Jinrong Qu1, Hongkai Zhang2, Xu Yan3, Shaoyu Wang4, and Thomas Benkert5
1Radiology, the Affiliated Cancer Hospital of Zhengzhou University & Henan Cancer Hospital, Zhengzhou, China, 2Radiology, the Affiliated Cancer Hospital of Zhengzhou University, Zhengzhou, China, 3MR Scientific Marketing, Siemens Healthcare, Shanghai, China, 4MR Scientific Marketing, Siemens Healthcare, Xi'an, China, 5Application Development, Siemens Healthcare GmbH, Erlangen, Germany
Synopsis
This
study evaluated a new diffusion weighted imaging (DWI) technique for assessing rectal
cancer. Based on a population of 12 patients diagnosed with rectal carcinoma,
images were acquired using both Read-out Segmented Echo-Planar Imaging (RESOLVE) and integrated
slice-specific shimming (iShim)-DWI sequences using the same field of view (FOV)
at 3T in assessment of rectal carcinoma. The quality of the images was compared based on
independent review by radiologists plus parameter data analysis. The results
showed that the image quality and lesion conspicuity of the iShim-DWI sequence were
significantly better than RESOLVE DWI sequence in assessment of rectal
carcinoma at 3T.
Background and Purpose
Diffusion weighted imaging (DWI) plays a valuable role
in assessing rectal cancer, such that the apparent diffusion coefficient (ADC)
of cancerous rectal tissue may quantitatively predict histopathological tumor (T)
staging and grade in a noninvasive manner1. Read-out Segmented
Echo-Planar Imaging (RESOLVE) and integrated slice-specific shimming (iShim)-DWI
sequences have shown greater advantages than conventional DWI, based on
previous studies.2
3 However, no previously published research was
found that analyzes the image quality (IQ)
of both RESOLVE
and iShim-DWI sequences
in rectal cancer. Therefore, the purpose of this study was to compare IQ between RESOLVE
and iShim-DWI sequences using the same field-of-view (FOV) at 3T in assessment
of rectal carcinoma.
Materials and Methods
This study was approved by
the Hospital Ethics Committee, and written informed consent was acquired. Participants
comprised 12
patients with rectal cancer who received magnetic resonance (MR) examinations
on a 3T scanner (MAGNETOM Prisma, Siemens Healthcare, Erlangen, Germany),
including RESOLVE and a prototype iShim-DWI
sequences. The detailed sequence parameters used are as follows: (1) RESOLVE-DWI:
thickness =3mm, repetition time/echo time (TR/TE) =4600-5200ms/53-56ms, matrix=142X142, FOV=220mm, scanning time=204s, b=50, 1000 s/mm²; (2) iShim-DWI:
thickness =3mm, TR/TE =7700ms/68ms, matrix=248X256, FOV=220mm, scanning time=78s, b=50, 1000 s/mm².The signal-to-noise ratio
(SNR) and contrast-to-noise ratio (CNR) were quantitatively evaluated using a paired
t-test. Two radiologists independently assessed subjective IQ parameters based
on: image sharpness, distortion, artifacts, lesion conspicuity, and overall
subjective IQ of both sequences. The Wilcoxon signed-rank test was used to
compare subjective IQ scores and tumor ADCs between RESOLVE-DWI and iShim-DWI. Results
CNR was significantly greater in iShim-DWI
(9.57 ± 2.49, [Figure 1; images A, C]) than that in the RESOLVE DWI (7.74 ±2.21,
P < 0.001 [Figure 1, Image B]). SNR was significantly higher in iShim-DWI (130.59
± 11.01) than that in RESOLVE DWI (37.16 ± 11.20, P < 0.001). The subjective IQ
parameters of iShim-DWI sequence (Figure 1; image A) were rated superior to
those of RESOLVE DWI (Figure 1; image B) sequence by both readers (P <
0.001). No significant difference was found between the mean tumor ADC values
of both sequences (iShim-DWI [0.991 ± 0.121]; RESOLVE DWI [0.100 ± 0.126 x 10-3
mm2 /s, P = 0.617]).
Conclusion
The iShim-DWI sequence provided significantly better IQ and lesion conspicuity
than RESOLVE DWI sequence in assessment of rectal carcinoma at 3T. The number of
cases is small, and larger sample size may provide more information.Acknowledgements
References
1. Peng Y, Li Z,
Tang H, et al. Comparison of reduced field-of-view diffusion-weighted imaging
(DWI) and conventional DWI techniques in the assessment of rectal carcinoma at
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