Bayesian Inference of Tissue Heterogeneity for Individualized Prediction of Glioma Growth

被引:2
|
作者
Liang, Baoshan [1 ]
Tan, Jingye [1 ]
Lozenski, Luke [2 ]
Hormuth, David A. [3 ]
Yankeelov, Thomas E. [3 ,4 ,5 ]
Villa, Umberto [6 ]
Faghihi, Danial [1 ]
机构
[1] SUNY Buffalo, Dept Mech & Aerosp Engn, Buffalo, NY 14260 USA
[2] Washington Univ St Louis, Dept Elect & Syst Engn, St Louis, MO 63112 USA
[3] Univ Texas Austin, Oden Inst Computat Engn & Sci, Livestrong Canc Inst, Austin, TX 78712 USA
[4] Univ Texas Austin, Dept Oncol, Austin, TX 78712 USA
[5] Univ Texas MD Anderson Canc Ctr, Dept Imaging Phys, Houston, TX 77030 USA
[6] Univ Texas Austin, Oden Inst Computat Engn & Sci, Austin, TX 78712 USA
关键词
Computational oncology; uncertainty quantification; biophysical tumor model; tumor shape prediction; quantitative MRI; ALGORITHMS; MODELS;
D O I
10.1109/TMI.2023.3267349
中图分类号
TP39 [计算机的应用];
学科分类号
081203 ; 0835 ;
摘要
Reliably predicting the future spread of brain tumors using imaging data and on a subject-specific basis requires quantifying uncertainties in data, biophysical models of tumor growth, and spatial heterogeneity of tumor and host tissue. This work introduces a Bayesian framework to calibrate the two-/three-dimensional spatial distribution of the parameters within a tumor growth model to quantitative magnetic resonance imaging (MRI) data and demonstrates its implementation in a pre-clinical model of glioma. The framework leverages an atlas-based brain segmentation of grey and white matter to establish subject-specific priors and tunable spatial dependencies of the model parameters in each region. Using this framework, the tumor-specific parameters are calibrated from quantitative MRI measurements early in the course of tumor development in four rats and used to predict the spatial development of the tumor at later times. The results suggest that the tumor model, calibrated by animal-specific imaging data at one time point, can accurately predict tumor shapes with a Dice coefficient $>$ 0.89. However, the reliability of the predicted volume and shape of tumors strongly relies on the number of earlier imaging time points used for calibrating the model. This study demonstrates, for the first time, the ability to determine the uncertainty in the inferred tissue heterogeneity and the model-predicted tumor shape.
引用
收藏
页码:2865 / 2875
页数:11
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