Patient-advocate-led global coalition adapting fit-for-purpose outcomes measures to assure meaningful inclusion of DEEs in clinical trials.

Therapeutic advances in rare disease Pub Date : 2024-06-22 eCollection Date: 2024-01-01 DOI:10.1177/26330040241249762
JayEtta Hecker, Gabrielle Conecker, Chere Chapman, Rebecca Hommer, Natasha N Ludwig, Gunes Sevinc, Sara Te, Mary Wojnaroski, Jenny Downs, Anne T Berg
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Abstract

Existing clinical tools that measure non-seizure outcomes lack the range and granularity needed to capture skills in developmental and epileptic encephalopathy (DEE)-affected individuals who also fall in the severe to profound range of intellectual disability. This effectively excludes those with severe impairments from clinical trials, impeding the ability of sponsors to evaluate disease-modifying therapies (DMTs). The Inchstone Project, an international, patient advocate-led collaboration, brings together leading researchers, clinicians, pharmaceutical companies, and advocates to develop an adapted, validated assessment battery within 5 years. The goal is to support trials of DMTs for the DEEs by providing sufficiently sensitive measurement tools to demonstrate therapeutic efficacy. An initial pilot study administered 7 established assessments to 10 individuals affected by SCN2A-DEE, identifying specific limitations of existing measures and areas for improvement. It was clear that most tools do not account for challenges throughout the DEE population, including vision impairments, significant motor impairments and profound intellectual disability, which need to be accounted for in creating a 'fit-for-purpose' battery for the DEE population. Several novel assessments, including two measures of responsivity developed for use in monitoring recovery after acquired brain injury as well as individualized Goal Attainment Scaling, showed promise in this group. The team also completed a DEE-wide survey with over 270 caregivers documenting their children's abilities and priorities for their improvement from new treatments. The Inchstone team is using this information to evaluate how existing tools might be updated to better capture what is most important to families and measure their child's small but important improvements over time. These efforts are building a coherent picture across multiple DEEs of what domains, or concepts of interest, have the greatest impact on most patients and families. The Inchstone team is on course to adapt non-seizure outcome measures that are (1) sufficiently sensitive to measure small increments of meaningful change ('Inchstones') and (2) applicable to multiple DEE conditions.

由患者倡导者领导的全球联盟调整适合目的的结果衡量标准,以确保将 DEE 纳入临床试验。
测量非癫痫发作结果的现有临床工具缺乏所需的范围和粒度,无法捕捉发育性和癫痫性脑病 (DEE) 患者的技能,而这些患者也属于重度至极重度智障。这实际上将有严重障碍的人排除在临床试验之外,阻碍了申办者评估疾病改变疗法(DMT)的能力。Inchstone 项目是一项由患者权益倡导者主导的国际合作项目,它汇集了顶尖的研究人员、临床医生、制药公司和权益倡导者,旨在 5 年内开发出一套经过调整和验证的评估电池。其目标是通过提供足够灵敏的测量工具来证明疗效,从而支持针对 DEE 的 DMT 试验。最初的试点研究对 10 名 SCN2A-DEE 患者进行了 7 项既定评估,确定了现有测量方法的具体局限性和需要改进的地方。很明显,大多数工具都没有考虑到整个 DEE 群体所面临的挑战,包括视力障碍、严重的运动障碍和严重的智力障碍。几种新的评估方法,包括两种用于监测后天性脑损伤后恢复情况的反应性测量方法以及个性化目标达成量表,在该群体中显示出了良好的前景。该团队还完成了一项针对整个 DEE 的调查,270 多名护理人员参与了调查,记录了他们孩子的能力以及通过新疗法改善他们能力的优先事项。Inchstone 团队正在利用这些信息评估如何更新现有工具,以便更好地捕捉对家庭来说最重要的内容,并衡量他们的孩子随着时间的推移所取得的微小但重要的进步。这些努力正在多个 DEE 之间建立起一幅连贯的图景,说明哪些领域或感兴趣的概念对大多数患者和家庭的影响最大。英克斯通团队正在调整非癫痫发作结果测量方法,这些方法(1)具有足够的灵敏度,能够测量有意义的微小变化("英克斯通");(2)适用于多种 DEE 条件。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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