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Published on: January 12, 2024
Efficacy of biologics and oral small molecules for atopic dermatitis: a systematic review and meta-analysis
Kelsey B Nusbaum1, Sarah Fleischer2, Alan B Fleischer3
1University of Cincinnati College of Medicine, Cincinnati, OH, USA.
Background:
As new targeted therapies continue to emerge for atopic dermatitis (AD), comparisons between agents are necessary to inform clinical decision-making.
Objectives:
Assess the efficacy of biologics and oral small molecules on the clinical signs, symptoms, and quality of life in AD.
Methods:
A systematic literature review identified phase II and III randomized clinical trials of biologics and oral small molecules in AD. Clinical benefit was assessed for three outcome measures: Eczema Area and Severity Index (EASI), Dermatology Life Quality Index (DLQI), and Peak Pruritus Numerical Rating Scale (PP-NRS) by performing a meta-analysis using the inverse variance heterogeneity model ((IVhet)).
Results:
The highest achievement of 75% reduction in EASI was seen with the higher dose of upadacitinib (30 mg) followed by abrocitinib and lebrikizumab, which outperformed dupilumab. Similarly, the highest proportion achieving at least a 4-point reduction of PP-NRS was seen with lebrikizumab followed by upadacitinib and abrocitinib which had greater reduction of itch than dupilumab. Abrocitinib had the greatest improvement in DLQI.
Conclusions:
Upadacitinib, abrocitinib, and lebrikizumab had greater improvement of clinical signs, symptoms, and quality of life in AD compared to dupilumab and other targeted therapies.
Insights
Newer targeted therapies like upadacitinib, abrocitinib, and lebrikizumab show superior efficacy for atopic dermatitis (AD) symptom relief and quality of life improvements compared to dupilumab.
Area of Science:
- Dermatology
- Pharmacology
- Clinical Trials
Background:
- Atopic dermatitis (AD) management is evolving with new targeted therapies.
- Clinical decision-making requires comparative efficacy data for these agents.
Purpose of the Study:
- To assess the efficacy of biologics and oral small molecules in treating atopic dermatitis (AD).
- To evaluate effects on clinical signs, symptoms, and quality of life.
Main Methods:
- Systematic literature review of phase II and III randomized clinical trials for AD treatments.
- Meta-analysis using the inverse variance heterogeneity model ((IVhet)) to assess Eczema Area and Severity Index (EASI), Dermatology Life Quality Index (DLQI), and Peak Pruritus Numerical Rating Scale (PP-NRS).
Main Results:
- Upadacitinib (30 mg), abrocitinib, and lebrikizumab demonstrated higher Eczema Area and Severity Index (EASI) reduction than dupilumab.
- Lebrikizumab, upadacitinib, and abrocitinib showed greater itch reduction (PP-NRS) compared to dupilumab.
- Abrocitinib achieved the most significant improvement in Dermatology Life Quality Index (DLQI).
Conclusions:
- Upadacitinib, abrocitinib, and lebrikizumab offer superior improvements in AD clinical signs, symptoms, and quality of life over dupilumab.
- These agents represent significant advancements in targeted atopic dermatitis therapy.
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