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Vascular tumor growth and treatment: Consequences of polyclonality, competition and dynamic vascular support

机译:血管肿瘤的生长和治疗:多克隆性,竞争和动态血管支持的后果

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A mathematical model is presented to describe the evolution of a vascular tumor in response to traditional chemotherapeutic treatment. Particular attention is paid to the effects of a dynamic vascular support system in a tumor comprised of competing cell populations that differ in proliferation rates and drug susceptibility. The model consists of a system of partial differential equations governing intratumoral drug concentration, cancer cell density, and blood vessel density. The balance between cell proliferation and death along with vessel production and destruction within the tumor generates a velocity field which drives the expansion or regression of the neoplasm. Radially symmetric solutions are obtained for the case when only one cell type is present and when the proportion of the tumor occupied by blood vessels remains constant. The stability of these solutions to asymmetric perturbations and to a small semi-drug resistant cell population is then investigated. The analysis shows that drug concentrations which are sufficient to insure eradication of a spherical tumor may be inadequate for the successful treatment of non-spherical tumors. When the drug is continuously infused, linear analysis predicts that whether or not a cure is possible is crucially dependent on the proliferation rate of the semi-resistant cells and on the competitive effect of the sensitive cells on the resistant population. When the blood vessel density is allowed to change dynamically, the model predicts a dramatic increase in the tumor's growth and decrease in its response to therapy. [References: 46]
机译:提出了数学模型来描述响应传统化学疗法的血管肿瘤的演变。特别注意动态血管支持系统在肿瘤中的作用,该肿瘤由竞争性细胞群组成,这些细胞群的增殖速率和药物敏感性不同。该模型由控制肿瘤内药物浓度,癌细胞密度和血管密度的偏微分方程系统组成。细胞增殖与死亡以及肿瘤内血管生成和破坏之间的平衡会产生一个速度场,该速度场驱动肿瘤的扩张或消退。当仅存在一种细胞类型并且肿瘤被血管占据的比例保持恒定时,可以得到径向对称解。然后研究了这些溶液对不对称扰动和小的半耐药细胞群的稳定性。分析表明,足以确保根除球形肿瘤的药物浓度可能不足以成功治疗非球形肿瘤。当连续输注药物时,线性分析预测是否可以治愈关键取决于半耐药细胞的增殖速率以及敏感细胞对耐药人群的竞争作用。当允许血管密度动态变化时,该模型预测肿瘤的生长会显着增加,对治疗的反应也会降低。 [参考:46]

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