Galvin Audrey Dunn, Vereda Andrea, Rodríguez del Río Pablo, Muraro Antonella, Jones Carla, Ryan Robert, Norval David, Jobrack Jennifer, Anagnostou Aikaterini, Wang Julie
University College Cork, Cork, Ireland.
Aimmune Therapeutics, a Nestlé Health Science Company, London, UK.
Clin Transl Allergy. 2022 Dec;12(12):e12213. doi: 10.1002/clt2.12213.
Health-related quality of life (HRQoL) is significantly and substantially reduced in individuals with peanut allergy due to many factors associated with unanticipated or potentially fatal reactions. Further insight on the impact of peanut oral immunotherapy in managing peanut allergy on HRQoL is needed. The aim of this analysis was to assess effects of peanut (Arachis hypogaea) allergen powder-dnfp (PTAH), a biologic drug for peanut oral immunotherapy, on HRQoL from three phase 3 and two follow-on trials of PTAH.
HRQoL assessments from participants aged 4-17 in the PALISADE (ARC003), ARC004 (PALISADE follow-on), ARTEMIS (ARC010), RAMSES (ARC007), and ARC011 (RAMSES follow-on) trials were included in this analysis. Responses on the Food Allergy Quality of Life Questionnaire (FAQLQ) and Food Allergy Independent Measure (FAIM) were evaluated by age group and respondent (self or caregiver proxy). Data were analyzed with descriptive statistics and Student t tests.
Baseline FAQLQ and FAIM total scores appeared comparable between PTAH- and placebo-treated participants. Self and caregiver proxy-reported total scores on the FAQLQ for PTAH-treated participants generally improved at trial exit versus baseline; FAIM total scores improved throughout all trials. The tendency for improvement in FAQLQ total scores from baseline for PTAH appeared larger in self versus caregiver proxy-reports. Between treatment groups, PTAH was generally favored in the PALISADE and ARTEMIS trials; differences varied in the RAMSES trial based on age and respondent types.
PTAH for the management of peanut allergy in children appeared to have a beneficial effect on HRQoL in trials. Improvements were seen despite rigors of trial participation.
由于与意外或潜在致命反应相关的多种因素,花生过敏个体的健康相关生活质量(HRQoL)显著且大幅降低。需要进一步了解花生口服免疫疗法对花生过敏管理中HRQoL的影响。本分析的目的是评估用于花生口服免疫疗法的生物药物花生(落花生)过敏原粉末-dnfp(PTAH)在三项3期试验和两项PTAH后续试验中对HRQoL的影响。
本分析纳入了PALISADE(ARC003)、ARC004(PALISADE后续试验)、ARTEMIS(ARC010)、RAMSES(ARC007)和ARC011(RAMSES后续试验)试验中4至17岁参与者的HRQoL评估。通过年龄组和受访者(自我或照顾者代理)对食物过敏生活质量问卷(FAQLQ)和食物过敏独立测量(FAIM)的回答进行评估。数据采用描述性统计和学生t检验进行分析。
PTAH治疗组和安慰剂治疗组参与者的基线FAQLQ和FAIM总分似乎相当。PTAH治疗组参与者的自我和照顾者代理报告的FAQLQ总分在试验结束时与基线相比总体有所改善;FAIM总分在所有试验中均有所改善。PTAH组FAQLQ总分从基线开始的改善趋势在自我报告中比照顾者代理报告中更大。在治疗组之间,PTAH在PALISADE和ARTEMIS试验中通常更受青睐;在RAMSES试验中,差异因年龄和受访者类型而异。
在试验中,用于儿童花生过敏管理的PTAH似乎对HRQoL有有益影响。尽管试验参与要求严格,但仍观察到了改善。