Neil P Jerome1,2, Matthew R Orton2, James A d'Arcy2, David J Collins2, Martin O Leach2, and Dow-Mu Koh3
1Department of Circulation and Medical Imaging, NTNU - Norwegian University of Science and Technology, Trondheim, Norway, 2Radiotherapy & Imaging, The Institute of Cancer Research, London, United Kingdom, 3Department of Radiology, The Royal Marsden Hospital, London, United Kingdom
Synopsis
Respiratory motion represents a serious confounding factor for
abdominal imaging; for more complex diffusion models such as IVIM, acquisition
of diffusion-weighted images in successive breath-holds offers control of
motion for sharper images. In this patient study, DWI was performed in
free-breathing and consecutive breath-holds, without registration, on
successive days without intervention to determine repeatability. Derived tumour
ROI parameters from ADC and IVIM models were not significantly affected between
breathing regimes, but observed coefficients of variation for free-breathing
were smaller for all pseudo-diffusion related parameters. Breath-holding is
time inefficient, and free-breathing allows more data collection for
development of robust DWI markers.
Introduction
The difficulty of imaging lesions in the abdomen is well
known (1); substantial blurring arising
from respiratory motion can severely compromise image quality,
and confound interpretation and analysis of functional MR images. The increased
use of longer, multiple-b-value diffusion-weighted imaging protocols such as
Intravoxel Incoherent Motion (IVIM) suggest a demand for motion-compensating or
control techniques at the point of acquisition, such as navigator-triggering or
breath-hold. Post-processing techniques, most commonly registration, offer
improvements to image appearance at the cost of off-line
computational effort (2). In this study, patients with
renal cell carcinoma underwent free-breathing (FB) and breath-holding (BH, in
expiration) multiple-b-value DWI protocols on successive days, in order to
assess the effect on derived diffusion parameter values and repeatability.Methods
Patients (n=11) with metastatic renal cell carcinoma gave
informed consent, and underwent diffusion-weighted imaging with the following
parameters: prototype single shot EPI, 3-scan-trace monopolar diffusion
weighting, 5 mm slices acquired coronally (n=5) or axially (n=6), FOV 380x380
mm, resolution 1.5x1.5 mm in-plane (interpolated), iPAT factor 2, and with
b-values 0, 20, 40, 60, 80, 100, 250, 500, and 750 mm-2s. For FB,
NSA = 5 for a total acquisition time of 9 minutes; for BH, each 20 s breath-hold
consisted of NSA = 1 for b = [0, X] where X is each successive non-zero b-value.
Including resting time, the total time for BH acquisition was approximately 7
minutes. All images were used for analysis, conducted using in-house software
(ADEPT, ICR, London UK) to fit both ADC and IVIM models, using a Markov Chain
Monte Carlo approach on a voxel-by voxel basis within ROIs drawn around the
tumour in 5 central imaging slices by an expert radiologist. Median values per
ROI were recorded, and the results for each parameter tested for significance
(p < 0.05) between successive days and breathing strategies using a
multi-way ANOVA. Repeat-measures Coefficients of Variation (CoV) were
calculated for each parameter and breathing strategy.Results
All FB data were acquired successfully on both days; data
for BH were excluded for two patients on one visit owing to image artefacts, and
so CoV calculations excluded these data. Lesions ranged in size from 30.5 to 1864.6 cm3, with CoV of voxel counts for BH and FB of 10.8 and 12.2%
respectively. Images acquired in breath-hold appeared visually to suffer less
from respiration blurring (Figure 1). The values for DWI
parameters (median in ROI) are given in Table 1 as cohort mean ± s.d., and show good repeatability for
ADC and D in both breathing regimes, with CoV values lower than 7%. The IVIM
parameters associated with pseudodiffusion, f, D*, and the compound parameter fD*, have
higher CoV values indicating lower repeatability, although in all cases
these are smaller for FB compared to BH. The comparison of all parameters is
shown in Figure 2; no significant difference was observed between BH and FB or
between successive day’s scans for any of the parameter values (p = 0.19 and
p = 0.40 respectively, ANOVA). The
values for D were significantly lower than those for ADC for the corresponding
day and breathing regime (p < 0.01, ANOVA), indicating the influence of
observed non-monoexponential decay when using the ADC model, which implicitly
assumes monoexponential behaviour.Discussion
The use of DWI parameters in lesion detection and
characterisation relies both on their sensitivity and their robustness, and so
acceptable repeatability is essential for critical assessment and
interpretation of results. The desire to reduce blurring in diffusion images is
borne of a visual frame of reference, but this contrasts with functional
imaging studies that typically involve post-processing and analysis at an ROI
level. In such cases, strategies to ameliorate respiratory motion may lead to
increased patient discomfort, while the reduced efficiency of data acquisition
compared to free-breathing does not benefit the accuracy or precision of
resulting parameters, similarly to navigator-triggered acquisitions (3). Acquisition of successive
breath-holds with a matched contrast (b=0) image may offer advantages for
registration techniques, which may circumvent the difficulty of co-registering
images with altered contrast; this introduces a considerable offline component
to the data analysis, and will be explored in future work. In this study,
parameters derived from a multiple-b-value abdominal DWI protocol in a patient
cohort show no benefit of breath-holding over free-breathing for ADC and IVIM
summary statistics in renal cell carcinoma; where robustness of analysis is improved by amount of
sampling, the scanning efficiency of free-breathing improves the repeatability
and thus performance of the resulting parameters for use as clinical
biomarkers.Acknowledgements
CRUK and EPSRC support to the Cancer Imaging Centre at The Institute of
Cancer Research and The Royal Marsden Hospital in association with the MRC and
Department of Health (England) (C1060/A10334, C1060/A16464) and NHS funding to
the NIHR Biomedical Research Centre and the Clinical Research Facility in
Imaging at The Royal Marsden and the ICR. We acknowledge support from Siemens
for use of work-in-progress DWI sequences.References
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D-M, Collins DJ, Orton MR. Intravoxel incoherent motion in body
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