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Transarterial chemoembolization combined with sorafenib for the treatment of hepatocellular carcinoma with hepatic vein tumor thrombus

OBJECTIVE: To compare the treatment outcomes of sorafenib plus transarterial chemoembolization (TACE) vs TACE alone in patients with hepatocellular carcinoma (HCC) and hepatic vein tumor thrombus (HVTT). METHODS: Twenty patients who were initially diagnosed with HCC and HVTT and received TACE combin...

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Autores principales: Zhang, Yong-Fa, Wei, Wei, Wang, Jia-Hong, Xu, Li, Jian, Pei-En, Xiao, Cheng-Zuo, Zhong, Xiao-Ping, Shi, Ming, Guo, Rong-Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4948732/
https://www.ncbi.nlm.nih.gov/pubmed/27471398
http://dx.doi.org/10.2147/OTT.S106659
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author Zhang, Yong-Fa
Wei, Wei
Wang, Jia-Hong
Xu, Li
Jian, Pei-En
Xiao, Cheng-Zuo
Zhong, Xiao-Ping
Shi, Ming
Guo, Rong-Ping
author_facet Zhang, Yong-Fa
Wei, Wei
Wang, Jia-Hong
Xu, Li
Jian, Pei-En
Xiao, Cheng-Zuo
Zhong, Xiao-Ping
Shi, Ming
Guo, Rong-Ping
author_sort Zhang, Yong-Fa
collection PubMed
description OBJECTIVE: To compare the treatment outcomes of sorafenib plus transarterial chemoembolization (TACE) vs TACE alone in patients with hepatocellular carcinoma (HCC) and hepatic vein tumor thrombus (HVTT). METHODS: Twenty patients who were initially diagnosed with HCC and HVTT and received TACE combined with sorafenib during February 2009 to October 2013 were included in the study. To minimize selection bias, these patients were compared with 60 case-matched controls selected from a pool of 81 patients (in a 1:3 ratio) who received TACE alone during the same period. The primary end point was overall survival (OS). The secondary end points were time to progression, disease control rate, and adverse events. RESULTS: After a median follow-up period of 12.5 months (range, 1.03–44.23 months), the OS of the combined group was found to be significantly higher compared with the monotherapy group (14.9 vs 6.1 months, P=0.010). The time to progression was found to be significantly longer in the combined group (4.9 vs 2.4 months, P=0.016). Univariate and multivariate analyses revealed that the treatment allocation was an independent predictor of OS. CONCLUSION: Sorafenib plus TACE was well tolerated and was more effective in treating patients with advanced HCC and HVTT. Future trials with prospective larger samples are required to validate these results.
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spelling pubmed-49487322016-07-28 Transarterial chemoembolization combined with sorafenib for the treatment of hepatocellular carcinoma with hepatic vein tumor thrombus Zhang, Yong-Fa Wei, Wei Wang, Jia-Hong Xu, Li Jian, Pei-En Xiao, Cheng-Zuo Zhong, Xiao-Ping Shi, Ming Guo, Rong-Ping Onco Targets Ther Original Research OBJECTIVE: To compare the treatment outcomes of sorafenib plus transarterial chemoembolization (TACE) vs TACE alone in patients with hepatocellular carcinoma (HCC) and hepatic vein tumor thrombus (HVTT). METHODS: Twenty patients who were initially diagnosed with HCC and HVTT and received TACE combined with sorafenib during February 2009 to October 2013 were included in the study. To minimize selection bias, these patients were compared with 60 case-matched controls selected from a pool of 81 patients (in a 1:3 ratio) who received TACE alone during the same period. The primary end point was overall survival (OS). The secondary end points were time to progression, disease control rate, and adverse events. RESULTS: After a median follow-up period of 12.5 months (range, 1.03–44.23 months), the OS of the combined group was found to be significantly higher compared with the monotherapy group (14.9 vs 6.1 months, P=0.010). The time to progression was found to be significantly longer in the combined group (4.9 vs 2.4 months, P=0.016). Univariate and multivariate analyses revealed that the treatment allocation was an independent predictor of OS. CONCLUSION: Sorafenib plus TACE was well tolerated and was more effective in treating patients with advanced HCC and HVTT. Future trials with prospective larger samples are required to validate these results. Dove Medical Press 2016-07-12 /pmc/articles/PMC4948732/ /pubmed/27471398 http://dx.doi.org/10.2147/OTT.S106659 Text en © 2016 Zhang et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Zhang, Yong-Fa
Wei, Wei
Wang, Jia-Hong
Xu, Li
Jian, Pei-En
Xiao, Cheng-Zuo
Zhong, Xiao-Ping
Shi, Ming
Guo, Rong-Ping
Transarterial chemoembolization combined with sorafenib for the treatment of hepatocellular carcinoma with hepatic vein tumor thrombus
title Transarterial chemoembolization combined with sorafenib for the treatment of hepatocellular carcinoma with hepatic vein tumor thrombus
title_full Transarterial chemoembolization combined with sorafenib for the treatment of hepatocellular carcinoma with hepatic vein tumor thrombus
title_fullStr Transarterial chemoembolization combined with sorafenib for the treatment of hepatocellular carcinoma with hepatic vein tumor thrombus
title_full_unstemmed Transarterial chemoembolization combined with sorafenib for the treatment of hepatocellular carcinoma with hepatic vein tumor thrombus
title_short Transarterial chemoembolization combined with sorafenib for the treatment of hepatocellular carcinoma with hepatic vein tumor thrombus
title_sort transarterial chemoembolization combined with sorafenib for the treatment of hepatocellular carcinoma with hepatic vein tumor thrombus
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4948732/
https://www.ncbi.nlm.nih.gov/pubmed/27471398
http://dx.doi.org/10.2147/OTT.S106659
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