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Real-World Effectiveness of Mepolizumab in Patients with Allergic and Non-Allergic Asthma

Authors :
Silver,Jared
Steffens,Andrea
Chastek,Benjamin
Deb,Arijita
Silver,Jared
Steffens,Andrea
Chastek,Benjamin
Deb,Arijita
Publication Year :
2024

Abstract

Jared Silver,1 Andrea Steffens,2 Benjamin Chastek,2 Arijita Deb3 1Medical Affairs, GSK, Durham, NC, USA; 2Optum, Eden Prairie, MN, USA; 3Value, Evidence and Outcomes, GSK, Upper Providence, PA, USACorrespondence: Arijita Deb, Value, Evidence and Outcomes, GSK, 1250 S Collegeville Road, Upper Providence, PA, 19426, USA, Tel +1 267 377-5717, Email arijita.x.deb@gsk.comPurpose: Real-world data on mepolizumab in patients with severe asthma and allergic and non-allergic phenotypes are limited. This study investigated the effectiveness of mepolizumab treatment in patients with severe asthma with allergic and non-allergic phenotypes.Patients and Methods: This retrospective cohort study (GSK ID: 214148) used administrative claims data from the Optum Research Database. Eligible patients were ≥ 6 years of age with asthma and had ≥ 2 mepolizumab claims post-index. Index date was the first mepolizumab claim/administration (January 2016–December 2018). Patients were divided into two cohorts: allergic and non-allergic asthma, based on diagnosis codes, medication use and lab test results. Outcomes included the rate of asthma-related exacerbations and oral corticosteroid (OCS) use during the 12 months before (baseline period) and 12 months after (follow-up period) mepolizumab initiation. Study ended in December 2019.Results: Overall, 240 (44.6%) and 298 (55.4%) patients were included in the allergic and non-allergic asthma cohorts, respectively. Mean (standard deviation [SD]) counts of asthma-related exacerbations were significantly reduced from baseline to follow-up in both the allergic and non-allergic asthma cohorts (3.2 [2.5] to 2.1 [2.1], p < 0.001 and 2.5 [2.2] to 1.7 [1.9], p < 0.001, respectively). The mean number of OCS pharmacy claims was significantly decreased by 33.3% and 41.4% from baseline to follow-up in the allergic and non-allergic cohorts, respectively (p < 0.001); mean daily OCS dose significantly decreased by 30.6% and 45.4%, respectively (p

Details

Database :
OAIster
Notes :
text/html, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1430690709
Document Type :
Electronic Resource