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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.
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.
Afiliação
  • Hartman L; Amsterdam Rheumatology and Immunology Center, Amsterdam University Medical Centers, Vrije Universiteit, Amsterdam, The Netherlands.
  • Rasch LA; Department of Epidemiology and Data Science, Amsterdam University Medical Centers, Vrije Universiteit, Amsterdam, The Netherlands.
  • Turk SA; Amsterdam Rheumatology and Immunology Center, Amsterdam University Medical Centers, Vrije Universiteit, Amsterdam, The Netherlands.
  • Ter Wee MM; Amsterdam Rheumatology and Immunology Center, Reade, Amsterdam, The Netherlands.
  • Kerstens PJSM; Department of Epidemiology and Data Science, Amsterdam University Medical Centers, Vrije Universiteit, Amsterdam, The Netherlands.
  • van der Laken CJ; Department of Rheumatology, Dijklander Ziekenhuis, Hoorn, The Netherlands.
  • Nurmohamed MT; Amsterdam Rheumatology and Immunology Center, Amsterdam University Medical Centers, Vrije Universiteit, Amsterdam, The Netherlands.
  • van Schaardenburg D; Amsterdam Rheumatology and Immunology Center, Amsterdam University Medical Centers, Vrije Universiteit, Amsterdam, The Netherlands.
  • van Tuyl LHD; Amsterdam Rheumatology and Immunology Center, Reade, Amsterdam, The Netherlands.
  • Voskuyl AE; Amsterdam Rheumatology and Immunology Center, Reade, Amsterdam, The Netherlands.
  • Boers M; Amsterdam Rheumatology and Immunology Center, Amsterdam University Medical Centers, Universiteit van Amsterdam, Amsterdam, The Netherlands.
  • Lems WF; Amsterdam Rheumatology and Immunology Center, Amsterdam University Medical Centers, Vrije Universiteit, Amsterdam, The Netherlands.
Rheumatology (Oxford) ; 62(6): 2098-2105, 2023 06 01.
Article em En | MEDLINE | ID: mdl-36205538
ABSTRACT

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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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Artrite Reumatoide / Antirreumáticos Tipo de estudo: Clinical_trials / Guideline / Prognostic_studies Limite: Humans Idioma: En Revista: Rheumatology (Oxford) Assunto da revista: REUMATOLOGIA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Holanda

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Artrite Reumatoide / Antirreumáticos Tipo de estudo: Clinical_trials / Guideline / Prognostic_studies Limite: Humans Idioma: En Revista: Rheumatology (Oxford) Assunto da revista: REUMATOLOGIA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Holanda