Keywords: Prostate, Diffusion/other diffusion imaging techniques
Diffusion-weighted imaging (DWI) plays an important role in assessing the significance of prostate cancer. DWI with Turbo Spin Echo readout (TSE-DWI) is robust to image distortion but suffers from low signal to noise ratio. In this study, we investigated the use of prototype AI-based reconstruction technique (SmartSpeed Precise Image) to improve the image quality of TSE-DWI images. The image quality was compared between conventional Compressed-SENSE (C-SENSE), SmartSpeed AI, and SmartSpeed Precise Image. Volunteer data demonstrated a significant improvement of sharpness in both b=0 and 1000 s/mm2 images as well as ADC map, compared with C-SENSE and SmartSpeed AI reconstructions.
1. American College of Radiology. PI-RADS Version 2.1. Prostate Imaging-Reporting Data Syst. Published online 2019:1-69. http://www.acr.org/~/media/ACR/Documents/PDF/QualitySafety/Resources/PIRADS/PIRADS V2.pdf
2. Hambrock T, Somford DM, Huisman HJ, et al. Relationship between Apparent Diffusion Coefficients at 3.0-T MR Imaging and Gleason Grade in Peripheral Zone Prostate Cancer. Radiology. 2011;259(2):453-461. doi:10.1148/radiol.11091409
3. Katahira K, Takahara T, Kwee TC, et al. Ultra-high-b-value diffusion-weighted MR imaging for the detection of prostate cancer: Evaluation in 201 cases with histopathological correlation. Eur Radiol. 2011;21(1):188-196. doi:10.1007/s00330-010-1883-7
4. Krishna S, Lim CS, McInnes MDF, et al. Evaluation of MRI for diagnosis of extraprostatic extension in prostate cancer. J Magn Reson Imaging. 2018;47(1):176-185. doi:10.1002/jmri.25729
5. Esses SJ, Taneja SS, Rosenkrantz AB. Imaging Facilities’ Adherence to PI-RADS v2 Minimum Technical Standards for the Performance of Prostate MRI. Acad Radiol. 2018;25(2):188-195. doi:10.1016/j.acra.2017.08.013
6. Pirasteh A, Johnson B, Dimitrov IE, et al. Turbo Spin-Echo Diffusion-Weighted Imaging in Prostate Magnetic Resonance Imaging of Men With Pelvic Hardware. J Comput Assist Tomogr. 2020;44(4):519-526. doi:10.1097/RCT.0000000000001067
7. Mori N, Mugikura S, Miyashita M, et al. Turbo spin-echo diffusion-weighted imaging compared with single-shot echo-planar diffusion-weighted imaging: Image quality and diagnostic performance when differentiating between ductal carcinoma in situ and invasive ductal carcinoma. Magn Reson Med Sci. 2021;20(1):60-68. doi:10.2463/mrms.mp.2019-0195
8. Tamada T, Ueda Y, Ueno Y, Kojima Y, Kido A, Yamamoto A. Diffusion-weighted imaging in prostate cancer. Magn Reson Mater Physics, Biol Med. 2021;(0123456789). doi:10.1007/s10334-021-00957-6
9. Yoneyama M, Yoshida T, Kwon J, Katsumata Y, Zhang S, Van Cauteren M. SNR enhancement in rapid high b-value prostate single-shot DW-EPI utilizing deep learning constrained Compressed SENSE reconstruction. In: ISMRM2022 #3712. ; 2022. doi:10.2214/AJR.09.3004.4.
10. Ueda T, Ohno Y, Yamamoto K, et al. Deep Learning Reconstruction of Diffusion-weighted MRI Improves Image Quality for Prostatic Imaging. Radiology. 2022;303(2):373-381. doi:10.1148/RADIOL.204097
11. Fan M, Liu Z, Xu M, et al. Generative adversarial network-based super-resolution of diffusion-weighted imaging: Application to tumour radiomics in breast cancer. NMR Biomed. 2020;33(8):1-12. doi:10.1002/nbm.4345
12. Pezzotti N, de Weerdt E, Yousefi S, et al. Adaptive-CS-Net: FastMRI with Adaptive Intelligence. arxiv. 2019;(NeurIPS). http://arxiv.org/abs/1912.12259
13. Peeters H, Chung H, Valvano G, et al. Philips SmartSpeed No compromise and robustness.
14. Li Y, Sixou B, Peyrin F. A Review of the Deep Learning Methods for Medical Images Super Resolution Problems. Irbm. 2021;42(2):120-133. doi:10.1016/j.irbm.2020.08.004
15. Chaudhari AS, Fang Z, Kogan F, et al. Super-resolution musculoskeletal MRI using deep learning. Magn Reson Med. 2018;80(5):2139-2154. doi:10.1002/mrm.27178
16. Kikinis R, Pieper SD, Vosburgh KG. 3D Slicer: A Platform for Subject-Specific Image Analysis, Visualization, and Clinical Support. In: Intraoperative Imaging and Image-Guided Therapy. Springer New York; 2014:277-289. doi:10.1007/978-1-4614-7657-3_19
17. 3D Slicer image computing platform. https://www.slicer.org/
Figure 1. Anatomical T2 weighted image (a) and corresponding EPI-DWI (b) and TSE-DWI (c) images, both acquired with b = 0 s/mm2. This representative EPI-DWI shows higher signal to noise ratio and severe image distortion in the proximity of rectum gas. TSE-DWI is less sensitive to such susceptibility difference, which results in anatomically more accurate delineation of prostate structure.
Figure 2. b = 0 (upper row), b = 1000 s/mm2 (middle row) images, and ADC maps (lower row) of the prostate in a healthy volunteer obtained with TSE-DWI, for C-SENSE (left), SmartSpeed AI (middle), and SmartSpeed Precise Image (right) reconstructions.
Figure 3. ADC maps of the prostate in a healthy volunteer obtained with TSE-DWI, for C-SENSE (a), SmartSpeed AI (b), and SmartSpeed Precise Image (c) reconstructions.
Figure 5. b = 0 (upper row), b = 2000 s/mm2 (middle row) images, and ADC maps (lower row) of the prostate in a healthy volunteer obtained with EPI-DWI, for C-SENSE (left), SmartSpeed AI (middle), and SmartSpeed Precise Image (right).