Aritrick Chatterjee1,2, Audrey Kim1, Batuhan Gundogdu1,2, Milica Medved1,2, Tatjana Antic1, Gregory Karczmar1,2, and Aytekin Oto1,2
1University of Chicago, CHICAGO, IL, United States, 2Sanford J. Grossman Center of Excellence in Prostate Imaging and Image Guided Therapy, Chicago, IL, United States
Synopsis
Keywords: Prostate, Diffusion/other diffusion imaging techniques
This
study compared the effect of echo times on the detection of prostate cancer on
DWI at high b-value and ADC maps. Contrast between benign tissue and cancer
increased significantly with higher TE on ADC maps. However, due to increased
noise at higher TEs, CNR (study endpoint) was highest at TE 57 ms; higher by
23, 26, 33% than that at TE 70, 150 and 200 ms on ADC maps. CNR, contrast ratio
AND auc are higher at lower TE on DWI high-b image. Therefore, the use of lower
echo times for DWI and ADC mapping may improve prostate cancer.
Introduction
Diffusion
weighted images (DWI) and apparent diffusion coefficient (ADC) maps remain an
integral part of prostate MRI as per the latest PIRADS v2.1 guidelines(1). However, PIRADS
guidelines provide very limited technical specifications which lead to
variation in multiparametric MRI protocols across imaging centers making
meta-data analysis and comparing images and radiologist performance across
institutions difficult. PIRADS recommends an echo time (TE) ≤90ms be utilized
for DWI. However, here is little information in the literature to back this up.
For
T2-weighted images, higher TE was shown to improve prostate cancer detection(2). Feng et. al
showed that quantitative IVIM parameters are clearly affected by TE(3). Therefore,
determining the optimal TE for detecting prostate cancer on DWI and ADC maps may
be useful for improving prostate cancer diagnosis and to standardize protocols
across institutions. This study aims to compare the effect of
different echo times on the detection of prostate cancer on DWI at high b-value
and ADC maps.Materials and Methods
This
study involved retrospective analysis of prospectively collected data. 35
participants (mean age 60 years, mean PSA 9.0ng/ml) with biopsy-confirmed
prostate cancer underwent MR imaging with a 3T Philips MR scanner prior to
radical prostatectomy. Axial images DW imagines were taken as part of the
Hybrid Multi-dimensional MRI and acquired using b-values of 0, 150, 750, 1500
s/mm2 at each TE of 57, 70, 150, and 200 ms using a spin-echo module,
single shot echoplanar imaging readout, fat saturation using spectrally
adiabatic inversion recovery, TR=5000ms, resolution= .50mm×1.50mm×3.00mm.
ADC
maps were calculated at each TE using a mono exponential fit. ROIs were taken
for the pathology confirmed index lesions and benign tissue on the
contralateral side on T2W and transferred to DWI high b-value image (b=1500 s/mm2)
and ADC maps for each TE keeping the size and shape the same. Mean ADC, signal
at high b was measured for cancer and benign ROIs. Noise
was measured as the standard deviation found in internal obturator muscles. We
calculated the contrast to noise ratio or CNR (difference in ADC or DWI signal
between cancer and benign tissue / noise) for each patient.
The
difference between metrics was assessed by Friedman’s test. Receiver operating characteristic (ROC) analysis was used to
evaluate the performance of parameters in differentiating cancer from benign prostatic
tissue. Results
Figure
1 and 2 shows a representative images for a Gleason 3+4 cancer. Table 1 has
detailed results of the study, summarizing the measured metrics.
The
average ADC values for benign tissue increased significantly with increased TE
(χ2=25.042,p<0.001). However, no
significant differences (χ2=3.379,p=0.34) in ADC values at
different TEs was found for cancers. The contrast between benign tissue and
cancer increased significantly (χ2=11.905, p=0.008) with higher TE.
Contrast at TE 57 was significantly lower than that at TE 150 (p=0.01) and 200
ms (p=0.01), while contrast at TE 70ms is lower than that at TE 150 (p=0.01)
and 200 ms (p=0.04). However, contrast is similar at TE 57 and 70ms (p=0.52). However,
due to higher noise at higher TEs, our study endpoint, CNR significantly
decreases at higher TE (χ2=12.158,p=0.007). CNR at TE 57 was
significantly higher than that at TE 150 (26% higher, p=0.03) and 200 ms (34%
higher, p=0.04), but not different from TE 70ms (p=0.17). Area under the ROC
curve (AUC) was highest (nominally) using
ADC values at TE 57ms (0.986) compared
to 0.961, 0.961 and 0.939 at TE 70,150 and 200 ms, respectively.
Due
to scaling differences contrast ratio between benign and cancer was used for
DWI signal at high b-value, with significantly (χ2=15.821p=0.001)
lower contrast ratio found at higher TEs (including post hoc tests). The CNR
for high b DWI was significantly higher at lower TE (χ2=31.933,p<0.001), with CNR at TE 57 ms significantly higher than others. There is
negative mean CNR at TE 200 ms, suggest cancers don’t show hyperintensity
compared to surrounding benign tissue on DWI high b. AUCs at TE 57 and 70ms was
significantly higher than at 150 and 200ms. Discussion
Contrast
on ADC maps improves at higher TE, especially as ADC of benign tissue increases
with higher TE, which is similar findings of a previous paper(4). However due to
higher noise at high TEs, CNR is better at lower TEs, which the other paper
didn’t investigate. Furthermore, CNR on DWI high b-value was also best at lower
TEs. This is supported by higher AUC for cancer diagnosis.
Cancer
has a higher fractional volume of epithelial cells which have lower T2(5). When higher TEs
are used, there is very little signal even on DWI b=0 images. So even after signal
suppression of fluid in lumen and stroma at higher b-values, cancers
may not show hyperintensity compared to surrounding benign tissue. This is why
we see negative CNR at TE 200ms at DWI high b. At lower TEs there is higher
signal at b=0 from cancer cells, which are then suppressed less than benign
tissue at higher b-value, showing higher CNR on DWI high b and ADC maps. Conclusion
The
use of lower echo times may improve prostate cancer detection with lower TEs
showing better CNR on DWI high b-value and ADC maps.Acknowledgements
This study was supported by NIH (R01 CA227036, 1R41CA244056-01A1, R01 CA17280, 1S10OD018448-01), and Sanford J. Grossman Charitable Trust.References
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