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Five-year real-world drug survival of dupilumab in severe atopic dermatitis and associate predictors.
- Source :
- Journal of Dermatological Treatment; Dec2024, Vol. 35 Issue 1, p1-8, 8p
- Publication Year :
- 2024
-
Abstract
- Background: Atopic dermatitis (AD) profoundly impacts patients' lives, necessitating long-term systemic treatments. Methods: This retrospective study involved 709 severe AD patients receiving dupilumab. Drug survival (DS) was analyzed using Kaplan-Meier curves, evaluating reasons for discontinuation. The log-rank test and Cox regression analysis were applied to assess differences in drug survival across baseline clinical characteristic groups. Results: Dupilumab showcased remarkable overall drug survival, reaching 74.1% at 65 months. Survival rates remained robust even when considering discontinuation solely due to primary or secondary inefficacy (86.4% at 65 months). For overall DS, the log-rank test did not reveal a statistically significant difference among the groups. Cox regression analysis showed that patients with nummular eczema-like as a phenotype have an increased risk of discontinuing dupilumab due to the development of psoriasis (p <.001, hazard ratio = 26.15, confidence interval [CI] 6.903–99.016). The multivariate logistic regression analysis confirmed these results (p <.001, OD = 18.956, CI 4.205–85.458), even when considering other clinical and epidemiological characteristics. Conclusion: This investigation establishes dupilumab's enduring efficacy and safety in severe AD, emphasizing its potential as a sustained therapeutic option over 5+ years. Baseline characteristics did not seem to influence DS, with the exception of the nummular eczema-like phenotype, which emerged as a significant predictor of psoriasis occurrence. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 09546634
- Volume :
- 35
- Issue :
- 1
- Database :
- Complementary Index
- Journal :
- Journal of Dermatological Treatment
- Publication Type :
- Academic Journal
- Accession number :
- 181738214
- Full Text :
- https://doi.org/10.1080/09546634.2024.2404718