Time-Dependent Diffusion MRI for Quantitative Microstructural Mapping of Prostate Cancer

被引:51
|
作者
Wu, Dan [1 ]
Jiang, Kewen [2 ]
Li, Hai [3 ,4 ]
Zhang, Zelin [1 ]
Ba, Ruicheng [1 ]
Zhang, Yi [1 ]
Hsu, Yi-Cheng [5 ]
Sun, Yi [5 ]
Zhang, Yu-Dong [2 ]
机构
[1] Zhejiang Univ, Coll Biomed Engn & Instrument Sci, Minist Educ, Key Lab Biomed Engn, Hangzhou, Peoples R China
[2] Nanjing Med Univ, Affiliated Hosp 1, Dept Radiol, Nanjing 210009, Peoples R China
[3] Nanjing Med Univ, Affiliated Hosp 1, Dept Pathol, Nanjing 210009, Peoples R China
[4] Nanjing Med Univ, Med Imaging Coll, AI Lab, Nanjing 210009, Peoples R China
[5] Siemens Healthcare, MR Collaborat, Shanghai, Peoples R China
基金
中国国家自然科学基金;
关键词
RESTRICTED DIFFUSION; CELL-SIZE; PATHOLOGY; TISSUE; TUMORS;
D O I
10.1148/radiol.211180
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Background: Recently developed time-dependent diffusion MRI has potential in characterizing cellular tissue microstructures; however, its value in imaging prostate cancer (PCa) remains unknown. Purpose: To investigate the feasibility of time-dependent diffusion MRI-based microstructural mapping for noninvasively characterizing cellular properties of PCa and for discriminating between clinically significant PCa and clinically insignificant disease. Materials and Methods: Men with a clinical suspicion of PCa were enrolled prospectively between October 2019 and August 2020. Time-dependent diffusion MRI data were acquired with pulsed and oscillating gradient diffusion MRI sequences at an equivalent diffusion time of 7.5-30 msec on a 3.0-T scanner. Time-dependent diffusion MRI-based microstructural parameters, including cell diameter, intracellular volume fraction, cellularity, and diffusivities, were estimated with a two-compartment model. These were compared for different International Society of Urological Pathology grade groups (GGs), and their performance in discriminating clinically significant PCa (GG > 1) from clinically insignificant disease (benign and GG 1) was determined with a linear discriminant analysis. The fitted microstructural parameters were validated by means of correlation with histopathologic measurements. Results: In the 48 enrolled men, the time-dependent diffusion MRI measurements showed that higher GG was correlated with higher intracellular volume fraction and higher cellularity (intracellular volume fraction = 0.22, 0.36, 0.34, 0.37, and 0.40 in GGs 1-5, respectively; P < .001 at one-way analysis of variance), while lower cell diameter was found at higher GGs (diameter = 23.4, 18.3, 19.2, 17.9, and 18.5 mm in GGs 1-5, respectively; P =.002). Among all measurements derived from time-dependent diffusion MRI, cellularity achieved the highest diagnostic performance, with an accuracy of 92% (44 of 48 participants) and area under the receiver operating characteristic curve of 0.96 (95% CI: 0.87, 0.99) in discriminating clinically significant PCa from clinically insignificant disease. Microstructural mapping was supported by positive correlations between time-dependent diffusion MRI-based and pathologic examination-based intracellular volume fraction (r = 0.83; P < .001). Conclusion: Time-dependent diffusion MRI-based microstructural mapping correlates with pathologic findings and demonstrates promise for characterizing prostate cancer. (C) RSNA, 2022
引用
收藏
页码:578 / 587
页数:10
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