Xing Meng1, Ailian Liu 1, Shifeng Tian1, Zhiwei Shen2, Tianjing Zhang2, Yishi Wang2, Yaxin Niu1, and Wan Dong1
1Department of Radiology, the First Affiliated Hospital of Dalian Medical University, Dalian, China, 2Philips Healthcare, Beijing, China
Synopsis
Amide proton transfer (APT)
combined with intravoxel incoherent motion (IVIM)
has been preliminarily applied in the diagnosis and differentiation of cervical
squamous cell carcinoma, but has not been in the identification of endometrial
lesions. We discussed the value of APT combined with IVIM in differentiating
endometrial carcinoma from endometrial benign
lesions. The AUC, sensitivity and specificity of APT combined IVIM were 0.979,
87.5% and 100%, respectively.
INTRODUCTION
Endometrial
carcinoma
and endometrial benign lesions have similar clinical manifestations with most
of which are irregular vaginal bleeding and fluid flow, but the treatment and
prognosis are quite different. Endometrial benign lesions can be treated with
hysteroscopy, while endometrial carcinoma surgery still needs appropriate adjuvant
treatment according to the condition. Therefore, an effective examination method
to differentiate and diagnose these two diseases before operation is
particularly important. As an endogenous chemical exchange saturation transfer
(CEST) imaging technique, amide protron transfer (APT) imaging has received
extensive attention in clinical practice [1]. Intravoxel
incoherent motion (IVIM) refers to the distribution of velocity in direction or
amplitude within a given voxel and measurement time, which can quantify the
pure diffusion movement of water molecules in tissues and organs, measure
microcirculation perfusion and other information, and comprehensively reflect
the pathophysiological state of tissues [2,3]. Previous studies have
shown that APT combined with IVIM technology has been preliminarily applied in
the diagnosis and differentiation of cervical squamous cell carcinoma [4]. In
this study, we discussed the value of APT combined with IVIM in the
differential diagnosis of endometrial carcinoma and endometrial benign lesions.METHODS
Data of 8 cases of
endometrial carcinoma and 6 cases of endometrial benign lesions (5 cases of
endometrial polyps and 1 case of endometrial hyperplasia) confirmed by surgery
and pathology were retrospectively analyzed. All patients underwent MRI , APT
and IVIM imaging on a 3.0 T MR scanner (Ingenia CX, Philips Healthcare, the
Netherlands) before surgery. The scanning parameters are shown in table 1. IVIM
adopted 11 b values (b= 0, 20, 50, 100, 150, 200, 400, 800, 1200, 2000, and 3000). Without
knowing the pathological results, the two observers identified the lesion area
of endometrium through T2WI and DWI. After the fusion of APT image and T2WI,
the ROI was delineated in the corresponding lesion area, and APT value was
obtained and recorded. ROI was mapped in the corresponding
region of IVIM imaging to obtain the lesion's pure diffusion coefficient (D),
pseudo-diffusion coefficient (D*) and perfusion fraction (f). Intra-group
correlation coefficient (ICC) was used to test the consistency of measurement
results between the two observers. The rank sum test was used to analyze the
difference of each parameter between the two groups, and ROC was used to
evaluate the diagnostic efficacy. This study has been
approved by the local IRB.RESULTS
The
results of parameter values and consistency test were measured by two observers
in the two groups, and the numerical consistency was good in each group with ICC>0.75.
APT value of endometrial carcinoma group was significantly higher than that of
benign lesion group and D value of endometrial carcinoma group was significantly
lower than that of benign lesion group (P<0.05). There was no statistically
significant difference between the two groups in D* value and f
value (P>0.05). The specific results were shown in table 2 and figure 1. The
AUC values of APT, D and their combination are shown in table 3.DISCUSSION AND CONCLUSIONS
APT
value in the endometrial carcinoma group was higher than that in the
endometrial benign lesion group. This may due to the tumor cells in endometrial
carcinoma were more metabolically active than those in the endometrial benign
lesion group, and changes in protein concentration and pH value caused an
increase in APT value [5]. The
D value reflects the microscopic movement of water molecules. The arrangement
of endometrial carcinoma cells is closer than that of endometrial benign
lesions, and hence the intercellular space becomes smaller, and the movement of
water molecules is limited causing the D value decreases, which is consistent
with the results of this study. The AUC, sensitivity and specificity of APT
combined IVIM were 0.979, 87.5% and 100%, respectively. Therefore, APT combined
with IVIM can effectively differentiate endometrial carcinoma from endometrial
benign lesions, which has promising clinical application value.Acknowledgements
No acknowledgement.References
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