Wal-yan Respiratory Research Centre, Telethon Kids Institute, University of Western Australia, Nedlands, Australia.
Department of Respiratory and Sleep Medicine, Perth Children's Hospital, Nedlands, Australia.
Trials. 2023 Mar 22;24(1):211. doi: 10.1186/s13063-023-07076-8.
Cystic fibrosis (CF) is a rare, inherited, life-limiting condition predominantly affecting the lungs, for which there is no cure. The disease is characterized by recurrent pulmonary exacerbations (PEx), which are thought to drive progressive lung damage. Management of these episodes is complex and generally involves multiple interventions targeting different aspects of disease. The emergence of innovative trials and use of Bayesian statistical methods has created renewed opportunities for studying heterogeneous populations in rare diseases. Here, we present the protocol for the BEAT CF PEx cohort, a prospective, multi-site, perpetual, platform enrolling adults and children with CF. The BEAT CF PEx cohort will be used to evaluate the comparative effectiveness of interventions for the treatment of PEx requiring intensive therapy (PERITs), with a primary focus on short-term improvements in lung function. This will be achieved through the conduct of cohort-nested studies, including adaptive clinical trials, within the BEAT CF PEx cohort. This protocol will outline key features of the BEAT CF PEx cohort, including the design, implementation, data collection and management, governance and analysis, and dissemination of results.
This platform will be conducted across multiple sites, commencing with CF treatment centers in Australia. People of all ages with a clinical diagnosis of CF will be eligible to participate, except those who have previously received a lung transplant. Data including demographic and clinical information, treatment details, and outcomes (including safety, microbiology, and patient-reported outcome measures including quality of life scores) will be systematically collected and securely stored via a digital centralized trial management system (CTMS). The primary endpoint is the absolute change in the percentage predicted forced expiratory volume in 1 s (ppFEV) from the commencement of intensive therapy to 7 to 10 days afterwards.
The BEAT CF PEx cohort will report clinical, treatment, and outcome data for PEx among people with CF and is intended to serve as a core (master) protocol for future nested, interventional trials evaluating treatment(s) for these episodes. The protocols for nested sub-studies are beyond the scope of this document and will be reported separately.
ANZCTR BEAT CF Platform - ACTRN12621000638831. Registration date: Sept. 26, 2022.
囊性纤维化(CF)是一种罕见的、遗传性的、危及生命的疾病,主要影响肺部,目前尚无治愈方法。该疾病的特征是反复发生的肺部恶化(PEx),据认为这些恶化会导致肺部进行性损伤。这些发作的管理非常复杂,通常需要针对疾病的不同方面进行多种干预。创新试验的出现和贝叶斯统计方法的使用为研究罕见疾病中的异质人群提供了新的机会。在这里,我们介绍了 BEAT CF PEx 队列的方案,这是一个前瞻性、多站点、永久性的平台,招募患有 CF 的成人和儿童。BEAT CF PEx 队列将用于评估需要强化治疗(PERITs)的 PEx 治疗干预措施的相对有效性,主要关注短期肺功能改善。这将通过在 BEAT CF PEx 队列中进行队列嵌套研究来实现,包括适应性临床试验。本方案将概述 BEAT CF PEx 队列的关键特征,包括设计、实施、数据收集和管理、治理和分析以及结果的传播。
该平台将在多个站点进行,首先在澳大利亚的 CF 治疗中心进行。所有年龄段的临床诊断为 CF 的人都有资格参加,除非他们之前接受过肺移植。数据包括人口统计学和临床信息、治疗细节和结果(包括安全性、微生物学和患者报告的结果测量,包括生活质量评分)将通过数字集中式试验管理系统(CTMS)系统地收集和安全存储。主要终点是从强化治疗开始到 7 至 10 天后预测的 1 秒用力呼气量(ppFEV)的绝对值变化。
BEAT CF PEx 队列将报告 CF 人群中 PEx 的临床、治疗和结果数据,旨在作为未来评估这些发作治疗的嵌套干预试验的核心(主)方案。嵌套子研究的方案超出了本文的范围,将单独报告。
ANZCTR BEAT CF 平台-ACTRN12621000638831。注册日期:2022 年 9 月 26 日。