Quantitative evaluation of skeletal tumours with dynamic FDG PET: SUV in comparison to Patlak analysis

Citation
H. Wu et al., Quantitative evaluation of skeletal tumours with dynamic FDG PET: SUV in comparison to Patlak analysis, EUR J NUCL, 28(6), 2001, pp. 704-710
Citations number
35
Categorie Soggetti
Radiology ,Nuclear Medicine & Imaging","Medical Research Diagnosis & Treatment
Journal title
EUROPEAN JOURNAL OF NUCLEAR MEDICINE
ISSN journal
03406997 → ACNP
Volume
28
Issue
6
Year of publication
2001
Pages
704 - 710
Database
ISI
SICI code
0340-6997(200106)28:6<704:QEOSTW>2.0.ZU;2-6
Abstract
This study was carried out to evaluate bone lesions using fluorine-18 fluor odeoxyglucose positron emission tomography (FDG PET) and to explore whether dynamic and quantitative PET data may help to differentiate benign lesions from malignant masses, Forty patients with primary bone lesions were studi ed. The final diagnosis was confirmed by histopathology. A 60-min dynamic F DG PET acquisition was undertaken in all subjects. From the dynamic PET ima ges, indices such as the average and maximal standardised uptake values (SU Vs), the tumour SUV-to-muscle SUV ratio (T/M) and the SUV at 60 min-to-SUV at 30 min ratio (averSUV60/30 min and maxSUV60/30 min) were produced. Patla k graphical analysis was used to obtain the influx constant (K,), and the m etabolic rate of FDG (MRFDG) was calculated. Based on the receiver operator characteristic curve, the sensitivity and specificity for each parameter i n differentiating between malignant and benign lesions were evaluated, The histological results revealed 21 malignant tumours and 19 benign lesions in this group. The MRFDG and SUV indices in malignant lesions were significan tly higher than those in benign lesions. However, each index showed a consi derable overlap between benign and malignant lesions. Average SUV correlate d positively with MRFDG (r=0.67). When a cut-off of 1.8 average SUV was use d, the sensitivity and specificity for discrimination of malignancy from be nign disease were 85% and 82.4%, respectively. MRFDG showed a similar sensi tivity (82.4%) and a better specificity (92.9%), A combination consisting o f a cut-off of average SUV (1.8) and averSUV60/30 min(1.1)resulted in an im provement of specificity to 93.3%, with a small reduction in sensitivity (8 1.3%) as compared with exclusive use of SUV, The results of this study indi cate that a detectable difference in glucose metabolism exists between mali gnant and benign skeletal lesions. The static FDG uptake indices alone may not enable adequate differentiation between benign and malignant lesions. Q uantitative dynamic imaging may provide more helpful information, but will not permit a definite diagnosis. The use of uptake indices may represent an alternative and interesting approach to the evaluation of bone lesions.