50
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Safety profile of upadacitinib over 15 000 patient-years across rheumatoid arthritis, psoriatic arthritis, ankylosing spondylitis and atopic dermatitis

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Objective

          To evaluate the long-term safety profile for upadacitinib across rheumatoid arthritis (RA), psoriatic arthritis (PsA), ankylosing spondylitis (AS) and atopic dermatitis (AD).

          Methods

          Safety data from clinical trials of upadacitinib 15 mg and upadacitinib 30 mg (AD only) for treating RA, PsA, AS and AD as of 30 June 2021 were analysed; some RA and PsA studies included adalimumab and methotrexate as active comparators. Treatment-emergent adverse events (TEAEs) were presented by disease as exposure-adjusted event rates per 100 patient years (E/100 PY).

          Results

          The analysis included 6991 patients (RA, n=3209; PsA, n=907; AS, n=182; AD, n=2693) who received at least one dose of upadacitinib, representing 15 425 PY of exposure (maximum duration 2.75–5.45 years) across diseases. Rates (E/100 PY) of any TEAE (205.5–278.1) and TEAE leading to discontinuation (4.5–5.4) were similar across diseases; serious TEAEs were numerically higher in patients with RA and PsA. Rates of herpes zoster (1.6–3.6), non-melanoma skin cancer (0–0.8) and elevations in creatine phosphokinase levels (4.4–7.9) were higher with upadacitinib than with active comparators in the RA and PsA populations. Deaths (0–0.8), serious infections (0–3.9), major adverse cardiovascular events (0–0.4), venous thromboembolism (<0.1–0.4) and malignancies (0.3–1.4) were observed, with rates generally lowest in AS and AD. Increased rates of acne were observed in patients with AD only.

          Conclusions

          Findings from this analysis demonstrate that upadacitinib is generally well tolerated with observed differences in safety profiles likely reflective of varying patient characteristics across RA, PsA, AS and AD populations.

          Trial registration numbers

          NCT02675426, NCT02706951, NCT02706847, NCT02629159, NCT02706873, NCT03086343, NCT03104374, NCT03104400, NCT03178487, NCT03569293, NCT03568318 and NCT03607422.

          Related collections

          Most cited references46

          • Record: found
          • Abstract: found
          • Article: not found

          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.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            JAK–STAT Signaling as a Target for Inflammatory and Autoimmune Diseases: Current and Future Prospects

            The Janus kinase/signal transduction and activator of transcription (JAK–STAT) signaling pathway is implicated in the pathogenesis of inflammatory and autoimmune diseases including rheumatoid arthritis, psoriasis, and inflammatory bowel disease. Many cytokines involved in the pathogenesis of autoimmune and inflammatory diseases use JAKs and STATs to transduce intracellular signals. Mutations in JAK and STAT genes cause a number of immunodeficiency syndromes, and polymorphisms in these genes are associated with autoimmune diseases. The success of small-molecule JAK inhibitors (Jakinibs) in the treatment of rheumatologic disease demonstrates that intracellular signaling pathways can be targeted therapeutically to treat autoimmunity. Tofacitinib, the first rheumatologic Jakinib, is US Food and Drug Administration (FDA) approved for rheumatoid arthritis and is currently under investigation for other autoimmune diseases. Many other Jakinibs are in preclinical development or in various phases of clinical trials. This review describes the JAK–STAT pathway, outlines its role in autoimmunity, and explains the rationale/pre-clinical evidence for targeting JAK–STAT signaling. The safety and clinical efficacy of the Jakinibs are reviewed, starting with the FDA-approved Jakinib tofacitinib, and continuing on to next-generation Jakinibs. Recent and ongoing studies are emphasized, with a focus on emerging indications for JAK inhibition and novel mechanisms of JAK–STAT signaling blockade.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: found

              2021 American College of Rheumatology Guideline for the Treatment of Rheumatoid Arthritis

              To develop updated guidelines for the pharmacologic management of rheumatoid arthritis.
                Bookmark

                Author and article information

                Journal
                RMD Open
                RMD Open
                rmdopen
                rmdopen
                RMD Open
                BMJ Publishing Group (BMA House, Tavistock Square, London, WC1H 9JR )
                2056-5933
                2023
                8 February 2023
                : 9
                : 1
                : e002735
                Affiliations
                [1 ]departmentDepartment of Rheumatology and Clinical Immunology , Charité Universitätsmedizin Berlin , Berlin, Germany
                [2 ]departmentDepartment of Rheumatology , Metroplex Clinical Research Center , Dallas, Texas, USA
                [3 ]departmentDivision of Infectious Diseases , Oregon Health and Science University , Portland, Oregon, USA
                [4 ]departmentSchool of Medicine , Griffith University School of Medicine , Brisbane, Queensland, Australia
                [5 ]departmentDepartment of Clinical Medicine , Trinity College Dublin , Dublin, Ireland
                [6 ]departmentWellcome-HRB Clinical Research Facility , St. James' Hospital , Dublin, Ireland
                [7 ]departmentRheumatology , Organización Medica de Investigación , Buenos Aires, Argentina
                [8 ]departmentThe First Department of Internal Medicine , University of Occupational and Environmental Health Japan , Kitakyushu, Japan
                [9 ]AbbVie Inc , North Chicago, Illinois, USA
                [10 ]AbbVie Ltd , Maidenhead, UK
                [11 ]departmentRheumatology Research Division , Swedish Medical Center/Providence St. Joseph Health , Seattle, Washington, USA
                [12 ]departmentDepartment of Dermatology and Laboratory for Inflammatory Skin Diseases , Icahn School of Medicine at Mount Sinai , New York, New York, USA
                Author notes
                [Correspondence to ] Professor Gerd R Burmester; gerd.burmester@ 123456charite.de
                Author information
                http://orcid.org/0000-0001-7518-1131
                http://orcid.org/0000-0002-9226-979X
                http://orcid.org/0000-0002-3892-6947
                http://orcid.org/0000-0002-2571-788X
                http://orcid.org/0000-0002-0807-7139
                http://orcid.org/0000-0002-6620-0457
                Article
                rmdopen-2022-002735
                10.1136/rmdopen-2022-002735
                9923346
                36754548
                94381869-c24b-4e4f-9b19-6e92e9808013
                © Author(s) (or their employer(s)) 2023. 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
                : 14 September 2022
                : 14 December 2022
                Categories
                Inflammatory Arthritis
                1506
                Original research
                Custom metadata
                unlocked

                arthritis, psoriatic,arthritis, rheumatoid,spondylitis, ankylosing,antirheumatic agents,inflammation

                Comments

                Comment on this article

                scite_
                0
                0
                0
                0
                Smart Citations
                0
                0
                0
                0
                Citing PublicationsSupportingMentioningContrasting
                View Citations

                See how this article has been cited at scite.ai

                scite shows how a scientific paper has been cited by providing the context of the citation, a classification describing whether it supports, mentions, or contrasts the cited claim, and a label indicating in which section the citation was made.

                Similar content419

                Cited by61

                Most referenced authors567