Please login or create an account. If you do not have access to this content, you will be shown a 30 second preview and licensing options.
- Presentation
Comparative Efficacy of Systemic Treatments for Adult Atopic Dermatitis
Description
The speaker discussed the rapidly expanding range of systemic treatments for adult atopic dermatitis and the difficulty of choosing among them because guidelines identify effective drugs but do not provide clear treatment algorithms. They emphasized that treatment decisions should consider efficacy, safety, patient age and comorbidities, cost, access, and patient preferences. Because placebo responses vary widely across trials, direct comparison of trial percentages can be misleading, so the group uses a living network meta-analysis to compare therapies indirectly across many studies. Their analyses suggest that cyclosporine and dupilumab are among the most effective older and targeted treatments, respectively, while higher-dose JAK inhibitors such as upadacitinib 30 mg and abrocitinib 200 mg tend to be the most effective overall, though differences from dupilumab are often small and clinically modest. Lower-dose JAKs and several biologics, including lebrikizumab, are similar to dupilumab, while tralokinumab, nemolizumab, and baricitinib appear somewhat less effective. The speaker noted that starting a JAK inhibitor at a lower dose and escalating if needed may be a reasonable strategy, and that long-term data may change how efficacy is judged because some newer drugs continue improving beyond 16 weeks.
View moreConclusions
- Network meta-analysis suggests that among older systemic treatments for adult atopic dermatitis, cyclosporine is the most effective short-term option, with methotrexate and azathioprine also effective but generally less potent.
- Across newer targeted therapies, the differences in efficacy are often small, but high-dose JAK inhibitors—especially upadacitinib 30 mg and abrocitinib 200 mg—tend to be the most effective.
- Lower-dose JAK inhibitor regimens appear closer in efficacy to dupilumab, supporting dose escalation strategies rather than automatic high-dose initiation.
- Among biologics, lebrikizumab appears broadly similar to dupilumab, while tralokinumab and nemolizumab are likely somewhat less effective on most measures.
- Nemolizumab may perform relatively better for itch specifically than for overall skin clearance or other disease outcomes.
- The overall ranking of treatments is broadly consistent across different outcome measures, including EASI, EASI-75, symptom scores, and quality-of-life measures.
- The pattern of comparative efficacy is similar whether trials include topical co-therapy or are monotherapy trials, suggesting the main conclusions are robust.
- Head-to-head trials have largely confirmed the network meta-analysis findings, particularly that high-dose JAK inhibitors outperform dupilumab but not by a dramatic margin.
- Short-term trial results at 16 weeks are informative, but emerging long-term data suggest some treatments may continue improving beyond that timepoint.
- Treatment choice should not be based on efficacy alone, because safety, age, comorbidities, cost, access, monitoring burden, and patient preference remain important in selecting systemic therapy.
- Davis DMR et al. JAAD. 2025;93(3):745.e1-745.e7.
- Ann Allergy Asthma Immunol. 2024. 132:274-312.
- Watt...Drucker. J Invest Dermatol. 2019 Jan;139(1):4-12.e1.
- Drucker et al. JAMA Dermatol. 2020 Jun 1;156(6):659-667.
- Drucker et al. JAMA Dermatol. 2024;158(5):523-532.
- Schram et al. Allergy. 2012 Jan;67(1):99-106.
- Basra et al., Dermatology, 2015, 230(1):27-33.
- Yosipovitch et al. Br J Dermatol 2019;181:761-769.
- Silverberg et al. Br J Dermatol. 2025;192:36-45.
- American Journal of Clinical Dermatology (2024) 25:179–193.