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特泽布尔单抗治疗重度、未控制哮喘的疗效:PATHWAY 和 NAVIGATOR 临床试验的汇总分析。

Efficacy of Tezepelumab in Severe, Uncontrolled Asthma: Pooled Analysis of the PATHWAY and NAVIGATOR Clinical Trials.

机构信息

David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, California.

Royal Brompton and Harefield Hospitals, London, United Kingdom.

出版信息

Am J Respir Crit Care Med. 2023 Jul 1;208(1):13-24. doi: 10.1164/rccm.202210-2005OC.

Abstract

Tezepelumab reduced exacerbations in patients with severe, uncontrolled asthma across a range of baseline blood eosinophil counts and fractional exhaled nitric oxide levels, and irrespective of allergy status, in the phase 2b PATHWAY (Study to Evaluate the Efficacy and Safety of MEDI9929 [AMG 157] in Adult Subjects With Inadequately Controlled, Severe Asthma; NCT02054130) and phase 3 NAVIGATOR (Study to Evaluate Tezepelumab in Adults & Adolescents With Severe Uncontrolled Asthma; NCT03347279) trials. To examine the efficacy and safety of tezepelumab in additional clinically relevant subgroups using pooled data from PATHWAY and NAVIGATOR. PATHWAY and NAVIGATOR were randomized, double-blind, placebo-controlled trials with similar designs. This pooled analysis included patients with severe, uncontrolled asthma (PATHWAY, 18-75 years old; NAVIGATOR, 12-80 years old) who received tezepelumab 210 mg or placebo subcutaneously every 4 weeks for 52 weeks. The annualized asthma exacerbation rate over 52 weeks and secondary outcomes were calculated in the overall population and in subgroups defined by inflammatory biomarker levels or clinical characteristics. Overall, 1,334 patients were included (tezepelumab,  = 665; placebo,  = 669). Tezepelumab reduced the annualized asthma exacerbation rate versus placebo by 60% (rate ratio, 0.40 [95% confidence interval, 0.34-0.48]) in the overall population, and clinically meaningful reductions in exacerbations were observed in tezepelumab-treated patients with type 2-high and type 2-low disease by multiple definitions. Tezepelumab reduced exacerbation-related hospitalization or emergency department visits and improved secondary outcomes compared with placebo overall and across subgroups. The incidence of adverse events was similar between treatment groups. Tezepelumab resulted in clinically meaningful reductions in exacerbations and improvements in other outcomes in patients with severe, uncontrolled asthma, across clinically relevant subgroups. Clinical trials registered with www.clinicaltrials.gov (NCT02054130 [PATHWAY], NCT03347279 [NAVIGATOR]).

摘要

特泽鲁单抗可降低重度、未控制型哮喘患者的恶化率,无论基线血嗜酸性粒细胞计数和呼出气一氧化氮(FeNO)水平如何,也与过敏状态无关,这在 2b 期 PATHWAY(评估 MEDI9929[AMG157]在控制不佳的重度哮喘成人受试者中的疗效和安全性的研究;NCT02054130)和 3 期 NAVIGATOR(评估特泽鲁单抗在重度未控制型哮喘成人和青少年中的疗效;NCT03347279)试验中得到了证实。本研究旨在通过 PATHWAY 和 NAVIGATOR 的汇总数据,进一步评估特泽鲁单抗在其他临床相关亚组中的疗效和安全性。PATHWAY 和 NAVIGATOR 是两项随机、双盲、安慰剂对照试验,设计相似。本汇总分析纳入了接受特泽鲁单抗 210mg 或安慰剂皮下注射、每 4 周 1 次、治疗 52 周的重度、未控制型哮喘患者(PATHWAY:18-75 岁;NAVIGATOR:12-80 岁)。52 周时,计算年化哮喘恶化率和次要终点在总体人群及根据炎症生物标志物水平或临床特征定义的亚组中的情况。共有 1334 例患者入组(特泽鲁单抗组 n=665;安慰剂组 n=669)。与安慰剂组相比,特泽鲁单抗组患者的年化哮喘恶化率降低了 60%(率比为 0.40[95%置信区间,0.34-0.48]),且采用多种定义,均观察到特泽鲁单抗治疗的 2 型高和 2 型低疾病患者的哮喘恶化有临床意义的降低。与安慰剂相比,特泽鲁单抗组患者的哮喘恶化相关住院或急诊就诊减少,次要终点改善。两组治疗相关不良事件发生率相似。在不同的临床相关亚组中,特泽鲁单抗可降低重度、未控制型哮喘患者的哮喘恶化率,并改善其他结局。临床试验注册于 www.clinicaltrials.gov(NCT02054130[PATHWAY],NCT03347279[NAVIGATOR])。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cee/10870853/5f9b6ca3a739/rccm.202210-2005OCf1a.jpg

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