Long-term effects of pollen allergoid tyrosine-adsorbed subcutaneous immunotherapy on allergic rhinitis and asthma

被引:3
|
作者
Vogelberg, Christian [1 ,2 ,6 ,7 ]
Klimek, Ludger [3 ]
Kruppert, Silvia [4 ]
Becker, Sven [5 ]
机构
[1] Tech Univ Dresden, Fac Med, Dept Pediat Pneumol & Allergol, Dresden, Germany
[2] Tech Univ Dresden, Univ Hosp Carl Gustav Carus Dresden, Dresden, Germany
[3] Ctr Rhinol & Allergy, Wiesbaden, Germany
[4] IQVIA, Frankfurt, Germany
[5] Univ Tubingen, Dept Otorhinolaryngol Head & Neck Surg, Tubingen, Germany
[6] Tech Univ Dresden, Fac Med, Dept Pediat Pneumol & Allergol, Dresden, Germany
[7] Tech Univ Dresden, Univ Hosp Carl Gustav Carus Dresden, Dresden, Germany
关键词
AIT; allergic rhinitis; asthma onset; long-term benefit; real-world evidence; ADVERSE SYSTEMIC REACTIONS; EUROPEAN SURVEY; EASSI;
D O I
10.1111/cea.14444
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: Allergen immunotherapy (AIT) may have a long-term disease-modifying effect. The aim of this study was to demonstrate the long-term effects of pollen allergoid tyrosine-adsorbed subcutaneous AIT on allergic rhinitis (AR) and asthma (AA) in clinical practice. Methods: This retrospective study, funded by an AIT manufacturer, analysed the impact of AIT on AR progression and onset of need for AA medication, using a German database covering similar to 35% of national prescriptions during 2008-2020. Anonymized prescription data of AR patients aged 5-65 years treated with grass or tree pollen AIT between 2009 and 2013 and followed for at least 2 years after AIT cessation were compared with matched control patients with seasonal AR. Results: 181,496 patients received AIT prescriptions. 5959 fulfilled the inclusion criteria. The median AIT treatment duration was 1092 days and the follow-up duration was 6.4 years. Less patients treated with AIT received prescriptions for symptomatic AR medication in the follow-up versus controls (AIT: OR: 0.37; 95% Confidence Interval (CI) 0.34, 0.40; p < .001, tyrosine-adsorbed AIT: OR: 0.27; 95% CI 0.20, 0.35 p < .001). Less asthmatic patients under AIT received prescriptions for AA medications versus controls (AIT: OR: 0.48; 95% CI 0.41, 0.55; p < .001, tyrosine-adsorbed AIT: OR: 0.48; 95% CI 0.29, 0.79; p = .004). AR and AA medication prescriptions for AIT patients were reduced in the follow-up versus baseline and controls (AIT: AR: 20.0%; 1.5 vs. 0.2 prescriptions; AA: 29.1%; 2.0 vs. 0.6 prescriptions, p < .001; tyrosine-adsorbed AIT: AR: 24.2%, 1.4 vs. 0.2 prescriptions; AA: 35.6%, 2.1 vs. 0.6 prescriptions, p < .001). The probability of AA medication onset in non-asthmatic patients during follow-up was reduced for AIT patients compared to controls (OR: 0.77, 95% CI 0.66, 0.90; p = .001). All endpoints were significant for children/adolescents and adults in stratified analyses. Conclusions: We found evidence for long-term effects up to 9.5 years for tyrosine-adsorbed AIT.
引用
收藏
页码:253 / 264
页数:12
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