To quantitatively compare the monoexponential, biexponential, and stretched-exponential diffusion-weighted imaging (DWI) models in differentiating benign from malignant solid hepatic lesions. The institutional review board approved this retrospective study and waived the informed consent requirement. A total of 188 patients with 288 hepatic lesions included 202 malignant lesions and 86 benign lesions were assessed (confirmed by pathology or clinical follow-up for 6 months). All patients underwent hepatic 3.0-T MRI, including multi-b DWI that used 12 b values. The ADC, Dp , Dt , perfusion fraction (fp ), α, and DDC values for normal liver, benign liver lesions, and malignant liver lesions were calculated. Independent sample t tests were used for comparisons. The diagnostic performance of the parameters was evaluated using ROC analysis. The AUC value for each model was also calculated. The value of Dp was significantly lower in benign lesions than in normal hepatic parenchyma while others were significantly higher (P < .001). Whereas Values of Dt and α in malignant hepatic lesions were significantly higher than in normal hepatic parenchyma (P < .001), and the Dp value was significantly lower (P < .001). Values of ADC, fp , DDC, and α for malignant hepatic lesions were significantly lower than those for benign hepatic lesions (P < .001). ROC analysis showed that the diagnostic value of the biexponential model of normal hepatic parenchyma vs benign hepatic lesions and normal hepatic parenchyma vs malignant hepatic lesions was high (0.946 and 0.876, respectively). In the differential diagnosis of benign and malignant hepatic lesions, DDC had the highest AUC value (0.819). The biexponential and stretched-exponential DWI may provide additional information and improve the differential diagnosis of benign and malignant hepatic lesions compared with the monoexponential DWI.
Keywords: diffusion-weighted imaging; exponential model; hepatic lesion; magnetic resonance imaging.
© 2018 The Authors. Cancer Medicine published by John Wiley & Sons Ltd.