Clinical outcomes and quality of life improvement in children with moderate-to-severe atopic dermatitis and atopic multimorbidity treated with dupilumab
Julia Levina (Moskva, Fédération de Russie), Elena Vishneva (Moscow, Fédération de Russie), Kamilla Efendieva (Moskva, Fédération de Russie), Vera Kalugina (Moscow, Fédération de Russie), Anna Alekseeva (Moskva, Fédération de Russie), Anastasia Lamasova (Mosc, Fédération de Russie), Leyla Namazova-Baranova (Moskva, Fédération de Russie)
Background

Atopic dermatitis (AD) is a prevalent chronic inflammatory skin condition in children, with approximately 20% affected and many cases debuting before 6 months of age. Despite various treatment options, disease control remains challenging, and severe AD is a known risk factor for other Type 2 (T2) inflammatory diseases. This study aimed to evaluate the efficacy and safety of dupilumab, a targeted therapy, in children with moderate-to-severe AD and other allergic conditions.

Method

The study included 15 children with moderate-to-severe AD, median age of 13.3 years (range: 5.1–15.9), 67% males. Disease severity was assessed using standard scales: SCORAD (Scoring Atopic Dermatitis) and EASI (Eczema Area and Severity Index). Quality of life was evaluated in patients aged over 4 years using the CDLQI (Children’s Dermatology Life Quality Index) before starting dupilumab therapy and at regular intervals (4, 8, 12 weeks). All patients had a multimorbid atopic phenotype, with two or more allergic diseases, such as allergic rhinitis, asthma, eosinophilic esophagitis and food allergy. Most patients (87%) had the onset of AD before 6 months of age.

Results

SCORAD-75 was achieved by 20% of patients by the 4th week, 20% by the 8th week, and 27% by the 12th week. However, 33% of patients did not achieve a 75% reduction in SCORAD by the 12th week. EASI-75 was achieved by 73% of patients by the 4th week, 20% by the 8th week, and 7% by the 12th week. All patients experienced a 75% reduction in EASI during the follow-up period. A 75% improvement in quality of life was observed in 38.4% of patients at 4 weeks, 23.1% at 8 weeks, and 15.4% at 12 weeks. By the 12th week, 23.1% of patients did not achieve a 75% improvement in CDLQI. Significant improvement was also observed in concomitant allergic conditions. Injection site reactions were noted in 13% patients, 14% reporting pain at the injection site, and 7% - itching. Conjunctivitis was observed in 6.7% patients. Erythema and swelling at the injection site were not reported.

Conclusion

The study demonstrated that dupilumab therapy significantly improved both clinical outcomes and quality of life in children with moderate-to-severe atopic dermatitis, even in those with atopic multimorbidity. The therapy demonstrated a favorable safety profile, with few and mild adverse events. Further studies are needed to optimize treatment strategies and assess long-term outcomes in children.