Hypereosinophilic syndrome in Europe: Retrospective study of treatment patterns, clinical manifestations, and healthcare resource utilization.


Journal

Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology
ISSN: 1534-4436
Titre abrégé: Ann Allergy Asthma Immunol
Pays: United States
ID NLM: 9503580

Informations de publication

Date de publication:
06 2023
Historique:
received: 07 12 2022
revised: 20 02 2023
accepted: 21 02 2023
medline: 5 6 2023
pubmed: 3 3 2023
entrez: 2 3 2023
Statut: ppublish

Résumé

The burden of hypereosinophilic syndrome (HES) in Europe is not well characterized. To evaluate real-world patient characteristics, treatment patterns, clinical manifestations, and healthcare resource utilization for patients with HES from France, Germany, Italy, Spain, and the United Kingdom. In this retrospective, noninterventional study, data for patients with a physician-confirmed diagnosis of HES were abstracted from medical chart reviews. Patients were aged 6 years or older at the time of HES diagnosis and had 1 or more years of follow-up from the index date (first clinic visit between January 2015 and December 2019). Data on treatment patterns, comorbidities, clinical manifestations, clinical outcomes, and healthcare resource utilization were collected from diagnosis or index date to end of follow-up. Data for 280 patients were abstracted from medical charts by 121 physicians treating HES, with multiple specialties. Most patients (55%) had idiopathic HES, and 24% had myeloid HES; the median number (interquartile range [IQR]) of diagnostic tests per patient was 10 (6-12). The most common comorbidities were asthma (45%) and anxiety or depression (36%). Most patients (89%) used oral corticosteroids; 64% used immunosuppressants or cytotoxic agents, and 44% used biologics. Patients had a median (IQR) of 3 clinical manifestations (1-5), most commonly constitutional (63%), lung (49%), and skin (48%). Twenty-three percent of patients experienced a flare, and 40% had a complete treatment response. Some patients (30%) were hospitalized with a median (IQR) stay of 9 days (5-15) for HES-related issues. Patients with HES across 5 European countries had a substantial disease burden despite extensive oral corticosteroids treatment, highlighting the need for additional targeted therapies.

Sections du résumé

BACKGROUND
The burden of hypereosinophilic syndrome (HES) in Europe is not well characterized.
OBJECTIVE
To evaluate real-world patient characteristics, treatment patterns, clinical manifestations, and healthcare resource utilization for patients with HES from France, Germany, Italy, Spain, and the United Kingdom.
METHODS
In this retrospective, noninterventional study, data for patients with a physician-confirmed diagnosis of HES were abstracted from medical chart reviews. Patients were aged 6 years or older at the time of HES diagnosis and had 1 or more years of follow-up from the index date (first clinic visit between January 2015 and December 2019). Data on treatment patterns, comorbidities, clinical manifestations, clinical outcomes, and healthcare resource utilization were collected from diagnosis or index date to end of follow-up.
RESULTS
Data for 280 patients were abstracted from medical charts by 121 physicians treating HES, with multiple specialties. Most patients (55%) had idiopathic HES, and 24% had myeloid HES; the median number (interquartile range [IQR]) of diagnostic tests per patient was 10 (6-12). The most common comorbidities were asthma (45%) and anxiety or depression (36%). Most patients (89%) used oral corticosteroids; 64% used immunosuppressants or cytotoxic agents, and 44% used biologics. Patients had a median (IQR) of 3 clinical manifestations (1-5), most commonly constitutional (63%), lung (49%), and skin (48%). Twenty-three percent of patients experienced a flare, and 40% had a complete treatment response. Some patients (30%) were hospitalized with a median (IQR) stay of 9 days (5-15) for HES-related issues.
CONCLUSION
Patients with HES across 5 European countries had a substantial disease burden despite extensive oral corticosteroids treatment, highlighting the need for additional targeted therapies.

Identifiants

pubmed: 36863663
pii: S1081-1206(23)00129-1
doi: 10.1016/j.anai.2023.02.022
pii:
doi:

Substances chimiques

Adrenal Cortex Hormones 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

768-775

Informations de copyright

Copyright © 2023 The Authors. Published by Elsevier Inc. All rights reserved.

Auteurs

Jeremiah Hwee (J)

Epidemiology, GSK, Mississauga, Ontario, Canada. Electronic address: Jeremiah.x.hwee@gsk.com.

Lynn Huynh (L)

Analysis Group, Inc., Boston, Massachusetts, United States.

Shawn Du (S)

Analysis Group, Inc., Boston, Massachusetts, United States.

Namhee Kwon (N)

Clinical Sciences, Respiratory, GSK, Brentford, Middlesex, United Kingdom.

Rupert W Jakes (RW)

Epidemiology, GSK, London, United Kingdom.

Rafael Alfonso-Cristancho (R)

Value Evidence and Outcomes, GSK, Collegeville, Pennsylvania, United States.

Lee Baylis (L)

Global Medical Affairs, GSK, Durham, North Carolina, United States.

Gema Requena (G)

Epidemiology, GSK, London, United Kingdom.

Anamika Khanal (A)

Analysis Group, Inc., Boston, Massachusetts, United States.

Marc E Rothenberg (ME)

Division of Allergy and Immunology, Department of Pediatrics, Cincinnati Children's Hospital Medical Center, University of Cincinnati School of Medicine, Cincinnati, Ohio, United States.

Mei Sheng Duh (M)

Analysis Group, Inc., Boston, Massachusetts, United States.

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Classifications MeSH