Efficacy and Risk Stratification of Janus Kinase Inhibitors in the Treatment of Moderate-to-Severe Atopic Dermatitis.
Shanthi NarlaJonathan Ian SilverbergPublished in: Dermatitis : contact, atopic, occupational, drug (2023)
Recently, 3 oral Janus kinase (JAK) inhibitors-abrocitinib, baricitinib, and upadacitinib-were approved in many regions around the world for the treatment of moderate-severe atopic dermatitis (AD). These JAK inhibitors generally have rapid onset of action and short half-life. Higher doses of abrocitinib and upadactinib even demonstrated superior efficacy to dupilumab. However, JAK inhibitors can be associated with rare serious and potentially life-threatening adverse events. Heterogeneity in study designs and lack of head-to-head studies make safety comparison between JAK inhibitors difficult. Dose reduction and patient selection are the most important considerations for risk mitigation. This narrative review examines the efficacy data for abrocitinib, baricitinib, and upadacitinib from large phase III double-blinded randomized controlled trials in AD and discusses risk stratification for oral JAK inhibitors in AD patients.
Keyphrases
- atopic dermatitis
- phase iii
- randomized controlled trial
- end stage renal disease
- clinical trial
- newly diagnosed
- early onset
- climate change
- chronic kidney disease
- ejection fraction
- high intensity
- open label
- single cell
- prognostic factors
- case report
- peritoneal dialysis
- tyrosine kinase
- electronic health record
- phase ii
- big data
- double blind
- optical coherence tomography
- replacement therapy
- smoking cessation