Samenvatting
OBJECTIVE. The purpose of this study is to compare dispersion MRI and Tofts model (TM) for analysis of quantitative dynamic contrast-enhanced (DCE) MRI (DCE-MRI) for localization of prostate cancer and to assess the correlation between quantitative DCE-MRI parameters and tumor grade. MATERIALS AND METHODS. This retrospective multicenter study included 80 patients with biopsy-proven prostate cancer who underwent DCE-MRI followed by radical prostatectomy. DCE-MRI parameters were extracted from dispersion MRI analysis (the dispersion parameter [kd], the flux rate [kep], and the intravascular mean transit time) and TM analysis (the forward volume transfer constant [Ktrans], kep, and the extravascular extracellular volume fraction [ve]). ROIs representing benign and malignant tissue were drawn on each DCE-MRI slice according to the histopathologic findings, and the diagnostic performance of the estimated parameters for the diagnosis of prostate cancer was evaluated using fivefold cross-validation and ROC curve analysis. Further analysis was conducted for the two most relevant parameters (i.e., kd [for dispersion MRI] and kep [for TM]), to investigate the correlation between DCE-MRI parameters and tumor grade. RESULTS. DCE-MRI parameters were significantly different between benign and malignant prostate tissue (p < 0.0001). The dispersion MRI parameter kd outperformed all other DCE-MRI parameters for prostate cancer diagnosis, showing the highest area under the ROC curve value (p < 0.0001). Only a weak linear correlation (Pearson r = 0.18; p < 0.05) was found between the dispersion parameter and the Gleason grade group. CONCLUSION. Dispersion MRI outperformed TM analysis, improving the diagnostic performance of quantitative DCE-MRI for prostate cancer localization. Of the DCE-MRI parameters, kd (for dispersion MRI) and kep (for TM) provided only poor characterization of tumor grade.
| Originele taal-2 | Engels |
|---|---|
| Pagina's (van-tot) | W242-W251 |
| Tijdschrift | American journal of Roentgenology |
| Volume | 211 |
| Nummer van het tijdschrift | 5 |
| DOI's | |
| Status | Gepubliceerd - 1 nov. 2018 |
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