丙酸氟替卡松口崩片(APT-1011)治疗嗜酸性粒细胞性食管炎的随机对照试验。

Fluticasone Propionate Orally Disintegrating Tablet (APT-1011) for Eosinophilic Esophagitis: Randomized Controlled Trial.

机构信息

Center for Esophageal Diseases and Swallowing, Division of Gastroenterology and Hepatology, University of North Carolina School of Medicine, Chapel Hill, North Carolina.

Division of Gastroenterology, General Hospital Tomelloso, Ciudad Real, Spain.

出版信息

Clin Gastroenterol Hepatol. 2022 Nov;20(11):2485-2494.e15. doi: 10.1016/j.cgh.2022.02.013. Epub 2022 Feb 16.

Abstract

BACKGROUND & AIMS: Topical steroids are effective treatments for eosinophilic esophagitis (EoE). The FLUTE (Fluticasone in EoE) trial evaluated safety and efficacy of APT-1011 (fluticasone propionate oral disintegrating tablet) vs placebo for treatment of EoE.

METHODS

In this randomized, double-blind, placebo-controlled, dose-finding, phase 2b trial, 106 adults with EoE received 1 of 4 APT-1011 doses or placebo for a 12-week induction period and 40 weeks of maintenance. Primary outcome was histologic response (≤6 eosinophils per high-power field) at Week 12. Secondary outcomes included endoscopic features and dysphagia frequency.

RESULTS

Histologic response rates were 0% for placebo, 80% for APT-1011 3 mg twice daily (BID), 67% for 3 mg at bedtime (HS), 86% for 1.5 mg BID, 48% for 1.5 mg HS (P < .001 for all groups vs placebo). At Week 12, mean Edema/Rings/Exudates/Furrows/Strictures (EoE Endoscopic Reference Score) total score (max, 9.0) improved from 4.5 to 2.3 for 3 mg BID, 5.3 to 2.1 for 3 mg HS, 4.6 to 1.7 for 1.5 mg BID, 5.3 to 2.9 for 1.5 mg HS vs 5.2 to 4.5 for placebo. Mean dysphagia frequency over 14 days improved from baseline to Week 12 with all active groups improving more than placebo. Improvements were sustained to Week 52. APT-1011 was safe and well-tolerated, with higher incidence of candidiasis noted at the higher twice daily doses.

CONCLUSION

APT-1011 dosing regimens were superior for histologic and endoscopic responses, and for reduction in dysphagia frequency vs placebo. Based on the symptom improvement and assessment of adverse events together with the histologic response rate, 3 mg once daily at bedtime dose showed the most favorable risk-benefit profile.

CLINICALTRIALS

gov, Number: NCT03191864.

摘要

背景与目的

局部皮质类固醇是治疗嗜酸性食管炎(EoE)的有效方法。FLUTE(EoE 中的氟替卡松)试验评估了 APT-1011(丙酸氟替卡松口腔崩解片)与安慰剂治疗 EoE 的安全性和疗效。

方法

在这项随机、双盲、安慰剂对照、剂量发现、2b 期试验中,106 名 EoE 成人接受了 4 种 APT-1011 剂量或安慰剂治疗 12 周诱导期和 40 周维持期。主要终点是第 12 周的组织学反应(每高倍视野≤6 个嗜酸性粒细胞)。次要终点包括内镜特征和吞咽困难频率。

结果

安慰剂组的组织学反应率为 0%,APT-1011 3mg 每日 2 次(BID)组为 80%,3mg 睡前(HS)组为 67%,1.5mg BID 组为 86%,1.5mg HS 组为 48%(所有组与安慰剂相比,P <.001)。第 12 周时,3mg BID 组的平均水肿/环/渗出/沟/狭窄(EoE 内镜参考评分)总评分(最高 9.0)从 4.5 降至 2.3,3mg HS 组从 5.3 降至 2.1,1.5mg BID 组从 4.6 降至 1.7,1.5mg HS 组从 5.3 降至 2.9,安慰剂组从 5.2 降至 4.5。14 天内平均吞咽困难频率从基线到第 12 周改善,所有活性组均优于安慰剂。改善持续到第 52 周。APT-1011 安全且耐受良好,较高的每日两次剂量组更易发生念珠菌病。

结论

与安慰剂相比,APT-1011 剂量方案在组织学和内镜反应以及减少吞咽困难频率方面更优。基于症状改善和不良事件评估以及组织学反应率,睡前 3mg 每日一次剂量显示出最佳的风险效益比。

临床试验

gov,编号:NCT03191864。

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