Imaging of Proliferation in Hepatocellular Carcinoma with the In Vivo Marker 18F-Fluorothymidine

Histology
DOI: 10.2967/jnumed.109.065896 Publication Date: 2009-08-19T03:34:15Z
ABSTRACT
We determined the ability of PET with thymidine analog 3'-deoxy-3'-(18)F-fluorothymidine ((18)F-FLT) to detect hepatocellular carcinoma (HCC).In this pilot study, (18)F-FLT was performed in 18 untreated patients clinically suspected HCC. Routine diagnostic procedures included ultrasound, MRI, or contrast-enhanced spiral CT upper gastrointestinal tract all patients. At 45-60 min after intravenous injection approximately 270-340 MBq (18)F-FLT, emission and transmission scanning a high-resolution scanner. Tracer uptake tumor surrounding liver tissue evaluated semiquantitatively by calculation mean maximum standardized values (SUVs). Results were correlated those conventional imaging methods.A total 13 tumors (sensitivity, 72%; 95% confidence interval [CI], 47%-90%) showed focal higher than activity detectable as hot lesions. Five characterized photopenic lesions contained mixture cold exhibiting comparable lower tissue. When considered, SUV 7.8 (range, 2.5-11.1), 9.3 2.9-14.3). Histology clinical follow-up revealed HCC 16 cholangiocarcinoma 2 In subgroup HCC, sensitivity for detection 69% (11/16; CI, 41%-89%). Correlation analysis demonstrated significant positive relationship between proliferation marker MIB-1 (r = 0.66, P 0.02). Survival (Cox proportional hazards regression) initial (mean SUVs) increased hazard ratios SUV, 1.20; 1.12), but because small number events, these results not statistically significant.In mixed pattern vivo (18)F-FLT. A that tissue, whereas remaining High seems be associated reduced overall survival could an important prognostic factor if tendency can confirmed larger prospective trial.
SUPPLEMENTAL MATERIAL
Coming soon ....
REFERENCES (31)
CITATIONS (38)