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Oncology-Clinical Diagnosis: Solid TumorsGI Cancers - Colorectal and Liver |
1 Mount Vernon Hospital, Northwood, United Kingdom; 2 University College Hospital, London, United Kingdom
445
Objectives: To assess the metabolic- perfusion relationship of primary colorectal adenocarcinoma at staging using 18- FDG PET-/CT and Perfusion CT.
Methods: Following institutional review board approval 10 prospective patients (7 male, 3 female, mean age 65.7years) with proven colorectal adenocarcinoma underwent imaging on a 64 detector PET/CT instrument (VCT Discovery, GE Healthcare). Immediately following the FDG PET study (190 MBq tracer IV; 60 minute uptake period; 2D acquisition; 10 minute per bed position), Perfusion CT study was performed (IV bolus 50 mls iohexol 350mg/ml; 4cm coverage; acquisition interval 2 sec; 150 sec study). Tumour SUVmax was recorded for each patient. Tumor blood flow, blood volume and permeability surface area product were determined using distributed parameter analysis (Perfusion 3.0 software, GE Healthcare). SUVmax and vascular parameters were compared using Pearson correlation; statistical significance was at 5%.
Results: 9/10 patients underwent surgery. Tumors were located in the cecum (3), sigmoid (4) and rectosigmoid (2); T stage: T3 (6), T4 (3); Dukes Stage: B (4), C/D (6). Mean (SE) SUVmax was 17.6 (1.2). Mean (SE) for tumor blood flow, volume and permeability surface area product were 90.7 (12.9) ml/min/100g tissue, 5.77 (0.51) ml/100g tissue, and 13.8 (2.5) ml/min/100g tissue. No correlation between vascular parameters and SUVmax was noted for higher stage tumors (Dukes C/D); there was a positive correlation between blood flow and volume and SUVmax for lower stage tumors (Dukes B) just above significance (r= 0.7, 0.9 respectively; p=0.07).
Conclusions: The metabolic- perfusion relationship is not consistent in colorectal cancer but may depend on stage.
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