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Oncology-Clinical Diagnosis: Solid TumorsClinical Diagnosis-Solid Tumors Posters |
1 LaTIM, INSERM U650, Brest, France; 2 Department of Oncology, CHU MORVAN, Brest, France
1482
Objectives: The use of FDG PET for prediction of therapy response in esophageal cancer (EC) is not yet widely accepted. FMISO targeting hypoxia may help in this context. Since hypoxia and angiogenesis are related, we designed a feasibility study combining functional imaging with FMISO and FDG with biological markers of angiogenesis in esophageal cancer.
Methods: At present, 8 patients with newly diagnosed EC have been included (7 patients with squamous cell and one with adenocarcinoma). All had advanced disease and were considered for exclusive radiochemotherapy. Before treatment all patients underwent an FDG and FMISO PET study (mean interval between the two studies of 7days). A dynamic FMISO PET protocol over the area of interest was used between 0-60 min with additional whole body acquisitions 2 and 3 hours after injection of a mean activity of 292 MBq. A standard whole body FDG acquisition was performed 60 min post-injection. Maximum SUVs and tumor to background ratios were calculated for all primary lesions. Epidermal growth factor receptor (EGFR) and endothelial growth factor (VEGF) expressions were assessed on blood samples before treatment. Response to therapy was evaluated using RECIST criteria by conventional imaging performed one month after treatment.
Results: Five patients have been classified as responders (R) and 3 as non responders (NR). SUVmax was 8.6 ± 3 using FDG (7 ± 2 vs. 11.2 ± 2.9 in R and NR respectively). FMISO uptake was low in the primary lesion for all patients with a SUVmax of 0.7 ± 0.2. (0.8 ± 0.3 for NR and 0.6 ± for R).
Conclusions: These preliminary results show that both tracers provide similar information concerning discrimination of responders and non responders to radiochemotherapy in esophageal cancer.
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