The development of brain tumours, after diagnosis, is routinely recorded by
different medical imaging techniques like computerised tomography (CT) or
magnetic resonance imaging (MRI). However, it is only through the formulati
on of mathematical models that an analysis of the spatio-temporal tumour gr
owth revealed on each patient serial scans can lead to a quantification of
parameters characterising the proliferative and expensive dynamic of the br
ain tumour. This paper reviews some of the results and limitations encounte
red in modelling the different stages of a brain tumour growth, namely befo
re and after diagnosis and therapy. It extends an original two-dimensional
approach by considering three-dimensional growth of brain tumours submitted
to the spatial constraints exerted by the skull and ventricles boundaries.
Considering the dynamic of both the pre-and post-diagnosis stages, the tum
our growth patterns obtained with various combinations of nonlinear growth
rates and cellular diffusion laws are considered and compared to real MRI s
cans taken in a patient with a glioblastoma and having undergone radiothera
py. From these simulations, we characterise the effects of different therap
ies on survival durations, with special attention to the effect of cell dif
fusion inside the resected brain region when surgical resection of the tumo
ur is carried out.