Points to consider for the treatment of immune-mediated inflammatory diseases with Janus kinase inhibitors: a consensus statement

Ann Rheum Dis. 2021 Jan;80(1):71-87. doi: 10.1136/annrheumdis-2020-218398. Epub 2020 Nov 6.

Abstract

Objectives: Janus kinase inhibitors (JAKi) have been approved for use in various immune-mediated inflammatory diseases. With five agents licensed, it was timely to summarise the current understanding of JAKi use based on a systematic literature review (SLR) on efficacy and safety.

Methods: Existing data were evaluated by a steering committee and subsequently reviewed by a 29 person expert committee leading to the formulation of a consensus statement that may assist the clinicians, patients and other stakeholders once the decision is made to commence a JAKi. The committee included patients, rheumatologists, a gastroenterologist, a haematologist, a dermatologist, an infectious disease specialist and a health professional. The SLR informed the Task Force on controlled and open clinical trials, registry data, phase 4 trials and meta-analyses. In addition, approval of new compounds by, and warnings from regulators that were issued after the end of the SLR search date were taken into consideration.

Results: The Task Force agreed on and developed four general principles and a total of 26 points for consideration which were grouped into six areas addressing indications, treatment dose and comedication, contraindications, pretreatment screening and risks, laboratory and clinical follow-up examinations, and adverse events. Levels of evidence and strengths of recommendations were determined based on the SLR and levels of agreement were voted on for every point, reaching a range between 8.8 and 9.9 on a 10-point scale.

Conclusion: The consensus provides an assessment of evidence for efficacy and safety of an important therapeutic class with guidance on issues of practical management.

Keywords: Autoimmune Diseases; Inflammation; Therapeutics.

Publication types

  • Consensus Development Conference
  • Practice Guideline
  • Research Support, Non-U.S. Gov't
  • Systematic Review

MeSH terms

  • Adamantane / analogs & derivatives
  • Adamantane / therapeutic use
  • Advisory Committees
  • Antirheumatic Agents / therapeutic use
  • Arthritis, Psoriatic / drug therapy*
  • Arthritis, Psoriatic / immunology
  • Arthritis, Rheumatoid / drug therapy*
  • Arthritis, Rheumatoid / immunology
  • Azetidines / therapeutic use
  • Cytokines / immunology
  • Drug Therapy, Combination
  • Europe
  • Heterocyclic Compounds, 3-Ring / therapeutic use
  • Humans
  • Inflammatory Bowel Diseases / drug therapy*
  • Inflammatory Bowel Diseases / immunology
  • Janus Kinase Inhibitors / therapeutic use*
  • Niacinamide / analogs & derivatives
  • Niacinamide / therapeutic use
  • Piperidines / therapeutic use
  • Psoriasis / drug therapy
  • Psoriasis / immunology
  • Purines / therapeutic use
  • Pyrazoles / therapeutic use
  • Pyridines / therapeutic use
  • Pyrimidines / therapeutic use
  • Rheumatology
  • Spondylarthropathies / drug therapy
  • Spondylarthropathies / immunology
  • Spondylitis, Ankylosing / drug therapy*
  • Spondylitis, Ankylosing / immunology
  • Sulfonamides / therapeutic use
  • Triazoles / therapeutic use

Substances

  • Antirheumatic Agents
  • Azetidines
  • Cytokines
  • GLPG0634
  • Heterocyclic Compounds, 3-Ring
  • Janus Kinase Inhibitors
  • Piperidines
  • Purines
  • Pyrazoles
  • Pyridines
  • Pyrimidines
  • Sulfonamides
  • Triazoles
  • Niacinamide
  • upadacitinib
  • tofacitinib
  • peficitinib
  • baricitinib
  • Adamantane