Real-Life Retention Rates and Reasons for Switching of Biological DMARDs in Rheumatoid Arthritis, Psoriatic Arthritis, and Ankylosing Spondylitis

Aims: To determine real-life biologic/targeted synthetic disease-modifying anti-rheumatic drug (b/tsDMARD) retention rates in rheumatoid arthritis (RA), psoriatic arthritis (PsA), and ankylosing spondylitis (AS), explore reasons for switching and to compare results to previously published data.Metho...

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Main Authors: Vandana Bhushan, Susan Lester, Liz Briggs, Raif Hijjawi, E. Michael Shanahan, Eliza Pontifex, Jem Ninan, Catherine Hill, Fin Cai, Jennifer Walker, Fiona Goldblatt, Mihir D. Wechalekar
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-09-01
Series:Frontiers in Medicine
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fmed.2021.708168/full
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author Vandana Bhushan
Vandana Bhushan
Susan Lester
Susan Lester
Liz Briggs
Raif Hijjawi
E. Michael Shanahan
E. Michael Shanahan
Eliza Pontifex
Eliza Pontifex
Jem Ninan
Catherine Hill
Catherine Hill
Fin Cai
Fin Cai
Jennifer Walker
Jennifer Walker
Fiona Goldblatt
Fiona Goldblatt
Mihir D. Wechalekar
Mihir D. Wechalekar
author_facet Vandana Bhushan
Vandana Bhushan
Susan Lester
Susan Lester
Liz Briggs
Raif Hijjawi
E. Michael Shanahan
E. Michael Shanahan
Eliza Pontifex
Eliza Pontifex
Jem Ninan
Catherine Hill
Catherine Hill
Fin Cai
Fin Cai
Jennifer Walker
Jennifer Walker
Fiona Goldblatt
Fiona Goldblatt
Mihir D. Wechalekar
Mihir D. Wechalekar
author_sort Vandana Bhushan
collection DOAJ
description Aims: To determine real-life biologic/targeted synthetic disease-modifying anti-rheumatic drug (b/tsDMARD) retention rates in rheumatoid arthritis (RA), psoriatic arthritis (PsA), and ankylosing spondylitis (AS), explore reasons for switching and to compare results to previously published data.Methods: Time-to-event analysis for mean treatment duration (estimated as the Restricted Mean Survival Time), b/tsDMARD failure, and b/tsDMARDs switching was performed for 230 patients (n = 147 RA, 46 PsA, 37 AS) who commenced their first b/tsDMARD between 2008 and 2018. Patients were managed in a dedicated “biologics” clinic in a tertiary hospital; the choice of b/tsDMARD was clinician driven based on medical factors and patient preferences. The effect of covariates on switching risk was analysed by a conditional risk-set Cox proportional-hazards model. Treatment retention data was compared to a historical analysis (2002–2008).Results: The proportions remaining on treatment (retention) were similar, throughout follow-up, for the first, second and third b/tsDMARDs across all patients (p = 0.46). When compared to RA patients, the risk of b/tsDMARD failure was halved in PsA patients [Hazard Ratio (HR) = 0.50], but no different in AS patients (HR = 1.0). The respective restricted mean (95%CI) treatment durations, estimated at 5 years of follow-up, were 3.1 (2.9, 3.4), 4.1 (3.7, 4.6), and 3.3 (2.8, 3.9) years, for RA, PsA, and AS, respectively. Age, gender, disease duration, smoking status and the use of concomitant csDMARDS were not associated with the risk of bDMARD failure. The most common reasons for switching in the first and subsequent years were secondary (n = 62) and primary (n = 35) failure. Comparison with historical data indicated no substantive differences in switching of the first biologic for RA and PsA.Conclusion: Similar retention rates of the second and third compared to the first b/tsDMARD in RA, PsA, and AS support a strategy of differential b/tsDMARDs use informed by patient presentation. Despite greater availability of b/tsDMARDs with differing mechanisms of action, retention rates of the first b/tsDMARD remain similar to previous years.
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spelling doaj.art-1e12a83da0a14ff0aaa971a0138dfa1f2022-12-21T18:28:44ZengFrontiers Media S.A.Frontiers in Medicine2296-858X2021-09-01810.3389/fmed.2021.708168708168Real-Life Retention Rates and Reasons for Switching of Biological DMARDs in Rheumatoid Arthritis, Psoriatic Arthritis, and Ankylosing SpondylitisVandana Bhushan0Vandana Bhushan1Susan Lester2Susan Lester3Liz Briggs4Raif Hijjawi5E. Michael Shanahan6E. Michael Shanahan7Eliza Pontifex8Eliza Pontifex9Jem Ninan10Catherine Hill11Catherine Hill12Fin Cai13Fin Cai14Jennifer Walker15Jennifer Walker16Fiona Goldblatt17Fiona Goldblatt18Mihir D. Wechalekar19Mihir D. Wechalekar20Rheumatology Unit, Flinders Medical Centre, Adelaide, SA, AustraliaDivision of Medicine, Flinders Medical Centre, Adelaide, SA, AustraliaRheumatology Unit, Queen Elizabeth Hospital, Adelaide, SA, AustraliaDiscipline of Medicine, The University of Adelaide, Adelaide, SA, AustraliaRheumatology Unit, Flinders Medical Centre, Adelaide, SA, AustraliaDivision of Medicine, Flinders Medical Centre, Adelaide, SA, AustraliaRheumatology Unit, Flinders Medical Centre, Adelaide, SA, AustraliaCollege of Medicine and Public Health, Flinders University, Adelaide, SA, AustraliaRheumatology Unit, Flinders Medical Centre, Adelaide, SA, AustraliaCollege of Medicine and Public Health, Flinders University, Adelaide, SA, AustraliaRheumatology Unit, Queen Elizabeth Hospital, Adelaide, SA, AustraliaRheumatology Unit, Queen Elizabeth Hospital, Adelaide, SA, AustraliaDiscipline of Medicine, The University of Adelaide, Adelaide, SA, AustraliaRheumatology Unit, Flinders Medical Centre, Adelaide, SA, AustraliaCollege of Medicine and Public Health, Flinders University, Adelaide, SA, AustraliaRheumatology Unit, Flinders Medical Centre, Adelaide, SA, AustraliaCollege of Medicine and Public Health, Flinders University, Adelaide, SA, AustraliaRheumatology Unit, Flinders Medical Centre, Adelaide, SA, AustraliaCollege of Medicine and Public Health, Flinders University, Adelaide, SA, AustraliaRheumatology Unit, Flinders Medical Centre, Adelaide, SA, AustraliaCollege of Medicine and Public Health, Flinders University, Adelaide, SA, AustraliaAims: To determine real-life biologic/targeted synthetic disease-modifying anti-rheumatic drug (b/tsDMARD) retention rates in rheumatoid arthritis (RA), psoriatic arthritis (PsA), and ankylosing spondylitis (AS), explore reasons for switching and to compare results to previously published data.Methods: Time-to-event analysis for mean treatment duration (estimated as the Restricted Mean Survival Time), b/tsDMARD failure, and b/tsDMARDs switching was performed for 230 patients (n = 147 RA, 46 PsA, 37 AS) who commenced their first b/tsDMARD between 2008 and 2018. Patients were managed in a dedicated “biologics” clinic in a tertiary hospital; the choice of b/tsDMARD was clinician driven based on medical factors and patient preferences. The effect of covariates on switching risk was analysed by a conditional risk-set Cox proportional-hazards model. Treatment retention data was compared to a historical analysis (2002–2008).Results: The proportions remaining on treatment (retention) were similar, throughout follow-up, for the first, second and third b/tsDMARDs across all patients (p = 0.46). When compared to RA patients, the risk of b/tsDMARD failure was halved in PsA patients [Hazard Ratio (HR) = 0.50], but no different in AS patients (HR = 1.0). The respective restricted mean (95%CI) treatment durations, estimated at 5 years of follow-up, were 3.1 (2.9, 3.4), 4.1 (3.7, 4.6), and 3.3 (2.8, 3.9) years, for RA, PsA, and AS, respectively. Age, gender, disease duration, smoking status and the use of concomitant csDMARDS were not associated with the risk of bDMARD failure. The most common reasons for switching in the first and subsequent years were secondary (n = 62) and primary (n = 35) failure. Comparison with historical data indicated no substantive differences in switching of the first biologic for RA and PsA.Conclusion: Similar retention rates of the second and third compared to the first b/tsDMARD in RA, PsA, and AS support a strategy of differential b/tsDMARDs use informed by patient presentation. Despite greater availability of b/tsDMARDs with differing mechanisms of action, retention rates of the first b/tsDMARD remain similar to previous years.https://www.frontiersin.org/articles/10.3389/fmed.2021.708168/fullbiologic DMARDsretentionswitchingrheumatoid arthritispsoriatic arthritisankylosing spondylitis
spellingShingle Vandana Bhushan
Vandana Bhushan
Susan Lester
Susan Lester
Liz Briggs
Raif Hijjawi
E. Michael Shanahan
E. Michael Shanahan
Eliza Pontifex
Eliza Pontifex
Jem Ninan
Catherine Hill
Catherine Hill
Fin Cai
Fin Cai
Jennifer Walker
Jennifer Walker
Fiona Goldblatt
Fiona Goldblatt
Mihir D. Wechalekar
Mihir D. Wechalekar
Real-Life Retention Rates and Reasons for Switching of Biological DMARDs in Rheumatoid Arthritis, Psoriatic Arthritis, and Ankylosing Spondylitis
Frontiers in Medicine
biologic DMARDs
retention
switching
rheumatoid arthritis
psoriatic arthritis
ankylosing spondylitis
title Real-Life Retention Rates and Reasons for Switching of Biological DMARDs in Rheumatoid Arthritis, Psoriatic Arthritis, and Ankylosing Spondylitis
title_full Real-Life Retention Rates and Reasons for Switching of Biological DMARDs in Rheumatoid Arthritis, Psoriatic Arthritis, and Ankylosing Spondylitis
title_fullStr Real-Life Retention Rates and Reasons for Switching of Biological DMARDs in Rheumatoid Arthritis, Psoriatic Arthritis, and Ankylosing Spondylitis
title_full_unstemmed Real-Life Retention Rates and Reasons for Switching of Biological DMARDs in Rheumatoid Arthritis, Psoriatic Arthritis, and Ankylosing Spondylitis
title_short Real-Life Retention Rates and Reasons for Switching of Biological DMARDs in Rheumatoid Arthritis, Psoriatic Arthritis, and Ankylosing Spondylitis
title_sort real life retention rates and reasons for switching of biological dmards in rheumatoid arthritis psoriatic arthritis and ankylosing spondylitis
topic biologic DMARDs
retention
switching
rheumatoid arthritis
psoriatic arthritis
ankylosing spondylitis
url https://www.frontiersin.org/articles/10.3389/fmed.2021.708168/full
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