Bordas, Stéphane [superviser], Skalli, Wafa [superviser], Rohan, Pierre-Yves [superviser], Sciumè, Giuseppe [superviser], Cristini, Vittorio [president of the jury], Gomez, Hector [member of the jury], Barrera, Olga [member of the jury], Grillo, Alfio [member of the jury]
We propose the modeling of glioblastoma isocitrate dehydrogenase wild-type (GBMwt) build on the following hypotheses: the brain tissue is a porous medium, the coupling of hypoxia consequences and mechanical interplay between extra-cellular matrix and tumor cells is the driver of the malignant evolution of the disease. In this thesis, a poromechanical model is developed with the aim of a clinical application in oncology. A review, with a large scope, is done on mechanical applications in clinical management of cancer. The model is first validated on in vitro experimental data of encapsulated multi-cellular spheroids. Then, a clinical collaboration is initiated with the Neuro-imaging center of Toulouse, and the targeted clinical application is the modeling of non- operable GBMwt. To this end, the model is first adapted to the specificity of brain tissue mechanics. Characteristic features of the disease are modeled: necrotic core, modified extra-cellular matrix production, emerging malignant phenotype and invasion. Clinical imaging data are pre- treated to inform the model in a patient specific basis. A proposition of modeling is provided with an evaluation against clinical data.