School and Chair of Allergology and Clinical Immunology, Department of Emergency and Organ Transplantation, University of Bari - Aldo Moro, Italy.
Department of Medical and Surgical Sciences, University of Foggia, Italy.
Pulm Pharmacol Ther. 2020 Oct;64:101974. doi: 10.1016/j.pupt.2020.101974. Epub 2020 Nov 1.
In the last decade, an increasing number of randomized controlled trials (RCTs) on biologic therapy in patients with severe asthma have included patient-reported outcomes (PROs) as secondary efficacy measures. The majority of these RCTs showed a benefit in symptoms and quality of life. However, the magnitude of this benefit remains uncertain, because it rarely exceeded the minimal important difference (MID), owing to a significant improvement in the control group (placebo effect). Real-life studies on biologic therapies assessing PRO are scarce. They may support and integrate RCT results through their different experimental design. This real-life retrospective study provides data on 15 patients with difficult-to-treat severe eosinophilic asthma treated with benralizumab up to 6 months. Asthma quality of life questionnaire (AQLQ) and asthma control test (ACT) were assessed and administered at each visit to minimize the Hawthorne effect. Changes in general accepted efficacy measures, such as forced expiratory volume in 1 s (FEV), peak expiratory flux (PEF), exacerbation rate and blood eosinophils, from baseline were also assessed. AQLQ and ACT improved from 3.9 ± 0.4 to 5.2 ± 0.4 and from 15.6 ± 5.7 to 18.1 ± 5.6, respectively. FEV increased of about 250 ml (+14%). PEF increased from 288 ± 107 to 333 ± 133 l/min. The number of exacerbations requiring OCS courses decreased from 2.8 ± 2.2 to 0.5 ± 0.8. Eosinophil counts dropped to 25.6 ± 15 cells/microliter. In conclusion, most patients reported improvements in AQLQ and ACT greater than MID, suggesting that these outcome represent a sensitive tool in real-life effectiveness studies. Our approach reduced the limitations of transition questions and the Hawthorne effect, increasing findings reliability.
在过去十年中,越来越多的严重哮喘患者生物治疗的随机对照试验(RCT)将患者报告的结局(PRO)作为次要疗效指标。这些 RCT 中的大多数显示症状和生活质量都有改善。然而,由于对照组(安慰剂效应)的显著改善,这种获益的幅度仍不确定,因为它很少超过最小有意义差异(MID)。在生物治疗的真实生活研究中,评估 PRO 的研究很少。它们可能通过不同的实验设计支持和整合 RCT 结果。这项真实生活的回顾性研究提供了 15 名接受 benralizumab 治疗的难治性严重嗜酸性粒细胞性哮喘患者的治疗数据,最长可达 6 个月。每次就诊时都评估和管理哮喘生活质量问卷(AQLQ)和哮喘控制测试(ACT),以最大程度地减少霍桑效应。还评估了从基线开始的一般公认的疗效指标的变化,例如 1 秒用力呼气量(FEV)、呼气峰流速(PEF)、恶化率和血液嗜酸性粒细胞计数。AQLQ 和 ACT 分别从 3.9±0.4 改善到 5.2±0.4 和从 15.6±5.7 改善到 18.1±5.6。FEV 增加了约 250ml(+14%)。PEF 从 288±107 增加到 333±133 l/min。需要 OCS 疗程的恶化次数从 2.8±2.2 减少到 0.5±0.8。嗜酸性粒细胞计数下降到 25.6±15 细胞/μl。总之,大多数患者报告 AQLQ 和 ACT 的改善大于 MID,这表明这些结果在真实生活中的有效性研究中是一种敏感的工具。我们的方法减少了过渡问题和霍桑效应的限制,提高了发现的可靠性。