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在阿尔茨海默病的自然病程背景下,淀粉样蛋白靶向疗法的长期疗效情景。

Scenarios for the long-term efficacy of amyloid-targeting therapies in the context of the natural history of Alzheimer's disease.

机构信息

Eli Lilly and Company, Indianapolis, Indiana, USA.

Clinical Memory Research Unit, Department of Clinical Sciences, Lund University, Lund, Sweden.

出版信息

Alzheimers Dement. 2024 Sep;20(9):6374-6383. doi: 10.1002/alz.14134. Epub 2024 Jul 29.

DOI:10.1002/alz.14134
PMID:39073291
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11497713/
Abstract

INTRODUCTION

Recent clinical trials of amyloid beta (Aβ)-targeting therapies in Alzheimer's disease (AD) have demonstrated a clinical benefit over 18 months, but their long-term impact on disease trajectory is not yet understood. We propose a framework for evaluating realistic long-term scenarios.

METHODS

Results from recent phase 3 trials of Aβ-targeting antibodies were integrated with an estimate of the long-term patient-level natural history trajectory of the Clinical Dementia Rating-Sum of Boxes (CDR-SB) score to explore realistic long-term efficacy scenarios.

RESULTS

Three distinct long-term efficacy scenarios were examined, ranging from conservative to optimistic. These extrapolations of positive phase 3 trials suggested treatments delayed onset of severe dementia by 0.3 to 0.6 years (conservative), 1.1 to 1.9 years (intermediate), and 2.0 to 4.2 years (optimistic).

DISCUSSION

Our study provides a common language for long-term impact of disease-modifying treatments. Our work calls for studies with longer follow-up and results from early intervention trials to provide a comprehensive assessment of these therapies' true long-term impact.

HIGHLIGHTS

We present long-term scenarios of the efficacy of AD therapies. In this framework, scenarios are defined relative to the natural history of AD. Long-term projections with different levels of optimism can be compared. It provides a common language for expressing beliefs about long-term efficacy.

摘要

简介

最近在阿尔茨海默病(AD)中进行的淀粉样蛋白 β(Aβ)靶向治疗的临床试验表明,在 18 个月以上具有临床获益,但它们对疾病轨迹的长期影响尚不清楚。我们提出了一个评估现实长期情况的框架。

方法

整合了最近的 Aβ靶向抗体的 3 期临床试验的结果,并根据临床痴呆评定量表总和评分(CDR-SB)的长期患者水平自然史轨迹的估计,探讨了现实的长期疗效情景。

结果

检查了三种不同的长期疗效情景,从保守到乐观。这些对 3 期阳性试验的推断表明,治疗可将严重痴呆的发病时间延迟 0.3 至 0.6 年(保守),1.1 至 1.9 年(中等)和 2.0 至 4.2 年(乐观)。

讨论

我们的研究为疾病修饰治疗的长期影响提供了共同的语言。我们的工作呼吁进行更长时间随访的研究,并从早期干预试验中获得结果,以全面评估这些疗法的真实长期影响。

重点

我们提出了 AD 治疗疗效的长期情景。在这个框架中,情景是相对于 AD 的自然史来定义的。可以比较不同乐观程度的长期预测。它为表达对长期疗效的信念提供了共同的语言。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/969e/11497713/f4398cb3ae26/ALZ-20-6374-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/969e/11497713/7613740c28e1/ALZ-20-6374-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/969e/11497713/53f7c84ac113/ALZ-20-6374-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/969e/11497713/f4398cb3ae26/ALZ-20-6374-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/969e/11497713/7613740c28e1/ALZ-20-6374-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/969e/11497713/53f7c84ac113/ALZ-20-6374-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/969e/11497713/f4398cb3ae26/ALZ-20-6374-g003.jpg

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