Quantitative techniques in 18FDG PET scanning in oncology
- PMID: 18475291
- PMCID: PMC2391128
- DOI: 10.1038/sj.bjc.6604330
Quantitative techniques in 18FDG PET scanning in oncology
Abstract
The clinical applications of (18)F-fluoro-2-deoxyglucose ((18)FDG) positron emission tomography (PET) in oncology are becoming established. While simple static scanning techniques are used for the majority of routine clinical examinations, increasing use of PET in clinical trials to monitor treatment response with (18)FDG and novel tracers reflecting different pharmacodynamic end points, often necessitates a more complex and quantitative analysis of radiopharmaceutical kinetics. A wide range of PET analysis techniques exist, ranging from simple visual analysis and semiquantitative methods to full dynamic studies with kinetic analysis. These methods are discussed, focusing particularly on the available methodologies that can be utilised in clinical trials.
Figures
References
-
- Borbely K, Nyary I, Toth M, Ericson K, Gulyas B (2006) Optimization of semi-quantification in metabolic PET studies with 18F-fluorodeoxyglucose and 11C-methionine in the determination of malignancy of gliomas. J Neurol Sci 246: 85–94 - PubMed
-
- Caraco C, Aloj L, Chen LY, Chou JY, Eckelman WC (2000) Cellular release of [18F]2-fluoro-2-deoxyglucose as a function of the glucose-6-phosphatase enzyme system. J Biol Chem 16: 18489–18494 - PubMed
-
- Cook GJR, Fogelman I, Maisey MN (1996) Normal physiological and benign pathological variants of 18-FDG PET scanning: potential for error in interpretation. Semin Nucl Med 26: 308–314 - PubMed
-
- Cook GJR, Lodge MA, Marsden PK, Dynes A, Fogelman I (1999) Non-invasive assessment of skeletal kinetics using 18F-fluoride positron emission tomography: evaluation of image and population derived arterial input functions. Eur J Nucl Med 26: 1424–1429 - PubMed
-
- Dimitrakopoulou-Strauss A, Strauss LG, Heichel T, Wu H, Burger C, Bernd L, Ewerbeck V (2002) The role of quantitative (18)F-FDG PET studies for the differentiation of malignant and benign bone lesions. J Nucl Med 43: 510–518 - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
