Why the study?
It was unknown whether prostate T2 varies across RSI compartments and in csPCa, and whether measuring compartmental T2 across multiple TEs improves csPCa detection over RSIrs.
Does the addition of compartmental T2 to Restriction Spectrum Imaging restriction score (RSIrs) improve the detection of clinically significant prostate cancer in patients with suspected or known prostate cancer?
Does the addition of compartmental T2 to Restriction Spectrum Imaging restriction score (RSIrs) improve the detection of clinically significant prostate cancer in patients with suspected or known prostate cancer?
While compartmental T2 differs between normal and cancerous prostatic tissue, its addition to diffusion-weighted imaging (RSIrs) does not significantly improve the detection of clinically significant prostate cancer.
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Compartmental T2 adds no incremental value to RSIrs for csPCa detection; leaves open optimal multiparametric protocols in prospective studies.
The Restriction Spectrum Imaging restriction score (RSIrs) has been shown to improve the accuracy for diagnosis of clinically significant prostate cancer (csPCa) compared to standard DWI. Both diffusion and T 2 properties of prostate tissue contribute to the signal measured in DWI, and studies have demonstrated that each may be valuable for distinguishing csPCa from benign tissue. The purpose of this retrospective study was to (1) determine whether prostate T 2 varies across RSI compartments and in the presence of csPCa, and (2) evaluate whether csPCa detection with RSIrs is improved by acquiring multiple scans at different TEs to measure compartmental T 2 (c T 2 ). Data includes two cohorts scanned for csPCa with 3T multi- b -value diffusion-weighted sequences acquired at multiple TEs. c T 2 values were computed from multi-TE RSI data and compared by compartment. CsPCa detection was compared between RSIrs and a logistic regression model (LRM) to predict the probability of csPCa using c T 2 in combination with RSI measurements. Two-sample t-tests ( α = 0.05) and the area under the receiver operating characteristic curve (AUC) were used for the statistical analyses. In both cohorts, T 2 was different ( p < 0.05) across the four RSI compartments ( C 1, C 2, C 3, C 4 ). Voxel-level, cohort 1: T 2 was different in csPCa for C 1, C 2, C 3 ( p < 0.001). Patient-level, cohort 1: T 2 was different in csPCa patients in C 3 ( p = 0.02); cohort 2: T 2 differed in csPCa patients in C 1 ( p = 0.01), C 3 ( p = 0.01) and C 4 ( p < 0.01). Voxel-level csPCa detection: c T 2 did not improve discrimination over RSIrs alone ( p = 0.9). Patient-level: RSIrs and the LRM performed better than diffusion alone ( p < 0.001), but the difference in AUCs between RSIrs and the LRM was not significantly different ( p = 0.54). In conclusion, significant differences in c T 2 were observed between normal and cancerous prostatic tissue. With our data, however, consideration of c T 2 in addition to diffusion did not significantly improve cancer detection performance.
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Domingo et al. (2024) studied this question.
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