Cummings J, Fox N
Cleveland Clinic Lou Ruvo Center for Brain Health, Las Vegas, NV, USA.
Dementia Research Centre, Department of Neurodegenerative Disease, UCL Institute of Neurology, University College London, London, United Kingdom.
J Prev Alzheimers Dis. 2017;4(2):109-115. doi: 10.14283/jpad.2017.12. Epub 2017 Apr 25.
Disease-modifying therapies (DMTs) are urgently needed to treat the growing number of individuals with Alzheimer's disease (AD) or at immanent risk for AD. A definition of DMT is required to facilitate the process of DMT drug development.
This is a review of the state of the science with regard to definition and development of DMTs.
A DMT is as an intervention that produces an enduring change in the clinical progression of AD by interfering in the underlying pathophysiological mechanisms of the disease process that lead to cell death. Demonstration of DMT efficacy is garnered through clinical trial designs and biomarkers. Evidence of disease modification in the drug development process is based on trial designs such as staggered start and delayed withdrawal showing an enduring effect on disease course or on combined clinical outcomes and correlated biomarker evidence of an effect on the underlying pathophysiological processes of the disease. Analytic approaches such as showing change in slope of cognitive decline, increasing drug-placebo difference over time, and delay of disease milestones are not conclusive by themselves but support the presence of a disease modifying effect. Neuroprotection is a related concept whose demonstration depends on substantiating disease modification. No single type of evidence in itself is sufficient to prove disease modification - consistency, robustness, and variety of sources of data will all contribute to convincing stakeholders that an agent is a DMT.
DMT is defined by its enduring effect on processes leading to cell death. A variety of types of data can be used to support the hypothesis that disease modification has occurred.
迫切需要疾病修饰疗法(DMTs)来治疗越来越多的阿尔茨海默病(AD)患者或有AD潜在风险的个体。需要对DMT进行定义,以促进DMT药物的研发进程。
这是一篇关于DMT定义和研发的科学现状综述。
DMT是一种通过干扰导致细胞死亡的疾病进程的潜在病理生理机制,从而对AD临床进展产生持久改变的干预措施。DMT疗效通过临床试验设计和生物标志物来证明。药物研发过程中疾病修饰的证据基于交错启动和延迟撤药等试验设计,这些设计显示对病程有持久影响,或对综合临床结局以及与疾病潜在病理生理过程相关的生物标志物证据有影响。诸如显示认知衰退斜率变化、药物 - 安慰剂差异随时间增加以及疾病里程碑延迟等分析方法本身并不具有决定性,但支持疾病修饰作用的存在。神经保护是一个相关概念,其证明依赖于证实疾病修饰。没有单一类型的证据本身足以证明疾病修饰——数据的一致性、稳健性和多样性都将有助于使利益相关者相信一种药物是DMT。
DMT通过其对导致细胞死亡的过程的持久影响来定义。可以使用多种类型的数据来支持疾病修饰已经发生的假设。