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Efficacy of synthetic and biological DMARDs: a systematic literature review informing the 2022 update of the EULAR recommendations for the management of rheumatoid arthritis.
Kerschbaumer, Andreas; Sepriano, Alexandre; Bergstra, Sytske Anne; Smolen, Josef S; van der Heijde, Désirée; Caporali, Roberto; Edwards, Christopher John; Verschueren, Patrick; de Souza, Savia; Pope, Janet E; Takeuchi, Tsutomu; Hyrich, Kimme L; Winthrop, Kevin L; Aletaha, Daniel; Stamm, Tanja A; Schoones, Jan W; Landewé, Robert B M.
Afiliação
  • Kerschbaumer A; Department of Medicine III, Division of Rheumatology, Medical University of Vienna, Vienna, Austria andreas.kerschbaumer@meduniwien.ac.at.
  • Sepriano A; CHRC Campus Nova Medical School, Universidade Nova de Lisboa, Lisboa, Portugal.
  • Bergstra SA; Department of Rheumatology, Leiden University Medical Center, Leiden, The Netherlands.
  • Smolen JS; Department of Rheumatology, Leiden University Medical Center, Leiden, The Netherlands.
  • van der Heijde D; Department of Medicine III, Division of Rheumatology, Medical University of Vienna, Vienna, Austria.
  • Caporali R; Department of Rheumatology, Leiden University Medical Center, Leiden, The Netherlands.
  • Edwards CJ; Department of Rheumatology, University of Milan, Milan, Italy.
  • Verschueren P; NIHR Southampton Clinical Research Facility, University Hospital Southampton NHS Foundation Trust, Southampton, UK.
  • de Souza S; Department of Rheumatology, University Hospitals Leuven and Skeletal Biology and Engineering Research Centre, KU Leuven, Leuven, Belgium.
  • Pope JE; Patient Research Partner Network, European Alliance of Associations for Rheumatology, Zurich, Switzerland.
  • Takeuchi T; Schulich School of Medicine, University of Western Ontario, London, Ontario, Canada.
  • Hyrich KL; Division of Rheumatology, Department of Internal Medicine, Keio University School of Medicine, Shinjuku-ku, Japan.
  • Winthrop KL; Centre for Epidemiology Versus Arthritis, The University of Manchester and NIHR Manchester Biomedical Research Centre, Manchester University NHS Trust, Manchester, UK.
  • Aletaha D; School of Public Health, Oregon Health & Science University, Portland, Oregon, USA.
  • Stamm TA; Department of Medicine III, Division of Rheumatology, Medical University of Vienna, Vienna, Austria.
  • Schoones JW; Section for Outcomes Research, Centre for Medical Statistics, Informatics, and Intelligent Systems, Medical University of Vienna, Vienna, Austria.
  • Landewé RBM; Ludwig Boltzmann Institute for Arthritis and Rehabilitation, Vienna, Austria.
Ann Rheum Dis ; 82(1): 95-106, 2023 01.
Article em En | MEDLINE | ID: mdl-36368906
ABSTRACT

OBJECTIVES:

To update the evidence on efficacy of DMARDs (disease-modifying antirheumatic drugs) and inform the taskforce of the 2022 update of the European Alliance of Associations for Rheumatology (EULAR) recommendations for management of rheumatoid arthritis (RA).

METHODS:

This systematic literature review (SLR) investigated the efficacy of conventional synthetic (cs), biological (b), biosimilar and targeted synthetic (ts)DMARDs in patients with RA. Medline, EMBASE, Cochrane CENTRAL and Web of Science were used to identify all relevant articles published since the previous update in 2019 to 14 January 2022.

RESULTS:

Of 8969 search results, 169 articles were selected for detailed review and 47 were finally included. Trials investigated the efficacy of csDMARDs, bDMARDs and tsDMARDs, DMARD switching, tapering and trials investigating different treatment strategies. The compounds investigated were csDMARDs (methotrexate (MTX), leflunomide, sulfasalazine, hydroxychloroquine), bDMARDs (abatacept, adalimumab, certolizumab-pegol, denosumab, etanercept, infliximab, levilimab, olokizumab, opineracept, rituximab, sarilumab, tocilizumab) and tsDMARDs (baricitinib, filgotinib, tofacitinib, upadacitinib). The efficacy of csDMARDs+ short-term glucocorticoids in early RA was confirmed and similar to bDMARD+MTX combination therapy. Interleukin-6 pathway inhibition was effective in trials on olokizumab and levilimab. Janus kinase inhibitor (JAKi) was efficacious in different patient populations. After insufficient response to JAKi, patients could respond to TNFi treatment. Tapering of DMARDs was feasible for a proportion of patients, who were able to taper therapy while remaining in low disease activity or remission.

CONCLUSION:

The results of this SLR, together with one SLR on safety of DMARD and one on glucocorticoids, informed the taskforce of the 2022 update of the EULAR recommendations for pharmacological management of RA.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Artrite Reumatoide / Reumatologia / Produtos Biológicos / Antirreumáticos / Medicamentos Biossimilares / Inibidores de Janus Quinases Tipo de estudo: Guideline / Systematic_reviews Limite: Humans Idioma: En Revista: Ann Rheum Dis Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Áustria

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Artrite Reumatoide / Reumatologia / Produtos Biológicos / Antirreumáticos / Medicamentos Biossimilares / Inibidores de Janus Quinases Tipo de estudo: Guideline / Systematic_reviews Limite: Humans Idioma: En Revista: Ann Rheum Dis Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Áustria