HyungJoon Cho1, Ellen Ackerstaff1, Sean Carlin1, Mihaela Lupu1, Ya Wang1, Asif Rizwan1, Joseph O'Donoghue1, Clifton Ling1, John Humm1, Pat Zanzonico1, Jason Koutcher1
1Memorial Sloan Kettering Cancer Center, New York, NY, USA
In vivo knowledge of the spatial distribution of viable, necrotic and hypoxic areas can provide prognostic information about the risk of developing metastases, the distribution of radiation sensitivity, and may possibly be used for localized dose escalation in radiation treatment. In this study, multimodality in vivo Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET) imaging using stereotactic fiduciary markers in the Dunning R3327-AT prostate tumor was performed, focusing on the relationship between Dynamic Contrast-Enhanced (DCE)-MRI using Magnevist (Gd-DTPA), and dynamic 18F-fluoromisonidazole (18F-Fmiso) PET. The non-invasive measurements were verified using tumor tissue sections stained for haematoxylin/eosin (H&E) and pimonidazole.