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Oncology-Clinical Diagnosis: Solid TumorsClinical Diagnosis-Solid Tumors Posters |
1 CMKP, Warsaw, Poland; 2 Oncology Center, Bydgoszcz, Poland; 3 CSK MSWiA, Warsaw, Poland; 4 RFH, London, United Kingdom
1553
Objectives: Prognostic significance of FDG PET in patients with poorly differentiated - PDNEC and well differentiated neuroendocrine carcinomas - WDNEC, base on progression free survival (PFS) and overall survival (OS).
Methods: This study comprised 31 pts, 17 with PDNEC, 14 with WDNEC. All had clinical, biochemical and imaging evaluation using anatomical and functional imaging of NET. In all of them FDG PET was performed as staging or restaging approach or evaluation of treatment (chemo) response. Active pathology was evaluated using clinical and radiological criteria. Kaplan-Meier survival curves were used to estimate PFS and OS, comparison between groups was performed using Cox-Mantel test.
Results: 12 PDNEC and 12 WDNEC patients presented progressive disease. There was significant SUV difference between PDNEC and WDNEC (8.4 vs. 4.9; p<0.05). Sensitivity of FDG PET/CT was 92%. Sensitivity WDNEC was 42%. OS and PFS in PDNEC with active disease were 21 and 7 months, in WDNEC, OS and PFS was 39 and 17 months, differences between OS in both groups (p=0.002). No significant difference between PFS. Only 2 of 12 patients with PDNEC and uptake of FDG were still alive during follow-up. In WDNEC only 2pts with high uptake of FDG died during follow-up.
Conclusions: Positive FDG PET/CT scan in patients with PDNEC, despite therapy, indicate active progressive disease with worse prognosis, compare to patients with negative FDG PET/CT. High sensitivity of FDG PET/CT could be routinely used to evaluation patients with PDNEC. Routine used of FDG PET in WDNEC due to low sensitivity is of limited value, high uptake is seen in selected cases with no additional prognostic value.
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