Meng-yao Wang1, Mei-yu Sun2, Xu Han2, Rui Fan2, and Lizhi Xie3
1radiology, the first Affiliated Hospital of Dalian Medical University, dalian, China, 2the First Affiliated Hospital of Dalian Medical University, dalian, China, 3GE Healthcare, Beijing, China
Synopsis
Preoperative
information about depth of myometrial invasion is therefore essential in
tailoring the surgical approach for patients in stage I. Consequently, we
investigate the feasibility of diffusion-kurtosis imaging(DKI) in distinguishing
the stage IA and IB of EC.
Introduction
Endometrial
carcinoma (EC) is one of the common gynecologic malignancies. Tumors confined
to the endometrium and those invading the superficial myometrium are designated
as stage IA, and tumors invading the deep myometrium are designated as stage IB
[1]. Depth of myometrial invasion is the most important morphologic prognostic
factor [1]. The incidence of lymph node metastases increases from 3% with
superficial myometrial invasion to 46% with deep myometrial invasion. Preoperative
information about the depth of myometrial invasion is therefore essential in
tailoring the surgical approach for patients in stage IA or IB [2]. To offer new ideas for
preoperative staging of endometrial carcinoma and guide clinical treatment, we investigate
the feasibility of diffusion-kurtosis imaging(DKI) in distinguishing the stage
IA and IB of endometrial carcinoma(EC).Materials and Methods
Twenty four
pathologically proved patients, classified into two groups as follows: 13 in
stage IA and 11 in stage IB, were enrolled, they were scanned by 1.5T MR unit
with DKI sequence before treatment. Fractional
anisotropy (FA), mean
diffusivity (MD), axial
diffusivity (Da), radial
diffusivity (Dr), fractional
anisotropy of kurtosis (FAk), mean kurtosis (MK), axial kurtosis (Ka) and radial kurtosis (Kr) were derived from DKI. The freehand ROI
was drawn three times to take average, along the border of the low signal
comprising the tumor to cover the maximum axial tumor parenchyma area. These
parameters were compared in different groups. ROC analysis was performed to
evaluate the diagnostic performance and to discover the corresponding
threshold.Results
MD and Da
values of stage IB group were significantly lower than that of stage IA group[(
0.93 ± 0.14 )um2/ms VS ( 1.09 ± 0.11 )um2/ms, P=0.011; (
1.16 ± 0.19 )um2/ms VS ( 1.35 ± 0.1 )um2/ms, P=0.018],
while MK, Ka and Kr values were significantly higher[( 1.02 ± 0.11 ) VS ( 0.89
± 0.05 ), P=0.001; ( 1.16 ± 0.16 ) VS ( 1.00 ± 0.09 ), P=0.035; ( 0.88 ± 0.09 )
VS ( 0.75 ± 0.07 ), P=0.001]. The rest parameters were not found to exhibit
significant difference between two groups. AUC was 0.874 for MK with
sensitivity of 84.6% and specificity of 90.9% when the cutoff value was 0.92.Discussion
Diffusion
kurtosis imaging (DKI), an extension of DWI, based on a non-Gaussian diffusion
model better reckons for restricted water diffusion within the complex
microstructure of the biological tissues [3]. We performed MD and Da values to
be lower, MK, Ka and Kr values to be significantly higher, in lesions staged
IB. A possible explanation is that there is more marked variation in cell size
and shape within lesions staged IB in comparison with lesions staged IA [4].Conclusion
The
pilot study demonstrated that DKI sequence can be used to distinguish stage IA
and IB of EC, and has potential value to be a non-enhancement quantitative
index for staging EC.Acknowledgements
No acknowledgement found. References
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