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Favourable effect of a ‘second hit’ after 13 weeks in early RA non-responders: the Amsterdam COBRA treat-to-target randomized trial

OBJECTIVE: The aim of this study was to investigate the effect of treat-to-target combination therapy with intensification at 13 weeks in early RA. METHODS: Early RA patients were classified as being at high or low risk of worsening RA based on disease activity and prognostic factors. High-risk pati...

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Autores principales: Hartman, Linda, Rasch, Linda A, Turk, Samina A, ter Wee, Marieke M, Kerstens, Pit J S M, van der Laken, Conny J, Nurmohamed, Michael T, van Schaardenburg, Dirkjan, van Tuyl, Lilian H D, Voskuyl, Alexandre E, Boers, Maarten, Lems, Willem F
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10234185/
https://www.ncbi.nlm.nih.gov/pubmed/36205538
http://dx.doi.org/10.1093/rheumatology/keac582
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author Hartman, Linda
Rasch, Linda A
Turk, Samina A
ter Wee, Marieke M
Kerstens, Pit J S M
van der Laken, Conny J
Nurmohamed, Michael T
van Schaardenburg, Dirkjan
van Tuyl, Lilian H D
Voskuyl, Alexandre E
Boers, Maarten
Lems, Willem F
author_facet Hartman, Linda
Rasch, Linda A
Turk, Samina A
ter Wee, Marieke M
Kerstens, Pit J S M
van der Laken, Conny J
Nurmohamed, Michael T
van Schaardenburg, Dirkjan
van Tuyl, Lilian H D
Voskuyl, Alexandre E
Boers, Maarten
Lems, Willem F
author_sort Hartman, Linda
collection PubMed
description OBJECTIVE: The aim of this study was to investigate the effect of treat-to-target combination therapy with intensification at 13 weeks in early RA. METHODS: Early RA patients were classified as being at high or low risk of worsening RA based on disease activity and prognostic factors. High-risk patients received COBRA-light (prednisolone 30 mg/day tapered to 7.5 mg/day, MTX increasing to 25 mg/week), and low-risk patients received MTX monotherapy increasing to 25 mg/week. The primary outcome (target) was DAS44 < 1.6 or EULAR good response at 26 weeks. At 13 weeks, non-responders were randomized to (open-label) intensification [high-risk patients: prednisolone 60 mg/day tapered to 7.5 mg/day, addition of SSZ (2 g/day) and HCQ (400 mg/day); low-risk patients: prednisolone 30 mg/day tapered to 7.5 mg/day] or continuation. RESULTS: In the high-risk group (n = 150), 110 patients (73%) reached the target at 13 weeks, and 9 dropped out. Non-responders were randomized to intensification (n = 15) or continuation (n = 16), and after 26 weeks, 12 (80%) vs 7 (44%) of these, respectively, reached the target [difference: 36%, (95% CI 2%, 71%); P = 0.04]. In the low-risk group (n = 40), 17 (43%) reached the target. Non-responders were randomized to intensification (n = 8) or continuation (n = 7); 4 vs 3, respectively, reached the target. Adverse event rates were higher in the high-risk group, and higher in the intensification subgroup of that group. Serious adverse events were rare. Protocol violations were frequent and mostly led to mitigation of actual treatment intensification. CONCLUSION: Initial combination therapy was very successful in high-risk RA, and early intensification was beneficial in patients not reaching the strict target. The low-risk group was too small for drawing conclusions. In routine practice, adherence to early intensification based on strict targets is difficult. TRIAL REGISTRATION: Netherlands Trial Register (NTR), NL4393, https://www.trialregister.nl/.
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spelling pubmed-102341852023-06-02 Favourable effect of a ‘second hit’ after 13 weeks in early RA non-responders: the Amsterdam COBRA treat-to-target randomized trial Hartman, Linda Rasch, Linda A Turk, Samina A ter Wee, Marieke M Kerstens, Pit J S M van der Laken, Conny J Nurmohamed, Michael T van Schaardenburg, Dirkjan van Tuyl, Lilian H D Voskuyl, Alexandre E Boers, Maarten Lems, Willem F Rheumatology (Oxford) Clinical Science OBJECTIVE: The aim of this study was to investigate the effect of treat-to-target combination therapy with intensification at 13 weeks in early RA. METHODS: Early RA patients were classified as being at high or low risk of worsening RA based on disease activity and prognostic factors. High-risk patients received COBRA-light (prednisolone 30 mg/day tapered to 7.5 mg/day, MTX increasing to 25 mg/week), and low-risk patients received MTX monotherapy increasing to 25 mg/week. The primary outcome (target) was DAS44 < 1.6 or EULAR good response at 26 weeks. At 13 weeks, non-responders were randomized to (open-label) intensification [high-risk patients: prednisolone 60 mg/day tapered to 7.5 mg/day, addition of SSZ (2 g/day) and HCQ (400 mg/day); low-risk patients: prednisolone 30 mg/day tapered to 7.5 mg/day] or continuation. RESULTS: In the high-risk group (n = 150), 110 patients (73%) reached the target at 13 weeks, and 9 dropped out. Non-responders were randomized to intensification (n = 15) or continuation (n = 16), and after 26 weeks, 12 (80%) vs 7 (44%) of these, respectively, reached the target [difference: 36%, (95% CI 2%, 71%); P = 0.04]. In the low-risk group (n = 40), 17 (43%) reached the target. Non-responders were randomized to intensification (n = 8) or continuation (n = 7); 4 vs 3, respectively, reached the target. Adverse event rates were higher in the high-risk group, and higher in the intensification subgroup of that group. Serious adverse events were rare. Protocol violations were frequent and mostly led to mitigation of actual treatment intensification. CONCLUSION: Initial combination therapy was very successful in high-risk RA, and early intensification was beneficial in patients not reaching the strict target. The low-risk group was too small for drawing conclusions. In routine practice, adherence to early intensification based on strict targets is difficult. TRIAL REGISTRATION: Netherlands Trial Register (NTR), NL4393, https://www.trialregister.nl/. Oxford University Press 2022-10-07 /pmc/articles/PMC10234185/ /pubmed/36205538 http://dx.doi.org/10.1093/rheumatology/keac582 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of the British Society for Rheumatology. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Clinical Science
Hartman, Linda
Rasch, Linda A
Turk, Samina A
ter Wee, Marieke M
Kerstens, Pit J S M
van der Laken, Conny J
Nurmohamed, Michael T
van Schaardenburg, Dirkjan
van Tuyl, Lilian H D
Voskuyl, Alexandre E
Boers, Maarten
Lems, Willem F
Favourable effect of a ‘second hit’ after 13 weeks in early RA non-responders: the Amsterdam COBRA treat-to-target randomized trial
title Favourable effect of a ‘second hit’ after 13 weeks in early RA non-responders: the Amsterdam COBRA treat-to-target randomized trial
title_full Favourable effect of a ‘second hit’ after 13 weeks in early RA non-responders: the Amsterdam COBRA treat-to-target randomized trial
title_fullStr Favourable effect of a ‘second hit’ after 13 weeks in early RA non-responders: the Amsterdam COBRA treat-to-target randomized trial
title_full_unstemmed Favourable effect of a ‘second hit’ after 13 weeks in early RA non-responders: the Amsterdam COBRA treat-to-target randomized trial
title_short Favourable effect of a ‘second hit’ after 13 weeks in early RA non-responders: the Amsterdam COBRA treat-to-target randomized trial
title_sort favourable effect of a ‘second hit’ after 13 weeks in early ra non-responders: the amsterdam cobra treat-to-target randomized trial
topic Clinical Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10234185/
https://www.ncbi.nlm.nih.gov/pubmed/36205538
http://dx.doi.org/10.1093/rheumatology/keac582
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