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Evaluation of dose-efficacy of sorafenib and effect of transarterial chemoembolization in hepatocellular carcinoma patients: a retrospective study.

Authors :
Wang-De Hsiao
Cheng-Yuan Peng
Po-Heng Chuang
Hsueh-Chou Lai
Ken-Sheng Cheng
Jen-Wei Chou
Yang-Yuan Chen
Cheng-Ju Yu
Chun-Lung Feng
Wen-Pang Su
Sheng-Hung Chen
Jung-Ta Kao
Hsiao, Wang-De
Peng, Cheng-Yuan
Chuang, Po-Heng
Lai, Hsueh-Chou
Cheng, Ken-Sheng
Chou, Jen-Wei
Chen, Yang-Yuan
Yu, Cheng-Ju
Source :
BMC Gastroenterology; 4/27/2016, Vol. 16, p1-9, 9p, 1 Diagram, 3 Charts, 1 Graph
Publication Year :
2016

Abstract

<bold>Background: </bold>Transarterial chemoembolization (TACE) and sorafenib are the therapeutic standard for intermediate and advanced stage hepatocellular carcinoma (HCC) patients respectively. High costs with adverse events (AE) of sorafenib might limit sorafenib dosage, further affecting therapeutic response. To attain greatest benefit, we evaluated the efficacy of different doses and effect of TACE during and after sorafenib discontinuation in patients representing Child-Pugh Classification Class A with venous or extra-hepatic invasion.<bold>Methods: </bold>A total 156 patients met the criteria and were divided into Groups I (n = 52) accepting 800 mg/day; II (n = 58) accepting 800 mg/day and reduced to 400 mg/day owing to AE; and III (n = 46) accepting 400 mg/day. TACE was performed during and after sorafenib discontinuation and therapeutic response bimonthly to four-monthly was rated thereafter.<bold>Results: </bold>Median duration of sorafenib treatment and patients' survival were 4.00 ± 0.45 and 7.50 ± 1.44 months in all cases; 2.50 ± 0.90 and 5.00 ± 1.10 months in Group I; 5.50 ± 1.27 and 16.50 ± 1.86 months in Group II; 4.00 ± 0.94 and 6.50 ± 2.49 months in Group III. Group II presented the best response and survival benefit (p = 0.010 and p = 0.011 respectively). Child-Pugh Classification score 5 (Hazard Ratio = 0.492, p = 0.049), absent AE (3.423, p = 0.015), tumor numbers ≤ 3 (0.313, p = 0.009), sorafenib duration ≤ 1 cycle (3.694, p = 0.004), and absent TACE (3.197, p = 0.008) significantly correlated with patient survival. TACE benefit appeared in separate and total cases during (p = 0.002, p = 0.595, p = 0.074, p = 0.002 respectively) and after discontinuation of sorafenib administration (p = 0.001, p = 0.034, p = 0.647, p = 0.001 respectively).<bold>Conclusions: </bold>Low-dosage sorafenib not only appeared tolerable and lowered economic pressure but also provided satisfactory results. TACE benefited patient's survival during and after sorafenib discontinuation. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
1471230X
Volume :
16
Database :
Complementary Index
Journal :
BMC Gastroenterology
Publication Type :
Academic Journal
Accession number :
115140150
Full Text :
https://doi.org/10.1186/s12876-016-0464-x