Effectiveness and Safety of Dupilumab for Prurigo Nodularis in China: A Multicentric and Observational Study

ABSTRACT Background The efficacy and safety of dupilumab in patients with refractory prurigo nodularis (PN) is well established in clinical trials, but there is a lack of multicenter data regarding its effectiveness and safety in real‐world settings. Methods Patients with moderate‐to‐severe PN who initiated dupilumab treatment between July 2023 and January 2024, with a follow‐up period of at least 16 weeks at 10 hospitals in China were included. We used peak pruritus numeric rating scale (PP‐NRS), investigator global assessment (IGA) for PN, and dermatology life quality index for adults or children (DLQI/CDLQI) to assess disease control status and quality of life impairment, and monitored adverse events to assess the safety. Results A total of 73 PN patients (33 female, 40 male; mean age 45.9 ± 21.5 years) were included. A clinically meaningful improvement of ≥ 4 points in PP‐NRS (PP‐NRS4) was achieved in 84.9% of patients at Week 12. The percentage of patients achieving IGA 0/1 significantly increasing from 0% to 37.0% and 46.6% at Week 12 and 16, respectively. Patient‐reported quality of life outcomes showed substantial improvement, with decreasing from 16.6 ± 6.8 at baseline to 7.2 ± 4.9 at Week 12, 6.4 ± 4.5 at Week 16. The safety profile of dupilumab was favorable, with one patient reporting dry eyes. Conclusion Dupilumab can effectively improve the pruritus, nodular lesions and quality of life for PN in real‐world settings.