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贝叶斯建模和模拟在罕见病药物开发早期决策中的应用:以杜氏肌营养不良症为例。

Bayesian modeling and simulation to inform rare disease drug development early decision-making: Application to Duchenne muscular dystrophy.

机构信息

Biomedical Engineering, University of Connecticut, Storrs, Connecticut, United States of America.

Metrum Research Group, Tariffville, Connecticut, United States of America.

出版信息

PLoS One. 2022 Apr 28;17(4):e0247286. doi: 10.1371/journal.pone.0247286. eCollection 2022.

Abstract

Rare disease clinical trials are constrained to small sample sizes and may lack placebo-control, leading to challenges in drug development. This paper proposes a Bayesian model-based framework for early go/no-go decision making in rare disease drug development, using Duchenne muscular dystrophy (DMD) as an example. Early go/no-go decisions were based on projections of long-term functional outcomes from a Bayesian model-based analysis of short-term trial data informed by prior knowledge based on 6MWT natural history literature data in DMD patients. Frequentist hypothesis tests were also applied as a reference analysis method. A number of combinations of hypothetical trial designs, drug effects and cohort comparison methods were assessed. The proposed Bayesian model-based framework was superior to the frequentist method for making go/no-go decisions across all trial designs and cohort comparison methods in DMD. The average decision accuracy rates across all trial designs for the Bayesian and frequentist analysis methods were 45.8 and 8.98%, respectively. A decision accuracy rate of at least 50% was achieved for 42 and 7% of the trial designs under the Bayesian and frequentist analysis methods, respectively. The frequentist method was limited to the short-term trial data only, while the Bayesian methods were informed with both the short-term data and prior information. The specific results of the DMD case study were limited due to incomplete specification of individual-specific covariates in the natural history literature data and should be reevaluated using a full natural history dataset. These limitations aside, the framework presented provides a proof of concept for the utility of Bayesian model-based methods for decision making in rare disease trials.

摘要

罕见病临床试验受到样本量小和缺乏安慰剂对照的限制,这给药物开发带来了挑战。本文以杜氏肌营养不良症(DMD)为例,提出了一种基于贝叶斯模型的罕见病药物开发早期决策方法,该方法基于对短期试验数据的贝叶斯模型分析,利用了来自 DMD 患者 6MWT 自然史文献数据的先验知识,进行长期功能结果的预测。还应用了频率主义假设检验作为参考分析方法。评估了多种假设性试验设计、药物效果和队列比较方法的组合。在 DMD 中,对于所有试验设计和队列比较方法,所提出的基于贝叶斯模型的框架在进行 Go/No-Go 决策方面优于频率主义方法。对于所有试验设计,贝叶斯和频率主义分析方法的平均决策准确率分别为 45.8%和 8.98%。在贝叶斯和频率主义分析方法下,分别有 42%和 7%的试验设计可以实现至少 50%的决策准确率。频率主义方法仅限于短期试验数据,而贝叶斯方法则利用短期数据和先验信息进行信息补充。由于自然史文献数据中个体特异性协变量的说明不完整,DMD 案例研究的具体结果受到限制,应使用完整的自然史数据集重新评估。尽管存在这些局限性,但所提出的框架为基于贝叶斯模型的方法在罕见病试验中的决策提供了概念验证。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dc5/9049549/e17b0955e77e/pone.0247286.g001.jpg

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本文引用的文献

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