Correlation of EGFR or KRAS mutation status with 18F-FDG uptake on PET-CT scan in lung adenocarcinoma.

Background: 18F-fluoro-2-deoxy-glucose (18F-FDG) positron emission tomography (PET) is a functional imaging modality based on glucose metabolism. The correlation between EGFR or KRAS mutation status and the standardized uptake value (SUV) of 18F-FDG PET scanning has not been fully elucidated.

Methods: Correlations between EGFR or KRAS mutation status and clinicopathological factors including SUVmax were statistically analyzed in 734 surgically resected lung adenocarcinoma patients.

The effect of glucagon on FDG uptake in skeletal muscle.

Glucagon is used as an anti-motility agent during gastrointestinal tract examinations. We experienced subjects with enhanced 18F-fluorodeoxyglucose (FDG) uptake in whole-body skeletal muscle when conducting positron emission tomography (PET). The subjects had been administered glucagon during gastroscopy just prior to PET.

[Imaging of cancer activity and range of tumor involvement--applying to breast cancer].

In recent years, PET using mainly fluorine-18 fluorodeoxyglucose (FDG) has played a very large role in the management of breast cancer. Systemic, functional images can be obtained by whole body PET and can provide information that is not obtained by anatomical imaging modalities such as conventional X-ray computed tomography, X-ray mammography, or ultrasonography. The utility of FDG-PET for breast cancer patients has been established in every phase of the management of breast cancer, such as the differential diagnosis of breast cancer primary lesion, cancer staging, and posttreatment monitoring.