Journal
EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING
Volume 33, Issue 11, Pages 1285-1289Publisher
SPRINGER
DOI: 10.1007/s00259-006-0164-9
Keywords
hepatology; PET; oncology; fluorocholine-(18F); PET/CT
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Purpose: The diagnostic accuracy of [F-18] fluorodeoxyglucose (FDG) PET is insufficient to characterise hepatocellular carcinoma (HCC) in liver masses and to diagnose all cases of recurrent HCC. HCC has been reported to take up [C-11] acetate, but routine use of this tracer is difficult. Choline is another tracer of lipid metabolism, present in large amounts in HCC. In a proof-of-concept study, we evaluated [F-18] fluorocholine (FCH) uptake by HCC and compared FCH PET/CT with FDG PET/CT. Methods: Twelve patients with newly diagnosed (n= 8) or recurrent HCC ( n= 4) were prospectively enrolled. HCC was assessed by histology in eight cases and by American Association for the Study of Liver Diseases (AASLD) criteria in four cases. All patients underwent whole-body PET/CT 10 min after injection of 4 MBq/kg FCH. Within 1 week, 9 of the 12 patients also underwent whole-body FDG PET/CT 1 h after injection of 5 MBq/kg FDG. Results: The per-patient analysis showed a detection rate of 12/12 using FCH PET/CT for both newly diagnosed and recurrent HCC. The median signal to noise ratio was 1.5 +/- 0.38. There was a trend towards a higher FCH SUVmax in well-differentiated HCC ( 15.6 +/- 7.9 vs 11.9 +/- 0.9, NS). Of the nine patients who underwent FCH and FDG PET/CT, all nine were positive with FCH whereas only five were positive with FDG. Conclusion: FCH provides a high detection rate for HCC, making it potentially useful in the initial evaluation of HCC or in the detection of recurrent disease. The favourable result of this proof-of-concept study opens the way to a phase III prospective study.
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