Patient specific tumor growth prediction using multimodal images.

Med Image Anal

Clinical Image Processing Service, Radiology and Imaging Sciences, NIH, United States. Electronic address:

Published: April 2014

AI Article Synopsis

  • A personalized tumor growth model based on multimodal imaging data (dual-phase CT and FDG-PET) is proposed to aid in tumor staging and therapy planning.
  • The Reaction-Advection-Diffusion model integrates factors like cancer cell proliferation, metabolic rates, and biomechanical responses by incorporating specific imaging metrics such as Intracellular Volume Fraction (ICVF) and Standardized Uptake Value (SUV).
  • The model's effectiveness was validated against observed tumors in six patients, showing close alignment with metrics like average surface distance and tumor volume differences.

Article Abstract

Personalized tumor growth model is valuable in tumor staging and therapy planning. In this paper, we present a patient specific tumor growth model based on longitudinal multimodal imaging data including dual-phase CT and FDG-PET. The proposed Reaction-Advection-Diffusion model is capable of integrating cancerous cell proliferation, infiltration, metabolic rate and extracellular matrix biomechanical response. To bridge the model with multimodal imaging data, we introduce Intracellular Volume Fraction (ICVF) measured from dual-phase CT and Standardized Uptake Value (SUV) measured from FDG-PET into the model. The patient specific model parameters are estimated by fitting the model to the observation, which leads to an inverse problem formalized as a coupled Partial Differential Equations (PDE)-constrained optimization problem. The optimality system is derived and solved by the Finite Difference Method. The model was evaluated by comparing the predicted tumors with the observed tumors in terms of average surface distance (ASD), root mean square difference (RMSD) of the ICVF map, average ICVF difference (AICVFD) of tumor surface and tumor relative volume difference (RVD) on six patients with pathologically confirmed pancreatic neuroendocrine tumors. The ASD between the predicted tumor and the reference tumor was 2.4±0.5mm, the RMSD was 4.3±0.4%, the AICVFD was 2.6±0.6%, and the RVD was 7.7±1.3%.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3992298PMC
http://dx.doi.org/10.1016/j.media.2014.02.005DOI Listing

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