TY - JOUR
T1 - Validation and parameter optimization of a hybrid embedded/homogenized solid tumor perfusion model
AU - Kremheller, Johannes
AU - Brandstaeter, Sebastian
AU - Schrefler, Bernhard A.
AU - Wall, Wolfgang A.
N1 - Funding Information:
The authors gratefully acknowledge the support of the Technical University of Munich – Institute for Advanced Study, funded by the German Excellence Initiative and the TÜV SÜD Foundation. Research reported in this publication was supported by the National Cancer Institute of the National Institutes of Health under Award Number U54CA210181. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health. The software QUEENS was provided by the courtesy of AdCo EngineeringGW GmbH, which is gratefully acknowledged. We would also like to thank the authors of REANIMATE, especially Paul W. Sweeney for sharing their data and making their code publicly available. In addition, we gratefully thank Barbara Wirthl and Anh‐Tu Vuong for discussions about various aspects of the two models. 13,14
Funding Information:
The authors gratefully acknowledge the support of the Technical University of Munich ? Institute for Advanced Study, funded by the German Excellence Initiative and the T?V S?D Foundation. Research reported in this publication was supported by the National Cancer Institute of the National Institutes of Health under Award Number U54CA210181. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health. The software QUEENS was provided by the courtesy of AdCo EngineeringGW GmbH, which is gratefully acknowledged. We would also like to thank the authors of REANIMATE,13,14 especially Paul W. Sweeney for sharing their data and making their code publicly available. In addition, we gratefully thank Barbara Wirthl and Anh-Tu Vuong for discussions about various aspects of the two models.
Publisher Copyright:
© 2021 The Authors. International Journal for Numerical Methods in Biomedical Engineering published by John Wiley & Sons Ltd.
PY - 2021/8
Y1 - 2021/8
N2 - The goal of this paper is to investigate the validity of a hybrid embedded/homogenized in-silico approach for modeling perfusion through solid tumors. The rationale behind this novel idea is that only the larger blood vessels have to be explicitly resolved while the smaller scales of the vasculature are homogenized. As opposed to typical discrete or fully resolved 1D–3D models, the required data can be obtained with in-vivo imaging techniques since the morphology of the smaller vessels is not necessary. By contrast, the larger vessels, whose topology and structure is attainable noninvasively, are resolved and embedded as one-dimensional inclusions into the three-dimensional tissue domain which is modeled as a porous medium. A sound mortar-type formulation is employed to couple the two representations of the vasculature. We validate the hybrid model and optimize its parameters by comparing its results to a corresponding fully resolved model based on several well-defined metrics. These tests are performed on a complex data set of three different tumor types with heterogeneous vascular architectures. The correspondence of the hybrid model in terms of mean representative elementary volume blood and interstitial fluid pressures is excellent with relative errors of less than 4%. Larger, but less important and explicable errors are present in terms of blood flow in the smaller, homogenized vessels. We finally discuss and demonstrate how the hybrid model can be further improved to apply it for studies on tumor perfusion and the efficacy of drug delivery.
AB - The goal of this paper is to investigate the validity of a hybrid embedded/homogenized in-silico approach for modeling perfusion through solid tumors. The rationale behind this novel idea is that only the larger blood vessels have to be explicitly resolved while the smaller scales of the vasculature are homogenized. As opposed to typical discrete or fully resolved 1D–3D models, the required data can be obtained with in-vivo imaging techniques since the morphology of the smaller vessels is not necessary. By contrast, the larger vessels, whose topology and structure is attainable noninvasively, are resolved and embedded as one-dimensional inclusions into the three-dimensional tissue domain which is modeled as a porous medium. A sound mortar-type formulation is employed to couple the two representations of the vasculature. We validate the hybrid model and optimize its parameters by comparing its results to a corresponding fully resolved model based on several well-defined metrics. These tests are performed on a complex data set of three different tumor types with heterogeneous vascular architectures. The correspondence of the hybrid model in terms of mean representative elementary volume blood and interstitial fluid pressures is excellent with relative errors of less than 4%. Larger, but less important and explicable errors are present in terms of blood flow in the smaller, homogenized vessels. We finally discuss and demonstrate how the hybrid model can be further improved to apply it for studies on tumor perfusion and the efficacy of drug delivery.
KW - 1D-3D coupling
KW - homogenization
KW - hybrid models
KW - microcirculation
KW - tissue perfusion
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U2 - 10.1002/cnm.3508
DO - 10.1002/cnm.3508
M3 - Article
C2 - 34231326
AN - SCOPUS:85110938850
VL - 37
JO - International Journal for Numerical Methods in Biomedical Engineering
JF - International Journal for Numerical Methods in Biomedical Engineering
SN - 2040-7939
IS - 8
M1 - e3508
ER -