Berkes Stefanie, Liddell Klara, Beyer Kirsten, Blumchen Katharina, Deschildre Antoine, Kukkonen Kaarina, Mäkelä Mika J, Patel Nandinee, Turner Paul J
National Heart & Lung Institute, Imperial College London, London, UK.
Division Department of Pediatric Respiratory Medicine, Immunology and Critical Care Medicine, Charité Universtãtsmedizin Berlin, Berlin.
Curr Opin Allergy Clin Immunol. 2025 Jun 1;25(3):185-193. doi: 10.1097/ACI.0000000000001077. Epub 2025 Apr 10.
Allergen immunotherapy (AIT) is increasingly popular as a treatment strategy for food allergy. Unfortunately, there is significant heterogeneity in reported outcomes, specifically in the dose-thresholds selected for evaluation and the symptoms used to define a "tolerated dose". These considerations are often investigator-driven and do not consider patient perspectives.
A systematic review by the EAACI CO-FAITH taskforce recently flagged the need to better standardize and harmonize outcomes used in clinical trials of food-AIT. Using less objective symptoms to define dose-limiting symptoms can underestimate the reaction threshold determined at baseline food challenge. As a consequence, this can overestimate the efficacy of food-AIT by 15%. In this review, we perform an individual patient data (IPD) meta-analysis using data from three randomized-controlled trials and one real-world registry, to evaluate how the definition of dose "tolerance" impacts upon reported desensitization rates.
This analysis provides insight into how clinical efficacy rates for food-AIT are impacted by using different dose thresholds and definitions for when a dose might be consider tolerated. Using more patient-centric outcomes may be a more useful metric to harmonize reporting of outcomes and inform clinical practice, paving the way towards reaching a consensus on outcome reporting in trials of food-AIT.
变应原免疫疗法(AIT)作为食物过敏的一种治疗策略越来越受欢迎。不幸的是,报告的结果存在显著异质性,特别是在选择用于评估的剂量阈值以及用于定义“耐受剂量”的症状方面。这些考量通常由研究者主导,并未考虑患者的观点。
欧洲变态反应和临床免疫学会(EAACI)CO-FAITH工作组最近的一项系统评价指出,有必要更好地规范和统一食物AIT临床试验中使用的结果。使用不太客观的症状来定义剂量限制症状可能会低估在基线食物激发试验中确定的反应阈值。因此,这可能会将食物AIT的疗效高估15%。在本综述中,我们使用来自三项随机对照试验和一项真实世界登记处的数据进行个体患者数据(IPD)荟萃分析,以评估剂量“耐受”的定义如何影响报告的脱敏率。
该分析深入探讨了使用不同的剂量阈值以及何时可认为剂量耐受的定义如何影响食物AIT的临床疗效率。采用更以患者为中心的结果可能是统一结果报告并为临床实践提供参考的更有用指标,为在食物AIT试验的结果报告上达成共识铺平道路。