long-term remission and biologic persistence rates: 12-year real-world data
title_full_unstemmed Long-term remission and biologic persistence rates: 12-year real-world data
title_short Long-term remission and biologic persistence rates: 12-year real-world data
title_sort long-term remission and biologic persistence rates: 12-year real-world data
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7807520/
https://www.ncbi.nlm.nih.gov/pubmed/33441191
http://dx.doi.org/10.1186/s13075-020-02380-z
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