Jutel Marek, Klimek Ludger, Richter Hartmut, Brüggenjürgen Bernd, Vogelberg Christian
ALL-MED Medical Research Institute, Wrocław, Poland.
Department of Clinical Immunology, Wroclaw Medical University, Wroclaw, Poland.
Allergy. 2024 Apr;79(4):1042-1051. doi: 10.1111/all.16052. Epub 2024 Mar 2.
The German Therapy Allergen Ordinance (TAO) triggered an ongoing upheaval in the market for house dust mite (HDM) allergen immunotherapy (AIT) products. Three HDM subcutaneous AIT (SCIT) products hold approval in Germany and therefore will be available after the scheduled completion of the TAO procedure in 2026. In general, data from clinical trials on the long-term effectiveness of HDM AIT are rare. We evaluated real-world data (RWD) in a retrospective, observational cohort study based on a longitudinal claims database including 60% of all German statutory healthcare prescriptions to show the long-term effectiveness of one of these products in daily life. Aim of this analysis was to provide a per product analysis on effectiveness of mite AIT as it is demanded by international guidelines on AIT.
Subjects between 5 and 70 years receiving their first (index) prescription of SCIT with a native HDM product (SCIT group) between 2009 and 2013 were included. The exactly 3:1 matched control group received prescriptions for only symptomatic AR medication (non-AIT group); the evaluation period for up to 6 years of follow-up ended in February 2017. Study endpoints were the progression of allergic rhinitis (AR) and asthma, asthma occurrence and time to the onset of asthma after at least 2 treatment years.
In total, 892 subjects (608 adults and 284 children/adolescents) were included in the SCIT group and 2676 subjects (1824 adults and 852 children/adolescents) in the non-AIT group. During the follow-up period after at least 2 years of SCIT, the number of prescriptions in the SCIT group was reduced by 62.8% (p < .0001) for AR medication and by 42.4% for asthma medication (p = .0003). New-onset asthma risk was significantly reduced in the SCIT vs non-AIT group by 27.0% (p = .0212). The asthma-preventive effect of SCIT occurred 15 months after start of the treatment. In the SCIT group, the time to onset of asthma was prolonged compared to the non-AIT group (p = .0010).
In this first product based RWD analysis on SCIT with a native HDM product, patients aged 5 to 70 years benefited from AIT in the long term in terms of reduced progression of AR and asthma after at least 2 years of treatment. The effects seemed to last for up to 6 years after treatment termination. A significantly reduced risk of asthma onset was observed, starting after 15 months of treatment.
德国治疗性变应原条例(TAO)引发了屋尘螨(HDM)变应原免疫疗法(AIT)产品市场的持续动荡。三种HDM皮下AIT(SCIT)产品在德国获得批准,因此将在2026年TAO程序按计划完成后上市。一般来说,关于HDM AIT长期有效性的临床试验数据很少。我们在一项回顾性观察队列研究中评估了真实世界数据(RWD),该研究基于一个纵向索赔数据库,其中包括德国所有法定医疗处方的60%,以显示这些产品之一在日常生活中的长期有效性。该分析的目的是按照AIT国际指南的要求,对螨AIT的有效性进行逐个产品分析。
纳入2009年至2013年间首次(索引)开具天然HDM产品SCIT处方的5至70岁受试者(SCIT组)。精确匹配的3:1对照组仅接受对症性AR药物处方(非AIT组);长达6年的随访评估期于2017年2月结束。研究终点为变应性鼻炎(AR)和哮喘的进展、哮喘的发生以及至少治疗2年后哮喘发作的时间。
SCIT组共纳入892名受试者(608名成人和284名儿童/青少年),非AIT组纳入2676名受试者(1824名成人和852名儿童/青少年)。在至少2年的SCIT治疗后的随访期内,SCIT组AR药物处方数量减少了62.8%(p <.0001),哮喘药物处方数量减少了42.4%(p =.0003)。与非AIT组相比,SCIT组新发哮喘风险显著降低27.0%(p =.0212)。SCIT的哮喘预防作用在治疗开始15个月后出现。与非AIT组相比,SCIT组哮喘发作时间延长(p =.0010)。
在这项首次基于产品的关于天然HDM产品SCIT的RWD分析中,5至70岁的患者在至少2年的治疗后,从AIT中获得了长期益处,AR和哮喘的进展有所减轻。这些效果在治疗终止后似乎持续长达6年。在治疗15个月后观察到哮喘发作风险显著降低。