Leiden University Medical Center Bunde, Netherlands
Sofia Ramiro1, Elena Nikiphorou2, Alexandre Sepriano3, Augusta Ortolan4, Casper Webers5, Xenofon Baraliakos6, Robert Landewé7, Filip Van den bosch8, Boryana Boteva9, Ann Bremander10, Philippe Carron11, Adrian Ciurea12, floris van Gaalen1, Pal Geher13, Lianne Gensler14, Josef Hermann15, Manouk de Hooge16, Marketa Husakova17, Uta Kiltz18, Clementina Lopez-Medina19, Pedro Machado20, Helena Marzo-Ortega21, Anna Molto22, Victoria Navarro-Compán23, Michael Nissen24, Fernando Pimentel-Santos25, Denis Poddubnyy26, Fabian Proft26, Martin Rudwaleit27, Mark Telkman9, Sizheng Zhao28, Nelly Ziade29 and Désirée van der Heijde30, 1Leiden University Medical Center, Leiden, Netherlands, 2Leiden University Medical Center & King's College London, London, United Kingdom, 3Leiden University Medical Centre, Portela Loures, Portugal, 4University of Padova/Leiden University Medical Center, Padova, Italy, 5Maastricht University Medical Centre, Maastricht, Netherlands, 6Rheumazentrum Ruhrgebiet Herne, Herne, Germany, 7Amsterdam University Medical Center, Meerssen, Netherlands, 8Department of Internal Medicine and Paediatrics, Ghent University and VIB Centre for Inflammation Research, Ghent, Belgium, 9Patients with Arthritis and Rheumatism (PARE) working group, EULAR, Zürich, Switzerland, 10Danish Hospital for Rheumatic Diseases, University Hospital of Southern Denmark, Sønderborg, Denmark, 11Ghent University Hospital, Ghent, Belgium, 12University Hospital Zurich, Zürich, Switzerland, 13Semmelweis University, Budapest, Hungary, 14Department of Medicine, Division of Rheumatology, University of California San Francisco, San Francisco, CA, 15Medical University of Graz, Graz, Austria, 16Ghent University Hospital, Luxembourg, Luxembourg, 17Department of Rheumatology, First Faculty of Medicine, Charles University and Rheumatology Institute, Prague, Prague, Czech Republic, 18Rheumazentrum Ruhrgebiet, Herne, Germany, 19Reina Sofia University Hospital, Rheumatology Department, Jaén, Spain, 20University College London, London, United Kingdom, 21Leeds Teaching Hospitals Trust and University of Leeds, Leeds, United Kingdom, 22Rheumatology Department, Hôpital Cochin,Assistance Publique- Hôpitaux de Paris, Paris, France, 23Department of Rheumatology, La Paz University Hospital, IdiPaz, Madrid, Spain, 24Hopitaux Universitaires de Genève, Geneva, Switzerland, 25NOVA Medical School; Universidade NOVA e Lisboa, Lisboa, Portugal, 26Department of Gastroenterology, Infectious Diseases and Rheumatology, Charité – Universitätsmedizin Berlin, Berlin, Germany, 27University of Bielefeld, Klinikum Bielefeld, Bielefeld; Germany Klinikum Bielefeld and Charité Berlin, Germany, and Gent University, Gent, Belgium, 28University of Manchester, Liverpool, United Kingdom, 29Saint-Joseph University, Beirut, Lebanon, 30Department of Rheumatology, Leiden University Medical Center, Leiden, The Netherlands, Leiden, Netherlands
Background/Purpose: Since the last update of the ASAS-EULAR recommendations for the management of axial spondyloarthritis (axSpA) in 2016, substantial new evidence has become available on the management of axSpA. Our aim was to update the ASAS-EULAR recommendations for the management of axSpA.
Methods: Following the EULAR Standardised Operating Procedures, two systematic literature reviews were conducted on non-pharmacological and pharmacological treatment of axSpA. During a task force meeting the evidence was presented, discussed and overarching principles and recommendations were updated, followed by voting.
Results: A total of 5 overarching principles (unchanged compared to the previous version of the recommendations) and 15 recommendations were formulated (Table). All recommendations included in the previous version were kept: eight unchanged (#2,3,6,7,8,13,14,15); three with minor edits, mostly on nomenclature (#1,4,5) and two with relevant updates (#9,12), while two newly formulated recommendations (#10,11) were added. The first 5 recommendations focus on personalised medicine, including treatment target and monitoring, non-pharmacological management and non-steroidal anti-inflammatory drugs (NSAIDs) as first choice pharmacological treatment. Recommendations 6-8 deal with analgesics and discourage long-term glucocorticoids and conventional synthetic DMARDs for pure axial involvement. Recommendation 9 describes the indication for biological DMARDs (bDMARDs i.e. TNFi, IL-17i) and this was expanded to targeted synthetic DMARDs (tsDMARDs i.e. JAKi). b/tsDMARDs are indicated for patients with elevated CRP, MRI inflammation of SI joints or radiographic sacroiliitis who have high disease activity (ASDAS≥2.1) and failed ≥2 NSAIDs (Figure). BASDAI is no longer recommended to assess treatment start. Current practice is to start a TNFi or IL-17i as there is more accumulated evidence, particularly on safety, and experience with these drug classes. The continuation of a b/tsDMARD should be considered if an improvement of ASDAS≥1.1 has been achieved after ≥12 weeks. The new recommendation 10 addresses extra-musculoskeletal manifestations, with TNF monoclonal antibodies preferred for recurrent uveitis or inflammatory bowel disease, and IL-17i for significant psoriasis. In light of overdiagnosis and overtreatment, treatment failure should trigger re-evaluation of the diagnosis and consideration of the presence of comorbidities (#11 - new). If active axSpA is confirmed after failing a b/tsDMARD, switching to another b/tsDMARD is recommended (#12). Tapering, but not immediate discontinuation of a bDMARD, can be considered in patients in sustained remission (#13). The unchanged recommendations #14 and #15 deal with surgery and spinal fractures.
Conclusion: The 2022 ASAS-EULAR recommendations provide up-to-date guidance on the management of patients with axSpA. ASAS-EULAR recommendations for the management of axial spondyloarthritis, 2022 update
ASAS-EULAR recommendations for the treatment of patients with axSpA with b/tsDMARDs Disclosures: S. Ramiro, AbbVie/Abbott, Eli Lilly, Galapagos, Merck/MSD, Novartis, Pfizer, UCB, Sanofi; E. Nikiphorou, Pfizer, Celltrion, Sanofi, Gilead, Galapagos, AbbVie, Lilly, Fresenius; A. Sepriano, UCB, Novartis; A. Ortolan, None; C. Webers, None; X. Baraliakos, AbbVie, Lilly, Galapagos, MSD, Novartis, Pfizer, UCB, Bristol-Myers Squibb, Janssen, Roche, Sandoz, Sanofi; R. Landewé, Abbott, Amgen, AstraZeneca, BMS, GSK, Novartis, Merck, Pfizer, Schering-Plough, UCB Pharma; F. Van den bosch, AbbVie, Lilly, Galapagos, Janssen, Merck, Novartis, Pfizer, UCB, Amgen, Bristol-Myers Squibb(BMS), Celgene; B. Boteva, None; A. Bremander, None; P. Carron, Biogen, AbbVie/Abbott, Eli Lilly, Fresenius Kabi, Galapagos, Merck/MSD, Pfizer, Sanofi, UCB; A. Ciurea, AbbVie, Novartis, Merck/MSD; f. van Gaalen, Stichting vrienden van Sole Mio, Stichting ASAS, Jacobus stichting, Novartis, UCB, MSD, AbbVie, Bristol Myers Squibb, Eli Lilly; P. Geher, AbbVie/Abbott; L. Gensler, Novartis, Pfizer Inc, UCB Pharma, AbbVie, Eli Lilly, Janssen, Gilead, Moonlake; J. Hermann, AbbVie/Abbott, Novartis, Janssen, Eli Lilly; M. de Hooge, None; M. Husakova, Novartis; U. Kiltz, AbbVie, Amgen, Biogen, Fresenius, GSK, Hexal, Novartis, Pfizer, Biocad, Lilly, Grünenthal, Janssen, MSD, Roche, UCB; C. Lopez-Medina, None; P. Machado, AbbVie/Abbott, Eli Lilly, UCB, Novartis, Orphazyme, Galapagos; H. Marzo-Ortega, None; A. Molto, Abbvie, UCB, Novartis, Gilead, Pfizer, Lilly, Jannsen; V. Navarro-Compán, AbbVie, Eli Lilly, Janssen, Merck/MSD, Novartis, Pfizer, UCB Pharma; M. Nissen, AbbVie/Abbott, Pfizer, Amgen, Novartis, Janssen; F. Pimentel-Santos, AbbVie/Abbott, Eli Lilly, Janssen, Novartis, Pfizer, UCB, Bial, Pharma Kern, Tecnimed, Biogen; D. Poddubnyy, AbbVie, Biocad, Bristol-Myers Squibb, Eli Lilly, Gilead, GlaxoSmithKline, MSD, Moonlake, Novartis, Pfizer, Samsung-Bioepis, UCB; F. Proft, AbbVie/Abbott, Amgen, Bristol-Myers Squibb(BMS), Celgene, Eli Lilly, Janssen, Merck/MSD, Novartis, Pfizer, Roche, UCB; M. Rudwaleit, AbbVie, Bristol-Myers Squibb (BMS), Boehringer-Ingelheim, Chugai, Eli Lilly, Janssen, Novartis, Pfizer, UCB Pharma; M. Telkman, None; S. Zhao, UCB; N. Ziade, Pfizer, Roche, AbbVie/Abbott, Eli Lilly, Boehringer-Ingelheim, Janssen; D. van der Heijde, AbbVie, Bayer, BMS, Cyxone, Eisai, Galapagos, Gilead, Glaxo-Smith-Kline, Janssen, Novartis, Pfizer, UCB, Imaging Rheumatology bv, Lilly.