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Combination Therapy after TACE for Hepatocellular Carcinoma with Macroscopic Vascular Invasion: Stereotactic Body Radiotherapy versus Sorafenib

Stereotactic body radiotherapy (SBRT) has shown promising results in the control of macroscopic vascular invasion in patients with hepatocellular carcinoma (HCC); however, its efficacy in comparison to sorafenib when combined with transarterial chemoembolization (TACE) remains to be determined. Betw...

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Autores principales: Shen, Lujun, Xi, Mian, Zhao, Lei, Zhang, Xuhui, Wang, Xiuchen, Huang, Zhimei, Chen, Qifeng, Zhang, Tianqi, Shen, Jingxian, Liu, Mengzhong, Huang, Jinhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6315557/
https://www.ncbi.nlm.nih.gov/pubmed/30558224
http://dx.doi.org/10.3390/cancers10120516
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author Shen, Lujun
Xi, Mian
Zhao, Lei
Zhang, Xuhui
Wang, Xiuchen
Huang, Zhimei
Chen, Qifeng
Zhang, Tianqi
Shen, Jingxian
Liu, Mengzhong
Huang, Jinhua
author_facet Shen, Lujun
Xi, Mian
Zhao, Lei
Zhang, Xuhui
Wang, Xiuchen
Huang, Zhimei
Chen, Qifeng
Zhang, Tianqi
Shen, Jingxian
Liu, Mengzhong
Huang, Jinhua
author_sort Shen, Lujun
collection PubMed
description Stereotactic body radiotherapy (SBRT) has shown promising results in the control of macroscopic vascular invasion in patients with hepatocellular carcinoma (HCC); however, its efficacy in comparison to sorafenib when combined with transarterial chemoembolization (TACE) remains to be determined. Between 2009 and 2017, 77 HCC patients with macroscopic vascular invasion receiving TACE–SBRT or TACE–sorafenib combination therapies were enrolled. The best treatment responses, overall survival (OS), and progression-free survival (PFS) of the two treatment arms were compared. Of the patients enrolled, 26 patients (33.8%) received TACE–SBRT treatment, and 51 (66.2%) received TACE–sorafenib treatment. The patients in the TACE–SBRT group were more frequently classified as elder in age (p = 0.012), having recurrent disease (p = 0.026), and showing lower rates of multiple hepatic lesions (p = 0.005) than patients in TACE–sorafenib group. After propensity score matching (PSM), 26 pairs of well-matched HCC patients were selected; patients in the TACE–SBRT group showed better overall response rates in trend compared to those in the TACE–sorafenib group. The hazard ratio (HR) of OS to PFS for the TACE–SBRT approach and the TACE–sorafenib approach was 0.36 (95% CI, 0.17–0.75; p = 0.007) and 0.35 (95% CI, 0.20–0.62; p < 0.001), respectively. For HCC patients with macrovascular invasion, TACE plus SBRT could provide improved OS and PFS compared to TACE–sorafenib therapy.
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spelling pubmed-63155572019-01-09 Combination Therapy after TACE for Hepatocellular Carcinoma with Macroscopic Vascular Invasion: Stereotactic Body Radiotherapy versus Sorafenib Shen, Lujun Xi, Mian Zhao, Lei Zhang, Xuhui Wang, Xiuchen Huang, Zhimei Chen, Qifeng Zhang, Tianqi Shen, Jingxian Liu, Mengzhong Huang, Jinhua Cancers (Basel) Article Stereotactic body radiotherapy (SBRT) has shown promising results in the control of macroscopic vascular invasion in patients with hepatocellular carcinoma (HCC); however, its efficacy in comparison to sorafenib when combined with transarterial chemoembolization (TACE) remains to be determined. Between 2009 and 2017, 77 HCC patients with macroscopic vascular invasion receiving TACE–SBRT or TACE–sorafenib combination therapies were enrolled. The best treatment responses, overall survival (OS), and progression-free survival (PFS) of the two treatment arms were compared. Of the patients enrolled, 26 patients (33.8%) received TACE–SBRT treatment, and 51 (66.2%) received TACE–sorafenib treatment. The patients in the TACE–SBRT group were more frequently classified as elder in age (p = 0.012), having recurrent disease (p = 0.026), and showing lower rates of multiple hepatic lesions (p = 0.005) than patients in TACE–sorafenib group. After propensity score matching (PSM), 26 pairs of well-matched HCC patients were selected; patients in the TACE–SBRT group showed better overall response rates in trend compared to those in the TACE–sorafenib group. The hazard ratio (HR) of OS to PFS for the TACE–SBRT approach and the TACE–sorafenib approach was 0.36 (95% CI, 0.17–0.75; p = 0.007) and 0.35 (95% CI, 0.20–0.62; p < 0.001), respectively. For HCC patients with macrovascular invasion, TACE plus SBRT could provide improved OS and PFS compared to TACE–sorafenib therapy. MDPI 2018-12-14 /pmc/articles/PMC6315557/ /pubmed/30558224 http://dx.doi.org/10.3390/cancers10120516 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Shen, Lujun
Xi, Mian
Zhao, Lei
Zhang, Xuhui
Wang, Xiuchen
Huang, Zhimei
Chen, Qifeng
Zhang, Tianqi
Shen, Jingxian
Liu, Mengzhong
Huang, Jinhua
Combination Therapy after TACE for Hepatocellular Carcinoma with Macroscopic Vascular Invasion: Stereotactic Body Radiotherapy versus Sorafenib
title Combination Therapy after TACE for Hepatocellular Carcinoma with Macroscopic Vascular Invasion: Stereotactic Body Radiotherapy versus Sorafenib
title_full Combination Therapy after TACE for Hepatocellular Carcinoma with Macroscopic Vascular Invasion: Stereotactic Body Radiotherapy versus Sorafenib
title_fullStr Combination Therapy after TACE for Hepatocellular Carcinoma with Macroscopic Vascular Invasion: Stereotactic Body Radiotherapy versus Sorafenib
title_full_unstemmed Combination Therapy after TACE for Hepatocellular Carcinoma with Macroscopic Vascular Invasion: Stereotactic Body Radiotherapy versus Sorafenib
title_short Combination Therapy after TACE for Hepatocellular Carcinoma with Macroscopic Vascular Invasion: Stereotactic Body Radiotherapy versus Sorafenib
title_sort combination therapy after tace for hepatocellular carcinoma with macroscopic vascular invasion: stereotactic body radiotherapy versus sorafenib
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6315557/
https://www.ncbi.nlm.nih.gov/pubmed/30558224
http://dx.doi.org/10.3390/cancers10120516
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