Hepatocellular Carcinoma Clinical Trial
Official title:
Evaluation of HCC Response to Systemic Therapy With Quantitative MRI
The incidence of hepatocellular carcinoma (HCC) has recently increased in the United States. Although imaging plays a major role in HCC screening and staging, the possibility of predicting HCC tumor grade, aggressiveness, angiogenesis and hypoxia with imaging are unmet needs. In addition, new antiangiogenic drugs now available to treat advanced HCC necessitate the use of new imaging criteria beyond size. The investigators would like to develop and validate non-invasive magnetic resonance imaging (MRI) methods based on advanced diffusion-weighted imaging (DWI), MR Elastography, BOLD (blood oxygen level dependent) MRI and perfusion-weighted imaging (PWI, using gadolinium contrast) to be used as non-invasive markers of major histopathologic features of HCC, and to predict and assess early response of HCC to systemic therapy. The investigators also would like to develop quality control tools to improve the quality and decrease variability of quantitative MRI metrics. These techniques combined could represent non-invasive correlates of histologic findings in HCC, could enable individualized therapy, and provide prognosis in patients with HCC.
The incidence of hepatocellular carcinoma (HCC) has recently increased in the US mostly due
to an increase in chronic hepatitis C infection. Angiogenesis is critical for the growth and
metastatic progression of HCC. With the development of new antiangiogenic drugs such as
sorafenib, imaging methods to predict and assess therapeutic response beyond changes in size
become critical. However, validated imaging methods to predict and assess early HCC response
to targeted agents are lacking.
In this study, the investigators would like to develop quantitative MRI methods interrogating
different features of HCC tumor biology and pathology, including tumor cellularity, grade,
angiogenesis and hypoxia. The investigators propose a multiparametric approach combining
advanced DWI (IVIM: intravoxel incoherent motion diffusion measuring perfusion fraction and
true diffusion coefficient), DCE-MRI (dynamic contrast-enhanced MRI, which measures arterial
and portal flow, mean transit time, blood volume and distribution volume), and BOLD MRI using
oxygen or carbogen challenge. This protocol will be performed in patients with HCC undergoing
hepatic resection. Routine and advanced histopathologic methods will be performed (tumor
grade, CK19 expression, presence of microvascular invasion, VEGF expression, microvessel
density, HIF 1-alpha expression). MRI metrics will be correlated with histopathologic
metrics.
The first portion of the proposal involves the development of a QC algorithm assessing MR
data quality and test-retest. The investigators will propose solutions to improve data
acquisition and processing. The last 2 years of the study will be dedicated to a prospective
randomized study comparing Yttrium 90 radioembolization to sorafenib, assessing the role of
baseline MRI metrics and early changes (at 2 weeks) in these metrics as markers of tumor
response and time to progression in patients with unresectable HCC.
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