Contrasting The Vascular Response To Sunitinib As Measured By Dce-Ct, Dce-Mri, And Dce-Us

378 Background: Medical imaging (DCE-MRI, DCE-CT, DCE-US) provides localized information about the integrity and hemodynamics of the tumor microvasculature.34 treatment (Rx) naive pts with mRCC and an abdominal tumor suitable for imaging received Sunitinib 50 mg on a 4wk-on/2wk-off schedule. DCE-US, DCE-CT, and DCE-MRI were done at baseline, during the first course of Rx and after 2wks off Rx. Imaging parameters obtained included vessel permeability (Ktrans), extracellular volume fraction (ve) and Ktrans/ve=Kep (by DCE-MRI), permeability surface product (PS, by DCE-CT), blood volume (BV, by DCE-CT and DCE-US), and blood flow (by DCE-US). We also developed a morphology parameter (MP) that relates the flow kinetics of an intravascular microbubble contrast agent to tumor vascular morphology using DCE-US.A range of imaging parameters that predicted for progression free survival (PFS) were identified in responding pts (N = 26). Baseline imaging parameters correlated with PFS: Ktrans by DCE-MR (r = 0.53, p = 0.01, N = 24), BV by DCE-CT (r = 0.48, p = 0.02, N = 25) and disorganized vessel morphology (large MP) by DCE-US (Spearman r = 0.-0.45, p = 0.02, N = 24). Changes from baseline imaging parameters correlated with PFS: BV by DCE-US at 2 wks (r = -0.46, p = 0.02, N = 24), Kep by DCE-MR at 2 wks (r = -0.45, p = 0.03, N = 24) and MP at 1wk (r = 0.67, p = 0.02, N = 12). There was a correlation between imaging methods: BV measured by DCE-CT correlated with BV by DCE-US (r = 0.46, p = 0.03, N = 23) and Kep by DCE-MR (r = 0.59, p = 0.003, N = 22); Permeability measured by DCE-MR (Ktrans) and DCE-CT (PS) correlated at 2wks (r = 0.56, p = 0.01, N = 21).This is the first study to contrast DCE-US, DCE-CT, and DCE-MRI imaging in pts receiving antiangiogenic therapy. Baseline parameters for all three methods can predict for PFS. Changes from baseline in DCE-US and DCE-MRI parameters also predict for PFS. There is a correlation between imaging methods in parameters that measure BV and permeability. A novel DCE-US parameter was developed (MP) that quantifies the degree of tumor vascular disorganization. Baseline values in MP and changes during Rx correlate with PFS.OCT1205, SU Timing RCC.