在临床试验中,我们可以使用血液生物标志物作为入场标准和监测药物治疗效果吗? 欧盟/美国CTAD特别工作组的报告
D Angioni1, O Hansson, R J Bateman
1D. Angioni, Gerontopole of Toulouse, Alzheimer's Disease Research and Clinical Center, Toulouse University Hospital, Toulouse, France, angioni.da@chu-toulouse.fr.
The journal of prevention of Alzheimer's disease
|June 25, 2023
概括
基于血液的标记物 (BBM) 对阿尔茨海默病 (AD) 临床试验有希望,可能取代昂贵的CSF和PET扫描. 需要进一步的研究来证实它们的可靠性,以便用于试验入门和监测.
科学领域:
- 神经学 神经学
- 生物标志物研究 生物标志物研究
- 临床试验设计 临床试验设计
背景情况:
- 目前阿尔茨海默病 (AD) 临床试验依赖于脑脊液 (CSF) 和正子发射断层扫描 (PET) 生物标志物.
- 这些方法资源密集,增加了成本,并限制了参与者在AD试验中的招生.
研究的目的:
- 评估血液基标记物 (BBM) 作为AD临床试验中CSF和PET生物标记物的替代品的潜力.
- 评估BBMs是否可以减少研究志愿者的负担,并简化试验流程.
主要方法:
- 对用于AD检测和监测的血生物标志物的现有数据的审查.
- 在随机临床试验 (RCT) 中使用BBM的可行性分析.
主要成果:
- 与CSF和PET生物标志物相比,基于血液的标志物 (BBM) 提供了一种资源密集度较低的方法.
- BBM可能会提高AD临床试验的效率和可访问性.
结论:
- 血生物标志物对提高ADRCT的设计和执行具有显著的前景.
- 需要进一步验证,以确定BBM是否可以完全取代已建立的CSF和PET生物标志物,用于试验标准和监测.
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