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      Safety and efficacy of the JAK inhibitor tofacitinib citrate in patients with alopecia areata

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          Abstract

          BACKGROUND. Alopecia areata (AA) is an autoimmune disease characterized by hair loss mediated by CD8 + T cells. There are no reliably effective therapies for AA. Based on recent developments in the understanding of the pathomechanism of AA, JAK inhibitors appear to be a therapeutic option; however, their efficacy for the treatment of AA has not been systematically examined.

          METHODS. This was a 2-center, open-label, single-arm trial using the pan-JAK inhibitor, tofacitinib citrate, for AA with >50% scalp hair loss, alopecia totalis (AT), and alopecia universalis (AU). Tofacitinib (5 mg) was given twice daily for 3 months. Endpoints included regrowth of scalp hair, as assessed by the severity of alopecia tool (SALT), duration of hair growth after completion of therapy, and disease transcriptome.

          RESULTS. Of 66 subjects treated, 32% experienced 50% or greater improvement in SALT score. AA and ophiasis subtypes were more responsive than AT and AU subtypes. Shorter duration of disease and histological peribulbar inflammation on pretreatment scalp biopsies were associated with improvement in SALT score. Drug cessation resulted in disease relapse in 8.5 weeks. Adverse events were limited to grade I and II infections. An AA responsiveness to JAK/STAT inhibitors score was developed to segregate responders and nonresponders, and the previously developed AA disease activity index score tracked response to treatment.

          CONCLUSIONS. At the dose and duration studied, tofacitinib is a safe and effective treatment for severe AA, though it does not result in a durable response. Transcriptome changes reveal unexpected molecular complexity within the disease.

          TRIAL REGISTRATION. ClinicalTrials.gov NCT02197455 and NCT02312882.

          FUNDING. This work was supported by the US Department of Veterans Affairs Office of Research and Development, National Institute of Arthritis and Musculoskeletal and Skin Diseases National Institutes of Health grant R01 AR47223 and U01 AR67173, the National Psoriasis Foundation, the Swedish Society of Medicine, the Fernström Foundation, the Locks of Love Foundation, the National Alopecia Areata Foundation, and the Ranjini and Ajay Poddar Resource Fund for Dermatologic Diseases Research.

          Abstract

          Tofacitinib citrate is a safe and effective treatment for severe alopecia areata at the dose and duration studied.

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          Author and article information

          Contributors
          Journal
          JCI Insight
          JCI Insight
          JCI Insight
          JCI Insight
          American Society for Clinical Investigation
          2379-3708
          22 September 2016
          22 September 2016
          22 September 2016
          : 1
          : 15
          : e89776
          Affiliations
          [1 ]Program in Epithelial Biology and Department of Dermatology, Stanford University School of Medicine, Stanford, California, USA.
          [2 ]Department of Dermatology,
          [3 ]Department of Pediatrics, and
          [4 ]Department of Internal Medicine, Yale University School of Medicine, New Haven, Connecticut, USA.
          [5 ]Department of Dermatology,
          [6 ]Department of Systems Biology, and
          [7 ]Department of Genetics and Development, Columbia University, New York, New York, USA.
          [8 ] Dermatology Service, Veterans Affairs Medical Center, Palo Alto, California, USA.
          Author notes
          Address correspondence to: Anthony Oro, Program in Epithelial Biology, 269 Campus Drive CCSR 2140, Stanford, California 94025, USA. Phone: 650.387.2278; E-mail: oro@ 123456stanford.edu . Or to: Brett A. King, Department of Dermatology, 333 Cedar Street, LCI 5040, New Haven, Connecticut 06520, USA. Phone: 203.785.4092; E-mail: brett.king@ 123456yale.edu .

          Authorship note: M.K. Crispin and J.M. Ko contributed equally to this work. A.E. Oro and B.A. King are cosenior authors.

          Author information
          http://orcid.org/0000-0002-8559-7314
          Article
          PMC5033755 PMC5033755 5033755 89776
          10.1172/jci.insight.89776
          5033755
          27699252
          5458a32c-ffb2-407e-9776-33a7220c72c9
          Copyright © 2016, American Society for Clinical Investigation
          History
          : 27 July 2016
          : 23 August 2016
          Categories
          Clinical Medicine

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