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Efficacy and safety of sorafenib in patients with advanced hepatocellular carcinoma according to baseline status: Subset analyses of the phase III Sorafenib Asia-Pacific trial

Authors
Cheng, Ann-LiiGuan, ZhongzhenChen, ZhendongTsao, Chao-JungQin, ShukuiKim, Jun SukYang, Tsai-ShengTak, Won YoungPan, HongmingYu, ShiyingXu, JianmingFang, FangZou, JessieLentini, GiuseppeVoliotis, DimitrisKang, Yoon-Koo
Issue Date
Jul-2012
Publisher
ELSEVIER SCI LTD
Keywords
Hepatocellular carcinoma; Sorafenib; Subset analyses
Citation
EUROPEAN JOURNAL OF CANCER, v.48, no.10, pp.1452 - 1465
Indexed
SCIE
SCOPUS
Journal Title
EUROPEAN JOURNAL OF CANCER
Volume
48
Number
10
Start Page
1452
End Page
1465
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/107960
DOI
10.1016/j.ejca.2011.12.006
ISSN
0959-8049
Abstract
Background: The phase III Sorafenib Asia-Pacific (AP) trial-conducted in China, Taiwan and South Korea - confirmed that sorafenib improves overall survival (OS) and is safe for patients with advanced hepatocellular carcinoma (HCC). We performed a series of exploratory subset analyses to determine whether baseline status affected response to sorafenib. Methods: In the Sorafenib AP trial, 226 patients with well-preserved liver function (>95% Child-Pugh A) were randomised 2: 1 to sorafenib 400 mg bid or matching placebo. Subanalyses were based on aetiology (hepatitis B virus present/absent); tumour burden (macroscopic vascular invasion and/or extrahepatic spread present/absent); presence or absence of either lung or lymph node metastasis at baseline, Eastern Cooperative Oncology Group performance status (0, 1-2); serum concentrations of alanine aminotransferase/aspartate aminotransferase (normal, mildly elevated, moderately elevated), alpha-fetoprotein (normal/elevated) and total bilirubin (normal/elevated); and whether or not there was a history of hepatectomy or transarterial chemoembolisation/embolisation. Subgroup assessments included OS, time to progression (TTP), disease control rate and safety. Findings: Sorafenib consistently improved both median OS and median TTP, compared with placebo (range of hazard ratios (HR), 0.32-0.87 and 0.31-0.75, respectively). The most common grade 3/4 adverse events were hand-foot skin reaction, diarrhoea and fatigue, the incidence of which was similar between subgroups. Interpretation: The efficacy and safety profiles of sorafenib in the subpopulations described were comparable with those in the overall study population. These exploratory analyses suggest that sorafenib is effective for patients from the AP region with advanced HCC, irrespective of baseline status. (C) 2011 Elsevier Ltd. All rights reserved.
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