© Spandidos Publications 2014. All rights reserved. A pulmonary lesion is an extremely common and clinically challenging disorder worldwide, and an accurate diagnosis of lung cancer is crucial for early treatment and management. The aim of the present study was to perform a comprehensive meta analysis to compare the diagnostic performance of 18 F-fluorothymidine ( 18 F-FLT) positron emission tomography (PET) with 18 F-fluorodeoxyglucose ( 18 F-FDG) PET in evaluating patients with pulmonary lesions. Relevant studies were identified using the PubMed, EMBASE and Cochrane library databases. The pooled estimated sensitivity, specificity, positive-likelihood ratio, negative-likelihood ratio, and diagnostic odds ratio (DOR) for 18 F-FLT PET versus 18 F-FDG PET were calculated as the main outcome measures. Summary receiver operating characteristic curves were also constructed by Meta-Disk 1.4 software using a Mose's constant of linear model. The meta analysis showed that 18 F-FLT PET had a higher specificity (0.70; 95% CI, 0.61-0.77), but lower sensitivity (0.81; 95% CI, 0.74-0.87) compared to 18 F-FDG PET (0.50; 95% CI, 0.41-0.58 for specificity; 0.92; 95% CI 0.86-0.95 for sensitivity). For DOR, 18 F-FLT PET (12.58; 95% CI, 6.81-23.24) was higher compared to 18 F-FDG PET (10.72; 95% CI, 5.51-20.87). The area under the curve was 0.8592 and 0.9240 for 18 F-FLT PET and 18 F-FDG PET, respectively (Z=0.976, P > 0.05). In conclusion, 18 F-FLT PET and 18 F-FDG PET had good diagnostic performance for the overall assessment of pulmonary lesions, and 18 F-FLT PET had a higher specificity compared to 18 F-FDG PET, but was less sensitive than 18 F-FDG PET. Therefore, 18 F-FLT and 18 F-FDG together could add diagnostic confidence for pulmonary lesions.
Mendeley helps you to discover research relevant for your work.
CITATION STYLE
LI, X.-F., DAI, D., SONG, X.-Y., LIU, J.-J., ZHU, Y.-J., & XU, W.-G. (2015). Comparison of the diagnostic performance of 18F-fluorothymidine versus 18F-fluorodeoxyglucose positron emission tomography on pulmonary lesions: A meta analysis. Molecular and Clinical Oncology, 3(1), 101–108. https://doi.org/10.3892/mco.2014.440