Tao Lin1, Jiazheng Wang2, Peng Sun2, Lihua Chen1, Qingwei Song1, Renwang Pu1, Ying Zhao1, Xue Ren1, Qihao Xu1, and Ailian Liu1
1The First Affiliated Hospital of Dalian Medical University, Dalian, China, 2Philips Healthcare, Beijing, China
Synopsis
Hepatocellular carcinoma (HCC), intrahepatic
cholangiocarcinoma (ICC) are the most common types of primary liver cancer,
which differ greatly in terms of pathogenesis, biological behavior,
histological morphology, treatment, and prognosis. This retrospective study revealed that APT combined
with quantitative DIXON technique could improve the performance for differentiating HCC
from ICC.
Introduction
Primary liver cancer mainly includes hepatocellular
carcinoma (HCC), intrahepatic cholangiocarcinoma (ICC), which differ greatly in
terms of pathogenesis, biological behavior, histological morphology, treatment,
and prognosis[1,2]. However, due to the similarity in typical
imaging findings, the differential
diagnosis of HCC and ICC is still challenging[3]. Amide
proton transfer (APT) imaging, a novel imaging tool based on endogenous amide
protons in mobile cellular proteins and peptides in tissue[4], has
shown great potentials for the diagnosis of central nervous system diseases and
cervical cancer[5,6]. Recent progress in fat quantification
techniques such as mDIXON Quant[7]
has provided additional information on liver functions. The purpose of this study was to explore the value of
a combination of APTw and mDIXON Quant imaging in the differential diagnosis of HCC and ICC.Materials and Methods
31
patients (with clinical symptoms and MRI image characteristics of primary
liver cancer) were recruited in this study, which
consisted of 21 HCC patients (20 men, 1 woman; mean age, 59 years; range, 33–76
years) and 10 ICC patients (8 men, 2 women; mean age, 62 years; range, 47–71
years). All patients were scanned using a 3.0 T MR scanner (Ingenia CX, Philips
Healthcare, the Netherlands) with a 16-channel abdominal array coil. The
detailed scan parameters were shown in Table 1. An experienced radiologist
manually placed the ROIs (100 - 200 mm2) on the axial slice of fusion
of T2WI and APT images, and parameter maps derived from mDIXON Quant (fat fraction (FF) and R2* maps)
with the largest lesions according to the high-resolution T2W images
(Figure 1). The values of APT, FF, and R2* were compared between the HCC and ICC
groups by using the Mann-Whitney U test, respectively. ROC curves were analyzed
to evaluate the diagnostic efficiency of APT, mDIXON Quant, and the joint use
of two methods for differentiating HCC from ICC. The diagnostic values of the
combination of APTw and mDIXON Quant were calculated by logistic regression. Spearman’s
bivariate correlation was employed to assess the correlation between the APT
values and mDIXON
Quant
(FF, R2*)
parameters. The difference
between AUCs derived from different parameters was compared using the Delong
test. A p-value < 0.05 was considered statistically
significant. Results
The measured values of APT, FF, and R2* from HCC and ICC patients were shown in Table 2.
The values of APT were lower for HCC than ICC, whereas the value of R2*
showed an opposite relationship. The
values of FF did not show statistically significant differences.
ROC analyses revealed the diagnostic performance of APT and R2* value in differentiating HCC from ICC,
with AUCs of 0.721 and 0.876 (Table 3). The AUC of the combination of APT and
R2* was 0.886, and the sensitivity
was 76.19%, the specificity was 90% (cut-off value 0.745) (Table 3, Figure 2).Discussion and conclusion
ICC is histologically
characterized by adenoid secretion or mucous secretion, and thus elevation of
mobile proteins and
peptides. This might be the reason why APT values are higher for ICC than HCC. Our results indicated that the R2* value was significantly
higher in HCC than ICC, which might be due to the faster cell proliferation and
more neovascularization. Compared with either APT or R2*, a
combination of APT and R2* increased the AUC from 0.721 to 0.886. In conclusion, a combination of APT and R2*
could enhance the diagnosis of HCC and ICC in primary liver cancer. Acknowledgements
No acknowledgments.References
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