Oncotarget

Clinical Research Papers:

Efficacy and safety of apatinib combined with transarterial chemoembolization for hepatocellular carcinoma with portal venous tumor thrombus: a retrospective study

Changfu Liu, Wenge Xing, Tongguo Si, Haipeng Yu and Zhi Guo _

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Oncotarget. 2017; 8:100734-100745. https://doi.org/10.18632/oncotarget.20140

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Abstract

Changfu Liu1,2,3,4, Wenge Xing1,2,3,4, Tongguo Si1,2,3,4, Haipeng Yu1,2,3,4 and Zhi Guo1,2,3,4

1Department of Interventional Treatment, Tianjin Medical University Cancer Institute and Hospital, Tianjin, China

2National Clinical Research Center for Cancer, Tianjin, China

3Key Laboratory of Cancer Prevention and Therapy, Tianjin, Tianjin, China

4Tianjin’s Clinical Research Center for Cancer, Tianjin, China

Correspondence to:

Zhi Guo, email: [email protected]

Keywords: hepatocellular carcinoma, portal vein tumor thrombosis, apatinib, transarterial chemoembolization, efficacy

Received: May 04, 2017     Accepted: July 29, 2017     Published: August 10, 2017

ABSTRACT

Objective: To investigate the efficacy and safety of combined therapy with apatinib and transarterial chemoembolization (TACE) for hepatocellular carcinoma with portal venous tumor thrombus (PVTT).

Materials and Methods: We retrospectively analyzed 19 patients with hepatocellular carcinoma with PVTT who were treated with apatinib and TACE at a single center between January 2015 and January 2017. Clinical information on the patients was collected. Adverse events, overall survival, progression-free survival, objective response rate, and disease-control rate based on mRECIST criteria (American Association for the Study of Liver Diseases, 2008) were reviewed and evaluated.

Results: All patients had complete follow-up records and the median follow-up time was 13 months (1–24 months). Among the 19 patients, 63.16% achieved a partial response and 21.05% achieved stable disease. The objective response and disease-control rates for the tumor were 63.16% and 84.21%, respectively, and the objective response and disease-control rates for PVTT were 10.93% and 89.47%, respectively. The median overall survival was 11.9 months, and the 6-month and 1-year overall survival rates were 94.7% and 48.8%, respectively. The median progression-free survival rate was 8.1 months, and the 6-month and 1-year rates were 73.3% and 22.9%, respectively. The most common apatinib-related adverse events were hand-foot-skin reaction, fatigue, dyspepsia, diarrhea, and hypertension, and the most common TACE-related adverse event was fever. No procedure-related mortality or grade 4 adverse events were observed, but grade 3 adverse events were observed in two patients.

Conclusions: This exploratory study suggested that apatinib combined with TACE treatment was safe and might improve overall and progression-free survival in patients with hepatocellular carcinoma with PVTT. Further randomized controlled trials are needed to clarify the potential role of apatinib in hepatocellular carcinoma with PVTT.


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