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Long-term treatment response in rheumatoid arthritis patients starting adalimumab or etanercept with or without concomitant methotrexate.
l'Ami, Merel J; Kneepkens, Eva L; Nurmohamed, Michael T; Krieckaert, Charlotte L M; Visman, Ingrid M; Wolbink, Gert-Jan.
Afiliação
  • l'Ami MJ; Amsterdam Rheumatology and Immunology Center, Reade, Amsterdam, The Netherlands. m.lami@reade.nl.
  • Kneepkens EL; Amsterdam Rheumatology and Immunology Center, Reade, Amsterdam, The Netherlands.
  • Nurmohamed MT; Amsterdam Rheumatology and Immunology Center, Reade; and Amsterdam Rheumatology and immunology Center, VU University Medical Center, Amsterdam, The Netherlands.
  • Krieckaert CLM; Amsterdam Rheumatology and Immunology Center, Reade, Amsterdam, The Netherlands.
  • Visman IM; Amsterdam Rheumatology and Immunology Center, Reade, Amsterdam, The Netherlands.
  • Wolbink GJ; Amsterdam Rheumatology and Immunology Center, Reade; and Immunopathology, Sanquin Research and Landsteiner Laboratory Academic Medical Center, Amsterdam, The Netherlands.
Clin Exp Rheumatol ; 35(3): 431-437, 2017.
Article em En | MEDLINE | ID: mdl-28079512
ABSTRACT

OBJECTIVES:

To observe long-term clinical response and drug survival in a prospective two-year cohort study in rheumatoid arthritis (RA) patients starting adalimumab or etanercept treatment, with or without methotrexate (MTX), after failure of conventional DMARD therapy, including MTX.

METHODS:

Disease activity score of 28 joints (DAS28) and Health Assessment Questionnaire (HAQ) were collected of 873 consecutive RA patients, treated with adalimumab or etanercept, prospectively at baseline, 4, 16, 28, 40, 52, 78 and 104 weeks of biological therapy. Sustained minimal disease activity (MDA), DAS28 <2.6 for at least 24 consecutive weeks, biological discontinuation, ΔHAQ and ΔDAS28 were compared between patients treated with or without concomitant MTX for etanercept and adalimumab separately.

RESULTS:

More patients treated with adalimumab and MTX (42%) achieved sustained MDA than patients without MTX (18%). The hazard ratio (HR) was 2.3 [1.4-3.9]. No significant difference was found in etanercept treatment (with MTX 33% vs. 28% without MTX), HR 1.1 [0.8-1.6]. More patients treated without MTX discontinued treatment than patients with MTX co-treatment in adalimumab (HR 2.1 [1.5-3.0]) and etanercept (HR 1.9 [1.0-3.4]). The mean decrease in DAS28 over time was higher for patients treated with MTX in adalimumab (regression coefficient (RC) 0.57, p<0.001), but was not significantly different in etanercept treatment (RC 0.05, p=0.427). No significant differences were found in ΔHAQ.

CONCLUSIONS:

Treatment discontinuation is lower in patients treated with MTX in both adalimumab and etanercept treatment. However, considering good clinical response, in contrast to etanercept, a synergetic effect of MTX is observed only in adalimumab treatment.
Assuntos
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Base de dados: MEDLINE Assunto principal: Artrite Reumatoide / Produtos Biológicos / Metotrexato / Antirreumáticos / Adalimumab / Etanercepte Tipo de estudo: Diagnostic_studies / Observational_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Clin Exp Rheumatol Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Holanda
Buscar no Google
Base de dados: MEDLINE Assunto principal: Artrite Reumatoide / Produtos Biológicos / Metotrexato / Antirreumáticos / Adalimumab / Etanercepte Tipo de estudo: Diagnostic_studies / Observational_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Clin Exp Rheumatol Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Holanda