Yu Chen1, Yanan Zhao1, Huadan Xue1, Zhuhua Zhang1, and Zhengyu Jin1
1Peking Union Medical College Hospital, Beijing, China
Synopsis
To investigate the feasibility of using
texture analysis (TA) of apparent diffusion coefficient (ADC) to distinguish
between well- and moderate- differentiated head and neck squamous cell
carcinoma (HNSCC). A total of 22 patients were retrospectively analyzed,
including: well-differentiated degree SCC (WSCC, n=11) and
moderate-differentiated degree SCC (MSCC, n=11). A Mean>101.38 at coarse
texture scale (SSF=6mm) identified WSCC and MSCC with the highest AUC of 0.843±0.083
(Se=72.7%, Sp=81.8%, PPV=80%, PV=75%, and accuracy=77.3%). Texture analysis of
ADC proved to be a feasible tool for differentiating WSCC from MSCC, and had
better diagnostic performance than ADC value.
Introduction/purpose
The
histopathological classification of malignancy proposed by the World Health
Classification (WHO, 2005) was based on the degree of cell differentiation and
allowed the classification of this malignancy into three categories, as well-,
moderately and poorly differentiated. This is increasingly challenged by new
non-invasive advanced MRI techniques and research into additional sequences to
improve radiological diagnostic accuracy. Texture analysis (TA) assessed the
distribution of gray-levels within an image to obtain texture features of
intra-lesional heterogeneity. The aim of our study is to investigate the
feasibility of using texture analysis (TA) of apparent diffusion coefficient
(ADC) to distinguish between well- and moderate- differentiated head and neck
squamous cell carcinoma (HNSCC).Methods
A
total of 22 patients undergoing MR examination with diffusion weighted image
(DWI) before treatment were retrospectively analyzed. All patients were
histological proven as HNSCC, including: well-differentiated degree SCC (WSCC, n=11)
and moderate-differentiated degree SCC (MSCC, n=11). The ADC mapping was
derived from DWI on workstation. The minimum, average and maximum ADC values
were compared between the WSCC and MSCC. The largest cross-section area of the
tumors were chosen for texture analysis using TexRAD software. Comparing of
texture parameters, mean gray-level intensity (Mean), standard deviation,
entropy, mean of positive pixels (MPP), skewness, and kurtosis were made for
the objective. Receiver operating characteristic (ROC) analysis was performed
and the area under the ROC curve was calculated for texture parameters that
were significantly different (P<0.05) for the purpose. Sensitivity (Se),
specificity (Sp), positive predictive value, negative predictive value, and
accuracy were calculated using the cut-off value of texture parameters with the
highest AUC.Results
The minimum, average and maximum
ADC values showed no significant difference between WSCC and MSCC. Compared to
MSCC, WSCC had significantly higher Mean from fine, medium and coarse texture
scale (P<0.05), higher SD from non-filtration and fine scale (P<0.05),
higher MPP from fine and medium scale (P<0.05), and lower entropy from all
scale (P<0.05). There was no significant difference in skewness or kurtosis
at any texture scale of ADC. A Mean>101.38 at coarse texture scale (SSF=6mm)
identified WSCC and MSCC with the highest AUC of 0.843±0.083
(Se=72.7%, Sp=81.8%, PPV=80%, PV=75%, and accuracy=77.3%).Discussion
This study demonstrated the
potential for TA of ADC to distinguish between the WSCC and MSCC by quantifying
heterogeneity, without additional imaging. TA is an easy post-processing step
that can be performed on existing DICOM format images. The results can in part
be explained by the correlation between tumour heterogeneity and tumour grade.Conclusions
Texture analysis of ADC proved to be a feasible tool for differentiating WSCC
from MSCC, and had better diagnostic performance than ADC value. Mean
quantified from coarse texture scale was the optimal diagnostic parameter for
estimating histologic differentiated degree of HNSCC.Acknowledgements
Thank you for the support from Professor Balaji Ganeshan, Institute of
Nuclear Medicine, University College London, University College Hospital.References
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