Nandita deSouza1, Matthew Orton1, Kate Downey1, Veronica Morgan1, David Collins1, Sharon Giles1, and Geoffrey Payne1
1CRUK/EPSRC Cancer Imaging Centre, The Institute of Cancer Research and The Royal Marsden NHS Foundation Trust, Sutton, United Kingdom
Synopsis
Diffusion-weighted MRI (DW-MRI) suffers from distortion
induced by susceptibility variation and eddy-currents. To correct this for endovaginal imaging of
the uterine cervix, we implemented the forward and reversed gradient technique
proposed by Chang and Fitzpatrick in the phase-encode direction and assessed
clinical utility of the technique. This
required acquisition of two images of the cervix under the same conditions. Correction of distortions significantly
improved diagnostic performance for an experienced observer when images were
viewed with the T2-W images. Correction
allowed definitive diagnosis in a third of cases with tumour volumes of
<0.2cm3 classified as equivocal on uncorrected images.Target Audience
Radiologists and physicists
interested in correcting and assessing distortions on clinical images.
Background and
Purpose
Diffusion-weighted MRI (DW-MRI) employed to improve the detection of
small cervical tumours suffers from distortion induced by susceptibility
variation and severe eddy-currents. Eddy-current related distortions are caused
by strong diffusion-sensitizing magnetic field gradients which have short ramp
times and depend on the magnitude and direction of the diffusion encoding field
gradients. This adds to the susceptibility induced distortions in EPI-based
sequences where residual eddy-currents cause translation (B0 eddy-current
field). To correct for spatial distortions on spin-echo MR images the forward
and reversed gradient technique proposed by Chang and Fitzpatrick requires the
acquisition of two images of the same object under the same conditions except
for the polarity of the frequency- encode line. For DW-EPI, we have implemented
a forward and reversed gradient technique in the phase-encode direction and
investigate the clinical utility of the technique when viewed with T2-W images.
Methods
Forty-one patients aged 25-72 years, (mean 40+11
years) with cervical cancer were imaged at 3.0T (Philips Achieva) using an
endovaginal receiver coil developed in-house [2]. T2 Weighted (T2-W) TSE images
were acquired in three planes orthogonal to the cervix (FOV 100mm, TE=80ms,
TR=3400ms, SPIR fat suppression, left-right phase encoding, 2 averages, image
acquisition matrix 288×288, 0.35mm resolution, 24 slices with 2mm slice
thickness and 0.2mm separation). Diffusion-weighted images were acquired
coronal to the cervix (single shot SE EPI, FOV 100mm, TE=52ms, TR=8000ms, SPIR
fat suppression, left-right phase encoding, 1 average, band-width 9.6Hz/pixel,
EPI factor 115, acquisition matrix 80×80, 1.25mm in-plane resolution, b-values
0, 100, 300, 500 and 800s/mm2, 24 slices with 2mm slice thickness
and 0.2mm separation). A left-right phase encoding was chosen rather than
anterior-posterior encoding to avoid artefacts through the cervix and the
gradient reversal method applied along the phase-encode (left-right) axis.
Acquisition time for the diffusion-weighted images was 4 min and 33 sec for
each gradient direction. Corrected images were generated using the
Chang-Fitzpatrick algorithm in MATLAB (The MathWorks, Natick, Massachusetts).
Images were scored as positive, negative or equivocal for tumor by two
independent observers of 20 years and 3 years experience of endovaginal MRI
respectively on viewing the T2-W and left gradient images together and the T2W
and right gradient images together. In the equivocal group, the T2-W+corrected
images were viewed together and scored either as positive or negative for
tumor. All cases that were scored as positive for tumor by the experienced
observer had tumor volume measured on the T2-W images by drawing a region of
interest around an intermediate signal intensity lesion that showed
corresponding diffusion restriction and multiplying the sum of the areas by the
slice thickness.
Results
Tumor volume
in these patients ranged from 0.07-18.4cm
3 (mean
+SD 4.4
+5.6cm
3).
Classification for tumor presence on uncorrected and corrected images are given
in Table 1 along with intraobserver agreement. Sensitivity and specificity against subsequent histology for corrected
images was 100% (8/8) and 50% (3/6) for observer 1 (Figure 1) and 50% and 20%
respectively for observer 2. Tumor volume for the uncorrected images classified
as positive was 4.4
+5.6cm
3, for the images
classified as equivocal it was 0.18
+0.44cm
3.
Discussion
Phase-based methods of
distortion correction [3] yield good corrections but they suffer from increased
acquisition time. For our work, the method of Chang and Fitzpatrick offered the
simplest solution, albeit requiring an extra image acquisition for the patient.
It also had the advantage that the corrected images generated from the combined
distorted left and right gradient images were expected to exhibit a
signal-to-noise ratio higher than either of the distorted images [4]. Also,
despite the limitation that an extra sequence was required incurring a time penalty,
the addition of distortion correction enabled the 34% of equivocal cases (maximum
tumor volume 1.5cm
3) to be further classified with high
sensitivity. The low specificity is likely related to the limits of the spatial
resolution of the technique in relation to tumor volume. The improvement in
diagnostic performance of the corrected images was primarily of benefit to an
experienced compared to a less experienced observer.
Distortions
encountered with an EPI based diffusion-weighted sequence were particularly
pronounced in our study because of the B0 field inhomogeneity induced by the
endovaginal coil, but the correction methods described here may be applied to
any situation or commercial coil where excessive B0 distortion is
encountered.
Conclusion
Application
of the reverse gradient algorithm for distortion correction of echo-planar
diffusion-weighted endovaginal images improved diagnostic performance in a
third of cases for a more experienced observer.
Acknowledgements
CRUK and EPSRC support to the Cancer Imaging Centre at ICR and RMH in association with MRC and Department of Health C1060/A10334, C1060/A16464 and NHS funding to the NIHR Biomedical Research Centre and the Clinical Research Facility in Imaging.References
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