EULAR recommendations for the management of psoriatic arthritis with pharmacological therapies: 2019 update.


Journal

Annals of the rheumatic diseases
ISSN: 1468-2060
Titre abrégé: Ann Rheum Dis
Pays: England
ID NLM: 0372355

Informations de publication

Date de publication:
06 2020
Historique:
received: 13 02 2020
revised: 30 04 2020
accepted: 01 05 2020
entrez: 22 5 2020
pubmed: 22 5 2020
medline: 8 7 2020
Statut: ppublish

Résumé

To update the European League Against Rheumatism (EULAR) recommendations for the pharmacological treatment of psoriatic arthritis (PsA). According to the EULAR standardised operating procedures, a systematic literature review was followed by a consensus meeting to develop this update involving 28 international taskforce members in May 2019. Levels of evidence and strengths of recommendations were determined. The updated recommendations comprise 6 overarching principles and 12 recommendations. The overarching principles address the nature of PsA and diversity of both musculoskeletal and non-musculoskeletal manifestations; the need for collaborative management and shared decision-making is highlighted. The recommendations provide a treatment strategy for pharmacological therapies. Non-steroidal anti-inflammatory drugs and local glucocorticoid injections are proposed as initial therapy; for patients with arthritis and poor prognostic factors, such as polyarthritis or monoarthritis/oligoarthritis accompanied by factors such as dactylitis or joint damage, rapid initiation of conventional synthetic disease-modifying antirheumatic drugs is recommended. If the treatment target is not achieved with this strategy, a biological disease-modifying antirheumatic drugs (bDMARDs) targeting tumour necrosis factor (TNF), interleukin (IL)-17A or IL-12/23 should be initiated, taking into account skin involvement if relevant. If axial disease predominates, a TNF inhibitor or IL-17A inhibitor should be started as first-line disease-modifying antirheumatic drug. Use of Janus kinase inhibitors is addressed primarily after bDMARD failure. Phosphodiesterase-4 inhibition is proposed for patients in whom these other drugs are inappropriate, generally in the context of mild disease. Drug switches and tapering in sustained remission are addressed. These recommendations provide stakeholders with an updated consensus on the pharmacological management of PsA, based on a combination of evidence and expert opinion.

Identifiants

pubmed: 32434812
pii: annrheumdis-2020-217159
doi: 10.1136/annrheumdis-2020-217159
pmc: PMC7286048
doi:

Substances chimiques

Anti-Inflammatory Agents, Non-Steroidal 0
Biological Products 0
Glucocorticoids 0
IL17A protein, human 0
Interleukin-17 0
Interleukin-23 0
Janus Kinase Inhibitors 0
Phosphodiesterase 4 Inhibitors 0
Synthetic Drugs 0
Tumor Necrosis Factor-alpha 0
Interleukin-12 187348-17-0

Types de publication

Journal Article Practice Guideline Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

700-712

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Informations de copyright

© Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: LG: AbbVie, Biogen, Celgene, Janssen, Lilly, Mylan, Novartis, Pfizer, Sandoz, Sanofi-Aventis, UCB. XB: AbbVie, Amgen, BMS, Celgene, Chugai, Hexal, Janssen, Lilly, MSD, Mylan, Novartis, Pfizer, Sandoz, UCB. AK: Bristol-Myers Squibb, Celgene, Eli Lilly, Gilead, Merck Sharp and Dohme, Novartis, Pfizer. MdW: Through Stichting Tools from AbbVie, BMS, Celgene, Eli Lilly, Janssen-Cilag, Novartis, Pfizer, Roche. IM: AbbVie, BMS, Lilly, Novartis, Celgene, Gilead, Janssen, Boehringer, UCB, Pfizer. MD: AbbVie, BMS, Janssen, Lilly, Novartis, Merck, Pfizer, UCB. JP: BMS, Pfizer. DGM: AbbVie, BMS, Celgene, Eli Lilly, Janssen, Merck, Novartis, Pfizer, UCB. DA: AbbVie, Amgen, Gilead, Lilly, Merck, Novartis, Pfizer, Roche, Sandoz, Sanofi/Genzyme, Sobi. AB: AbbVie, Amgen, AstraZeneca, Angelini, AlfaSigma, BMS, Berlin-Chemie, Egis, Ewopharma, GSK, Lilly, Mylan, MSD, Novartis, Pfizer, Roche, Sandoz, Sanofi, Teva, UCB, Zentiva. PVB: AbbVie, Celgene, Lilly, MSD, Novartis, Pfizer, Richter. HB: Pfizer. W-HB: AbbVie, Almirall, BMS, Celgene, Leo, Lilly, Novartis, Pfizer, UCB. GRB: AbbVie, Celgene, Lilly, MSD, Novartis, Pfizer. JDC: Celgene, Eli Lilly, Gilead, Janssen, Novartis, Pfizer, UCB. NSD: AbbVie, Boehringer Ingelheim, Gedeon Richter, Lilly, Novartis, Pfizer, Roche. TWK: Bristol-Myers Squibb, Eli Lilly, Novartis, Pfizer, UCB. TKK: AbbVie, Amgen, Biogen, BMS, Celltrion, Egis, Eli Lilly, Ewopharma, Hikma, Hospira/Pfizer, MSD, Mylan, Orion Pharma, Roche, Sandoz, Sanofi, UCB. RBML: AbbVie, Boehringer Ingelheim, Bristol-Myers Squibb, Celgene, Eli Lilly, Galapagos, Gilead, MSD, Novartis, Pfizer, UCB. RJUL is Director of Rheumatology Consultancy; AbbVie, Celgene, Eli Lilly, Janssen, Novartis, Pfizer, UCB. HM-O: AbbVie, Celgene, Eli Lilly, Janssen, Novartis, Pfizer, Takeda, UCB. DP: AbbVie, BMS, Celgene, Janssen, Lilly, MSD, Novartis, Pfizer, Roche, UCB. SARM: Janssen, MSD, Novartis. GS: AbbVie, BMS, Celgene, Gilead, Janssen, Lilly, Novartis, Pfizer, Roche, UCB. DJV: AbbVie, Biogen, Boehringer Ingelheim, HealthBeacon, Janssen, Lilly, MSD, Novartis, Pfizer, Roche, UCB. FEVdB: AbbVie, Celgene, Eli Lilly, Galapagos/Gilead, Janssen, Merck, Novartis, Pfizer, UCB. DvdH: AbbVie, Amgen, Astellas, AstraZeneca, BMS, Boehringer Ingelheim, Celgene, Cyxone, Daiichi, Eisai, Eli Lilly, Galapagos, Gilead, GlaxoSmithKline, Janssen, Merck, Novartis, Pfizer, Regeneron, Roche, Sanofi, Takeda, UCB Pharma; Director of Imaging Rheumatology. JSS: grants to institution from AbbVie, AstraZeneca, Janssen, Lilly, Merck Sharp & Dohme, Pfizer and Roche; speaker for AbbVie, Amgen, AstraZeneca, Astro, Bristol-Myers Squibb, Celgene, Celltrion, Chugai, Gilead, ILTOO Pharma, Janssen, Lilly, Merck Sharp & Dohme, Novartis-Sandoz, Pfizer, Roche, Samsung, Sanofi and UCB.

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Auteurs

Laure Gossec (L)

Institut Pierre Louis d'Epidémiologie et de Santé Publique, INSERM, Sorbonne Universite, Paris, France laure.gossec@gmail.com.
APHP.Sorbonne Universite, Rheumatology Department, Hopital Universitaire Pitie Salpetriere, Paris, France.

Xenofon Baraliakos (X)

Ruhr-Universität Bochum, Rheumazentrum Ruhrgebiet, Herne, Germany.

Andreas Kerschbaumer (A)

Division of Rheumatology, Department of Medicine 3; 2nd Department of Medicine, Hietzing Hospital, Medical University of Vienna, Vienna, Austria.

Iain McInnes (I)

Institute of Infection, Immunity and Inflammation, University of Glasgow, Glasgow, UK.

Maxime Dougados (M)

Hopital Cochin, Rheumatology, Université Paris Descartes, Paris, France.

Jette Primdahl (J)

Danish Hospital for Rheumatic Diseases, University Hospital of Southern Denmark, Sønderborg, Denmark.
Department of Regional Health Research, University of Southern Denmark, Odense, Denmark.

Dennis G McGonagle (DG)

LTHT, Leeds NIHR Biomedical Research Centre, Leeds, UK.
Leeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds, Leeds, UK.

Daniel Aletaha (D)

Division of Rheumatology, Department of Medicine 3, Medical University of Vienna, Vienna, Austria.

Andra Balanescu (A)

Research Center of Rheumatic Diseases, Sf Maria Hospital, Carol Davila University of Medicine and Pharmacy, Bucharest, Romania.

Peter V Balint (PV)

3rd Department of Rheumatology, National Institute of Rheumatology and Physiotherapy, Budapest, Hungary.

Heidi Bertheussen (H)

Patient Research Partner, EULAR, Oslo, Norway.

Wolf-Henning Boehncke (WH)

Dermatology, University Hospitals of Geneva, Geneva, Switzerland.

Gerd R Burmester (GR)

Rheumatology and Clinical Immunology, Charite University Hospital Berlin, Berlin, Germany.

Juan D Canete (JD)

Arthritis Unit, Department of Rheumatology and IDIBAPS, Hospital Clinic, Barcelona, Spain.

Nemanja S Damjanov (NS)

Institute of Rheumatology, Belgrade University School of Medicine, Belgrade, Serbia.

Tue Wenzel Kragstrup (TW)

Department of Biomedicine, Aarhus University, Aarhus C, Denmark.
Department of Rheumatology, Aarhus Universitetshospital, Aarhus, Denmark.

Tore K Kvien (TK)

Rheumatology, Diakonhjemmet Hospital, Oslo, Norway.

Robert B M Landewé (RBM)

Amsterdam Rheumatology Center, AMC, Amsterdam, The Netherlands.
Rheumatology, Zuyderland MC, Heerlen, The Netherlands.

Rik Jozef Urbain Lories (RJU)

Laboratory of Tissue Homeostasis and Disease, Skeletal Biology and Engineering Research Center, KU Leuven, Leuven, Flanders, Belgium.
Rheumatology, KU Leuven University Hospitals Leuven, Leuven, Flanders, Belgium.

Helena Marzo-Ortega (H)

LTHT, Leeds NIHR Biomedical Research Centre, Leeds, UK.
Leeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds, Leeds, UK.

Denis Poddubnyy (D)

Department of Rheumatology, Infectious Diseases and Rheumatology, Charité Universitätsmedizin Berlin, Berlin, Germany.
Epidemiology, German Rheumatism Research Center Berlin, Berlin, Germany.

Santiago Andres Rodrigues Manica (SA)

Rheumatology, Hospital de Egas Moniz, Lisboa, Portugal.
Universidade Nova de Lisboa Centro de Estudos de Doencas Cronicas, Lisboa, Portugal.

Georg Schett (G)

Internal Medicine, University of Erlangen-Nuremberg, Erlangen, Germany.

Douglas J Veale (DJ)

Centre for Arthritis and Rheumatic Disease, Dublin Academic Medical Centre, St Vincent's University Hospital, Dublin, Ireland.

Filip E Van den Bosch (FE)

Department of Internal Medicine and Pediatrics, VIB Center for Inflammation Research, Ghent University, Gent, Belgium.

Désirée van der Heijde (D)

Rheumatology, Diakonhjemmet Hospital, Oslo, Norway.
Rheumatology, Leiden University Medical Center, Leiden, The Netherlands.

Josef S Smolen (JS)

Division of Rheumatology, Department of Medicine 3, Medical University of Vienna, Vienna, Wien, Austria.
2nd Department of Medicine, Hietzing Hospital, Vienna, Wien, Austria.

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