F-FDG PET/CT predicts survival after Y transarterial radioembolization in unresectable hepatocellular carcinoma.

作者信息

Jreige Mario, Mitsakis Periklis, Van Der Gucht Axel, Pomoni Anastasia, Silva-Monteiro Marina, Gnesin Silvano, Boubaker Ariane, Nicod-Lalonde Marie, Duran Rafael, Prior John O, Denys Alban, Schaefer Niklaus

机构信息

Department of Nuclear Medicine and Molecular Imaging, Lausanne University Hospital, Rue du Bugnon 46, CH-1011, Lausanne, Switzerland.

Institute of Radiation Physics, Lausanne University Hospital, Lausanne, Switzerland.

出版信息

Eur J Nucl Med Mol Imaging. 2017 Jul;44(7):1215-1222. doi: 10.1007/s00259-017-3653-0. Epub 2017 Feb 23.

Abstract

PURPOSE

To compare the value of pretreatment functional and morphological imaging parameters for predicting survival in patients undergoing transarterial radioembolization using yttrium-90 (Y-TARE) for unresectable hepatocellular carcinoma (uHCC).

METHODS

We analysed data from 48 patients in our prospective database undergoing Y-TARE treatment for uHCC (31 resin, 17 glass). All patients underwent F-FDG PET/CT and morphological imaging (CT and MRI scans) as part of a pretherapeutic work-up. Patients did not receive any treatment between these imaging procedures and Y-TARE. Kaplan-Meier estimates of progression-free survival (PFS) and overall survival (OS) were used to assess the prognostic value of F-FDG PET/CT metabolic parameters, including SUV, tumour-to-liver (T/L) uptake ratio and SUV of healthy liver, and morphological data, including number and size of lesions, portal-venous infiltration (PVI). Relevant prognostic factors for HCC including Child-Pugh class, Barcelona Clinic Liver Cancer (BCLC) stage, tumour size, PVI and serum AFP level were compared with metabolic parameters in univariate and multivariate analyses.

RESULTS

The median follow-up in living patients was 16.2 months (range 11.4-50.1 months). Relapse occurred in 34 patients (70.8%) at a median of 7.4 months (range 1.4-27.9 months) after Y-TARE, and relapse occurred in 24 of 34 patients (70.8%) who died from their disease at a median of 8.1 months (range 2.2-35.2 months). Significant prognostic markers for PFS were the mean and median lesion SUV (both P = 0.01; median PFS 10.2 vs. 7.4 months), and significant prognostic markers for OS were the first quarter (Q1) cut-off values for lesion SUV and T/L uptake ratio (both P = 0.02; median OS 30.9 vs. 9 months). The multivariate analysis confirmed that lesion SUV and T/L uptake ratio were independent negative predictors of PFS (hazard ratio, HR, 2.7, 95% CI 1.2-6.1, P = 0.02, for mean SUV; HR 2.6, 95% CI 1.1-5.9, P = 0.02, for median SUV:) and OS (HR 3.2, 95% CI 1-10.9, P = 0.04 for Q1 SUV; HR 3.7, 95% CI 1.1-12.2, P = 0.03, for Q1 T/L uptake ratio), respectively, when testing with either the BCLC staging system or serum AFP level.

CONCLUSION

Lesion SUV and T/L uptake ratio as assessed by F-FDG PET/CT, but not morphological imaging, were predictive markers of survival in patients undergoing Y-TARE for uHCC.

摘要

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