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Abstract #0824

Dynamic Contrast-enhanced MRI in Renal Tumors: Common Subtype Differentiation using Pharmacokinetics

Haiyi Wang1, Lu Ma1, Zihua Su2, Ning Huang2, Xiao Xu3, Zhipeng Sun4, Aitao Guo5, and Huiyi Ye1

1Department of Radiology, Chinese PLA General Hospital, Beijing, People's Republic of China, 2Lift Science, Advanced Application Team, GE Healthcare China, Beijing, People's Republic of China, 3Lift Science, Advanced Application Team, GE Healthcare China, Shanghai, People's Republic of China, 4Department of Radiology, No.1 Hospital of Zhangjiakou, Zhangjiakou, People's Republic of China, 5Department of Pathology, Chinese PLA General Hospital, Beijing, People's Republic of China

Synopsis

In this prospective study on pharmacokinetic parameters (Ktrans & Ve) of renal tumors, we enrolled the patients with five common subtypes of renal tumor - clear cell renal cell carcinoma (ccRCC), papillary renal cell carcinoma (pRCC), chromophobic renal cell carcinoma (cRCC), uroepithelial carcinoma (UEC), and fat poor angiomyolipoma (fpAML) to undergo DCE-MRI pharmacokinetic studies. Our results demonstrated that ccRCC, pRCC, cRCC, UEC and fpAML are pharmacokinetically different (Ktrans & Ve). Ktrans could distinguish ccRCC from non-ccRCC (pRCC & cRCC) and differentiate fpAML with non-ccRCC with high specificity and sensitivity, which probably can facilitate the precise treatment of renal tumors in the future clinical practice.

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