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

Abstract 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...

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Main Authors: Kieran Murray, Matthew Turk, Yousef Alammari, Francis Young, Phil Gallagher, Tajvur Saber, Ursula Fearon, Douglas J. Veale
Format: Article
Language:English
Published: BMC 2021-01-01
Series:Arthritis Research & Therapy
Subjects:
Online Access:https://doi.org/10.1186/s13075-020-02380-z
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spelling doaj-6300f7fa7db14cc0b3710f5ce94f54ac2021-01-17T12:57:59ZengBMCArthritis Research & Therapy1478-63622021-01-0123111010.1186/s13075-020-02380-zLong-term remission and biologic persistence rates: 12-year real-world dataKieran Murray0Matthew Turk1Yousef Alammari2Francis Young3Phil Gallagher4Tajvur Saber5Ursula Fearon6Douglas J. Veale7Department of Rheumatology, St Vincent’s University HospitalDepartment of Rheumatology, St Vincent’s University HospitalDepartment of Rheumatology, St Vincent’s University HospitalDepartment of Rheumatology, St Vincent’s University HospitalDepartment of Rheumatology, St Vincent’s University HospitalLady Reading HospitalMolecular Rheumatology, School of Medicine, Trinity Biomedical Sciences Institute, Trinity College DublinDepartment of Rheumatology, St Vincent’s University HospitalAbstract 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.https://doi.org/10.1186/s13075-020-02380-zRheumatoid arthritisPsoriatic arthritisBiologicsRemission
collection DOAJ
language English
format Article
sources DOAJ
author Kieran Murray
Matthew Turk
Yousef Alammari
Francis Young
Phil Gallagher
Tajvur Saber
Ursula Fearon
Douglas J. Veale
spellingShingle Kieran Murray
Matthew Turk
Yousef Alammari
Francis Young
Phil Gallagher
Tajvur Saber
Ursula Fearon
Douglas J. Veale
Long-term remission and biologic persistence rates: 12-year real-world data
Arthritis Research & Therapy
Rheumatoid arthritis
Psoriatic arthritis
Biologics
Remission
author_facet Kieran Murray
Matthew Turk
Yousef Alammari
Francis Young
Phil Gallagher
Tajvur Saber
Ursula Fearon
Douglas J. Veale
author_sort Kieran Murray
title 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_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_sort long-term remission and biologic persistence rates: 12-year real-world data
publisher BMC
series Arthritis Research & Therapy
issn 1478-6362
publishDate 2021-01-01
description Abstract 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.
topic Rheumatoid arthritis
Psoriatic arthritis
Biologics
Remission
url https://doi.org/10.1186/s13075-020-02380-z
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