HepatoCellular Carcinoma Clinical Trial
Official title:
Stratification of Patients With Chronic Liver Disease Using Multi Spectral CT
The purpose of this study is to evaluate the feasibility to stratify liver fibrosis in patients with chronic liver disease through non-invasive, spectral CT.
This is a retrospective study, in which a FDA approved imaging device (spectral CT scanner)
currently used for several clinical applications will be evaluated for feasibility of
studying chronic liver disease (this application has not yet been validated).
Tomographic imaging has assumed a fundamental role in patients with Chronic Liver Disease
(CLD) to screen patients for hepatocellular carcinoma (HCC), and, is increasingly being
explored as a noninvasive alternative for characterizing liver fibrosis. The overarching
goal of this study is to improve noninvasive characterization of liver fibrosis through
spectral CT.
Hypothesis: concentration of iodine-based contrast agent in the liver parenchyma during the
delayed phase, as measured with spectral CT imaging, increases monotonically with Ishak
fibrosis score obtained from liver biopsy. This hypothesis is supported by the literature
and our preliminary data, described in the references section (Lamb et al. 2015).
We will evaluate multiphase spectral CT images consisting of the arterial phase, 2-minute
delayed phase, and 5-minute delayed phase. Fibrosis will be assessed on both delayed phase
images, where it is assumed that any remaining contrast agent, in the liver, is due to the
presence of fibrosis. This type of multiphase protocol can still be used to image CLD
patients with spectral CT for HCC detection and, thus, will not interfere with liver lesion
workup and evaluation.
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