
Proceedings Paper
Complementary tumor vascularity imaging in a single PET-CT routine using FDG early dynamic blood flow and contrast-enhanced CT texture analysisFormat | Member Price | Non-Member Price |
---|---|---|
$17.00 | $21.00 |
Paper Abstract
A feasibility study of improved PET-CT tumor imaging approach is presented. A single PET-CT routine includes three different techniques: 18F-FDG early dynamic blood flow intended for perfusion assessment; standard late 18F-FDG uptake; and high-resolution contrast-enhanced CT enabling tissue texture analysis. Both PET protocols utilize the same single standard radiotracer dose administration. Quantitative volumetric arterial perfusion maps are derived from the reconstructed dynamic PET images corresponding to successive acquisition time intervals of 3 seconds only. For achieving high accuracy, the analysis algorithm differentiates the first-pass arterial flow from other interfering dynamic effects, and a noise reduction scheme based on adaptive total-variation minimization aims to provide appreciable quantitative map in physical conditions of high noise and low spatial resolution. The CT texture analysis comprises a practical and robust method for generating volumetric tissue irregularity maps. A local map value is represented by the entropy function which is derived from a weighted co-occurrence matrix histogram of the corresponding image voxel three-dimensional vicinity. Unique entropy scaling scheme and parameter optimization process, as well as appropriate scaling for varying image noise levels and contrast agent concentrations, improve the results toward quantitative absolute measure with respect to diverse scanning conditions and key analysis parameters. Representative imaging results are demonstrated on several clinical cases involving different organs and cancer types. In these cases, significant tumor characterization relative to the normal surrounding tissues is seen on the quantitative maps of all three imaging techniques. This proof of concept can lead the way to a new practical diagnostic imaging application.
Paper Details
Date Published: 13 March 2014
PDF: 14 pages
Proc. SPIE 9038, Medical Imaging 2014: Biomedical Applications in Molecular, Structural, and Functional Imaging, 90380R (13 March 2014); doi: 10.1117/12.2036420
Published in SPIE Proceedings Vol. 9038:
Medical Imaging 2014: Biomedical Applications in Molecular, Structural, and Functional Imaging
Robert C. Molthen; John B. Weaver, Editor(s)
PDF: 14 pages
Proc. SPIE 9038, Medical Imaging 2014: Biomedical Applications in Molecular, Structural, and Functional Imaging, 90380R (13 March 2014); doi: 10.1117/12.2036420
Show Author Affiliations
Raz Carmi, Philips Healthcare (Israel)
Nikolay Yefremov, Rabin Medical Ctr. (Israel)
Assuta Medical Ctr. (Israel)
Nikolay Yefremov, Rabin Medical Ctr. (Israel)
Assuta Medical Ctr. (Israel)
Hanna Bernstine, Rabin Medical Ctr. (Israel)
Tel Aviv Univ. (Israel)
David Groshar, Rabin Medical Ctr. (Israel)
Tel Aviv Univ. (Israel)
Assuta Medical Ctr. (Israel)
Tel Aviv Univ. (Israel)
David Groshar, Rabin Medical Ctr. (Israel)
Tel Aviv Univ. (Israel)
Assuta Medical Ctr. (Israel)
Published in SPIE Proceedings Vol. 9038:
Medical Imaging 2014: Biomedical Applications in Molecular, Structural, and Functional Imaging
Robert C. Molthen; John B. Weaver, Editor(s)
© SPIE. Terms of Use
