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Determining Glucose Metabolism Kinetics Using 18F-FDG Micro-PET/CT
Published on: May 2, 2017
Diabetes Decreases FDG Accumulation in Primary Lung Cancer
Tatsuo Torizuka1, Kenneth R. Zasadny, Richard L. Wahl
1Division of Nuclear Medicine, Department of Internal Medicine, University of Michigan, Ann Arbor, MI, USA
Diabetes impairs 2-[fluorine-18]-fluoro-2-deoxy-D-glucose (FDG) uptake in primary lung tumors. This reduced FDG accumulation in diabetic patients may decrease the sensitivity of positron emission tomography (PET) for lung cancer detection.
Area of Science:
- Oncology
- Nuclear Medicine
- Metabolic Research
Background:
- Positron Emission Tomography (PET) with 2-[fluorine-18]-fluoro-2-deoxy-D-glucose (FDG) is a key imaging modality for lung cancer.
- Diabetes mellitus affects glucose metabolism, potentially influencing FDG uptake in tumors.
Purpose of the Study:
- To compare the kinetics and accumulation of FDG in primary lung cancer between diabetic and non-diabetic patients using PET.
- To investigate the impact of diabetes on FDG uptake parameters and tumor-to-background ratios.
Main Methods:
- Dynamic FDG-PET scans were performed on 5 diabetic and 21 non-diabetic patients with untreated primary lung cancers.
- Standardized uptake value normalized for lean body mass (SUL) was measured in tumor, blood, muscle, and lung.
- A 3-compartment metabolic model analyzed FDG kinetics in tumors.
Main Results:
- Diabetic patients exhibited significantly decreased tumor SUL, tumor/blood, and tumor/muscle SUL ratios compared to non-diabetic patients (P < 0.02).
- The rate constant for FDG phosphorylation (k3) and influx constant (Ki) were significantly lower in diabetic patients (P < 0.02).
- A trend towards a decreased tumor/lung SUL ratio was observed in diabetic patients (P = 0.064).
Conclusions:
- FDG accumulation and tumor targeting are impaired in primary lung cancers of diabetic patients.
- Diabetes may reduce the diagnostic sensitivity of FDG-PET for detecting lung cancer.
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