Oden Institute for Computational Engineering and Sciences, The University of Texas at Austin, 201 E. 24th Street, POB 4.102, 1 University Station (C0200), Austin, TX, 78712-1229, USA.
Livestrong Cancer Institutes, The University of Texas at Austin, Austin, TX, USA.
Ann Biomed Eng. 2019 Jul;47(7):1539-1551. doi: 10.1007/s10439-019-02262-9. Epub 2019 Apr 8.
The spatiotemporal variations in tumor vasculature inevitably alters cell proliferation and treatment efficacy. Thus, rigorous characterization of tumor dynamics must include a description of this phenomenon. We have developed a family of biophysical models of tumor growth and angiogenesis that are calibrated with diffusion-weighted magnetic resonance imaging (DW-MRI) and dynamic contrast-enhanced (DCE-) MRI data to provide individualized tumor growth forecasts. Tumor and blood volume fractions were evolved using two, coupled partial differential equations consisting of proliferation, diffusion, and death terms. To evaluate these models, rats (n = 8) with C6 gliomas were imaged seven times. The tumor volume fraction was estimated using DW-MRI, while DCE-MRI provided estimates of the blood volume fraction. The first three time points were used to calibrate model parameters, which were then used to predict growth at the remaining four time points and compared directly to the measurements. The best performing model predicted tumor growth with less than 10.3% error in tumor volume and with less than 9.4% error at the voxel-level at all prediction time points. The best performing model resulted in less than 9.3% error in blood volume at the voxel-level. This pre-clinical study demonstrates the potential for image-based, mechanistic modeling of tumor growth and angiogenesis.
肿瘤血管的时空变化不可避免地改变了细胞增殖和治疗效果。因此,严格描述肿瘤动力学必须包括对这一现象的描述。我们已经开发了一系列肿瘤生长和血管生成的生物物理模型,这些模型使用扩散加权磁共振成像 (DW-MRI) 和动态对比增强 (DCE-) MRI 数据进行校准,以提供个体化的肿瘤生长预测。肿瘤和血液体积分数使用两个耦合的偏微分方程演变,这些方程由增殖、扩散和死亡项组成。为了评估这些模型,对 8 只 C6 胶质细胞瘤大鼠进行了 7 次成像。使用 DW-MRI 估计肿瘤体积分数,而 DCE-MRI 提供血液体积分数的估计。前三个时间点用于校准模型参数,然后使用这些参数来预测剩余四个时间点的生长,并直接与测量值进行比较。表现最好的模型预测肿瘤生长的误差小于肿瘤体积的 10.3%,在所有预测时间点的体素水平上的误差小于 9.4%。表现最好的模型在体素水平上的血液体积误差小于 9.3%。这项临床前研究表明,基于图像的肿瘤生长和血管生成的机制建模具有潜力。