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First published online April 16, 2009, 10.2967/jnumed.108.060574
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Journal of Nuclear Medicine Vol. 50 No. 5 682-687
© 2009 by Society of Nuclear Medicine

doi: 10.2967/jnumed.108.060574

Clinical Investigation

Prediction of Tumor Recurrence by 18F-FDG PET in Liver Transplantation for Hepatocellular Carcinoma

Jeong Won Lee1,2, Jin Chul Paeng1,3, Keon Wook Kang1–3, Hyun Woo Kwon1, Kyung-Suk Suh4, June-Key Chung1–3, Myung Chul Lee1,3 and Dong Soo Lee1–3

1 Department of Nuclear Medicine, Seoul National University College of Medicine, Seoul, Korea; 2 Cancer Research Institute, Seoul National University College of Medicine, Seoul, Korea; 3 Institute of Radiation Medicine, Medical Research Center, Seoul National University, Seoul, Korea; and 4 Department of Surgery, Seoul National University College of Medicine, Seoul, Korea

Correspondence: For correspondence or reprints contact: Jin Chul Paeng, Department of Nuclear Medicine, Seoul National University College of Medicine, 28 Yeongeon-dong, Jongno-gu, Seoul, 110-744, Korea. E-mail: paengjc{at}snu.ac.kr

Although several prognostic factors are used to predict recurrence and to select adequate candidates for liver transplantation for hepatocellular carcinoma (HCC), these prognostic factors have some clinical limitations. The purpose of this study was to evaluate 18F-FDG PET as a prognostic factor and to optimize its ability to predict tumor recurrence in liver transplantation for HCC. Methods: The study included a total of 59 HCC patients (45 men and 15 women; mean age ± SD, 56 ± 8 y) who underwent 18F-FDG PET and subsequent orthotopic liver transplantation. All patients were followed up for more than 1 y (mean, 29 ± 17 mo), and recurrence of tumor was monitored. Three PET parameters—maximal standardized uptake value (SUVmax), ratio of tumor SUVmax to normal-liver SUVmax (TSUVmax/LSUVmax), and ratio of tumor SUVmax to normal-liver mean SUV (TSUVmax/LSUVmean)—were tested as prognostic factors and compared with conventional prognostic factors. Results: Among the 3 parameters tested, TSUVmax/LSUVmax was the most significant in the prediction of tumor recurrence, with a cutoff value of 1.15. In a multivariate analysis of various prognostic factors including TSUVmax/LSUVmax, serum {alpha}-fetoprotein, T stage, size of tumor, and vascular invasion of tumor, TSUVmax/LSUVmax was the most significant, and only vascular invasion of tumor had additional significance. According to TSUVmax/LSUVmax, the 1-y recurrence-free survival rate above the cutoff was markedly different from the rate below the cutoff (97% vs. 57%, P < 0.001). Conclusion: In this study, 18F-FDG PET was an independent and significant predictor of tumor recurrence. In liver transplantation for HCC, 18F-FDG PET can provide effective information on the prognosis for tumor recurrence and the selection of adequate candidates for liver transplantation.

Key Words: FDG • liver transplantation • PET • recurrence • prognosis

COPYRIGHT © 2009 by the Society of Nuclear Medicine, Inc.


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