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用于评估 CAR T 细胞治疗疗效和变异性的随机框架。

A stochastic framework for evaluating CAR T cell therapy efficacy and variability.

机构信息

Department of Mathematical Sciences, New Mexico State University, Las Cruces, NM 88001, USA.

Institute for Modeling Collaboration and Innovation, University of Idaho, Moscow, ID 83844, USA.

出版信息

Math Biosci. 2024 Feb;368:109141. doi: 10.1016/j.mbs.2024.109141. Epub 2024 Jan 6.

Abstract

Based on a deterministic and stochastic process hybrid model, we use white noises to account for patient variabilities in treatment outcomes, use a hyperparameter to represent patient heterogeneity in a cohort, and construct a stochastic model in terms of Ito stochastic differential equations for testing the efficacy of three different treatment protocols in CAR T cell therapy. The stochastic model has three ergodic invariant measures which correspond to three unstable equilibrium solutions of the deterministic system, while the ergodic invariant measures are attractors under some conditions for tumor growth. As the stable dynamics of the stochastic system reflects long-term outcomes of the therapy, the transient dynamics provide chances of cure in short-term. Two stopping times, the time to cure and time to progress, allow us to conduct numerical simulations with three different protocols of CAR T cell treatment through the transient dynamics of the stochastic model. The probability distributions of the time to cure and time to progress present outcome details of different protocols, which are significant for current clinical study of CAR T cell therapy.

摘要

基于确定性和随机过程混合模型,我们使用白噪声来解释治疗结果中患者的变异性,使用超参数来表示队列中患者的异质性,并根据 Ito 随机微分方程构建一个随机模型,以测试三种不同的 CAR T 细胞治疗方案的疗效。该随机模型有三个遍历不变测度,分别对应于确定性系统的三个不稳定平衡点,而遍历不变测度在某些肿瘤生长条件下是吸引子。由于随机系统的稳定动力学反映了治疗的长期结果,因此瞬态动力学为短期的治愈机会提供了可能。两个停止时间,即治愈时间和进展时间,允许我们通过随机模型的瞬态动力学对三种不同的 CAR T 细胞治疗方案进行数值模拟。治愈时间和进展时间的概率分布呈现了不同方案的结果细节,这对于当前的 CAR T 细胞治疗临床研究具有重要意义。

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