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The prognostic and predictive value of vascular response parameters measured by dynamic contrast-enhanced-CT, -MRI and -US in patients with metastatic renal cell carcinoma receiving sunitinib
Authors:John?M.?Hudson  mailto:john.hudson@mail.utoronto.ca"   title="  john.hudson@mail.utoronto.ca"   itemprop="  email"   data-track="  click"   data-track-action="  Email author"   data-track-label="  "  >Email author,Colleen?Bailey,Mostafa?Atri,Greg?Stanisz,Laurent?Milot,Ross?Williams,Alex?Kiss,Peter?N.?Burns,Georg?A.?Bjarnason  mailto:georg.bjarnason@sunnybrook.ca"   title="  georg.bjarnason@sunnybrook.ca"   itemprop="  email"   data-track="  click"   data-track-action="  Email author"   data-track-label="  "  >Email author
Affiliation:1.Department of Medical Biophysics,University of Toronto,Toronto,Canada;2.Sunnybrook Research Institute,University of Toronto,Toronto,Canada;3.Department of Medical Imaging,University of Toronto Health Network,Toronto,Canada;4.Department of Medical Imaging,Sunnybrook Health Sciences Centre,Toronto,Canada;5.Department of Health Policy, Management and Evaluation,University of Toronto,Toronto,Canada;6.Division of Medical Oncology,Sunnybrook Odette Cancer Centre, Sunnybrook Health Sciences Centre,Toronto,Canada
Abstract:

Objectives

To identify dynamic contrast-enhanced (DCE) imaging parameters from MRI, CT and US that are prognostic and predictive in patients with metastatic renal cell cancer (mRCC) receiving sunitinib.

Methods

Thirty-four patients were monitored by DCE imaging on day 0 and 14 of the first course of sunitinib treatment. Additional scans were performed with DCE-US only (day 7 or 28 and 2 weeks after the treatment break). Perfusion parameters that demonstrated a significant correlation (Spearman p < 0.05) with progression-free survival (PFS) and overall survival (OS) were investigated using Cox proportional hazard models/ratios (HR) and Kaplan-Meier survival analysis.

Results

A higher baseline and day 14 value for Ktrans (DCE-MRI) and a lower pre-treatment vascular heterogeneity (DCE-US) were significantly associated with a longer PFS (HR, 0.62, 0.37 and 5.5, respectively). A larger per cent decrease in blood volume on day 14 (DCE-US) predicted a longer OS (HR, 1.45). We did not find significant correlations between any of the DCE-CT parameters and PFS/OS, unless a cut-off analysis was used.

Conclusions

DCE-MRI, -CT and ultrasound produce complementary parameters that reflect the prognosis of patients receiving sunitinib for mRCC. Blood volume measured by DCE-US was the only parameter whose change during early anti-angiogenic therapy predicted for OS and PFS.

Key Points

? DCE-CT, -MRI and ultrasound are complementary modalities for monitoring anti-angiogenic therapy. ? The change in blood volume measured by DCE-US was predictive of OS/PFS. ? Baseline vascular heterogeneity by DCE-US has the strongest prognostic value for PFS.
Keywords:
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