A minimal model of tumor growth with angiogenic inhibition using bevacizumab

D. Drexler, Johanna Sápi, L. Kovács
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引用次数: 22

Abstract

Modeling the tumor growth under angiogenic inhibition is an important step towards designing tumor treatment therapies based on mathematical tools. Our goal is to create a model for tumor growth that describes the underlying physiological processes adequately while being as simple as possible. We propose a second-order model containing linear terms and one bilinear term modeling the dynamics of tumor volume and inhibitor level, and work out the parametric identification process for the model. The parametric identification of the model is done using measurements from experiments on C57Bl/6 mice with C38 colon adenocarcinoma treated with bevacizumab. The control group of the mice received one injection at the beginning of the experiment, these measurement data are used for parametric identification, while the case group of mice received injection at each day of the treatment, these measurements are used to validate the model. The validation showed that the proposed model is capable of describing the tumor growth dynamics.
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肿瘤生长与血管生成抑制的最小模型使用贝伐单抗
模拟血管生成抑制下的肿瘤生长是基于数学工具设计肿瘤治疗方法的重要一步。我们的目标是创建一个肿瘤生长的模型,它能充分描述潜在的生理过程,同时尽可能简单。我们提出了一个包含线性项和双线性项的二阶模型来模拟肿瘤体积和抑制剂水平的动态变化,并给出了模型的参数识别过程。模型的参数识别是通过贝伐单抗治疗C38结肠腺癌的C57Bl/6小鼠的实验测量来完成的。对照组小鼠在实验开始时注射一次,这些测量数据用于参数识别,而病例组小鼠在治疗的每一天注射一次,这些测量数据用于验证模型。验证结果表明,该模型能够较好地描述肿瘤的生长动态。
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