Foley Catherine, Mackey Michael C
Department of Mathematics and Centre for Nonlinear Dynamics, Mcgill University, 3655 Promenade Sir William Osler, Montreal, Quebec, Canada H3G 1Y6.
J Theor Biol. 2009 Mar 7;257(1):27-44. doi: 10.1016/j.jtbi.2008.09.043. Epub 2008 Nov 1.
Granulocyte-colony stimulating factor (G-CSF) is used clinically for treating chemotherapy-induced neutropenia (low neutrophil levels). Here we present a delay differential equation model for the regulation of neutrophil production that accounts for the effects of G-CSF. Using a combination of analysis and numerical simulations, we use this model to study the effects of delaying G-CSF treatment following chemotherapy for two recombinant forms of G-CSF (filgrastim and pegfilgrastim). We also examine the consequences of varying the duration of filgrastim treatment. We found that varying the starting day or the duration of G-CSF treatment can lead to different qualitative responses in the neutrophil count. These changes can be explained by the coexistence of two stable solutions in the mathematical model.
粒细胞集落刺激因子(G-CSF)在临床上用于治疗化疗引起的中性粒细胞减少症(中性粒细胞水平低)。在此,我们提出一个用于调节中性粒细胞生成的延迟微分方程模型,该模型考虑了G-CSF的作用。通过分析和数值模拟相结合的方法,我们使用这个模型来研究化疗后延迟使用两种重组形式的G-CSF(非格司亭和聚乙二醇化非格司亭)治疗的效果。我们还研究了改变非格司亭治疗持续时间的后果。我们发现,改变G-CSF治疗的起始日或持续时间会导致中性粒细胞计数出现不同的定性反应。这些变化可以通过数学模型中两个稳定解的共存来解释。