Department of Physics, Stockholm University, Stockholm, Sweden; Department of Oncology and Pathology, Karolinska Institutet, Solna, Sweden.
Department of Physics, Stockholm University, Stockholm, Sweden; Department of Oncology and Pathology, Karolinska Institutet, Solna, Sweden.
J Theor Biol. 2022 Aug 21;547:111175. doi: 10.1016/j.jtbi.2022.111175. Epub 2022 May 26.
Tumor oxygenation is one of the key features influencing the response of cells to radiation and chemo therapies. This study presents a novel in silico tumor model simulating realistic 3D microvascular structures and related oxygenation maps, featuring regions with different levels and typologies of hypoxia (chronic, acute and anemic). Such model, if integrated into a treatment planning system, could allow evaluations and comparisons of various scenarios when deciding the therapy to administer.
Spherical tumors between 0.6 and 1.5 cm in diameter encompassed uniformly by vascular trees generated starting from pseudo-fractal principles were simulated with a voxel resolution of 10 µm. The approach ensures a continuous transition from a well-perfused rim to a core with poor vascularization. The oxygen diffusion equation in the tumor is solved by a finite difference method. Several quantities, such as the fractal dimension (FD), the microvascular density (MVD) and the hypoxic fraction (HF) were assessed and compared.
Different tumors with various degrees of chronic hypoxia were simulated by varying the tumor size and the number of bifurcations in the vascular networks. The simulations showed that for the case of chronically hypoxic tumors, in well-oxygenated volumes FD = 2.53 ± 0.07, MVD = 3460 ± 2180 vessels/mm and HF = 4.0 ± 3.4%, while in hypoxic volumes FD = 2.34 ± 0.09, MVD = 365 ± 156 vessels/mm, HF = 49.8 ± 18.3%. The superimposition of acute or anemic hypoxia accentuated the oxygen deprivation in the core of the volumes.
Tumors varying in diameter and extension of their vasculature were simulated, showing features that define two distinctive subvolumes in terms of oxygenation. The model could be regarded as a testbed for simulations of key radiobiological features governing the tumor response to radio- and chemotherapy and thus for treatment outcome simulations.
肿瘤氧合是影响细胞对放疗和化疗反应的关键特征之一。本研究提出了一种新的计算肿瘤模型,模拟真实的 3D 微血管结构和相关的氧合图,具有不同水平和缺氧类型(慢性、急性和贫血性)的区域。如果将这种模型集成到治疗计划系统中,可以在决定治疗方案时对各种情况进行评估和比较。
直径在 0.6 到 1.5 厘米之间的球形肿瘤被模拟,它们被均匀地包裹在由伪分形原理生成的血管树中,体素分辨率为 10 微米。该方法确保了从灌注良好的边缘到血管化较差的核心的连续过渡。肿瘤中的氧扩散方程通过有限差分法求解。评估并比较了几个数量,如分形维数(FD)、微血管密度(MVD)和缺氧分数(HF)。
通过改变肿瘤的大小和血管网络的分叉数量,模拟了具有不同程度慢性缺氧的不同肿瘤。模拟结果表明,对于慢性缺氧肿瘤,在氧合良好的体积中 FD=2.53±0.07,MVD=3460±2180 个血管/毫米,HF=4.0±3.4%,而在缺氧体积中 FD=2.34±0.09,MVD=365±156 个血管/毫米,HF=49.8±18.3%。急性或贫血性缺氧的叠加加剧了体积核心的缺氧。
模拟了直径和血管扩展不同的肿瘤,显示了氧合方面定义两个不同亚体积的特征。该模型可以被视为模拟控制肿瘤对放疗和化疗反应的关键放射生物学特征以及治疗结果模拟的试验台。