Literature DB >> 28606961

Long-term outcomes after disease activity-guided dose reduction of TNF inhibition in rheumatoid arthritis: 3-year data of the DRESS study - a randomised controlled pragmatic non-inferiority strategy trial.

Chantal Am Bouman1, Noortje van Herwaarden1, Frank Hj van den Hoogen1,2, Jaap Fransen2, Ronald F van Vollenhoven3,4, Johannes Wj Bijlsma5, Aatke van der Maas1, Alfons A den Broeder1,2.   

Abstract

OBJECTIVE: Tumour necrosis factor inhibitors (TNFi) are effective in rheumatoid arthritis (RA), but disadvantages include adverse events (AEs) and high costs. This can be improved by disease activity-guided dose reduction (DR). We aimed to assess long-term outcomes of TNFi DR in RA by using 3-year data from the DRESS study (Dose REduction Strategy of Subcutaneous TNF inhibitors study).
METHODS: In the intervention phase (month 0-18) of the DRESS study (Dutch trial register, NTR 3216), patients were randomised to DR or usual care (UC). In the extension phase (month 18-36), treatment strategies in both groups converged to continuation of protocolised tight control and allowed dose optimisation. Intention-to-treat analyses were done on flare, disease activity (28 joint count-based disease activity score with C reactive protein (DAS28-CRP)), functioning (health assessment questionnaire-disability index (HAQ-DI)), quality of life (Euroqol 5 dimensions 5 levels questionnaire (EQ5D-5L)), medication use, radiographic progression (Sharp van der Heijde score (SvdH)) and AE.
RESULTS: 172/180 patients included in the DRESS study were included in the extension phase. Cumulative incidences of major flare were 10% and 12% (-2%, 95% CI -8 to 15) in DR and UC groups in the extension phase, and 17% and 14% (3%, 95% CI -9 to 13) from 0 to 36 months. Cumulative incidences of short-lived flares were 43% (33 to 52%)%) and 35% (23 to 49%)%) in DR and UC groups in the extension phase, and 83% (75 to 90%)%) and 44% (31 to 58%)%) from 0 to 36 months. Mean DAS28-CRP, HAQ-DI, EQ5D-5L and SvdH remained stable and not significantly different between groups. TNFi use remained low in the DR group and decreased in the UC group. Cumulative incidences of AE were not significantly different between groups.
CONCLUSIONS: Safety and efficacy of disease activity guided TNFi DR in RA are maintained up to 3 years, with a large reduction in TNFi use, but no other benefits. Implementation of DR would vastly improve the cost-effective use of TNFi. © Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2017. All rights reserved. No commercial use is permitted unless otherwise expressly granted.

Entities:  

Keywords:  TNF inhibitor; flare; rheumatoid arthritis; treatment optimization

Mesh:

Substances:

Year:  2017        PMID: 28606961     DOI: 10.1136/annrheumdis-2017-211169

Source DB:  PubMed          Journal:  Ann Rheum Dis        ISSN: 0003-4967            Impact factor:   19.103


  13 in total

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Authors:  Johanna Sigaux; Florian Bailly; David Hajage; Xavier Mariette; Jacques Morel; Frédérique Gandjbakhch; Violaine Foltz; Laure Gossec; Florence Tubach; Bruno Fautrel
Journal:  RMD Open       Date:  2017-09-12

2.  Dosage reduction and discontinuation of biological disease-modifying antirheumatic drugs in patients with rheumatoid arthritis, psoriatic arthritis and axial spondyloarthritis: protocol for a pragmatic, randomised controlled trial (the BIOlogical Dose OPTimisation (BIODOPT) trial).

Authors:  Line Uhrenholt; Annette Schlemmer; Ellen-Margrethe Hauge; Robin Christensen; Lene Dreyer; Maria E Suarez-Almazor; Salome Kristensen
Journal:  BMJ Open       Date:  2019-07-09       Impact factor: 2.692

3.  Impact of tapering targeted therapies (bDMARDs or JAKis) on the risk of serious infections and adverse events of special interest in patients with rheumatoid arthritis or spondyloarthritis: a systematic analysis of the literature and meta-analysis.

Authors:  D Vinson; L Molet-Benhamou; Y Degboé; A den Broeder; F Ibrahim; C Pontes; R Westhovens; J Závada; T Pham; T Barnetche; A Constantin; A Ruyssen-Witrand
Journal:  Arthritis Res Ther       Date:  2020-04-29       Impact factor: 5.156

4.  Efficacy of pharmacological treatment in rheumatoid arthritis: a systematic literature research informing the 2019 update of the EULAR recommendations for management of rheumatoid arthritis.

Authors:  Andreas Kerschbaumer; Alexandre Sepriano; Josef S Smolen; Désirée van der Heijde; Maxime Dougados; Ronald van Vollenhoven; Iain B McInnes; Johannes W J Bijlsma; Gerd R Burmester; Maarten de Wit; Louise Falzon; Robert Landewé
Journal:  Ann Rheum Dis       Date:  2020-02-07       Impact factor: 19.103

5.  Tapering of biological antirheumatic drugs in rheumatoid arthritis patients is achievable and cost-effective in daily clinical practice: data from the Brussels UCLouvain RA Cohort.

Authors:  Stéphanie Dierckx; Tatiana Sokolova; Bernard R Lauwerys; Aleksandra Avramovska; Laurent Meric de Bellefon; Adrien Nzeusseu Toukap; Maria Stoenoiu; Frédéric A Houssiau; Patrick Durez
Journal:  Arthritis Res Ther       Date:  2020-04-28       Impact factor: 5.156

6.  Sample Size Calculation Guide - Part 6: How to calculate the sample size for a non-inferiority or an equivalence clinical trial.

Authors:  Ahmed Negida
Journal:  Adv J Emerg Med       Date:  2019-11-27

7.  Extra-articular findings with FDG-PET/CT in rheumatoid arthritis patients: more harm than benefit.

Authors:  Evy Ulijn; Alfons A den Broeder; Nadine Boers; Martin Gotthardt; Chantal A M Bouman; Robert Landewé; Nathan den Broeder; Noortje van Herwaarden
Journal:  Rheumatol Adv Pract       Date:  2022-02-18

8.  Switching from TNFα inhibitor to tacrolimus as maintenance therapy in rheumatoid arthritis after achieving low disease activity with TNFα inhibitors and methotrexate: 24-week result from a non-randomized, prospective, active-controlled trial.

Authors:  Sang Youn Jung; Jung Hee Koh; Ki-Jo Kim; Yong-Wook Park; Hyung-In Yang; Sung Jae Choi; Jisoo Lee; Chan-Bum Choi; Wan-Uk Kim
Journal:  Arthritis Res Ther       Date:  2021-07-08       Impact factor: 5.156

Review 9.  Hypersensitivity reactions to monoclonal antibodies: Classification and treatment approach (Review).

Authors:  Irena Pintea; Carina Petricau; Dinu Dumitrascu; Adriana Muntean; Daniel Constantin Branisteanu; Daciana Elena Branisteanu; Diana Deleanu
Journal:  Exp Ther Med       Date:  2021-07-03       Impact factor: 2.447

10.  Using adalimumab serum concentration to choose a subsequent biological DMARD in rheumatoid arthritis patients failing adalimumab treatment (ADDORA-switch): study protocol for a fully blinded randomised superiority test-treatment trial.

Authors:  Maike H M Wientjes; Sadaf Atiqi; Gerrit Jan Wolbink; Michael T Nurmohamed; Maarten Boers; Theo Rispens; Annick de Vries; Ronald F van Vollenhoven; Bart J F van den Bemt; Alfons A den Broeder
Journal:  Trials       Date:  2021-06-19       Impact factor: 2.279

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