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. 2015 Dec;4(4):253-62.
doi: 10.1159/000367743. Epub 2015 Oct 21.

Effectiveness of Sorafenib in Patients with Transcatheter Arterial Chemoembolization (TACE) Refractory and Intermediate-Stage Hepatocellular Carcinoma

Affiliations

Effectiveness of Sorafenib in Patients with Transcatheter Arterial Chemoembolization (TACE) Refractory and Intermediate-Stage Hepatocellular Carcinoma

Tadaaki Arizumi et al. Liver Cancer. 2015 Dec.

Abstract

Background and aims: Patients with intermediate-stage hepatocellular carcinoma (HCC) refractory to transcatheter arterial chemoembolization (TACE) are considered to be candidates for sorafenib. The aim of this study was to evaluate the superiority of conversion of treatment to sorafenib on overall survival (OS) for cases refractory to TACE.

Methods: This was a retrospective cohort study carried out on 497 patients with HCC who were treated with TACE therapy at our hospital between January 2008 and December 2013. Fifty-six patients were diagnosed as refractory to TACE during their clinical course and they were divided into two cohorts, (1) those who switched from TACE to sorafenib and (2) those who continued TACE. The overall survival (OS) after the time of being refractory to TACE was evaluated between the two groups.

Results: After refractoriness to TACE therapy was confirmed, 24 patients continued with TACE (TACE-group) and 32 patients underwent treatment conversion to sorafenib (sorafenib-group). The median OS was 24.7 months in the sorafenib-group and 13.6 months in the TACE-group (p=0.002).

Conclusions: Conversion to sorafenib significantly improves the OS in patients refractory to TACE therapy with intermediate-stage HCC. Administration of sorafenib is therefore recommended in such circumstances of TACE treatment failure.

Keywords: Child-Pugh score; Hepatocellular carcinoma; Overall survival; Sorafenib; Transarterial chemoembolization.

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Figures

Fig. 1
Fig. 1
Comparison of OS between TACE and sorafenib among patients deemed refractory to TACE. Kaplan-Meier curves of the OS of 56 patients who underwent treatment with continued TACE or conversion to sorafenib after being deemed refractory to TACE. The median OS of patients assigned to the TACE and sorafenib groups was 13.6 and 24.7 months, respectively, after being deemed refractory to TACE (p=0.002 by log-rank test).
Fig. 2
Fig. 2
Overall comparison of Child-Pugh score between the sorafenib conversion group and the TACE continuation group over time. a A significant difference was noted in Child-Pugh score 6 months after patients were deemed refractory to TACE (p=0.005 by Mann-Whitney U test). Each bar represents 25th-75th percentile. The dashed line indicates the alteration in the median value of the TACE group and solid line represents the sorafenib group. b No significant difference was noted in the plasma bilirubin at 3 or 6 months after patients were deemed refractory to TACE. c A significant difference was noted in plasma albumin at 6 months after patients were deemed refractory to TACE (p=0.043 by Mann-Whitney U test). d A significant difference was noted in the PT at 6 months after patients were deemed refractory to TACE (p=0.0041 by Mann-Whitney U test).

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