Jones Leslie Braziel, Secomb Timothy W, Dewhirst Mark W, El-Kareh Ardith W
Department of Mathematics, University of Arizona, Tucson, AZ, USA.
Department of Physiology, University of Arizona, Tucson, AZ, USA.
J Theor Biol. 2014 Sep 21;357:10-20. doi: 10.1016/j.jtbi.2014.04.032. Epub 2014 May 4.
Mathematical models to describe dose-dependent cellular responses to drug combinations are an essential component of computational simulations for predicting therapeutic responses. Here, a new model, the additive damage model, is introduced and tested in cases where varying concentrations of two drugs are applied with a fixed exposure schedule. In the model, cell survival is determined by whether cellular damage, which depends on the concentrations of the drugs, exceeds a lethal threshold, which varies randomly in the cell population with a prescribed statistical distribution. Cellular damage is assumed to be additive, and is expressed as a sum of separate terms for each drug. Each term has a saturable dependence on drug concentration. The model has appropriate behavior over the entire range of drug concentrations, and is predictive, given single-agent dose-response data for each drug. The proposed model is compared with several other models, by testing their ability to fit 24 data sets for platinum-taxane combinations and 21 data sets for various other combinations. The Akaike Information Criterion is used to assess goodness of fit, taking into account the number of unknown parameters in each model. Overall, the additive damage model provides a better fit to the data sets than any previous model. The proposed model provides a basis for computational simulations of therapeutic responses. It predicts responses to drug combinations based on data for each drug acting as a single agent, and can be used as an improved null reference model for assessing synergy in the action of drug combinations.
描述细胞对药物组合剂量依赖性反应的数学模型是预测治疗反应的计算模拟的重要组成部分。在此,引入了一种新模型——累加损伤模型,并在以固定暴露方案应用两种药物不同浓度的情况下进行了测试。在该模型中,细胞存活取决于细胞损伤是否超过致死阈值,细胞损伤取决于药物浓度,而致死阈值在细胞群体中以规定的统计分布随机变化。假定细胞损伤是累加性的,并表示为每种药物单独项的总和。每个项对药物浓度具有饱和依赖性。该模型在整个药物浓度范围内具有适当的行为,并且在给出每种药物的单药剂量反应数据时具有预测性。通过测试它们拟合24个铂类-紫杉烷组合数据集和21个其他各种组合数据集的能力,将所提出的模型与其他几个模型进行了比较。使用赤池信息准则来评估拟合优度,同时考虑每个模型中未知参数数量。总体而言,累加损伤模型比以往任何模型都能更好地拟合数据集。所提出的模型为治疗反应的计算模拟提供了基础。它基于每种药物作为单一药物的数据预测对药物组合的反应,并且可以用作评估药物组合作用中协同作用的改进零参考模型。