Suppr超能文献

在临床试验中使用生物标志物和未来的发展,这将有助于识别新的生物标志物。

Use of biomarkers in clinical trials and future developments that will help identify novel biomarkers.

机构信息

Professor of Neurology, Queen Square MND Centre, Instute of Neurology, London, United Kingdom.

出版信息

Int Rev Neurobiol. 2024;176:171-207. doi: 10.1016/bs.irn.2024.04.010. Epub 2024 May 22.

Abstract

Engineering new solutions for therapeutic benefit in Amyotrophic Lateral Sclerosis (ALS) has proved a difficult task to accomplish. This is largely the reflection of complexities at multiple levels, that require solutions to improve cost-effectiveness and outcomes. The main obstacle related to the condition's clinical heterogeneity, chiefly the broad difference in survival observed among ALS patients, imposes large populations studies and long follow-up to evaluate any efficacy. The emerging solution is composite clinical and biological parameters enabling prognostic stratification into homogeneous phenotypes for more affordable studies. From a therapeutic development perspective, the choice of a medicinal product requires the availability of treatment-specific biomarkers of target engagement to identify off-target effects based on the compound's putative modality of action. More importantly, there are no established biomarkers of treatment response that can complement clinical outcome measures and support futility and end of treatment analyses of efficacy. Ultimately the onus rests on the development of biomarkers encompassing the unmet needs of clinical trial design, from inclusion to efficacy. These readouts of the pathological process may be used in combination with clinical and paraclinical outcome measured, significantly reducing the time and financial burden of clinical studies. Progress towards a biomarker-driven clinical trial design in ALS has been possible thanks to the accurate detection of neurofilaments and of other immunological mediators in biological fluids with the disease progression, a step change enabling the testing of novel therapeutic agents in a new clinical trial setting. However, further progress remains to be made to find treatment specific target engagement biomarkers along with readouts of treatment response that can be reliably applied to all emerging therapies and clinical studies. Here we will cover the basic notions of biomarker development in ALS clinical trials, the most crucial unanswered questions and the unmet needs in the ALS biomarkers space.

摘要

在肌萎缩侧索硬化症(ALS)中为治疗获益开发新的解决方案已被证明是一项艰巨的任务。这主要反映了多个层面的复杂性,需要解决方案来提高成本效益和结果。与该病症临床异质性相关的主要障碍,主要是 ALS 患者之间观察到的生存率存在广泛差异,需要进行大型人群研究和长期随访,以评估任何疗效。新兴的解决方案是综合临床和生物学参数,使预后分层为同质表型,以进行更具成本效益的研究。从治疗开发的角度来看,选择一种药物需要有治疗特异性的靶标结合生物标志物,以便根据化合物的假定作用模式来识别脱靶效应。更重要的是,目前还没有公认的治疗反应生物标志物,可以补充临床终点测量,并支持疗效的无效性和治疗结束分析。最终,需要开发涵盖临床试验设计从纳入到疗效各个方面未满足需求的生物标志物。这些病理过程的检测结果可与临床和临床前测量的结果结合使用,显著减少临床试验的时间和财务负担。由于在生物体液中能够准确检测到神经丝和其他免疫介质随疾病进展而发生的变化,因此在 ALS 中实现基于生物标志物的临床试验设计取得了进展,这是一个改变游戏规则的进展,使新型治疗剂能够在新的临床试验环境中进行测试。然而,仍需要进一步努力,以找到针对治疗的靶标结合生物标志物,以及可可靠应用于所有新兴疗法和临床研究的治疗反应检测结果。在这里,我们将介绍 ALS 临床试验中生物标志物开发的基本概念、最关键的未解答问题以及 ALS 生物标志物领域的未满足需求。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验