Three-dimensional image-based mechanical modeling for predicting the response of breast cancer to neoadjuvant therapy

被引:49
|
作者
Weis, Jared A. [1 ]
Miga, Michael I. [1 ,2 ,3 ]
Yankeelov, Thomas E. [4 ,5 ,6 ]
机构
[1] Vanderbilt Univ, Dept Biomed Engn, Nashville, TN 37235 USA
[2] Vanderbilt Univ, Dept Neurosurg, 221 Kirkland Hall, Nashville, TN 37235 USA
[3] Vanderbilt Univ, Dept Radiol & Radiol Sci, 221 Kirkland Hall, Nashville, TN 37235 USA
[4] Univ Texas Austin, Inst Computat Engn & Sci, Austin, TX 78712 USA
[5] Univ Texas Austin, Dept Biomed Engn, Austin, TX 78712 USA
[6] Univ Texas Austin, Dept Internal Med, Austin, TX 78712 USA
基金
美国国家卫生研究院;
关键词
Tumor; Mechanics; Mathematical; Computational; Oncology; Finite element; DIFFUSION-WEIGHTED MRI; SIMPLE MATHEMATICAL-MODEL; CONTRAST-ENHANCED MRI; TUMOR-GROWTH; EXTRACELLULAR-MATRIX; APPARENT DIFFUSION; PATHOLOGICAL RESPONSE; CELL MORPHOLOGY; GROWING TUMOR; IN-VIVO;
D O I
10.1016/j.cma.2016.08.024
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The use of quantitative medical imaging data to initialize and constrain mechanistic mathematical models of tumor growth has demonstrated a compelling strategy for predicting therapeutic response. More specifically, we have demonstrated a data driven framework for prediction of residual tumor burden following neoadjuvant therapy in breast cancer that uses a biophysical mathematical model combining reaction diffusion growth/therapy dynamics and biomechanical effects driven by early time point imaging data. Whereas early work had been based on a limited dimensionality reduction (two-dimensional planar modeling analysis) to simplify the numerical implementation, in this work, we extend our framework to a fully volumetric, three-dimensional biophysical mathematical modeling approach in which parameter estimates are generated by an inverse problem based on the adjoint state method for numerical efficiency. In an in silico performance study, we show accurate parameter estimation with error less than 3% as compared to ground truth. We apply the approach to patient data from a patient with pathological complete response and a patient with residual tumor burden and demonstrate technical feasibility and predictive potential with direct comparisons between imaging data observation and model predictions of tumor cellularity and volume. Comparisons to our previous two-dimensional modeling framework reflect enhanced model prediction of residual tumor burden through the inclusion of additional imaging slices of patient-specific data. (C) 2016 Elsevier B.V. All rights reserved.
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页码:494 / 512
页数:19
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