4.1 Article

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

Journal

NUCLEAR MEDICINE COMMUNICATIONS
Volume 30, Issue 6, Pages 455-461

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/MNM.0b013e32832bdcac

Keywords

dual-phase acquisition; F-18-FDG-PET; kinetic modelling; non-small-cell lung cancer; oncology

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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.

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