Yachao Liu1, Mu Lin2, Xu Yan2, and Baixuan Xu1
1PLA 301 General Hospital, Nuclear Medicine Department, Beijing, China, 2Siemens Healthcare, MR Collaborations NE Asia, Shanghai, China
Synopsis
The
combined use of diffusion-weighted and 11C-Choline PET images can provide
complementary information on prostate cancer. However, it is still unknown how to combine
these multiple parameters to give a simple indication for malignant lesions.
Based on a scatterplot analysis of standardized uptake values (SUVs) and
apparent diffusion coefficient (ADC) values, we clustered voxels into groups
corresponding to different tissue types. The proposed method shows promising
results in differentiating the lesion of tumor from normal tissue.
Introduction
Diffusion-weighted
magnetic resonance imaging (DW-MRI) and imaging of glucose metabolism by
positron emission tomography (PET) can provide complementary information on tissue
biology, and is potentially useful for the evaluation of prostate lesions
including primary and recurrent cancers 1. However, due to the tumor
heterogeneity and large amount of data, it is still unknown how to combine these
multiple parameters as a reliable indicator for prostate cancer. In this study,
based on standardized uptake values (SUVs) and apparent diffusion coefficient (ADC)
values, we propose to use voxelwise analysis to delineate lesions and investigate
the tissue characterization within them.Methods
Nine male
patients with evaluated prostate-specific antigen were scanned with 11C-Choline
PET/MRI (Biograph mMR, Siemens Healthcare, Erlangen, Germany), then received
standardized ultrasound guided sextant core biopsy. The PET/MRI protocol
consists of T1W, T2W, a readout-segmented DWI (RESOLVE) sequence prototype and
15 minutes list-mode PET (injection is counted from 0 minute) for the pelvis
region; this was followed by T1W, T2W, single-shot DWI from throat to pelvis
regions. PET and MR images were coregistered using a 3D rigid transformation
and voxel interpolation. In total, the VOI of each patient was selected based on
suspicious findings in T2W, DWI 2 and high
uptake in 11C-Choline PET images.
For
each VOI, voxelwise analysis of ADC and SUV from PET/MR data was conducted
using MATLAB (Mathworks, Natick, MA, USA). Based on the ADC and SUV values,
clustering analysis was performed, where each cluster was characterized with a
bivariate Gaussian distribution described by the mean and covariance matrix.
The voxels in each cluster were mapped to the position of corresponding SUV and
ADC images. Each voxel was assigned to either cancer group or healthy group
according to the results of clustering.
Results
The scatterplots of two typical patients were shown in
Figure 1 and 2. It should be noted that the previous biopsy was reported as
false negative for them. This is due to the spatial location of the lesions
(tip of prostate), which is difficult to reach. For the first patient (69 years old, PSA 10.3 ng/ml, Gleason
score 3+4), two clusters were found with ADCmean
= 1.1×10-3 ,1.5×10-3 mm2/s and
SUVmean = 4.7, 2.1 (Figure 1). For the second patient (50 years old,
PSA 11.8 ng/ml, Gleason score 4+4), three clusters were identified with ADCmean
= 0.5×10-3 ,1.1×10-3, 0.6 ×10-3 mm2/s and
SUVmean = 4.9, 3.4, 2.8 (Figure 2). This is consistent with a
previous study, which showed that low ADC could be observed in areas with high
glucose metabolism but also in regions of low glucose metabolism 3. As expected,
the cancer group had higher SUV values and lower ADC values than the normal
group, the ratio between SUV and ADC could even better differentiate cancer
from normal tissue (Figure 3).Discussion
In all the patients with prostate
cancer including those not shown, at least two clusters can be found separated
by SUV values. For example, in Patient 1 (Figure 1), the cluster with high SUV
should correspond to tumor tissue, and the other cluster with low SUV should
represent normal tissue. In some other patients, the low SUV cluster can be
further divided into 2 sub-clusters with regard of their ADC values.
Specifically, in Patient 2 (Figure 2), 69% of the low-SUV voxels show high ADC (Cluster 2) and may indicate
normal tissue. 31% of the low-SUV voxels showed low-ADC values (Cluster 3).
These voxels surround cancer tissue and could relate
to inflammatory tissue 4. Thus, a voxelwise analysis allows for differentiation
of tumor properties from other tissue and might facilitate the delineation of lesion
for a targeted regional therapy. Furthermore, the quantitative cluster analysis
reveals an additional value of this method in the diagnosis of cancer as the combination SUV/ADC outperforms the single ADC or SUV in
differentiating tumor group from normal tissue group 5 (Figure 3). Further
evaluation on the clinical usage of voxelwise scatterplot analysis in a larger
primary prostate population is necessary. In the future, a comparison should
also be made between the segmentation of tumor by cluster analysis and pathological
section images.Conclusion
The combined use of ADC and SUV maps are feasible for
prostate cancer patient and can provide additional diagnostic value compared to
single MR or PET. Although we only have a limited number of cases, the clustering
analysis of SUV and ADC for each VOI shows promising results in the
differentiation of tumor from normal tissue. Acknowledgements
No acknowledgement found.References
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