Abstract
Glioblastoma is the most aggressive tumor originated in the central nervous system. Modeling its evolution is of great interest for therapy planning and early response to treatment assessment. Using a continuous multi-scale growth model, which considers the angiogenic process, oxygen supply and different phenotype expressions, a new method is proposed for setting the initial values of the celular variables, based on a spatiotemporal characterization of their distribution in controlled synthetic simulations. The method is applied to a real case showing an improvement on the dynamic stability, compared to the usual method.
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Acknowledgments
This work was partially supported by Project TIN2013- 43457-R funded by the Ministerio de Economia y Competitividad of Spain, the GLIOMARKERS project funded by the INBIO joint action between UPV and IIS HUPLF, and the CURIAM-FDFT project funded by ITACA-UPV EMBLEMA action. E. Fuster-Garcia acknowledges the financial support from the UPV PAID-10–14 grant.
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Ortiz-Pla, J., Fuster-Garcia, E., Juan-Albarracin, J., Garcia-Gomez, J.M. (2016). GBM Modeling with Proliferation and Migration Phenotypes: A Proposal of Initialization for Real Cases. In: Tsaftaris, S., Gooya, A., Frangi, A., Prince, J. (eds) Simulation and Synthesis in Medical Imaging. SASHIMI 2016. Lecture Notes in Computer Science(), vol 9968. Springer, Cham. https://doi.org/10.1007/978-3-319-46630-9_7
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DOI: https://doi.org/10.1007/978-3-319-46630-9_7
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