Real-World Effect of Ruxolitinib Cream: Decreased Use of Additional Topical Therapies and Limited Escalation to Systemic Treatments
摘要
Ruxolitinib cream has demonstrated efficacy and safety in patients aged ≥ 2 years with mild to moderate atopic dermatitis (AD) in clinical trials. Early real-world data have demonstrated results consistent with clinical trial observations and have indicated that initiation of ruxolitinib cream may reduce the need for other AD therapies, both topical and systemic. This analysis investigated the longer-term (18-month) effect of ruxolitinib cream on AD treatment patterns.
MethodsIn this retrospective, observational study, US claims data from the Healthcare Integrated Research Database (HIRD®) were used to identify new ruxolitinib cream users aged ≥ 12 years between October 1, 2021 and July 31, 2022. The 6 months prior to the index date (first claim for ruxolitinib cream) comprised the baseline period. The 18-month follow-up period was divided into months 1–6, 7–12, and 13–18 to evaluate short- and long-term effects of ruxolitinib cream on AD treatment patterns.
ResultsA total of 1269 patients were included in the analysis. The mean (SD; range) number of ruxolitinib cream fills during the 18-month follow-up period was 2.4 (2.3; 1–19). By months 13–18 of follow-up, claims for topical corticosteroids, topical calcineurin inhibitors, and topical PDE4 inhibitors were reduced from baseline by 52%, 63%, and 70%, respectively. Use of oral corticosteroids was reduced by 28%, with a 32% reduction in the mean cumulative prednisone-equivalent dose. Among patients with baseline biologic AD therapy (n = 231), 35.5% did not receive biologics during months 13–18 of follow-up. Additionally, among patients without baseline biologic use (n = 1038), > 90% remained off biologics.
ConclusionUse of both topical and systemic AD therapies, including biologics, decreased over 18 months following initiation of ruxolitinib cream. These data suggest that ruxolitinib cream may reduce the need for additional topical therapies and limit escalation to systemic therapies for adults and adolescents with AD.