Guy's and St. Thomas' National Health Service Foundation Trust and Kings College, London.
Aimmune Therapeutics, Nestlé Health Science, Brisbane, CA.
NEJM Evid. 2023 Nov;2(11):EVIDoa2300145. doi: 10.1056/EVIDoa2300145. Epub 2023 Oct 23.
Peanut allergy is a common childhood allergy, and the only approved treatment for children 4 to 17 years of age is peanut allergen powder-dnfp (PTAH) oral immunotherapy. METHODS: For this phase 3, randomized, double-blind, placebo-controlled trial, we enrolled peanut-allergic children 1 to <4 years of age who experienced dose-limiting symptoms from ≤300 mg peanut protein during a screening double-blind, placebo-controlled food challenge (DBPCFC). Participants received PTAH or placebo, randomized in a 2:1 ratio, for approximately 12 months. At the trial conclusion, all participants underwent an exit BDPCFC. The primary end point was desensitization (i.e., tolerating a ≥600-mg single dose of peanut protein with only mild allergy symptoms). RESULTS: In the PTAH-treated group (n=98), 73.5% of participants tolerated a single dose of ≥600 mg peanut protein at exit DBPCFC compared with 6.3% in the placebo group (n=48). Most participants experienced an adverse event (98.0% of PTAH-treated and 97.9% of placebo-treated participants), which was mild or moderate in grade for 93.2% of participants (92.9% in PTAH-treated and 93.8% in placebo-treated participants). Treatment-related adverse events, which were mild to moderate, were experienced by 75.5% of PTAH-treated and 58.3% of placebo-treated participants. Three treatment-related systemic allergic reactions, none of which were severe or serious in grade, were noted in two PTAH-treated participants (2%). CONCLUSIONS: In peanut-allergic children 1 to <4 years of age treated with PTAH for approximately 12 months, the majority tolerated all peanut protein dose levels assessed. PTAH-treated patients had more treatment-related adverse events, which were mild to moderate severity. (Funded by Aimmune Therapeutics; ClinicalTrials.gov number, NCT03736447.)
花生过敏是一种常见的儿童过敏,唯一批准用于 4 至 17 岁儿童的治疗方法是食用花生过敏原粉-dnfp(PTAH)口服免疫疗法。方法:在这项 3 期、随机、双盲、安慰剂对照试验中,我们招募了 1 至 <4 岁的花生过敏儿童,这些儿童在筛选性双盲、安慰剂对照食物挑战(DBPCFC)中,摄入≤300mg 花生蛋白时出现剂量限制症状。参与者以 2:1 的比例随机接受 PTAH 或安慰剂治疗,约 12 个月。在试验结束时,所有参与者均进行了出口 DBPCFC。主要终点是脱敏(即耐受 600mg 以上单剂量的花生蛋白,仅出现轻度过敏症状)。结果:在 PTAH 治疗组(n=98)中,73.5%的参与者在出口 DBPCFC 时耐受 600mg 以上的单剂量花生蛋白,而安慰剂组(n=48)中仅为 6.3%。大多数参与者发生不良事件(98.0%的 PTAH 治疗组和 97.9%的安慰剂治疗组),93.2%的参与者(92.9%的 PTAH 治疗组和 93.8%的安慰剂治疗组)为轻度或中度。75.5%的 PTAH 治疗组和 58.3%的安慰剂治疗组出现与治疗相关的不良事件,为轻度至中度。两名 PTAH 治疗组患者(2%)各有 1 例出现与治疗相关的全身性过敏反应,均为轻度至中度,无严重或严重程度。结论:在接受 PTAH 治疗约 12 个月的 1 至 <4 岁花生过敏儿童中,大多数人耐受了评估的所有花生蛋白剂量水平。PTAH 治疗组患者发生更多与治疗相关的不良事件,为轻度至中度。(由 Aimmune Therapeutics 资助;临床试验编号,NCT03736447。)