Debosmita Biswas1,2, Dariya Malyarenko3, Wesley Surento1, Johannes Peeters4, Hye Shin Ahn1,5, Dallas Turley6, Habib Rahbar1, Wei Huang7, Thomas L Chenevert3, and Savannah C Partridge1,2
1Department of Radiology, University of Washington, Seattle, WA, United States, 2Department of Bioengineering, University of Washington, Seattle, WA, United States, 3Department of Radiology, University of Michigan, Ann Arbor, MI, United States, 4MR Clinical Science, Philips, Best, Netherlands, 5Department of Radiology, College of Medicine, Chung-Ang University Hospital, Seoul, Korea, Republic of, 6Philips Healthcare, Bothell, WA, United States, 7Advanced Imaging Research Center, Oregon Health and Science University, Portland, OR, United States
Synopsis
Keywords: Breast, Gradients, Gradient Non linearity
Motivation: Improve accuracy of ADC measurement by correcting spatial nonuniformity of diffusion weighting caused by gradient nonlinearity (GNL) using novel vendor implemented on-scanner tools
Goal(s): Evaluate GNL correction of breast tumor ADC in a treatment response study
Approach: Implement on-scanner GNL correction, evaluate uncorrected and corrected tumor ADCs, evaluate GNL bias and ADC changes pre-treatment and post one cycle of neoadjuvant chemotherapy.
Results: Preliminary results from this study indicate adequate performance of the vendor implemented GNL correction of ADC in breast DWI assessment of response to neoadjuvant chemotherapy.
Impact: This pilot study demonstrates vendor-implemented GNL-correction
(GNC) of spatially dependent b-value bias can dramatically simplify the process
of obtaining more accurate ADC measures, which can improve robustness of ADC as
a biomarker for treatment response.
Introduction
Apparent Diffusion Coefficient (ADC) has shown potential as a non-invasive
biomarker to predict tumor response in neoadjuvant chemotherapy (NAC) trials [1].
Previous retrospective studies have demonstrated that offline correction for spatial non-uniformity of diffusion
weighting (DW) b-values caused by system-specific gradient nonlinearity (GNL) can
improve ADC accuracy. The bias in ADC measures is mainly
determined by the gradient platform and the tissue offset from magnet isocenter
[2]. In longitudinal studies such as for monitoring response to therapy,
scanner system and patient positioning may vary between MRI examinations. Emerging vendor provided GNL correction (GNC) tools can generate
accurate ADC maps in real time, increasing feasibility of integration in
clinical workflow [3]. The purpose of this study was to prospectively explore
the utility of on-scanner GNL correction for breast cancer ADC measures in a
longitudinal NAC response study. Method
Study Cohort: In this ongoing prospective IRB approved study,
women diagnosed with breast cancer and recommended for NAC as a part of their
clinical care were enrolled to undergo longitudinal MRI monitoring during
treatment. They underwent research MRIs at four treatment timepoints: 1) pre-treatment
(baseline), 2) after one cycle of NAC (post-NACx1), 3) mid-treatment, and 4) after
completion of NAC and prior to surgery. For this preliminary analysis of GNC
efficacy, we evaluated only the first two treatment timepoints (pre-treatment
and post-NACx1).
MRI Acquisition: MRI acquisitions were
performed on a 3T clinical scanner using a 16-channel
breast coil (Achieva [60 cm bore diameter with Mammotrak coil] or Ingenia system [70 cm bore with dStream coil], Philips, Best, Netherlands). Data were acquired according to ACR guidelines, including DCE, T2w
TSE, and DWI. DWI was acquired with b = 0, 100, 600, 800 s/mm2,
TR/TE = 3500/66 ms, SENSE = 2.8, MB SENSE = 2, EPI factor = 67, and 1.8 ×
1.8 ×
4 mm3 resolution. DWI and ADC maps before and after GNC were created
on the scanner in real time.
Image Processing: Tumor regions of interest (ROIs) were segmented
on b=800 s/mm2 images using a semi-automated threshold tool, supervised
by a fellowship trained radiologist. The tumor ROIs were propagated to the
scanner generated ADC maps. All image processing was performed in the MATLAB
environment. Fractional Bias was calculated as (ADC-ADCGNC)/ADCGNC
for ROI-mean ADC values.
Statistical Analysis: Paired Wilcoxon signed-rank test was
used to compare mean ADC values between visits and between ADC and ADCGNC
values. All statistical analysis was performed in R.Results
On-scanner
GNL-corrected ADC maps were generated for 10 women at baseline and post-NACx1
visits. Of these, 80% (8/10) cases were invasive ductal carcinomas (IDC), 10%
(1/10) were invasive lobular carcinomas (ILC) and 1 was a mixture of IDC and ILC.
The tumor ROI sizes ranged between 18 and 43 voxels. The ADCGNC map,
percentage fractional bias map and the percent GNL model bias map for a patient
on the Achieva scanner system are shown in Fig1, indicating good agreement
between predicted and observed fractional bias. 30%
(6/20) of the exams were scanned on the Achieva system and the remaining on the
Ingenia system. The %fractional bias in tumor ADC was higher for the Ingenia versus
Achieva gradient systems, which is consistent with the % GNL bias model for these
systems (Fig2). GNL corrected tumor ADC measures were significantly lower than uncorrected
ADC measures for all visits (Table 1). Observed mean tumor fractional bias was
4.7% and 5.8% for the baseline and post NACx1 visits, respectively, for the
entire cohort. Larger unexpected fractional bias was also observed in some
patients. (Fig 3). Discussion
On-scanner
ADC GNC maps can be generated in real time, which can dramatically simplify data
processing. Observed differences in % fractional bias of tumor ADC measures by
scanner system could be attributed in part to the differences in bore
diameter, breast coil geometry, and table position. Previous studies have shown that predicted GNL bias for typical breast
DWI FOV on gradient systems used here should be positive and within 10% [2]. Larger
fractional bias deviations (> 10%) with negative excursions were observed
for some low SNR cases, which will be investigated with off-scanner ADC analyses
and bias model comparisons. Implementing the on-scanner GNL correction can
potentially improve the accuracy of ADC as a biomarker for treatment response
while accounting for scanner platform and patient positioning variations. Increasing
availability of GNL correction on multi-vendor
platforms should help standardize this technique for accurate ADC measurements.
Preliminary results from this study indicate adequate performance of the
vendor provided GNL correction on breast DWI.Acknowledgements
This study was funded by grants from National Institutes of Health
R01 CA248192 and academic industrial partnership R01 CA190299.References
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