TY - JOUR
T1 - Image guided personalization of reaction-diffusion type tumor growth models using modified anisotropic eikonal equations
AU - Konukoglu, Ender
AU - Clatz, Olivier
AU - Menze, Bjoern H.
AU - Stieltjes, Bram
AU - Weber, Marc André
AU - Mandonnet, Emmanuel
AU - Delingette, Hervé
AU - Ayache, Nicholas
N1 - Funding Information:
Manuscript received June 09, 2009; June 09, 2009; accepted June 15, 2009. First published July 14, 2009; current version published January 04, 2010. This work was supported in part by the European Health-e-Child under Project IST-2004-027749, in part by the CompuTumor project, and in part by Microsoft Research, Cambridge. The work of B. H. Menze was supported by the German Academy of Sciences Leopoldina under the Leopoldina Fellowship Program (LPDS 2009-10). Asterisk indicates corresponding author. *E. Konukoglu is with INRIA, Asclepios Research Project, 06902 Sophia-Antipolis, France (e-mail: [email protected]).
PY - 2010/1
Y1 - 2010/1
N2 - Reaction-diffusion based tumor growth models have been widely used in the literature for modeling the growth of brain gliomas. Lately, recent models have started integrating medical images in their formulation. Including different tissue types, geometry of the brain and the directions of white matter fiber tracts improved the spatial accuracy of reaction-diffusion models. The adaptation of the general model to the specific patient cases on the other hand has not been studied thoroughly yet. In this paper, we address this adaptation. We propose a parameter estimation method for reaction-diffusion tumor growth models using time series of medical images. This method estimates the patient specific parameters of the model using the images of the patient taken at successive time instances. The proposed method formulates the evolution of the tumor delineation visible in the images based on the reaction-diffusion dynamics; therefore, it remains consistent with the information available. We perform thorough analysis of the method using synthetic tumors and show important couplings between parameters of the reaction-diffusion model. We show that several parameters can be uniquely identified in the case of fixing one parameter, namely the proliferation rate of tumor cells. Moreover, regardless of the value the proliferation rate is fixed to, the speed of growth of the tumor can be estimated in terms of the model parameters with accuracy. We also show that using the model-based speed, we can simulate the evolution of the tumor for the specific patient case. Finally, we apply our method to two real cases and show promising preliminary results.
AB - Reaction-diffusion based tumor growth models have been widely used in the literature for modeling the growth of brain gliomas. Lately, recent models have started integrating medical images in their formulation. Including different tissue types, geometry of the brain and the directions of white matter fiber tracts improved the spatial accuracy of reaction-diffusion models. The adaptation of the general model to the specific patient cases on the other hand has not been studied thoroughly yet. In this paper, we address this adaptation. We propose a parameter estimation method for reaction-diffusion tumor growth models using time series of medical images. This method estimates the patient specific parameters of the model using the images of the patient taken at successive time instances. The proposed method formulates the evolution of the tumor delineation visible in the images based on the reaction-diffusion dynamics; therefore, it remains consistent with the information available. We perform thorough analysis of the method using synthetic tumors and show important couplings between parameters of the reaction-diffusion model. We show that several parameters can be uniquely identified in the case of fixing one parameter, namely the proliferation rate of tumor cells. Moreover, regardless of the value the proliferation rate is fixed to, the speed of growth of the tumor can be estimated in terms of the model parameters with accuracy. We also show that using the model-based speed, we can simulate the evolution of the tumor for the specific patient case. Finally, we apply our method to two real cases and show promising preliminary results.
UR - http://www.scopus.com/inward/record.url?scp=73949157513&partnerID=8YFLogxK
U2 - 10.1109/TMI.2009.2026413
DO - 10.1109/TMI.2009.2026413
M3 - Article
C2 - 19605320
AN - SCOPUS:73949157513
SN - 0278-0062
VL - 29
SP - 77
EP - 95
JO - IEEE Transactions on Medical Imaging
JF - IEEE Transactions on Medical Imaging
IS - 1
M1 - 5165028
ER -