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Efficacy of biologics and oral small molecules for atopic dermatitis: a systematic review and meta-analysis.

AbstractBACKGROUND:
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.
AuthorsKelsey B Nusbaum, Sarah Fleischer, Alan B Fleischer Jr
JournalThe Journal of dermatological treatment (J Dermatolog Treat) Vol. 33 Issue 5 Pg. 2534-2544 (Aug 2022) ISSN: 1471-1753 [Electronic] England
PMID34620047 (Publication Type: Journal Article, Meta-Analysis, Systematic Review)
Chemical References
  • Biological Products
Topics
  • Biological Products (therapeutic use)
  • Dermatitis, Atopic (diagnosis, drug therapy)
  • Double-Blind Method
  • Humans
  • Pruritus (drug therapy)
  • Quality of Life
  • Severity of Illness Index
  • Treatment Outcome

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