Purpose:To determine the feasibility of in vivo diffusionweighted imaging (DWI) to distinguish between normal liver, viable tumor and necrosis compared to postmortem DWI in a rat model with vascular-targeting treatment.
Materials and Methods:Fifteen rats with liver implantation of 30 rhabdomyosarcomas were treated with combretastatin A-4-phosphate (CA4P) at 10 mg/kg. Two days after treatment, T2-weighted imaging, precontrast T1-weighted imaging, postcontrast T1-weighted imaging, and DWI were performed in vivo and postmortem with a 1.5T scanner. Apparent diffusion coefficients (ADCs) calculated from DWIs with b values of 0, 50, and 100 seconds/mm 2 (ADC low ), 500, 750, and 1000 seconds/mm 2 (ADC high ), 0, 500, and 1000 seconds/mm 2 (ADC 3b ), and 0 -1000 seconds/mm 2 (ADC 10b ) for tumor, liver, therapeutic necrosis, and phantoms were compared and validated with ex vivo microangiographic and histopathologic findings.Results: Except ADC low between tumor and necrosis, in vivo ADCs successfully differentiated liver, viable tumor, and necrosis (P Ͻ 0.05). Compared to in vivo outcomes, postmortem ADCs significantly dropped in tumor and liver (P Ͻ 0.05) except ADC high of tumor, but not in necrosis and phantoms. Compared to ADC low , ADC high was less affected by vital status.
Conclusion:Advantageous over postmortem DWI, in vivo DWI provides a noninvasive easy-performing tool for distinguishing between liver, viable tumor, and necrosis. ADC low and ADC high better reflect tissue perfusion and water diffusion, respectively.