Dupilumab Treatment Reduces Hospitalizations in Adults With Moderate-to-Severe Atopic Dermatitis

Refractory disease, flares, or infections in atopic dermatitis (AD) can lead to hospitalizations. To compare hospitalization rates among adults with moderate-to-severe AD treated with dupilumab versus control. Data from 7 randomized, placebo-controlled trials of dupilumab (300 mg every 2 weeks [q2w]...

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Published in:The journal of allergy and clinical immunology in practice (Cambridge, MA) Vol. 10; no. 5; pp. 1279 - 1285.e1
Main Authors: Silverberg, Jonathan I., Rubini, Norma P.M., Pires, Mario C., Rossi, Ana B., Zhang, Annie, Chen, Zhen, Levit, Noah A., Chao, Jingdong, Shumel, Brad, Bégo-Le Bagousse, Gaëlle
Format: Journal Article
Language:English
Published: United States Elsevier Inc 01-05-2022
Elsevier Limited
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Summary:Refractory disease, flares, or infections in atopic dermatitis (AD) can lead to hospitalizations. To compare hospitalization rates among adults with moderate-to-severe AD treated with dupilumab versus control. Data from 7 randomized, placebo-controlled trials of dupilumab (300 mg every 2 weeks [q2w] and/or weekly [qw]; with or without topical corticosteroids) were analyzed. Patients in the dupilumab 300 mg q2w, qw, and combined dupilumab (q2w and qw; n = 1,841) groups compared with patients in the control group (n = 1,091) had lower rates of all-cause hospitalizations (5.8, 2.7, and 3.8 events, respectively, vs 9.0 events per 100 patient-years [PY]; all P < .05 [49%, 71%, and 62% risk reduction, respectively]); AD-related hospitalizations (2.0, 0.4, 1.0 events vs 4.1 events per 100 PY; P < .05 for qw and dupilumab combined [91% and 79% risk reduction, respectively]); as well as reduced overall duration of AD-related hospitalization (10.9, 7.3, and 8.6 d vs 38.9 d per 100 PY). Among adults with moderate-to-severe AD, treatment with dupilumab versus control was associated with significant reductions in all-cause and AD-related hospitalization rates, and shorter duration of AD-related hospitalization.
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ISSN:2213-2198
2213-2201
DOI:10.1016/j.jaip.2021.11.034