Assessment of compression-induced solid stress, fluid pressure and mechanopathological parameters in cancersin vivousing poroelastography.

Objective.Compression-induced solid stress (SSc) and fluid pressure (FPc) during ultrasound poroelastography (USPE) experiments are correlated with two markers of cancer growth and treatment effectiveness: growth-induced solid stress (SSg) and interstitial fluid pressure (IFP). The spatio-temporal distributions of SSg and IFP are determined by the transport properties of the vessels and interstitium in the tumor microenvironment.Approach.We propose a new USPE method for the non-invasive imaging of the local cancer mechanical parameters and dynamics of fluid flow. When performing poroelastography experiments, it may be difficult to implement a typical creep compression protocol, which requires to maintain a constant normally applied force. In this paper, we investigate the use of a stress relaxation protocol, which might be a more convenient choice for clinical poroelastography applications.Main results.Based on our finite element and ultrasound simulations study, we demonstrate that the SSc, FPc and their spatio-temporal distribution related parameters, interstitial permeability and vascular permeability, can be determined from stress relaxation experiments with errors below 10% as compared to the ground truth and accuracy similar to that of corresponding creep tests, respectively. We also demonstrate the feasibility of the new methodology forin vivoexperiments using a small animal cancer model.Significance.The proposed non-invasive USPE imaging methods may become an effective tool to assess local tumor pressure and mechanopathological parameters in cancers.

Ultrasound estimation of strain time constant and vascular permeability in tumors using a CEEMDAN and linear regression-based method.

Ultrasound poroelastography focuses on the estimation of the spatio-temporal mechanical behavior of tissues using data often corrupted with non-stationary noise. The cumulative strain calculated from prolonged temporal acquisition of RF data can face the problem of aggregate noise. This noise can significantly affect the accuracy of curve fitting techniques necessary to estimate the clinically significant strain Time Constant (TC) and related parameters. We present a new technique, which decomposes the non-linear temporal behavior of the differential strain to extract the monotonic decaying trend by using the time-domain and data-driven Complete Ensemble Empirical Mode Decomposition with Adaptive Noise (CEEMDAN) algorithm. A linear regression scheme is then used to obtain the slope of the transformed non-linear trend, which carries information about the strain TC. Assessment of Vascular Permeability (VP), a transport parameter indicative of tumor growth, requires accurate strain TC estimations. Finite Element (FE), ultrasound simulations and in vivo experiments are used to investigate the performance of the proposed technique. Based on the simulation analysis, the average Percentage Relative Error (PRE) values of our method are 4.15% (for TC estimation) and 5.00% (for VP estimation) at 20 dB SNR level for different Percentage of Good Frames (PGF) (i.e., 20%, 50%, 75%, and 100%). These PRE values are substantially lower than those obtained using other conventional elastographic techniques. Our proposed method could become a new data-adaptive tool for analyzing the non-linear time-dependent response of complex tissues such as cancers.