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

被引:5
作者
Hwee, Jeremiah [1 ,8 ]
Huynh, Lynn [2 ]
Du, Shawn [2 ]
Kwon, Namhee [3 ]
Jakes, Rupert W. [4 ]
Alfonso-Cristancho, Rafael [5 ]
Baylis, Lee [6 ]
Requena, Gema [4 ]
Khanal, Anamika [2 ]
Rothenberg, Marc E. [7 ]
Duh, Mei Sheng [2 ]
机构
[1] GSK, Epidemiol, Mississauga, ON, Canada
[2] Anal Grp Inc, Boston, MA USA
[3] GSK, Clin Sci, Resp, Brentford, Middx, England
[4] GSK, Epidemiol, London, England
[5] GSK, Value Evidence & Outcomes, Collegeville, PA USA
[6] GSK, Global Med Affairs, Durham, NC USA
[7] Univ Cincinnati, Cincinnati Childrens Hosp Med Ctr, Dept Pediat, Div Allergy & Immunol,Sch Med, Cincinnati, OH USA
[8] GSK, Value Evidence & Outcomes, 100 Milverton Dr, Mississauga L5R 4H1, ON, Canada
关键词
MANAGEMENT; MEPOLIZUMAB; EFFICACY; SAFETY; ASTHMA; MAB;
D O I
10.1016/j.anai.2023.02.022
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
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 health-care 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 diag-nosis 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 spe-cialties. 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 treat-ment 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.& COPY; 2023 American College of Allergy, Asthma & Immunology. Published by Elsevier Inc. This is an open access arti-cle under the CC BY license (http://creativecommons.org/licenses/by/4.0/)
引用
收藏
页码:768 / 775
页数:8
相关论文
共 34 条
  • [1] American Academy of Allergy Asthma and Immunology, HYP SYNDR
  • [2] 38-Year-Old Man With Asthma and Eosinophilia
    Andersen, Carl
    Yadav, Hemang
    Iyer, Vivek N.
    [J]. MAYO CLINIC PROCEEDINGS, 2017, 92 (08) : E111 - E115
  • [3] [Anonymous], 1994, NOMENCLATURE CRITERI, V9th, P253
  • [4] Guideline for the investigation and management of eosinophilia
    Butt, Nauman M.
    Lambert, Jonathan
    Ali, Sahra
    Beer, Philip A.
    Cross, Nicholas C. P.
    Duncombe, Andrew
    Ewing, Joanne
    Harrison, Claire N.
    Knapper, Steven
    McLornan, Donal
    Mead, Adam J.
    Radia, Deepti
    Bain, Barbara J.
    [J]. BRITISH JOURNAL OF HAEMATOLOGY, 2017, 176 (04) : 553 - 572
  • [5] HYPEREOSINOPHILIC SYNDROME - ANALYSIS OF 14 CASES WITH REVIEW OF LITERATURE
    CHUSID, MJ
    DALE, DC
    WEST, BC
    WOLFF, SM
    [J]. MEDICINE, 1975, 54 (01) : 1 - 27
  • [6] Cogan E, 2012, EXPERT REV HEMATOL, V5, P275, DOI [10.1586/EHM.12.14, 10.1586/ehm.12.14]
  • [7] Incidence of myeloproliferative hypereosinophilic syndrome in the United States and an estimate of all hypereosinophilic syndrome incidence
    Crane, Martin M.
    Chang, Cindy Ma
    Kobayashi, Monica G.
    Weller, Peter F.
    [J]. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2010, 126 (01) : 179 - 181
  • [8] Diagnosis and Novel Approaches to the Treatment of Hypereosinophilic Syndromes
    Dispenza, Melanie C.
    Bochner, Bruce S.
    [J]. CURRENT HEMATOLOGIC MALIGNANCY REPORTS, 2018, 13 (03) : 191 - 201
  • [9] EMA, EU304213 ORPH DES TR
  • [10] EMA, MEP NUC SUMM PROD CH