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JAK inhibitors in the treatment of atopic dermatitis
1Department of Dermatology, Northwestern University Feinberg School of Medicine, Chicago, Ill.
Abstract:
Atopic dermatitis (AD) is a chronic inflammatory skin disorder associated with heterogenous presentation and often immense patient burden. Safe, targeted treatment options are currently limited. This focused review of the published literature, including clinical trial results, case reports, and abstracts, as well as presentations from scientific meetings and data from industry press releases, describes the use of topical and systemic Janus kinase (JAK) inhibitors in the treatment of AD. New topical JAK inhibitors include ruxolitinib (JAK1/2) and delgocitinib (pan-JAK). Ruxolitinib cream met all primary and secondary endpoints in phase 3 clinical trials for mild-to-moderate AD with minimal treatment-emergent adverse events. Delgocitinib ointment was recently approved in Japan for pediatric and adult AD. Oral JAK inhibitors include baricitinib (JAK1/2), abrocitinib (JAK1-selective), and upadacitinib (JAK1-selective). All 3 met primary and secondary endpoints across numerous trials for moderate-to-severe AD. Treatment-emergent adverse events were mainly mild to moderate and included acne, nausea, headache, upper respiratory tract infection, and to a lesser degree, herpes infection and selected laboratory abnormalities. JAK inhibitors hold great promise as the next generation of targeted AD therapy. While their outstanding efficacy is balanced by a favorable safety profile in clinical trials, real-world data are needed to better understand long-term safety, durability, and treatment success.
Insights
Janus kinase (JAK) inhibitors, including topical and oral options, show promise for treating atopic dermatitis (AD). Clinical trials demonstrate efficacy with manageable side effects, but real-world data are needed for long-term insights.
Area of Science:
- Dermatology
- Immunology
- Pharmacology
Background:
- Atopic dermatitis (AD) is a chronic inflammatory skin condition with limited targeted therapies.
- Current treatment options for AD often present challenges in terms of safety and efficacy.
- The patient burden associated with AD is significant, necessitating novel therapeutic approaches.
Purpose of the Study:
- To review the efficacy and safety of topical and systemic Janus kinase (JAK) inhibitors for atopic dermatitis (AD).
- To summarize findings from clinical trials, case reports, and scientific presentations on JAK inhibitors in AD treatment.
- To highlight the potential of JAK inhibitors as a new class of targeted therapies for AD.
Main Methods:
- Focused literature review of published studies, clinical trial results, case reports, and scientific meeting abstracts.
- Inclusion of data from industry press releases regarding JAK inhibitor development and trials.
- Analysis of both topical (ruxolitinib, delgocitinib) and systemic (baricitinib, abrocitinib, upadacitinib) JAK inhibitors.
Main Results:
- Topical JAK inhibitors like ruxolitinib and delgocitinib demonstrated efficacy in clinical trials for mild-to-moderate AD with minimal adverse events.
- Oral JAK inhibitors (baricitinib, abrocitinib, upadacitinib) met primary and secondary endpoints in trials for moderate-to-severe AD.
- Commonly reported side effects for oral JAK inhibitors were mild to moderate, including acne, nausea, and headache.
Conclusions:
- Janus kinase (JAK) inhibitors represent a promising next generation of targeted therapies for atopic dermatitis.
- Clinical trial data indicate a favorable safety and efficacy profile for both topical and systemic JAK inhibitors in AD.
- Further real-world data are essential to fully understand the long-term safety, durability, and treatment success of JAK inhibitors in AD management.
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