Wu Zhou1, Hanqiu Ju1, Wanwei Jian1, Hui Huang1, Shaoyang Men1, and Honglai Zhang1
1School of Medical Information Engineering, Guangzhou University of Chinese Medicine, Guangzhou, China
Synopsis
Microvascular invasion (MVI) of
hepatocellualr carcinoma(HCC) is regarded as the most important factor associated
with the success of curative resection and the outcome after liver
transplation. As the MVI prediction can only be ultimately determined
by the histopathological features of the tumor cells, numerous works have attempted
to predict the MVI of HCC based on noninvasively preoperative images.
Diffusion-weighted MR has also shown to be effective for MVI prediction based
on signal intensities of lesions and the apparent diffusion coefficient (ADC). In
this work, the emerging deep learning technique is used for MVI prediction of
HCC based on DWI.
Introduction
Preoperative
prediction of microvascular invasion (MVI) of hepatocellular carcinoma (HCC) is
remarkably significant and helpful for prognosis, treatment strategy and patient
management1. The prediction of MVI cannot be diagnosed before surgery or
biopsy and can only be ultimately determined by the histopathological features
of the tumor cells. Many works have
been predicting MVI of HCCs using radiological or radimoics features extracted
from preoperative images2,3. Diffusion-weighted MR has also shown to be
effective for MVI prediction based on signal intensities of lesions and the apparent
diffusion coefficient (ADC)4. As deep learning technique can learn increasing
high-level features of images that can optimally represent the characteristics
of the data, we anticipate that deep feature derived from Diffusion weighted MR
(DWI) might be better than ADC for MVI prediction. The purpose of this study is
to investigate whether DWI can be useful for MVI prediction of HCC using a deep
learning evaluation. Method
This study was approved by the local
institutional review board and the patients’ informed consent was waived due to
its retrospective properties. In this retrospective study, consecutive 54
subjects with fifty-four HCCs from July 2012 to May 2017 with resected HCC were
retrieved (50 male, 4 female, aged 50.26±12.32 years within an age range of 27
to 76 years). The histology information of MVI in HCC was retrieved from the
archived clinical histology report, where tumor size, differentiation, the
presence or absence of microvascular invasion, the surgical resection margin,
and the presence or absence of fibrosis or cirrhosis of the HCCs were
described. Of the 54 lesions, twenty-six were pathologically determined as the
absence of MVI, while twenty-eight were pathologically determined as the
presence of MVI. All subjects with DWI examinations were acquired using a 3.0 Tesla
MR scanner (Signa Excite HD 3.0T, GE Healthcare, Milwaukee, WI, USA). DWI
examinations were performed with a single-shot echo-planar imaging and a
breath-hold routine after CE-MR examinations. DWI parameters were: three b
values of 0,100,600 sec/mm2; TR/TE 1800/35ms; flip angle, 90; a
matrix of 128×128;slice
thickness: 8 mm; interslice gap, 1 mm. First, ADC images were computed by
mono-exponentially fitting the three b-value points. Then, multiple 2D axial patches
(28×28) of
HCCs from b0, b100, b600 and ADC images were extracted to increase the dataset
for training the convolutional neural network. Furthermore, deep features were separately
extracted from b0, b100, b600 and ADC based on the CNN for MVI prediction. Finally,
fusion of deep features derived from three b-value images and ADC was conducted
for MVI prediction. Figure 1 showed the framework of the proposed deep fusion
model with DWI for MVI prediction. Values of prediction performance in
differentiating the presence and absence of MVI were denoted as mean±standard
deviation as a result of four-folded cross-validation with 10 repetitions on
the data set.Results
Table 1 showed the characterization
performance of deep features using different image sets for MVI prediction. Deep
feature
in higher b values (b600) yielded better performance for MVI prediction than
that of the lower b values (b0 and b100). Comparatively, deep feature in the
ADC did not obtain promising results for MVI prediction, which was much lower
than that of the higher b value (b600). Furthermore, fusion of deep features
from the b0, b100, b600 and ADC images yielded best results for MVI prediction.Discussion
Our
study suggests that deep feature derived from higher b value yields better
performance for MVI prediction, implying that DWI imaging with higher b value might
be better for MVI prediction. In the present study, deep feature from higher b
value image obtained better performance than that from the ADC image for MVI
prediction, inferring that image features from higher b value image can be more
representative than that from the ADC image. Furthermore, our study also suggests
that fusion of deep features derived from original b0, b100, b600 and ADC images
results in improved performance compared with that of the single image, demonstrating
that multiple b value images and ADC image can be taken full advantage to yield
better performance for MVI characterization.
Conclusion
Our
study suggests that fusion of deep features derived from DWI image with respect
to the three b-value images and ADC image yields better performance for MVI
prediction. It can be believed that the
proposed fusion model may be broadly used for MVI prediction with DWI images in
clinical practice.Acknowledgements
This research is sponsored by the
grants from National Natural Science Foundation of China (81771920). References
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