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Oncology-Clinical Diagnosis: Solid TumorsClinical Diagnosis-Solid Tumors Posters |
1 Rambam HealthCare Campus, Haifa, Israel; 2 Carmel Medical Center, Haifa, Israel; 3 German Cancer Research Center, Heidelberg, Germany
1470
Objectives: Present study evaluates a kinetic FDG-PET model as an indicator for defining tumor aggressiveness and prognosis in patients (pts) with pancreatic cancer.
Methods: Fifty pts with known or suspected cancer of the pancreas were referred for FDG-PET/CT. A dynamic single field of view PET acquisition over the region of the pancreas was initiated with the administration of 15 mCi FDG and sequential data were sampled for 60 minutes. Tracer kinetics were measured. Fractional blood volume associated with vessel density (VB), kinetic parameters (K1, K2, K3, K4) and global FDG influx were calculated using a two-compartmental model and the fractal dimension (FD) using a non-compartmental model. Whole body PET/CT was performed at 2 hours post-injection. Statistical significance was assessed using Cox proportional-hazards for overall survival analysis and logistic multivariate analysis to compare kinetic tracer behavior in FDG-avid pancreatic cancer in pts with localized vs. metastatic disease.
Results: No increased FDG uptake was found in 22 pts and 28 pancreatic lesions were FDG-avid. Pancreatic cancer was diagnosed in 24 pts including 12 with localized and 12 with metastatic lesions. 11 pts died during a follow up period of 12 months. K1 was the single statistically significant variable predicting overall survival (P<0.01). There was no significant difference in kinetic parameters in the primary tumor between pts with localized and metastatic disease.
Conclusions: Present results suggest that K1 may represent the prognostic kinetic variable predicting outcome in patients with newly diagnosed cancer of the pancreas.
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