Assessment of dual-time-point 18F-FDG-PET imaging for pulmonary lesions

被引:53
作者
Laffon, Eric [1 ,5 ,6 ]
de Clermont, Henri [1 ]
Begueret, Hugues [2 ]
Vernejoux, Jean-Marc [3 ]
Thumerel, Matthieu [4 ]
Marthan, Roger [5 ,6 ]
Ducassou, Dominique [1 ]
机构
[1] Hop Haut Leveque, Nucl Med Serv, CHU Bordeaux, F-33604 Pessac, France
[2] Hop Haut Leveque, Serv Anat Pathol, F-33604 Pessac, France
[3] Hop Haut Leveque, Serv Pneumol, F-33604 Pessac, France
[4] Hop Haut Leveque, Serv Chirurg Thorac, F-33604 Pessac, France
[5] Univ Bordeaux 2, Lab Physiol Cellulaire Resp, F-33076 Bordeaux, France
[6] INSERM, Bordeaux, France
关键词
dual-phase acquisition; F-18-FDG-PET; kinetic modelling; non-small-cell lung cancer; oncology; POSITRON-EMISSION-TOMOGRAPHY; FDG-PET; NONINVASIVE ESTIMATION; NODULES; MALIGNANCY; TISSUES; TUMOR; QUANTIFICATION; QUANTIFY; GLUCOSE;
D O I
10.1097/MNM.0b013e32832bdcac
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Objective The objective of this study was to assess suitability of dual-time-point F-18-FDG [(F-18)-fluoro-2-deoxyglucose]-PET imaging for differentiating between malignant and benign pulmonary lesions, whose size and maximal standardized uptake values (SUVs) are greater than 10 mm and 2.5, respectively. Methods A total of 38 patients, 27 with malignant lesions (n = 30), and 11 with benign lesions (n = 22), were investigated by performing two static acquisitions started at mean times t = 79 and t = 158 min after the tracer injection. A model analysis involving tissue F-18-FDG uptake and release has been developed and applied. Results Malignant lesions showed a SUV increase between the two acquisitions for 27 of 30 lesions, and a SUV decrease or constancy for the other three. Benign lesions showed a SUV increase in 19 of 22 lesions, and a SUV decrease in three (both increase and decrease were observed for multiple benign lesions in two patients). Conclusion It is recommended that dual-time-point F-18-FDG-PET imaging is not indicated to differentiate between malignant and benign pulmonary lesions, whose size and maximal SUV are greater than 10 mm and 2.5, respectively. Furthermore, a model analysis suggests that the variation in SUV observed between early and delayed scans may be explained by different values of the F-18-FDG release/uptake ratio. Nucl Med Commun 30:455-461 (C) 2009 Wolters Kluwer Health Lippincott Williams & Wilkins.
引用
收藏
页码:455 / 461
页数:7
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