Erschienen in:
14.12.2016 | Magnetic Resonance
T2-weighted MRI-derived textural features reflect prostate cancer aggressiveness: preliminary results
verfasst von:
Gabriel Nketiah, Mattijs Elschot, Eugene Kim, Jose R. Teruel, Tom W. Scheenen, Tone F. Bathen, Kirsten M. Selnæs
Erschienen in:
European Radiology
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Ausgabe 7/2017
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Abstract
Purpose
To evaluate the diagnostic relevance of T2-weighted (T2W) MRI-derived textural features relative to quantitative physiological parameters derived from diffusion-weighted (DW) and dynamic contrast-enhanced (DCE) MRI in Gleason score (GS) 3+4 and 4+3 prostate cancers.
Materials and Methods
3T multiparametric-MRI was performed on 23 prostate cancer patients prior to prostatectomy. Textural features [angular second moment (ASM), contrast, correlation, entropy], apparent diffusion coefficient (ADC), and DCE pharmacokinetic parameters (Ktrans and Ve) were calculated from index tumours delineated on the T2W, DW, and DCE images, respectively. The association between the textural features and prostatectomy GS and the MRI-derived parameters, and the utility of the parameters in differentiating between GS 3+4 and 4+3 prostate cancers were assessed statistically.
Results
ASM and entropy correlated significantly (p < 0.05) with both GS and median ADC. Contrast correlated moderately with median ADC. The textural features correlated insignificantly with Ktrans and Ve. GS 4+3 cancers had significantly lower ASM and higher entropy than 3+4 cancers, but insignificant differences in median ADC, Ktrans, and Ve. The combined texture-MRI parameters yielded higher classification accuracy (91%) than the individual parameter sets.
Conclusion
T2W MRI-derived textural features could serve as potential diagnostic markers, sensitive to the pathological differences in prostate cancers.
Key Points
• T2W MRI-derived textural features correlate significantly with Gleason score and ADC.
• T2W MRI-derived textural features differentiate Gleason score 3+4 from 4+3 cancers.
• T2W image textural features could augment tumour characterization.