Quantitative techniques in 18FDG PET scanning in oncology

被引:58
作者
Castell, F. [2 ]
Cook, G. J. R. [1 ]
机构
[1] Royal Marsden NHS Fdn Trust, Dept Nucl Med & PET, Sutton SM2 5PT, Surrey, England
[2] Royal Marsden NHS Fdn Trust, Dept Radiotherapy, Sutton SM2 5PT, Surrey, England
关键词
(18)FDG; PET; oncology; quantitation; kinetic analysis;
D O I
10.1038/sj.bjc.6604330
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The clinical applications of F-18-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.
引用
收藏
页码:1597 / 1601
页数:5
相关论文
共 33 条
[1]   Optimization of semi-quantification in metabolic PET studies with 18F-fluorodeoxyglucose and 11C-methionine in the determination of malignancy of gliomas [J].
Borbely, Katalin ;
Nyary, Istvan ;
Toth, Maria ;
Ericson, Kaj ;
Gulyas, Balazs .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 2006, 246 (1-2) :85-94
[2]   Cellular release of [18F]2-fluoro-2-deoxyglucose as a function of the glucose-6-phosphatase enzyme system [J].
Caracó, C ;
Aloj, L ;
Chen, LY ;
Chou, JY ;
Eckelman, WC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (24) :18489-18494
[3]   Non-invasive assessment of skeletal kinetics using fluorine-18 fluoride positron emission tomography: evaluation of image and population-derived arterial input functions [J].
Cook, GJR ;
Lodge, MA ;
Marsden, PK ;
Dynes, A ;
Fogelman, I .
EUROPEAN JOURNAL OF NUCLEAR MEDICINE, 1999, 26 (11) :1424-1429
[4]   Normal physiological and benign pathological variants of 18-fluoro-2-deoxyglucose positron-emission tomography scanning: Potential for error in interpretation [J].
Cook, GJR ;
Fogelman, I ;
Maisey, MN .
SEMINARS IN NUCLEAR MEDICINE, 1996, 26 (04) :308-314
[5]  
Dimitrakopoulou-Strauss A, 2002, J NUCL MED, V43, P510
[6]  
Dimitrakopoulou-Strauss A, 2001, J NUCL MED, V42, P713
[7]   Recovery correction for quantitation in emission tomography: a feasibility study [J].
Geworski, L ;
Knoop, BO ;
de Cabrejas, ML ;
Knapp, WH ;
Munz, DL .
EUROPEAN JOURNAL OF NUCLEAR MEDICINE, 2000, 27 (02) :161-169
[8]  
Hoekstra CJ, 2002, J NUCL MED, V43, P1304
[9]   Monitoring response to therapy in cancer using [18F]-2-fluouo-2-deoxy-D-glucose and positron emission tomography:: an overview of different analytical methods [J].
Hoekstra, CJ ;
Paglianiti, I ;
Hoekstra, OS ;
Smit, EF ;
Postmus, PE ;
Teule, GJJ ;
Lammertsma, AA .
EUROPEAN JOURNAL OF NUCLEAR MEDICINE, 2000, 27 (06) :731-743
[10]  
Huang SC, 2000, NUCL MED BIOL, V27, P643