Zheng Ye1, Shan Yao1, Ting Yang1, Qing Li2, Robert Grimm3, Zhenlin Li1, and Bin Song1
1Department of Radiology, West China Hospital, Sichuan University, Chengdu, China, 2MR collaborations, Siemens Healthcare Ltd., Shanghai, China, 3MR Application Predevelopment, Siemens Healthcare GmbH, Erlangen, Germany
Synopsis
Keywords: Quantitative Imaging, Diffusion/other diffusion imaging techniques
Although diffusion weighted MR imaging is of great
importance in the diagnosis and evaluation of hepatocellular carcinoma (HCC),
it is limited by long acquisition times. Simultaneous multi-slice (SMS)
technique can reduce scan time and has been proved to be feasible in liver
imaging. Our study included twenty patients with HCC, and acquired conventional
and SMS-accelerated diffusion data with different models (DWI, DKI and IVIM). By analyzing quantitative parametric maps, we found SMS technique did not affect the quantitative
measurements of HCC. However, the difference of mean kurtosis between
conventional and SMS-accelerated DKI in liver parenchyma should be noted.
Introduction
Diffusion weighted imaging (DWI) plays an essential
role in the detection and diagnosis of hepatocellular carcinoma (HCC)1.
In addition, previous studies have shown that quantitative diffusion parameters
can predict tumor aggressiveness and evaluate treatment response of HCC2,3.
Despite the great clinical potential, liver DWI still suffers from many
practical problems4. Notably, the relatively long acquisition time
of DWI with multiple b-values or advanced diffusion models, such as diffusion
kurtosis imaging (DKI) and intravoxel incoherent motion (IVIM), may hamper its
widespread application in clinical practice. With recent advances in MR
imaging, simultaneous multi-slice (SMS) acceleration technique has been
developed to reduce scan time5. The feasibility of SMS technique has
been demonstrated in abdominal DWI with shortened acquisition time and
comparable image quality6,7. However, the impact of SMS technique on
quantitative measurements in
different diffusion models, especially in diseased tissues, remains
unknown.Purpose
To investigate whether SMS technique affects the
quantitative measurements of diffusion weighted MR imaging sequences in HCC and
liver parenchyma.Materials and Methods
Institutional review board approved this prospective
study and all participants provided written informed consent. A total of twenty
patients (sixteen men and four women; mean age ± standard deviation [SD], 55.15
years ± 11.47) with pathology-proven HCC were included from June 2021 to
October 2021. Preoperative MR examinations were performed on a 3 T scanner (MAGNETOM Skyra, Siemens Healthineers, Erlangen, Germany) with an
18-channel body coil. Conventional (CON) and SMS-accelerated diffusion weighted
sequences, including CON-DWI, SMS-DWI, CON-DKI, SMS-DKI, CON-IVIM, SMS-IVIM, were
conducted sequentially in free-breathing manner (Figure 1). All images were
transferred to syngo.via frontiers workstation and analyzed by a prototype MR Body
Diffusion toolbox (v1.4.0), yielding apparent diffusion coefficient (ADC) for DWI,
mean kurtosis (MK) and mean diffusivity (MD) for DKI, as well as true diffusion
coefficient (D), perfusion-related diffusion (D*) and perfusion
fraction (f) for IVIM. Two experienced researchers independently performed
region of interest (ROI) analysis for quantitative measurements (Figure 2
and Figure 3). For HCC lesion, a free-hand ROI was drawn along the tumor
margin at the slice of largest tumor diameter, excluding necrotic and
hemorrhage areas. For liver parenchyma, three circle ROIs were placed on the
right liver lobe, avoiding major vessels, tumor, and artifact. Statistical differences between
conventional and SMS-accelerated diffusion
parameters of HCC and liver parenchyma were assessed using pair t test or
Wilcoxon signed rank test, where appropriate. Bland-Altman method was used to
evaluate the distribution and concordance of quantitative parameters of HCC
between conventional
and SMS-accelerated sequences.Results
The acquisition times of SMS-DWI, SMS-DKI and SMS-IVIM were approximately 37.35%, 44.44%
and 30.69% faster than that of the conventional sequences, respectively. As
shown in Figure 4, there was no significant difference of quantitative
measurements between conventional and SMS- accelerated diffusion-weighted
sequences in HCC (all p value > 0.05). For liver parenchyma, the
MK value from CON-DKI was significantly
lower than that of SMS-DKI (0.83 ± 0.86 versus 0.91 ± 0.12, p = 0.016), while other quantitative
diffusion parameters did not differ significantly between conventional and SMS-accelerated
sequences (all p value > 0.05). As shown in Figure 5, Bland-Altman
plots demonstrated good agreement of quantitative
parameters in HCC
between conventional and SMS-accelerated diffusion sequences, with acceptable
absolute mean biases and most measurements within the limits of agreement
(LOA).Discussion
Thanks to the specialized multiband radiofrequency
(RF) pulse and the information from coil sensitivity, SMS technique can
simultaneously excite multiple slices and acquire image data at the same time.
Recently, Xu et al. found SMS technique provided considerable scan time
reduction for abdominal DWI with equivalent quantitative parameters compared
with the nonaccelerated sequences, which was in good accordance with our study7.
In addition to the good agreement of conventional and SMS-accelerated diffusion
parameters in HCC, we also found the MK value in the CON-DKI was significantly lower than that of SMS-DKI in liver parenchyma.
Similarly, the trend of increased liver MK with increased acceleration factor
was also reported8. Moreover, other studies have shown mixed results
regarding the difference between CON-ADC and SMS-ADC in the liver5,9,
probably because the scanning protocols were different among these studies.Conclusion
SMS technique can significantly accelerate the
acquisition of diffusion weighted sequences, and SMS-accelerated diffusion
sequences provide quantitative parameters similar to conventional sequences in HCC, showing great promise in
clinical applications.Acknowledgements
None.References
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