将多态模型与临床试验数据相结合,加深对复杂疾病过程的理解。

IF 2.2 3区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL Clinical Trials Pub Date : 2024-10-01 Epub Date: 2024-08-02 DOI:10.1177/17407745241267862
Terry M Therneau, Fang-Shu Ou
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引用次数: 0

摘要

临床试验是所有参与人员的一项重大承诺,也是一项巨大的财务义务,因为其成本高昂;因此,通过尽可能多的学习来充分利用所有收集到的数据是明智之举。多态模型是描述纵向事件的通用框架;多态危险模型可将多个中间/最终临床终点作为结果,并同时估计协变量的影响。比例危险模型是拟合模型(每个转变一个),可用于计算绝对风险,即在给定时间内处于某一状态的概率、进入某一状态的预期次数以及在某一状态下花费的预期时间。为了展示多态危险模型的实用性,我们使用了 R 生存软件包中三个公开的临床试验数据集:结肠、骨髓和 rhDNase。结肠数据集是一个非常著名且使用广泛的数据集,在该数据集中,我们发现左旋咪唑+氟尿嘧啶治疗延长了无复发状态的时间,超过了延长总生存期的时间,从而减少了复发状态的时间,这就是典型的 "压缩发病率 "的例子。在骨髓数据集中,我们发现完全应答(CR)是持久的,接受 B 治疗的患者比接受 A 治疗的患者在 CR 状态下的停留时间更长,而突变状态并不影响向 CR 的转变率,但对 CR 状态下的停留时间有很大影响。我们还发现,接受治疗 A 的更多患者在没有 CR 的情况下接受了移植,而接受治疗 B 的更多患者在 CR 后接受了移植。此外,突变状态对 CR 到移植的转换率也有很大影响。如果没有多态模型,我们就不可能对这三个数据集进行观察。我们鼓励读者花更多时间深入研究临床试验数据。只要我们统计学家愿意去寻找,它就能提供比简单的 "是/否 "答案更多的信息。
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Using multistate models with clinical trial data for a deeper understanding of complex disease processes.

A clinical trial represents a large commitment from all individuals involved and a huge financial obligation given its high cost; therefore, it is wise to make the most of all collected data by learning as much as possible. A multistate model is a generalized framework to describe longitudinal events; multistate hazards models can treat multiple intermediate/final clinical endpoints as outcomes and estimate the impact of covariates simultaneously. Proportional hazards models are fitted (one per transition), which can be used to calculate the absolute risks, that is, the probability of being in a state at a given time, the expected number of visits to a state, and the expected amount of time spent in a state. Three publicly available clinical trial datasets, colon, myeloid, and rhDNase, in the survival package in R were used to showcase the utility of multistate hazards models. In the colon dataset, a very well-known and well-used dataset, we found that the levamisole+fluorouracil treatment extended time in the recurrence-free state more than it extended overall survival, which resulted in less time in the recurrence state, an example of the classic "compression of morbidity." In the myeloid dataset, we found that complete response (CR) is durable, patients who received treatment B have longer sojourn time in CR than patients who received treatment A, while the mutation status does not impact the transition rate to CR but is highly influential on the sojourn time in CR. We also found that more patients in treatment A received transplants without CR, and more patients in treatment B received transplants after CR. In addition, the mutation status is highly influential on the CR to transplant transition rate. The observations that we made on these three datasets would not be possible without multistate models. We want to encourage readers to spend more time to look deeper into clinical trial data. It has a lot more to offer than a simple yes/no answer if only we, the statisticians, are willing to look for it.

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来源期刊
Clinical Trials
Clinical Trials 医学-医学:研究与实验
CiteScore
4.10
自引率
3.70%
发文量
82
审稿时长
6-12 weeks
期刊介绍: Clinical Trials is dedicated to advancing knowledge on the design and conduct of clinical trials related research methodologies. Covering the design, conduct, analysis, synthesis and evaluation of key methodologies, the journal remains on the cusp of the latest topics, including ethics, regulation and policy impact.
期刊最新文献
Challenges in conducting efficacy trials for new COVID-19 vaccines in developed countries. Society for Clinical Trials Data Monitoring Committee initiative website: Closing the gap. A comparison of computational algorithms for the Bayesian analysis of clinical trials. Comparison of Bayesian and frequentist monitoring boundaries motivated by the Multiplatform Randomized Clinical Trial. Efficient designs for three-sequence stepped wedge trials with continuous recruitment.
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