Shang Wan1, Yi Wei1, Hehan Tang1, Lisha Nie2, Xiaocheng Wei2, and Bin Song3
1Radiology, West China Hospital, Sichuan University, Cheng Du, China, 2GE Healthcare Beijing China, Beijing, China, 3West China Hospital, Sichuan University, Cheng Du, China
Synopsis
Gd-EOB-DTPA has been
widely used in liver MR imaging for the evaluation of hepatic lesion, whereas, the long
intervals between the dynamic enhanced imaging and hepatobiliary phase imaging usually
influence patient throughput. Notably, the adjustment of diffusion weighted
imaging (DWI) sequence’s scanning order from pre-contrast to post-contrast is crucial
to overcome this limitation. However, few studies have investigated the apparent diffusion coefficient (ADC) values that at low
and high b values should be affected, respectively, thus, we aimed to prospectively
determine whether DWI at both low and high b-values should be affected before
and after gadoxetic acid-enhanced MR imaging.
Introduction
Liver cancer is the second most frequency cause
of cancer-related deaths of men worldwide1,2. At present,
Gd-EOB-DTPA has been widely used in liver MR imaging which enables not only the
traditional arterial phase imaging of hepatic lesions but further provide the
specific hepatobiliary phase. However, the hepatobiliary phase can be obtained
about 20 minutes delay after the
contrast agent injection, and patient throughput will be influenced
if no sequences were scanned during the long period time. Evidence has shown
that the adjustment of diffusion weighted imaging (DWI) sequence’s scanning
order from pre-contrast to post-contrast may help to overcome this limitation3-5, they found that the acquisition and optimization
of DWI during the interval between dynamic MRI and hepatobiliary imaging can be
effective and time-saving without compromising contrast-to-noise ration (CNR)
and apparent diffusion coefficient (ADC) values of focal hepatic
lesions5. However, most of these reports just explored the fitting ADC
values of both low and high b valve DWI, and few studies have investigated the
ADC values that at low and high b values should be affected, respectively. Therefore, the purpose of this paper was to determine
whether the DWI at both low and high b-values should be affected before and
after Gd-EOB-DTPA enhancement.Methods
This prospective study was
approved by the institutional review board, and written informed consent was
obtained from all patients. From July to November 2019, prospectively
acquired data of 73 patients with 97
focal hepatic lesions underwent gadoxetic acid-enhanced MR imaging were
included. MR imaging was carried out by using a 3.0 T MR system (Discovery MR
750w, GE Healthcare, Milwaukee, USA). Routine liver MRI protocols include: T1-weighted
imaging using in-phase and out-of-phase spoiled gradient echo (SPGR), dynamic
T1-weighted imaging using 3-dimentional (3D) liver imaging with volume acceleration-flexible (LAVA-FLEX),
T2-weighted imaging using fast spin echo (FSE) with PROPELLER technique and
chemical-shift fat saturation, single-shot-fast-spin-echo
with echo-planner-imaging (SSFSE-EPI) DWI with respiratory trigger (RT)
and multi-b-value (b=0, 50, 800, 1000 and 1200 s/mm2), 3D T1WI
LAVA-FLEX in hepatobiliary phase (HBP) were performed before and after
injecting gadoxetic acid. Detailed information of the MR parameters was shown in Figure
1. All the patients underwent with multi-b-value DWI before and after
contrast agent. The drawing methods of region
of interests (ROIs) were shown in Figure 2. Two abdominal radiologists reviewed all MR
images, and the contrast intensity ratio (CIR) value and ADC values at each value were calculated. The CIR of lesions at each b value images were calculated from the signal intensity
(SI) by using the following equation: CIR= (SI(lesion)
- SI(liver))/SI(muscle)4: Mann-Whitney U test was
used to compare the CIR and ADC values of each group and the receiver operating
characteristics (ROC) curves was used to determine the diagnostic
performance.Results
CIRs and ADC of
focal hepatic lesions were comparable on pre- and post-contrast images at each
b-value (all p>0.05) (Figure 3,
Figure 4). The ADC of liver parenchymal on the post-contrast was lower
than pre-contrast (all p<0.05).
The ADCs of malignant lesion were smaller than benign lesion on DWI with high
b-values (800, 1000, 1200 s/mm2) (all p<0.01), while no statistical difference was
shown between ADC of malignant tumors and benign tumors at b-value=50 s/mm2
(p(pre) = 0.606; p(post) = 0.637). The
b value of 1200 s/mm2 had the largest AUC value of 0.889 among 4 b-values of
DWI with enhancement, and subsequent with
the b value = 1000 (AUC=0.868), and 800 (AUC=0.866) s/mm2.Discussion
Our results indicated that DWI scanned
between the interval of dynamic enhanced imaging and hepatobiliary phase
imaging can save overall scanning time without influencing on CIRs, ADCs and diagnostic
capabilities of hepatic lesions at both low and high b-value. The result showed
that Gd-EOB-DTPA injection has no effect on the ADC value of focal hepatic
lesions without uptake of contrast agents, which was similar to previous
reports4,5,6,7. Unlike previous
reports that only discussed one single ADC value, this study evaluated the ADCs
at four b-values (50, 800, 1000, 1200 s/mm2). We also found that at
the high b-value (800, 1000, 1200 s/mm2), the ADC values of malignant
tumors (hepatocellular carcinomas(HCC) and metastases) were lower than benign lesions (cysts and hemangiomas)
in both pre- and post-contrast images, which was similar with Choi’s report5. This study also found
the diagnostic ability of ADCs at low b-value (50
s/mm2) DW images couldn’t distinguish the
malignant lesion from benign lesions. It may related to the principle, in which
the ADC maps obtained by low b-value DWI reflected more blood perfusion
information than water molecule movement8.
In addition, this study also compared the diagnostic ability of ADCs at
different b-values and found that, among the high b-value DWI images, the ADC1200
had the largest AUC, although it was not statistically different from ADC1000
and ADC800. It may be related to the principle, in which the water molecular
diffusion weight is heavier at higher b-value DWI9.Conclusions
Our study demonstrated that DWI acquisition
can be performed between dynamic enhanced scans and delayed hepatobiliary scans
to save overall scan time. Regardless of the high or the low b-value of DWI,
the ADC values of the lesion were not affected by the injection of Gd-EOB-DTPA.Acknowledgements
No acknowledgement found.References
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