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Oncology-Clinical Diagnosis: Solid TumorsClinical Diagnosis-Solid Tumors Posters |
1 CHU Cote de Nacre, Caen, France
1465
Objectives: FDG-PET has a low sensitivity (40%)in the diagnosis of HCC. We postulate that insulin resistance in cirrhosis increased FDG liver uptake (background noise) and decrease HCC contrast with surrounding liver. Octreotide treatment can correct insulin resistance in cirrhosis .In a preliminary study of 26 patients (13 cirrhotic/13 healthy liver) mean SUVbw was significantly lower in healthy liver. This study evaluate the interest of insulin resistance correction to improve FDG-PET detection of HCC on cirrhosis.
Methods: In 5 cirrhotic patients euglycemic insulin clamp was achieved before any treatment to verify insulin resistance status and after 4 days of octreotide treatment (200 µg/day IV) to be sure that insulin resistance is corrected. Each patient underwent 2 FDG PET : first within 7 days before octreotide treatment and the second on the day 4. Ratio T/N was calculated : mean SUVbw HCC/ mean SUVbw surrounding liver using same Region Of Interest size.
Results: 16 HCC nodules were evaluated. All patients treated with octreotide showed reduction of their insulin resistance by decreasing the fasting hyperinsulinemia (9.76 ± 3.8 vs 2.5 ± 6 mU / l, p <0.05) and increasing glucose utilization during the clamp. The tumor mean SUVbw increased significantly after octreotide (3.77 ± 1.95 vs. 5.74 ± 4.79, p <0.05) whereas the mean SUV bw in cirrhotic non-tumoral liver did not significally change (2.26 ± 0.47 vs 2.82 ± 0.69; NS). In 3/5 patients mean SUVbw T/N ratio (contrast) was increased and an additional HCC nodule was visualised.
Conclusions: Correction of insulin resistance by octreotide improves HCC contrast in FDG PET in the majority of case (3/5). But FDG increased uptake in HCC is not clearly associated with lower background uptake of the liver.
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