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EULAR recommendations for the management of rheumatoid arthritis with synthetic and biological disease-modifying antirheumatic drugs: 2019 update
by
den Broeder, Alfons A
, Takeuchi, Tsutomu
, Sepriano, Alexandre
, Buch, Maya H
, Gottenberg, Jacques-Eric
, Gossec, Laure
, Balsa, Alejandro
, Voshaar, Marieke
, Smolen, Josef S
, Kerschbaumer, Andreas
, Cutolo, Maurizio
, Burmester, Gerd R
, Boers, Maarten
, da Silva, Jose A P
, Dougados, Maxime
, Li, Zhanguo
, van Eijk-Hustings, Yvonne
, Koloumas, Marios
, Cardiel, Mario Humberto
, Huizinga, Tom W J
, Caporali, Roberto
, Hetland, Merete Lund
, Aringer, Martin
, Mariette, Xavier
, Aletaha, Daniel
, Landewé, Robert B M
, Mysler, Eduardo F
, Rubbert-Roth, Andrea
, de Wit, Maarten
, Finckh, Axel
, van Vollenhoven, Ronald F
, De Cock, Diederik
, Müller-Ladner, Ulf
, Saag, Kenneth G
, Edwards, Christopher John
, van der Heijde, Désirée
, Codreanu, Catalin
, McInnes, Iain B
, Westhovens, René
, Ruyssen-Witrand, Adeline
, Bijlsma, Johannes W J
, Buttgereit, Frank
, Pope, Janet E
, Strangfeld, Anja
, Askling, John
, Emery, Paul
, Poór, Gyula
in
Antibiotics
/ Antirheumatic Agents - economics
/ Antirheumatic Agents - therapeutic use
/ Arthritis, Rheumatoid - drug therapy
/ Autoantibodies
/ Biological products
/ Biological Products - economics
/ Biological Products - therapeutic use
/ Clinical trials
/ Consensus
/ Costs
/ DMARDs (biologic)
/ DMARDs (synthetic)
/ Drug Therapy, Combination
/ Drugs
/ economic evaluations
/ Etanercept
/ Europe
/ Glucocorticoids
/ Humans
/ Immunomodulators
/ Immunotherapy
/ Infliximab
/ Janus kinase
/ Janus Kinase Inhibitors - therapeutic use
/ Leflunomide
/ Life Sciences
/ Medical personnel
/ Methotrexate
/ Monoclonal antibodies
/ Patients
/ Recommendation
/ Regulatory approval
/ Remission
/ Rheumatoid arthritis
/ Rheumatology
/ Risk factors
/ Rituximab
/ Societies, Medical
/ Sulfasalazine
/ Synthetic Drugs - economics
/ Synthetic Drugs - therapeutic use
/ Systematic Reviews as Topic
/ Task forces
/ treatment
/ Tumor Necrosis Factor-alpha - antagonists & inhibitors
/ Tumor necrosis factor-α
/ Tumors
2020
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EULAR recommendations for the management of rheumatoid arthritis with synthetic and biological disease-modifying antirheumatic drugs: 2019 update
by
den Broeder, Alfons A
, Takeuchi, Tsutomu
, Sepriano, Alexandre
, Buch, Maya H
, Gottenberg, Jacques-Eric
, Gossec, Laure
, Balsa, Alejandro
, Voshaar, Marieke
, Smolen, Josef S
, Kerschbaumer, Andreas
, Cutolo, Maurizio
, Burmester, Gerd R
, Boers, Maarten
, da Silva, Jose A P
, Dougados, Maxime
, Li, Zhanguo
, van Eijk-Hustings, Yvonne
, Koloumas, Marios
, Cardiel, Mario Humberto
, Huizinga, Tom W J
, Caporali, Roberto
, Hetland, Merete Lund
, Aringer, Martin
, Mariette, Xavier
, Aletaha, Daniel
, Landewé, Robert B M
, Mysler, Eduardo F
, Rubbert-Roth, Andrea
, de Wit, Maarten
, Finckh, Axel
, van Vollenhoven, Ronald F
, De Cock, Diederik
, Müller-Ladner, Ulf
, Saag, Kenneth G
, Edwards, Christopher John
, van der Heijde, Désirée
, Codreanu, Catalin
, McInnes, Iain B
, Westhovens, René
, Ruyssen-Witrand, Adeline
, Bijlsma, Johannes W J
, Buttgereit, Frank
, Pope, Janet E
, Strangfeld, Anja
, Askling, John
, Emery, Paul
, Poór, Gyula
in
Antibiotics
/ Antirheumatic Agents - economics
/ Antirheumatic Agents - therapeutic use
/ Arthritis, Rheumatoid - drug therapy
/ Autoantibodies
/ Biological products
/ Biological Products - economics
/ Biological Products - therapeutic use
/ Clinical trials
/ Consensus
/ Costs
/ DMARDs (biologic)
/ DMARDs (synthetic)
/ Drug Therapy, Combination
/ Drugs
/ economic evaluations
/ Etanercept
/ Europe
/ Glucocorticoids
/ Humans
/ Immunomodulators
/ Immunotherapy
/ Infliximab
/ Janus kinase
/ Janus Kinase Inhibitors - therapeutic use
/ Leflunomide
/ Life Sciences
/ Medical personnel
/ Methotrexate
/ Monoclonal antibodies
/ Patients
/ Recommendation
/ Regulatory approval
/ Remission
/ Rheumatoid arthritis
/ Rheumatology
/ Risk factors
/ Rituximab
/ Societies, Medical
/ Sulfasalazine
/ Synthetic Drugs - economics
/ Synthetic Drugs - therapeutic use
/ Systematic Reviews as Topic
/ Task forces
/ treatment
/ Tumor Necrosis Factor-alpha - antagonists & inhibitors
/ Tumor necrosis factor-α
/ Tumors
2020
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EULAR recommendations for the management of rheumatoid arthritis with synthetic and biological disease-modifying antirheumatic drugs: 2019 update
by
den Broeder, Alfons A
, Takeuchi, Tsutomu
, Sepriano, Alexandre
, Buch, Maya H
, Gottenberg, Jacques-Eric
, Gossec, Laure
, Balsa, Alejandro
, Voshaar, Marieke
, Smolen, Josef S
, Kerschbaumer, Andreas
, Cutolo, Maurizio
, Burmester, Gerd R
, Boers, Maarten
, da Silva, Jose A P
, Dougados, Maxime
, Li, Zhanguo
, van Eijk-Hustings, Yvonne
, Koloumas, Marios
, Cardiel, Mario Humberto
, Huizinga, Tom W J
, Caporali, Roberto
, Hetland, Merete Lund
, Aringer, Martin
, Mariette, Xavier
, Aletaha, Daniel
, Landewé, Robert B M
, Mysler, Eduardo F
, Rubbert-Roth, Andrea
, de Wit, Maarten
, Finckh, Axel
, van Vollenhoven, Ronald F
, De Cock, Diederik
, Müller-Ladner, Ulf
, Saag, Kenneth G
, Edwards, Christopher John
, van der Heijde, Désirée
, Codreanu, Catalin
, McInnes, Iain B
, Westhovens, René
, Ruyssen-Witrand, Adeline
, Bijlsma, Johannes W J
, Buttgereit, Frank
, Pope, Janet E
, Strangfeld, Anja
, Askling, John
, Emery, Paul
, Poór, Gyula
in
Antibiotics
/ Antirheumatic Agents - economics
/ Antirheumatic Agents - therapeutic use
/ Arthritis, Rheumatoid - drug therapy
/ Autoantibodies
/ Biological products
/ Biological Products - economics
/ Biological Products - therapeutic use
/ Clinical trials
/ Consensus
/ Costs
/ DMARDs (biologic)
/ DMARDs (synthetic)
/ Drug Therapy, Combination
/ Drugs
/ economic evaluations
/ Etanercept
/ Europe
/ Glucocorticoids
/ Humans
/ Immunomodulators
/ Immunotherapy
/ Infliximab
/ Janus kinase
/ Janus Kinase Inhibitors - therapeutic use
/ Leflunomide
/ Life Sciences
/ Medical personnel
/ Methotrexate
/ Monoclonal antibodies
/ Patients
/ Recommendation
/ Regulatory approval
/ Remission
/ Rheumatoid arthritis
/ Rheumatology
/ Risk factors
/ Rituximab
/ Societies, Medical
/ Sulfasalazine
/ Synthetic Drugs - economics
/ Synthetic Drugs - therapeutic use
/ Systematic Reviews as Topic
/ Task forces
/ treatment
/ Tumor Necrosis Factor-alpha - antagonists & inhibitors
/ Tumor necrosis factor-α
/ Tumors
2020
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EULAR recommendations for the management of rheumatoid arthritis with synthetic and biological disease-modifying antirheumatic drugs: 2019 update
Journal Article
EULAR recommendations for the management of rheumatoid arthritis with synthetic and biological disease-modifying antirheumatic drugs: 2019 update
2020
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Overview
ObjectivesTo provide an update of the European League Against Rheumatism (EULAR) rheumatoid arthritis (RA) management recommendations to account for the most recent developments in the field.MethodsAn international task force considered new evidence supporting or contradicting previous recommendations and novel therapies and strategic insights based on two systematic literature searches on efficacy and safety of disease-modifying antirheumatic drugs (DMARDs) since the last update (2016) until 2019. A predefined voting process was applied, current levels of evidence and strengths of recommendation were assigned and participants ultimately voted independently on their level of agreement with each of the items.ResultsThe task force agreed on 5 overarching principles and 12 recommendations concerning use of conventional synthetic (cs) DMARDs (methotrexate (MTX), leflunomide, sulfasalazine); glucocorticoids (GCs); biological (b) DMARDs (tumour necrosis factor inhibitors (adalimumab, certolizumab pegol, etanercept, golimumab, infliximab), abatacept, rituximab, tocilizumab, sarilumab and biosimilar (bs) DMARDs) and targeted synthetic (ts) DMARDs (the Janus kinase (JAK) inhibitors tofacitinib, baricitinib, filgotinib, upadacitinib). Guidance on monotherapy, combination therapy, treatment strategies (treat-to-target) and tapering on sustained clinical remission is provided. Cost and sequencing of b/tsDMARDs are addressed. Initially, MTX plus GCs and upon insufficient response to this therapy within 3 to 6 months, stratification according to risk factors is recommended. With poor prognostic factors (presence of autoantibodies, high disease activity, early erosions or failure of two csDMARDs), any bDMARD or JAK inhibitor should be added to the csDMARD. If this fails, any other bDMARD (from another or the same class) or tsDMARD is recommended. On sustained remission, DMARDs may be tapered, but not be stopped. Levels of evidence and levels of agreement were mostly high.ConclusionsThese updated EULAR recommendations provide consensus on the management of RA with respect to benefit, safety, preferences and cost.
Publisher
BMJ Publishing Group Ltd and European League Against Rheumatism,Elsevier Limited,BMJ Publishing Group
Subject
/ Antirheumatic Agents - economics
/ Antirheumatic Agents - therapeutic use
/ Arthritis, Rheumatoid - drug therapy
/ Biological Products - economics
/ Biological Products - therapeutic use
/ Costs
/ Drugs
/ Europe
/ Humans
/ Janus Kinase Inhibitors - therapeutic use
/ Patients
/ Synthetic Drugs - therapeutic use
/ Tumor Necrosis Factor-alpha - antagonists & inhibitors
/ Tumors
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