Reduction in hospitalisations with dupilumab in Japanese adults with atopic dermatitis in a real‐world setting

Author:

Igawa Ken1ORCID,Fujita Hiroyuki2ORCID,Tajima Yuki2,Lubwama Robert3,Daoud Moataz4,Wang Zhixiao5,Arima Kazuhiko2ORCID

Affiliation:

1. Dokkyo Medical University Tochigi Japan

2. Sanofi K.K. Tokyo Japan

3. Sanofi Bridgewater New Jersey USA

4. Sanofi Cambridge Massachusetts USA

5. Regeneron Pharmaceuticals, Inc Tarrytown New York USA

Abstract

AbstractBackgroundIn a recent post hoc analysis of multinational clinical trial data, dupilumab treatment for patients with moderate or severe atopic dermatitis (AD) reduced all‐cause and AD‐related hospitalisations.ObjectivesWe studied the impact of dupilumab on health care resource utilisation (HCRU) and AD medication by comparing use during the 6 months either side of starting dupilumab (index) in a real‐world setting.MethodsThis observational, retrospective, cohort study used Japanese hospital claims data (1 April 2018 to 28 February 2019). A total of 357 patients (mean [range] age 45 [15–92] years; 65.5% male) with ≥1 AD diagnosis and ≥1 dupilumab prescription were included. Outcome variables included AD treatments and HCRU during the 6 months pre‐ and post‐index.ResultsThe number of all‐cause hospitalisations decreased by 43.1% (from 51 in the 6 months before to 29 in the 6 months after dupilumab initiation), with a 96.0% reduction in skin/subcutaneous tissue disease‐related hospitalisations (25 to 1). Use of nonsteroidal systemic immunosuppressants, phototherapy and systemic corticosteroids decreased (by 59.8%, 59.5% and 30.6%, respectively) after dupilumab initiation. At 180 days after dupilumab initiation, 86.8% of patients were still taking dupilumab.ConclusionsOverall, these results suggest that dupilumab can reduce skin/soft tissue‐related hospitalisations and use of various other AD medications in a real‐world setting.

Funder

Regeneron Pharmaceuticals

Sanofi

Publisher

Wiley

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