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      Effectiveness of TNF-inhibitors, abatacept, IL6-inhibitors and JAK-inhibitors in 31 846 patients with rheumatoid arthritis in 19 registers from the ‘JAK-pot’ collaboration

      research-article
      1 , 2 , , 3 , 3 , 4 , 5 , 6 , 7 , 8 , 9 , 7 , 8 , 10 , 7 , 8 , 11 , 2 , 12 , 13 , 14 , 2 , 15 , 15 , 16 , 17 , 18 , 19 , 20 , 21 , 22 , 23 , 24 , 11 , 25 , 9 , 26 , 3 , 3
      Annals of the Rheumatic Diseases
      BMJ Publishing Group
      Epidemiology, Biological Therapy, Tumor Necrosis Factor Inhibitors, Arthritis, Rheumatoid, Therapeutics

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          Abstract

          Background

          JAK-inhibitors (JAKi), recently approved in rheumatoid arthritis (RA), have changed the landscape of treatment choices. We aimed to compare the effectiveness of four current second-line therapies of RA with different modes of action, since JAKi approval, in an international collaboration of 19 registers.

          Methods

          In this observational cohort study, patients initiating tumour necrosis factor inhibitors (TNFi), interleukin-6 inhibitors (IL-6i), abatacept (ABA) or JAKi were included. We compared the effectiveness of these treatments in terms of drug discontinuation and Clinical Disease Activity Index (CDAI) response rates at 1 year. Analyses were adjusted for patient, disease and treatment characteristics, including lines of therapy and accounted for competing risk.

          Results

          We included 31 846 treatment courses: 17 522 TNFi, 2775 ABA, 3863 IL-6i and 7686 JAKi. Adjusted analyses of overall discontinuation were similar across all treatments. The main single reason of stopping treatment was ineffectiveness. Compared with TNFi, JAKi were less often discontinued for ineffectiveness (adjusted HR (aHR) 0.75, 95% CI 0.67 to 0.83), as was IL-6i (aHR 0.76, 95% CI 0.67 to 0.85) and more often for adverse events (aHR 1.16, 95% CI 1.03 to 1.33). Adjusted CDAI response rates at 1 year were similar between TNFi, JAKi and IL-6i and slightly lower for ABA.

          Conclusion

          The adjusted overall drug discontinuation and 1 year response rates of JAKi and IL-6i were similar to those observed with TNFi. Compared with TNFi, JAKi were more often discontinued for adverse events and less for ineffectiveness, as were IL-6i.

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          Most cited references27

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          The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) statement: guidelines for reporting observational studies.

          Much of biomedical research is observational. The reporting of such research is often inadequate, which hampers the assessment of its strengths and weaknesses and of a study's generalizability. The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) Initiative developed recommendations on what should be included in an accurate and complete report of an observational study. We defined the scope of the recommendations to cover three main study designs: cohort, case-control, and cross-sectional studies. We convened a 2-day workshop in September 2004, with methodologists, researchers, and journal editors to draft a checklist of items. This list was subsequently revised during several meetings of the coordinating group and in e-mail discussions with the larger group of STROBE contributors, taking into account empirical evidence and methodological considerations. The workshop and the subsequent iterative process of consultation and revision resulted in a checklist of 22 items (the STROBE Statement) that relate to the title, abstract, introduction, methods, results, and discussion sections of articles. Eighteen items are common to all three study designs and four are specific for cohort, case-control, or cross-sectional studies. A detailed Explanation and Elaboration document is published separately and is freely available on the web sites of PLoS Medicine, Annals of Internal Medicine, and Epidemiology. We hope that the STROBE Statement will contribute to improving the quality of reporting of observational studies.
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            Cardiovascular and Cancer Risk with Tofacitinib in Rheumatoid Arthritis

            Increases in lipid levels and cancers with tofacitinib prompted a trial of major adverse cardiovascular events (MACE) and cancers in patients with rheumatoid arthritis receiving tofacitinib as compared with a tumor necrosis factor (TNF) inhibitor.
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              Baricitinib versus Placebo or Adalimumab in Rheumatoid Arthritis.

              Baricitinib is an oral, reversible inhibitor of the Janus kinases JAK1 and JAK2 that may have therapeutic value in patients with rheumatoid arthritis.
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                Author and article information

                Journal
                Ann Rheum Dis
                Ann Rheum Dis
                annrheumdis
                ard
                Annals of the Rheumatic Diseases
                BMJ Publishing Group (BMA House, Tavistock Square, London, WC1H 9JR )
                0003-4967
                1468-2060
                October 2022
                15 June 2022
                : 81
                : 10
                : 1358-1366
                Affiliations
                [1 ] departmentDivision of Rheumatology, Department of Internal Medicine and Department of Medicine, Faculty of Medicine , Geneva University Hospitals , Geneve, Switzerland
                [2 ] departmentCentre for Epidemiology versus Arthritis, Centre for Musculoskeletal Research, Faculty of Biology, Medicine and Health , University of Manchester, Manchester Academic Health Science Centre , Manchester, UK
                [3 ] departmentDivision of Rheumatology, Department of Internal Medicine and Department of Medicine, Faculty of Medicine , Geneva University Hospitals , Geneva, Switzerland
                [4 ] departmentRheumatology , Leiden University Medical Center , Leiden, The Netherlands
                [5 ] Institut de recherche en rhumatologie de Montréal , Montreal, Quebec, Canada
                [6 ] departmentRheumatology , University of Medicine and Pharmacy, Center of Rheumatic Diseases , Bucharest, Romania
                [7 ] departmentDepartments of Clinical Medicine and Rheumatology , Aarhus University and Aarhus University Hospital , Aalborg, Denmark
                [8 ] DANBIO , Glostrup, Denmark
                [9 ] departmentDepartment of Development and Regeneration , KU Leuven , Leuven, Belgium
                [10 ] departmentDepartment of Rheumatology, Sackler Faculty of Medicine , Tel Aviv University, Sourasky Medical Center , Tel Aviv, Israel
                [11 ] departmentEpidemiology Unit , German Rheumatism Research Center (DRFZ) , Berlin, Germany
                [12 ] NIHR Manchester Biomedical Research Centre, Manchester University NHS Foundation Trust, Manchester Academic Health Science Centre , Manchester, UK
                [13 ] GISEA, DETO – Rheumatology Unit, University of Bari , Bari, Italy
                [14 ] Division of Rheumatology, School of Medicine, Marmara University , Istanbul, Turkey
                [15 ] Division of Rheumatology and Research, Diakonhjemmet Hospital , Oslo, Norway
                [16 ] BioReg , Vienna, Austria
                [17 ] Private Office , Hollabrunn, Austria
                [18 ] V.A. Nasonova Research Institute of Rheumatology, A. S. Loginov Moscow Clinical Scientific Center, Russian Federation , Moscow, Russian Federation
                [19 ] departmentDepartments of Medicine and Rheumatology , ROB-FIN, Helsinki University Hospital and Helsinki University , Helsinki, Finland
                [20 ] departmentRheumatology Department , Charles University , Prag, Czech Republic
                [21 ] Rheumatology Service, Hospital Clinico Universitario , Santiago de Compostela, Spain
                [22 ] departmentDepartment of Rheumatology , biorx.si, University Medical Centre , Ljubljana, Slovenia
                [23 ] Faculty of Medicine, University of Ljubljana , Ljubljana, Slovenia
                [24 ] departmentRheumatology Department , Hospital Garcia de Orta, on behalf of Reuma.pt , Almada, Portugal
                [25 ] Charité University Medicine , Berlin, Germany
                [26 ] departmentDivision of Rheumatology , KU Leuven University Hospitals , Leuven, Belgium
                Author notes
                [Correspondence to ] Dr Kim Lauper, Rheumatology, Geneva University Hospitals, Geneve, Switzerland; Kim.Lauper@ 123456hcuge.ch
                Author information
                http://orcid.org/0000-0002-4315-9009
                http://orcid.org/0000-0002-7136-5248
                http://orcid.org/0000-0002-5656-6236
                http://orcid.org/0000-0001-8242-9262
                http://orcid.org/0000-0003-0474-5344
                http://orcid.org/0000-0003-0377-1575
                http://orcid.org/0000-0002-8441-3093
                http://orcid.org/0000-0002-2524-4883
                http://orcid.org/0000-0002-7946-1365
                http://orcid.org/0000-0002-6233-022X
                http://orcid.org/0000-0002-0340-3580
                http://orcid.org/0000-0002-1956-2607
                http://orcid.org/0000-0002-1210-4347
                Article
                annrheumdis-2022-222586
                10.1136/annrheumdis-2022-222586
                9484385
                35705376
                4b2a1b29-0111-491e-b792-8b1c50fac628
                © Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

                This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See:  http://creativecommons.org/licenses/by-nc/4.0/.

                History
                : 01 April 2022
                : 26 May 2022
                Funding
                Funded by: Galapagos;
                Funded by: FundRef http://dx.doi.org/10.13039/100004319, Pfizer;
                Funded by: FundRef http://dx.doi.org/10.13039/100006483, AbbVie;
                Categories
                Rheumatoid Arthritis
                1506
                2311
                2502
                Custom metadata
                unlocked

                Immunology
                epidemiology,biological therapy,tumor necrosis factor inhibitors,arthritis, rheumatoid,therapeutics

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