Abstract
2-[18F] Fluoro-2-deoxy-D-glucose (2-[18F]FDG or FDG) is by far the most frequently used PET tracer in nuclear medical diagnostics. The high sensitivity of FDG PET to detect oncologic disease reflects an increased rate of glycolysis or/and glucose transport in most neoplasms relative to normal tissues. However, from a biochemical point of view FDG is not an ideal means of diagnosis because both normal and neoplastic cells metabolize glucose. As the metabolism of a tumor cell does not generally differ from that of a normal cell, other metabolic oncologic tracers also cannot be judged by exclusivity (i.e., accumulation solely in the tumor cell, no accumulation in normal cells) either. Furthermore, the metabolic rate, i.e., glucose consumption, is not a sensitive parameter in characteristically slow growing neoplasms, such as prostate cancer. Thus, tracers based on other biochemical concepts are valuable tools in nuclear medicinal diagnosis (for an overview see [120]). The development of the adequate selective tracers, which will allow deeper insight to tumor biochemistry from outside the human body using PET, is one of the most active areas in current radiopharmaceutical research.
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Rösch, F., Wester, HJ., DeGrado, T.R. (2000). Current developments of 18F-labeled PET tracers in oncology. In: Wieler, H.J., Coleman, R.E. (eds) PET in Clinical Oncology. Steinkopff, Heidelberg. https://doi.org/10.1007/978-3-642-57703-1_7
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DOI: https://doi.org/10.1007/978-3-642-57703-1_7
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