Sara Lewis1, Steven Peti2, Stefanie Hectors1, Michael King2, Juan Putra3, Swan Thung3, and Bachir Taouli1
1Translational and Molecular Imaging Institute, Icahn School of Medicine at Mount Sinai, New York, NY, United States, 2Department of Radiology, Icahn School of Medicine at Mount Sinai, New York, NY, 3Department of Pathology, Icahn School of Medicine at Mount Sinai, New York, NY, United States
Synopsis
ADC
measurement using DWI have shown promise for characterizing focal liver lesions.
In this study, we assessed the ability of advanced ADC histogram parameters to
distinguish the histological diagnosis and the grade of primary malignant liver
cancers. We found that both ADC mean and ADC percentiles could distinguish
between tumor types; ADC percentiles were also predictive of tumor grade for
HCC and ICC. Advanced ADC histogram analysis may be useful for accurate tumor
diagnosis and prediction of tumor grade.
Purpose
Primary
liver cancers, including hepatocellular carcinoma (HCC), intrahepatic
cholangiocarcinoma (ICC) and “combined” hepatocellular-cholangiocarcinoma
(HCC-ICC) share common risk factors, are rising in incidence and differ in
terms of treatment strategy and prognosis. ADC quantification is useful for
liver lesion detection, however, is limited for lesion characterization given
overlap in mean ADC values for malignant and benign liver lesions (1,2). ADC values have also shown inverse
correlation with pathologic tumor grade for HCC and ICC (3,4). ADC histogram analysis with quantification
of advanced metrics characterizing the distribution of ADC values within a
lesion, have shown promise for differentiating between liver tumor types and pathologic
tumor grades (5). The goal of this preliminary study was to evaluate the ability of
quantitative ADC histogram parameters to characterize primary liver neoplasms
and determine its role for predicting tumor grade.Methods and Materials
In this
IRB-approved retrospective study, we included 34 consecutive patients (mean age
59.9±11.8y, 24M/11F) with pathology proven primary liver cancers that underwent
MRI including single shot echo-planar (SS-EPI) DWI (b 50, 400, 800), from
12/2013 to 5/2016. Diffusion restriction pattern was qualitatively assessed on
high b-values. Lesion volume of interest measurements (VOI) were placed on DWI
images excluding areas of necrosis to extract the following ADC histogram
parameters: ADC mean, median, min, max, skewness, kurtosis, and 5th, 10th,
25th, 75th, 90th and 95th percentiles. Tumor grade was categorized
pathologically as well (G1), moderately (G2), or poorly differentiated (G3).
ADC histogram metrics were compared between different tumor types and tumor
grades using the Kruskal-Wallis test. The Mann-Whitney test was used to compare
ADC metrics with histopathologic tumor grade (G1+2 vs. G3). Spearman
correlation was computed to assess correlation between ADC histogram metrics
and tumor grade. Results
Preliminary results from 34
patients with 35 lesions (mean size 65 ± 30 mm) are reported. Lesions included HCC
[n=14; G1 (n=3), G2 (n=8), G3 (n=3)], ICC [n=12; G2 (n=6), G3 (n=6)] and combined
HCC-ICC [n=9; G1 (n=3), G2 (n=2), G3 (n=4)]. On high b-value DWI, 11/14 (79%)
HCCs, 12/12 (100%) ICCs and 9/9 (100%) combined tumors were hyperintense (Figure 1). ADC histogram values are
shown in Table 1. For discrimination
between tumor types, ADC mean was borderline significant (p=0.05); ADCmax,
75th, 90th and 95th percentiles were all significant (p values 0.03, 0.02, 0.01
and 0.01, respectively) (Figure 2). For
distinguishing G3 tumors vs G1+2, the 5th percentile ADC values were
significant for HCC (p=0.03) and the 10th percentile ADC values were borderline
significant for ICC (p=0.05). A trend towards significance was observed when
correlating ICC tumor grade and ADCmean (r -0.53, p=0.09); there was no
significant correlation for HCC or combined tumor grade and ADC metrics. There
was no significant difference in ADC median, minimum, skewness, kurtosis or
other percentile values for different tumor types or tumor grades (all p-values
> 0.13).Discussion and Conclusions
Diagnosis of primary liver
cancer is often an imaging diagnosis, and accurate prospective tumor diagnosis
is essential to direct appropriate management, as patients with ICC and
combined tumors should not be transplanted, as patients with ICC and combined
tumors should not be transplanted. However, there are overlapping appearances
between all primary liver cancers. Histogram quantification enables derivation
of additional metrics and can minimize the effect of outlier ADC measurements. Our
preliminary results demonstrate that primary liver cancers are highly
conspicuous on DWI and may potentially be distinguishable based on the advanced
ADC metrics, possibly in combination with qualitative imaging findings. Statistical
percentile parameters reflecting the shape of the right side and left side of
the ADC histogram may be useful for distinction of tumor type and tumor grade,
respectively. There was a trend towards correlation between ADC and ICC tumor
grade, which was not found in HCC or combined tumors. Skewness or kurtosis values
were not predictive of tumor type or grade, which could be due to inadequate
sample size. ADC histogram quantification may potentially be useful for
characterization of histopathologic diagnosis and tumor grade. These results
need to be confirmed with a larger number of cases.Acknowledgements
No acknowledgement found.References
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