Royal Brompton & Harefield NHS Foundation Trust, London, United Kingdom; National Heart and Lung Institute, Imperial College London, United Kingdom.
Translational Medicine, Hospital for Sick Children, Toronto, Canada.
J Cyst Fibros. 2020 Jul;19(4):602-607. doi: 10.1016/j.jcf.2019.11.006. Epub 2019 Nov 24.
The lung clearance index (LCI), derived from the Multiple Breath Washout (MBW) test, is sensitive to treatment effects and compared with spirometry has higher feasibility in younger children and requires smaller sample sizes. As a result, the LCI has been endorsed by the European CF Society Clinical Trials Network for use as a primary outcome measure in CF clinical trials.
Here we describe the implementation of standardised protocols for MBW test performance, data collection and quality control to successfully incorporate LCI as a novel outcome measure in a large multicentre phase III clinical trial.
Three regional (North America (NA), Europe (EU), Australia (AUS)) central over-reading centres (CORC) were established to provide a collaborative platform for MBW training, certification and quality control of data. One hundred and thirty-two naïve operators from 53 sites across NA, EU and AUS were successfully trained and certified to perform MBW testing. Incorporation of a re-screening opportunity in the study protocol resulted a final screening feasibility rate of 93%, success remained high throughout the study resulting in an overall feasibility of MBW study data of 88.1% (1107/1257). MBW test acceptability was similar between geographical regions: NA (88%), EU (89%) and AUS (89%).
With this approach we achieved high MBW test feasibility and sustained collection of good quality data, demonstrating the utility of LCI as an effective primary endpoint in the first international phase III clinical trial to report LCI as the primary outcome.
从多呼吸测洗(MBW)试验中得出的肺清除指数(LCI)对治疗效果敏感,与肺活量测定法相比,在年幼儿童中具有更高的可行性,且所需样本量更小。因此,LCI 已被欧洲 CF 学会临床试验网络认可,可作为 CF 临床试验中的主要结局指标。
本文描述了实施 MBW 试验性能、数据收集和质量控制标准化方案,以成功地将 LCI 作为一种新的结局指标纳入一项大型多中心 III 期临床试验。
设立了三个区域(北美(NA)、欧洲(EU)、澳大利亚(AUS))中央审核中心(CORC),为 MBW 培训、认证和数据质量控制提供了协作平台。来自 NA、EU 和 AUS 53 个站点的 132 名新手操作人员成功接受了培训和认证,可进行 MBW 测试。在研究方案中纳入了重新筛选机会,最终的筛选可行性率为 93%,整个研究过程中成功率一直很高,导致 MBW 研究数据的总体可行性为 88.1%(1107/1257)。MBW 测试的可接受性在地理区域之间相似:NA(88%)、EU(89%)和 AUS(89%)。
通过这种方法,我们实现了高 MBW 测试可行性和高质量数据的持续收集,证明了 LCI 作为首个报告 LCI 为主要结局的国际 III 期临床试验的有效主要终点的实用性。