IMAGE-DRIVEN BIOPHYSICAL TUMOR GROWTH MODEL CALIBRATION

被引:4
作者
Scheufele, Klaudius [1 ]
Subramanian, Shashank [2 ]
Mang, Andreas [3 ]
Biros, George [2 ]
Mehl, Miriam [1 ]
机构
[1] Univ Stuttgart, Inst Parallel & Distributed Syst, Univ Str 38, D-70569 Stuttgart, Germany
[2] Univ Austin, Oden Inst Computat Engn & Sci, 201 E 24th St, Austin, TX 78712 USA
[3] Univ Houston, Dept Math, 3551 Cullen Blvd, Houston, TX 77204 USA
关键词
tumor progression inversion; biophysical model calibration; image registration; PDE-constrained optimization; Picard iteration; PDE-CONSTRAINED OPTIMIZATION; PARAMETER-ESTIMATION; DEFORMABLE REGISTRATION; INDIVIDUAL PATIENTS; INVERSE PROBLEM; ADJOINT METHOD; GLIOMA GROWTH; OPTICAL-FLOW; BRAIN-TUMORS; DIFFUSION;
D O I
10.1137/19M1275280
中图分类号
O29 [应用数学];
学科分类号
070104 ;
摘要
We present a novel formulation for the calibration of a biophysical tumor growth model from a single-time snapshot, multiparametric magnetic resonance imaging (MRI) scan of a glioblastoma patient. Tumor growth models are typically nonlinear parabolic partial differential equations (PDEs). Thus, we have to generate a second snapshot to be able to extract significant information from a single patient snapshot. We create this two-snapshot scenario as follows. We use an atlas (an average of several scans of healthy individuals) as a substitute for an earlier, pretumor, MRI scan of the patient. Then, using the patient scan and the atlas, we combine image-registration algorithms and parameter estimation algorithms to achieve a better estimate of the healthy patient scan and the tumor growth parameters that are consistent with the data. Our scheme is based on our recent work (Scheufele et al., Comput. Methods Appl. Mech. Engrg., to appear), but we apply a different and novel scheme where the tumor growth simulation in contrast to the previous work is executed in the patient brain domain and not in the atlas domain yielding more meaningful patient-specific results. As a basis, we use a PDE-constrained optimization framework. We derive a modified Picard-iteration-type solution strategy in which we alternate between registration and tumor parameter estimation in a new way. In addition, we consider an l(1) sparsity constraint on the initial condition for the tumor and integrate it with the new joint inversion scheme. We solve the sub-problems with a reduced space, inexact Gauss-Newton-Krylov/quasi-Newton method. We present results using real brain data with synthetic tumor data that show that the new scheme reconstructs the tumor parameters in a more accurate and reliable way compared to our earlier scheme.
引用
收藏
页码:B549 / B580
页数:32
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