在 2B 期随机对照试验 AMBAR 中使用潜伏生长混合模型对阿尔茨海默病的认知疗效进行事后评估。

Nicolai D Ayasse, Walter F Stewart, Richard B Lipton, David Gomez-Ulloa, M Chris Runken
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引用次数: 0

摘要

背景:阿尔茨海默氏痴呆症(AD)的疾病进展通常表现为认知和功能的加速衰退:阿尔茨海默氏痴呆症(AD)的疾病进展通常以认知和功能的加速衰退为特征,其中的异质性轨迹可能会影响观察到的治疗反应:我们假设,未观察到的异质性可能会掩盖阿尔茨海默氏症的治疗效果。我们在阿尔茨海默病白蛋白替代治疗(AMBAR)2b 期试验数据中对未观察到的异质性的影响进行了经验量化。在最初拟合治疗组的 2 类潜在增长混合模型中,对 ADAS-Cog 12 认知终点进行了重新分析。然后将拟合效果最好的模型应用于两个治疗组,并应用于一个更大的(n=1000)模拟数据集,该数据集代表了 AMBAR 试验的认知数据:观察到两类患者:一类认知轨迹稳定,另一类高度多变。将后者(48 人,22%)从分析中剔除,并重新拟合疗效模型,将稳定型患者与完全安慰剂患者进行比较,结果显示认知疗效显著(P=0.007,Cohen's D=-0.4)。在模拟数据集中比较各治疗组的稳定类药物,发现疗效有显著差异,模拟稳定类药物的治疗效果更佳:这项事后探索性分析表明,解决未观察到的异质性的预设策略可能会改善AD试验中的效应检测。该分析策略的推广性受到仅治疗组潜在分层的限制,因为 AMBAR 中的安慰剂组规模较小。模拟建模部分解决了这一局限性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Post-Hoc Assessment of Cognitive Efficacy in Alzheimer's Disease Using a Latent Growth Mixture Model in AMBAR, a Phase 2B Randomized Controlled Trial.

Background: Disease progression in Alzheimer's Dementia (AD) is typically characterized by accelerated cognitive and functional decline, where heterogeneous trajectories can impact the observed treatment response.

Methods: We hypothesized that unobserved heterogeneity could obscure treatment benefits in AD. The effect of unobserved heterogeneity was empirically quantified within the Alzheimer's Management By Albumin Replacement (AMBAR) phase 2b trial data. The ADAS-Cog 12 cognition endpoint was reanalyzed in a 2-class latent growth mixture model initially fit to the treatment arm. The model with the best fit was then applied across both treatment arms to a larger (n=1000) simulated dataset that was representative of AMBAR trial cognitive data.

Results: Two classes of patients were observed: a stable cognitive trajectory class and a highly variable class. Removal of the latter (n=48, 22%) from the analysis and refitting efficacy models comparing the stable class to full placebo yielded significant treatment efficacy on cognition (p=0.007, Cohen's D=-0.4). Comparison of the stable class of each arm within the simulated dataset revealed a significant difference in treatment efficacy favoring the simulated stable treatment arm.

Conclusion: This post hoc exploratory analysis suggests that prespecified strategies for addressing unobserved heterogeneity may yield improved effect detection in AD trials. The generalizability of the analytic strategy is limited by latent stratification in only the treatment arm, a requirement given the small placebo arm in AMBAR. This limitation was partially addressed by the simulation modeling.

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