首页> 外文期刊>Journal of Asthma and Allergy >Onset of Effect, Changes in Airflow Obstruction and Lung Volume, and Health-Related Quality of Life Improvements with Benralizumab for Patients with Severe Eosinophilic Asthma: Phase IIIb Randomized, Controlled Trial (SOLANA)
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Onset of Effect, Changes in Airflow Obstruction and Lung Volume, and Health-Related Quality of Life Improvements with Benralizumab for Patients with Severe Eosinophilic Asthma: Phase IIIb Randomized, Controlled Trial (SOLANA)

机译:效果,气流梗阻和肺部变化的变化,以及与Benralizumab对患有严重嗜酸性哮喘的患者的健康有关的生活质量改善:IIIB阶段随机,受控试验(索兰)

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Objective: In the SOLANA trial, we sought to physiologically characterize benralizumab’s onset of effect and maintenance of that effect for patients with severe eosinophilic asthma. Methods: SOLANA (NCT02869438) was a multicenter, randomized, double-blind, parallel-group, placebo-controlled, Phase IIIb study conducted at 49 centers in six countries (Chile, Germany, Hungary, the Philippines, South Korea, and the United States). Eligible patients with baseline blood eosinophil counts ≥ 300 cells/μL were randomized to subcutaneous benralizumab (30 mg) or placebo administered at Days 0, 28, and 56. The primary endpoint was the average change from baseline in prebronchodilator forced expiratory volume in 1 s (pre-BD FEVsub1/sub) during the Day 28?Day 84 period for benralizumab vs placebo. Secondary endpoints included patient-reported outcomes (PROs). A subset of patients participated in a whole-body plethysmography substudy. Safety was also assessed. Results: In total, 233 patients were randomized to benralizumab (n=118) or placebo (n=115). Improvement from baseline in pre-BD FEVsub1/sub with benralizumab 30 mg was not statistically significant compared with placebo (least-squares mean change difference [95% confidence interval] 57 mL [? 22 to 135]; p=0.16). Compared with placebo, benralizumab demonstrated early (Day 7) nonstatistically significant improvements in whole-body plethysmography assessments of hyperinflation and clinically meaningful improvements in PRO measures (Asthma Control Questionnaire 6 at Day 14 and St. George’s Respiratory Questionnaire at Day 28), which were maintained over the treatment period. Benralizumab’s safety profile was commensurate with previously reported studies. Conclusion: The observed early changes in lung volume despite relatively small improvements in airflow obstruction suggest that the anti-inflammatory effect of benralizumab may be manifested as deflation over time for patients with hyperinflation, who potentially have a greater degree of airway remodeling. This early effect could partially explain the rapid PRO improvements observed for certain patients.
机译:目的:在索拉纳审判中,我们试图在生理学上表征Benralizumab对患有严重嗜酸性哮喘患者的效果和维持这种效果。方法:Solana(NCT02869438)是多中心,随机,双盲,并行组,安慰剂控制,在六个国家的49个中心(智利,德国,匈牙利,菲律宾,韩国和曼联的49个中心)状态)。符合基线血液粒细胞计数≥300个细胞/μl的符合条件的患者被随机化为皮下来的Benralizumab(30mg)或安慰剂在0,28和56天施用。初级终点是从伯伯丙酮的基线中的平均变化在1 s中的呼气呼气量(BD FEV 1 )在第28天?Benralizumab VS安慰剂的第84天。次要终点包括患者报告的结果(专业人士)。患者的一部分患者参与了全身体积描绘血小杂化。还评估了安全性。结果:总共233名患者随机分配给Benralizumab(n = 118)或安慰剂(n = 115)。与BDE-Hev 1 中的基线改善30mg与安慰剂(最小二乘性变化差[95%置信区间] 57ml [22至135]; p = 0.16)。与安慰剂相比,Benralizumab早期(第7天)在Pro措施中的流血性和临床有意义的改进的全身体积描记评估(第14天的哮喘控制问卷6和第28天的呼吸问卷调查问卷)的临床有意义的改善保持在治疗期间。 Benralizumab的安全性曲线与先前报告的研究相称。结论:由于气流阻塞的改善,观察到肺卷的早期变化表明,对于流过敏患者,北中腺素的抗炎作用可能表现为随着时间的推移,潜在的气道改造患者。这种早期效果可以部分解释某些患者观察到的快速亲改进。

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