Jie Yuan1, Mengxiao Liu2, Songhua Zhan1, Zhigang Gong1, and Qiang Shen1
1Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, Shanghai, China, 2MR scientific Marketing, Diagnostic Imaging, Siemens Healthineers Ltd, Shanghai, China
Synopsis
It is
important to combine histopathological and non-invasive imaging measurements to
assess tumor components and predict tumor invasiveness to define disease
treatment and prognostic assessment. In this study, we assessed the
relationships between DKI and IVIM parameter measurements and the corresponding
tumor tissue composition, regardless of the status of the malignant tumor. To
this end, we selected a range of tissue parameters informative for important
biological properties of the tumor, such as Ki-67, the tumor: stroma ratio,
CD34 etc.
Purpose
To correlate non-invasive quantitative diffusion kurtosis
imaging (DKI) and intravoxel incoherent motion-derived (IVIM) parameters with rectal
cancer composition assessed by the expression of caudal-type homeobox 2 (CDX-2),
Vimentin (VIM) and CD34 on resected tissues, as well as the tumor stroma ratio
(TSR) and the results of H&E and Masson staining.
Materials
and Methods
A prospective study of 26 patients with
rectal cancer were included in this
study. All patients underwent magnetic resonance (MR) imaging, including DKI and
IVIM at a 3 T scanner(Magnetom Skyra, Siemens Healthcare, Erlangen, Germany) with a 18
channel coil. Oblique axial DKI with b values
of 0, 700, 1400, 2100 sec/mm2 (with no. of averages=1, 2, 8, 8,
respectively) and IVIM with b values
of 0, 20, 50, 70, 150, 400 and 800 sec/mm2 were performed using a
single-shot echo-planar imaging sequence with similar parameters. Primary tumor
was harvested and fixed for H&E, immunohistochemistry and Masson staining.
Results
Here, we document a number of correlations between non-invasive MR
imaging parameters and the composition of rectal cancer tissue after resection.
The apparent diffusion coefficient (ADC)DKI exhibited
a weak negative correlation with CDX-2 (r=-0.367,
P=0.068) whereas MKDKI showed a moderate negative correlation with this
marker (r=-0.422, P=0.04) and a moderate positive correlation with CD34
(r=0.421, P=0.041). ADCIVIM exhibited a
moderate positive correlation with Masson staining (r=0.426, P=0.048) and a weak
negative correlation with CDX-2 (r=-0.394, P=0.007). The fIVIM was weakly
negatively correlated with the TSR (r=-0.364, P=0.088). DIVIM showed
a moderate negative correlation with CDX-2 (r=-0.58, P=0.005) and a moderate
positive correlation with CD34 (r=0.403, P=0.063). DIVIM showed a
weak negative correlation with Ki-67 (r=-0.378, P=0.075) and a weak positive correlation
with Masson (r=0.39, P=0.072). Finally, D*IVIM showed a moderate
positive correlation with VIM (r=0.445, P=0.033) and a weak positive
correlation with CD34 (r=0.38, P=0.073).
Conclusion
The present prospective study linked DKI and IVIM
to tissue structure assessed by histopathology after rectal resection. By
comparing DKI and IVIM parameters and histological sections, this work revealed
correlations between MRI parameters and the composition of rectal cancer
tissue. Thus, this study documents the use of DKI and IVIM values to non-invasively
establish tumor biological properties in rectal cancer.Acknowledgements
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