Yasuo Takatsu1,2, Masafumi Nakamura3, Satoshi Kobayashi4, and Tosiaki Miyati4
1Department of Radiological Technology, Faculty of Health and Welfare, Tokushima Bunri University, Sanuki-city, Japan, 2Department of System Control Engineering, Graduate School of Engineering, Tokushima Bunri University, Sanuki-city, Japan, 3Department of Radiology, Otsu City Hospital, Otsu, Japan, 4Division of Health Sciences, Graduate School of Medical Sciences, Kanazawa University, Kanazawa, Japan
Synopsis
The hepatobiliary
phase image using Gd–EOB–DTPA in the liver MRI is assessed by the quantitative
liver–spleen contrast ratio (Q-LSC) , the cutoff value at which tumors can be
easily determined is 1.5. However, Q-LSC is found unsuitable for cases of splenectomy
and when there is splenic deposition of Gamna–Gandy bodies. Therefore, the quantitative
liver-portal vein contrast ratio (Q-LPC) is useful instead of Q-LSC. The cutoff
value of Q-LPC was at 1.462, the sensitivity and the specificity were higher than
Q-LSC at the cutoff value. Q-LPC cutoff value can be used for hepatobiliary phase MR image
evaluation.
Background
Gadolinium–ethoxybenzyl–diethylenetriamine
penta-acetic acid (Gd–EOB–DTPA) has been widely used in diagnosing liver tumors
in magnetic resonance imaging (MRI). Gd–EOB–DTPA is found to accumulate in the
liver cells over time [1]; therefore, the contrast between the liver parenchyma
and tumor is enhanced in the hepatobiliary phase (HBP). The quantitative liver–spleen contrast ratio (Q-LSC) has
been well-reported as an evaluation method [2], and the cutoff value at which
tumors can be easily determined is 1.5 [3]. However, Q-LSC is found unsuitable
for cases of splenectomy and when there is splenic deposition of Gamna–Gandy
bodies. Therefore, instead of the spleen, the contrast between the portal vein
and the liver parenchyma can be measured. Referred to as
the quantitative liver-portal vein contrast ratio (Q-LPC) [4], it is reported
to have a high correlation with Q-LSC. [4] However, the cutoff value for Q-LPC has
yet to be determined, and therefore, there is no way to assess it in HBP
images.Purpose
The
aim of the present study was to calculate the quantitative liver-portal vein contrast
ratio (Q-LPC) cutoff value based on tumor detectability by using receiver
operating characteristic curves (ROC).Methods
This study enrolled 74 patients with tumor (46 males and 28
females; age, 71.0 ± 8.1 years) who underwent liver MRI using Gd–EOB–DTPA. Some
patients were found to have multiple tumors. In total, 102 tumor images were evaluated
for Q-LSC and Q-LPC 10 minutes after administration of Gd–EOB–DTPA. MRI was
performed using a 3-T MRI unit (Ingenia, anterior coil; Philips Medical
Systems, Best, the Netherlands) with fat-saturated three-dimensional gradient
echo sequences. the contrast between normal liver parenchyma and spleen [5] and
normal liver parenchyma and portal vein were calculated as follows: Q-LSC = SIL/SIS,
Q-LPC = SIL/SIPV, where SIL is the mean signal intensity (SI)
value of the ROI for the normal liver parenchyma, SIS is the
mean SI value of a homogeneous area of the spleen, and SIPV
is the mean SI value of the portal vein.We
compared Q-LPC with Q-LSC in order to assess its cutoff value and usefulness. ROC evaluation was performed
using the 50-point continuous confidence method, with a free scale of 50 mm. A
score of 30 or more out of 50 points was considered good. Cutoff values of
Q-LPC and Q-LSC were then calculated. The areas under the curve (AUCs) were also
examined and compared.Results
The AUC–ROC
for Q-LPC was 0.858, 95% confidence interval (CI), 0.783–0.933. The cutoff
value was determined to be at 1.462. Sensitivity was 0.747, and specificity was
0.852 at the cutoff value. The AUC–ROC for Q-LSC was 0.710, 95% CI, 0.597–0.822).
The cutoff value was at 1.543, the sensitivity was 0.560, and the specificity
was 0.778 at the cutoff value. A significant difference was noted between the
AUCs (P = 0.0016). (Fig. 1)Conclusions
We
conclude that Q-LPC cutoff value can be used for hepatobiliary phase magnetic
resonance image evaluation.Acknowledgements
No acknowledgement found.References
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