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436A AASLD ABSTRACTS HEPATOLOGY, October, 2015 7.5% of the patients (n=5) in group 2 died within 3 months post-sorafenib initiation (p=0.196). In group 1, 29 patients (45%) had additional therapy either adjuvant or for recurrence (including TACE, chemotherapy (CT), sorafenib, thermo-ablation, additional resection) and one was transplanted. In group 2, 20 (30%) patients had additional therapy either in addition to sorafenib or as second line (including TACE, CT, radiotherapy or radioembolization). Median overall survival (OS) was 12.0 months (IC95%:5.5-18.5) in group 1 and 12.9 months (IC95%: 8.3-17.5) in group 2 (p=0.61). Taking into account the imbalance in baseline characteristics, a propensity analysis was performed, identifying 57 patients with similar characteristics with a median OS of 7.2 months (IC95%: 3.7-10.6) in the “resection” group and 12.6 months (IC95%: 7.1-18.0) in the “sorafenib” group (p=0.89). In multivariate analysis, prognostic factors associated with survival in the whole population (resection + sorafenib) were PT time 50 mm HR=1.69, p=0.046), MVI involving 1st order branch or main trunk (HR=1.948, p=0.042) and additionnal therapy (HR=0.500, p=0.024). Median OS in the resection+additional therapy group of patients (n=29) was 25.2 [8.8-41.6] months and 24.3 [15.9-32.7] months in the sorafenib+additional therapy group (n=20), (p=0.82). Conclusion: In patients with HCC+ MVI amenable to surgical resection, a survival similar to that observed on standard of care, sorafenib, can be achieved. Palliative surgery may be a valuable alternative in this setting. A multimodal treatment strategy was associated with prolonged survival. Disclosures: Françoise Roudot-Thoraval - Advisory Committees or Review Panels: Roche; Consulting: LFB biomedicaments; Speaking and Teaching: gilead, Janssen, BMS, Roche Nathalie Ganne-Carrié - Advisory Committees or Review Panels: Roche; Speaking and Teaching: BMS, Gilead, Bayer Olivier Seror - Board Membership: Bayer Healthcare; Consulting: Olympus; Speaking and Teaching: Angiodynamics Didier Samuel - Consulting: Astellas, MSD, BMS, Roche, Novartis, Gilead, LFB, Janssen-Cilag, Biotest, Abbvie Christophe Duvoux - Advisory Committees or Review Panels: Novartis, Roche, Novartis, Roche, Novartis, Roche, Novartis, Roche; Speaking and Teaching: Astellas, Astellas, Astellas, Astellas The following authors have nothing to disclose: Charlotte E. Costentin, Eric Vibert, Thomas Decaens, Bernard Paule, Christian Letoublon, Mélanie Chiaradia, Julien Calderaro, Rene Adam, Ivan Bricault, Giuliana Amaddeo, Daniel Cherqui, Ariane Mallat, Alexis Laurent 450 Prediction of liver decompensation and survival after TACE for hepatocellular carcinoma. Is there a role for non-invasive markers of fibrosis? Jean-Baptiste Hiriart 1 , François Franques 1 , Julien Vergniol 1 , Christophe Cassinotto 2 , Faiza Chermak 1 , Bruno Lapuyade 2 , Juliette Foucher 1 , Wassil Merrouche 1 , Jean-Frédéric Blanc 3 , Victor de Ledinghen 1 ; 1 Hepatology, Hôpital Haut-Lévêque, Pessac, France; 2 Diagnostic and Interventional Imaging, Hôpital Haut-Lévêque, Pessac, France; 3 Hepatology, Hôpital Saint-André, Bordeaux, France Introduction: Non-invasive markers of liver fibrosis are useful to predict survival and liver-related events in patients with chronic liver disease. The aim of this study was to investigate the performance of these markers to predict hepatic decompensation and death after transarterial chemoembolization (TACE) for hepatocellular carcinoma (HCC). Patients and methods: From 2008 to 2012, all consecutive patients undergoing a first TACE for HCC with a FibroScan and serum biomarkers (Fibrotest, APRI, Hepascore, FIB-4, AST/ALT ratio, NAFLD score) performed at baseline were included. Liver decompensation was defined as the occurrence of at least one of the following events within 6 weeks after TACE: ascites, increase of bilirubin levels above 50 mmol/L, acute kidney injury. Child-Pugh score and MELD score were calculated the day before TACE and one month after. Incident cases of death were prospectively collected. Results: 103 patients were included (mean age 66 years, 85% men). In univariate analysis, factors associated with decompensation were albumin level 200 ng/ml (OR=2.51, CI95% 1.24-5.08, p=0.01) and albumin
HEPATOLOGY, VOLUME 62, NUMBER 1 (SUPPL) AASLD ABSTRACTS 437A for 70.9% and 12.6% of the total HCC cases (1292 patients) respectively. Out of the total cohort enrolled from 1980 to 2005, the ratio of cryptogenic to CHB patients was 1:6.7; while from 2006 to 2015, the ratio of cryptogenic to CHB patients has increased significantly to 1:3.9. Both groups were comparable with regards to gender, Chinese ethnicity, smoking status, Child’s score, stage of HCC, portal vein invasion, AFP and platelet count. Relative to CHB group, cryptogenic HCC patients were older (68 versus 60 years old; p
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1000A AASLD ABSTRACTS HEPATOLOGY, O
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1312A AUTHOR INDEX HEPATOLOGY, Octo
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1366A CATEGORY INDEX HEPATOLOGY, Oc
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