Approaches and outcomes of adalimumab discontinuation in patients with well-controlled inflammatory arthritis: a systematic search and review

Abstract Objective This systematic search and review aimed to evaluate the available literature on discontinuation of adalimumab and other tumor necrosis factor inhibitors (TNFi) for patients with well-controlled chronic inflammatory arthritides. Methods We conducted a publication search on adalimum...

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Main Authors: Erin Balay-Dustrude, Jessica Fennell, Kevin Baszis, Y. Ingrid Goh, Daniel B. Horton, Tzielan Lee, Chloe Rotman, Anna Sutton, Marinka Twilt, Olha Halyabar, for the CARRA JIA Inactive Disease Workgroup
Format: Article
Language:English
Published: BMC 2024-12-01
Series:Pediatric Rheumatology Online Journal
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Online Access:https://doi.org/10.1186/s12969-024-01046-3
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author Erin Balay-Dustrude
Jessica Fennell
Kevin Baszis
Y. Ingrid Goh
Daniel B. Horton
Tzielan Lee
Chloe Rotman
Anna Sutton
Marinka Twilt
Olha Halyabar
for the CARRA JIA Inactive Disease Workgroup
author_facet Erin Balay-Dustrude
Jessica Fennell
Kevin Baszis
Y. Ingrid Goh
Daniel B. Horton
Tzielan Lee
Chloe Rotman
Anna Sutton
Marinka Twilt
Olha Halyabar
for the CARRA JIA Inactive Disease Workgroup
author_sort Erin Balay-Dustrude
collection DOAJ
description Abstract Objective This systematic search and review aimed to evaluate the available literature on discontinuation of adalimumab and other tumor necrosis factor inhibitors (TNFi) for patients with well-controlled chronic inflammatory arthritides. Methods We conducted a publication search on adalimumab discontinuation from 2000–2023 using PubMed, CINAHL, EMBASE, and Cochrane Library. Included studies evaluated adalimumab discontinuation approaches, tapering schemes, and outcomes including successful discontinuation and recapture after flare, in patients with well-controlled disease. Studies included evaluated rheumatoid arthritis, ankylosing spondylitis, psoriatic arthritis, and juvenile idiopathic arthritis (JIA). Results Forty-nine studies were included. Studies evaluating adalimumab alone were limited, and many reported TNFi outcomes as a single entity. Studies on rheumatoid arthritis (RA) (32, 8 RCTs) reported flare rates from 33–87%. Flares with medication tapering were slightly lower than with abrupt stop, and successful recapture was generally high (80–100%). Studies on spondyloarthropathy (12, 4 RCTs), focused on tapering, noting lower flare rates in tapering rather than abruptly stopping, and high recapture rates (~ 90%). Studies on JIA (5) were observational and demonstrated modestly lower flare rates with tapering (17–63%) versus abrupt stopping (28–82%). There was notable variability in study design, follow-up duration, specificity for TNFi results, and controlled pediatric studies. Conclusion The literature evaluating adalimumab and other TNFi discontinuation, flare rates, and recapture success within the inflammatory arthritis population demonstrated less flare when medications were tapered, over abrupt stop in the RA, spondyloarthropathy, and JIA populations. When medications were restarted after flare, recapture of well-controlled disease was generally high in RA and spondyloarthropathy, and generally favorable in JIA.
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spelling doaj-art-2910ad30af814fb5bf1348d7af496ff72025-01-05T12:11:14ZengBMCPediatric Rheumatology Online Journal1546-00962024-12-0122111410.1186/s12969-024-01046-3Approaches and outcomes of adalimumab discontinuation in patients with well-controlled inflammatory arthritis: a systematic search and reviewErin Balay-Dustrude0Jessica Fennell1Kevin Baszis2Y. Ingrid Goh3Daniel B. Horton4Tzielan Lee5Chloe Rotman6Anna Sutton7Marinka Twilt8Olha Halyabar9for the CARRA JIA Inactive Disease WorkgroupSeattle Children’s Hospital and Research CenterPediatric Rheumatology, Connecticut Children’s, Department of Pediatrics, University of ConnecticutDivision of Rheumatology & Immunology, Department of Pediatrics, Washington University School of Medicine, Saint Louis Children’s HospitalDivision of Rheumatology, The Hospital for Sick ChildrenDepartment of Pediatrics, Rutgers Robert Wood Johnson Medical SchoolPediatric Rheumatology, Stanford Medicine Children’s Health, Stanford University School of MedicineMedical Library, Boston Children’s HospitalDepartment of Epidemiology, University of WashingtonDepartment of Pediatrics, Alberta Children’s Hospital, Cumming School of Medicine, University of CalgaryDivision of Immunology, Boston Children’s Hospital, Harvard Medical SchoolAbstract Objective This systematic search and review aimed to evaluate the available literature on discontinuation of adalimumab and other tumor necrosis factor inhibitors (TNFi) for patients with well-controlled chronic inflammatory arthritides. Methods We conducted a publication search on adalimumab discontinuation from 2000–2023 using PubMed, CINAHL, EMBASE, and Cochrane Library. Included studies evaluated adalimumab discontinuation approaches, tapering schemes, and outcomes including successful discontinuation and recapture after flare, in patients with well-controlled disease. Studies included evaluated rheumatoid arthritis, ankylosing spondylitis, psoriatic arthritis, and juvenile idiopathic arthritis (JIA). Results Forty-nine studies were included. Studies evaluating adalimumab alone were limited, and many reported TNFi outcomes as a single entity. Studies on rheumatoid arthritis (RA) (32, 8 RCTs) reported flare rates from 33–87%. Flares with medication tapering were slightly lower than with abrupt stop, and successful recapture was generally high (80–100%). Studies on spondyloarthropathy (12, 4 RCTs), focused on tapering, noting lower flare rates in tapering rather than abruptly stopping, and high recapture rates (~ 90%). Studies on JIA (5) were observational and demonstrated modestly lower flare rates with tapering (17–63%) versus abrupt stopping (28–82%). There was notable variability in study design, follow-up duration, specificity for TNFi results, and controlled pediatric studies. Conclusion The literature evaluating adalimumab and other TNFi discontinuation, flare rates, and recapture success within the inflammatory arthritis population demonstrated less flare when medications were tapered, over abrupt stop in the RA, spondyloarthropathy, and JIA populations. When medications were restarted after flare, recapture of well-controlled disease was generally high in RA and spondyloarthropathy, and generally favorable in JIA.https://doi.org/10.1186/s12969-024-01046-3AdalimumabMedication discontinuationRheumatoid arthritisSpondyloarthritisJuvenile idiopathic arthritis
spellingShingle Erin Balay-Dustrude
Jessica Fennell
Kevin Baszis
Y. Ingrid Goh
Daniel B. Horton
Tzielan Lee
Chloe Rotman
Anna Sutton
Marinka Twilt
Olha Halyabar
for the CARRA JIA Inactive Disease Workgroup
Approaches and outcomes of adalimumab discontinuation in patients with well-controlled inflammatory arthritis: a systematic search and review
Pediatric Rheumatology Online Journal
Adalimumab
Medication discontinuation
Rheumatoid arthritis
Spondyloarthritis
Juvenile idiopathic arthritis
title Approaches and outcomes of adalimumab discontinuation in patients with well-controlled inflammatory arthritis: a systematic search and review
title_full Approaches and outcomes of adalimumab discontinuation in patients with well-controlled inflammatory arthritis: a systematic search and review
title_fullStr Approaches and outcomes of adalimumab discontinuation in patients with well-controlled inflammatory arthritis: a systematic search and review
title_full_unstemmed Approaches and outcomes of adalimumab discontinuation in patients with well-controlled inflammatory arthritis: a systematic search and review
title_short Approaches and outcomes of adalimumab discontinuation in patients with well-controlled inflammatory arthritis: a systematic search and review
title_sort approaches and outcomes of adalimumab discontinuation in patients with well controlled inflammatory arthritis a systematic search and review
topic Adalimumab
Medication discontinuation
Rheumatoid arthritis
Spondyloarthritis
Juvenile idiopathic arthritis
url https://doi.org/10.1186/s12969-024-01046-3
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