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Multicenter Study
. 2019 Jul 18;10(1):3170.
doi: 10.1038/s41467-019-11007-0.

Multicenter study demonstrates radiomic features derived from magnetic resonance perfusion images identify pseudoprogression in glioblastoma

Affiliations
Multicenter Study

Multicenter study demonstrates radiomic features derived from magnetic resonance perfusion images identify pseudoprogression in glioblastoma

Nabil Elshafeey et al. Nat Commun. .

Abstract

Pseudoprogression (PsP) is a diagnostic clinical dilemma in cancer. In this study, we retrospectively analyse glioblastoma patients, and using their dynamic susceptibility contrast and dynamic contrast-enhanced perfusion MRI images we build a classifier using radiomic features obtained from both Ktrans and rCBV maps coupled with support vector machines. We achieve an accuracy of 90.82% (area under the curve (AUC) = 89.10%, sensitivity = 91.36%, 67 specificity = 88.24%, p = 0.017) in differentiating between pseudoprogression (PsP) and progressive disease (PD). The diagnostic performances of the models built using radiomic features from Ktrans and rCBV separately were equally high (Ktrans: AUC = 94%, 69 p = 0.012; rCBV: AUC = 89.8%, p = 0.004). Thus, this MR perfusion-based radiomic model demonstrates high accuracy, sensitivity and specificity in discriminating PsP from PD, thus provides a reliable alternative for noninvasive identification of PsP versus PD at the time of clinical/radiologic question. This study also illustrates the successful application of radiomic analysis as an advanced processing step on different MR perfusion maps.

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Conflict of interest statement

Meng Law receives Honorarium and Research Grant Support from Bracco Diagnostics. The remaining authors declare no competing interests.

Figures

Fig. 1
Fig. 1
Image post-processing radiomic workflow. a relative cerebral blood volume (rCBV) and Ktrans maps of perfusion MRI are acquired. b Segmentation of the region of interest using 3D slicer software. c Radiomic feature extraction from the whole tumor volume. d Statistical analysis: radiomic and clinical features are analyzed to determince their diagnostic and predictive values
Fig. 2
Fig. 2
Model building and evaluation using the selected Ktrans features (60 features). a, b ROC curve depicts the predictive model building using C5.0 (P-value 1.512e−11) and SVM methods (P-value 0.003744) respectively. c, d 10-fold cross-validation ROC curve (P-value 1.512e−11) and Leave-One-Out Cross-Validation (LOOCV) ROC curve (P-value 0.004) depicts the performance of the model
Fig. 3
Fig. 3
Model building and evaluation using the selected rCBV features (160 features). a, b ROC curve depicts the predictive model building using C5.0 (P-value 1.512e−11) and SVM methods (P-value 0.012) respectively. c, d 10-fold cross-validation ROC curve (P-value 1.512e−11) and Leave-One-Out Cross-Validation (LOOCV) ROC curve (P-value 0.012) depicts the performance of the model
Fig. 4
Fig. 4
Model building and evaluation using the selected merged Ktrans and rCBV features (60 features). a, b ROC curve depicts the predictive model building using C5.0 (P-value 1.512e−11) and SVM methods (P-value 0.017), respectively. c, d 10-fold cross-validation ROC curve (P-value 1.512e−11) and Leave-One-Out Cross-Validation (LOOCV) ROC curve (P-value 0.02) depicts the performance of the model

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