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Evaluation of D-TACE combined with endovascular brachytherapy for HCC with MPVTT

BACKGROUND: Hepatocellular carcinoma (HCC) patients with main portal vein tumor thrombus (MPVTT) may be able to have TACE through stent implantation into the portal vein with thrombosis to recover portal blood flow. PURPOSE: The goal of this study was to compare clinical results of conventional tran...

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Autores principales: Huang, Wei, Gong, Ju, Wang, Qingbing, Wang, Ziyin, Liu, Qin, Liu, Jingjing, Gu, Junwei, Ding, Xiaoyi, Wu, Zhiyuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9434401/
https://www.ncbi.nlm.nih.gov/pubmed/36059634
http://dx.doi.org/10.3389/fonc.2022.973357
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author Huang, Wei
Gong, Ju
Wang, Qingbing
Wang, Ziyin
Liu, Qin
Liu, Jingjing
Gu, Junwei
Ding, Xiaoyi
Wu, Zhiyuan
author_facet Huang, Wei
Gong, Ju
Wang, Qingbing
Wang, Ziyin
Liu, Qin
Liu, Jingjing
Gu, Junwei
Ding, Xiaoyi
Wu, Zhiyuan
author_sort Huang, Wei
collection PubMed
description BACKGROUND: Hepatocellular carcinoma (HCC) patients with main portal vein tumor thrombus (MPVTT) may be able to have TACE through stent implantation into the portal vein with thrombosis to recover portal blood flow. PURPOSE: The goal of this study was to compare clinical results of conventional transcatheter arterial chemoembolization (C-TACE) and doxorubicin-eluting bead transcatheter arterial chemoembolization (D-TACE) combined with endovascular brachytherapy in HCC patients with MPVTT. METHODS: This study was a retrospective controlled study with follow-up dates spanning from Mar 2015 to Feb 2020. Patients with both HCC and MPVTT were divided into two groups. Portal vein stents with iodine-125 seed strands were implanted first; then, C-TACE or D-TACE was administered to all patients. Objective response rates were assessed. RESULTS: A total of 26 patients were enrolled, with 13 in each group. During follow-up, the portal stent patency times were 112.3 ± 98.2 days in the C-TACE group and 101.7 ± 90.4 days in the D-TACE group. The time to disease progression was 42 days in the C-TACE group and 120 days in the D-TACE group (p=0.03). The overall survival time from the first intervention procedure was 216 days in the C-TACE group and 239 days in the D-TACE group (p=0.047). The D-TACE group was superior to the C-TACE group in terms of progression-free survival (PFS) and overall survival (OS) times. CONCLUSION: Endovascular implantation of brachytherapy combined with TACE is safe and effective in HCC patients with MPVTT. This combination therapy may be helpful for survival benefits to patients with stage BCLC-C HCC.
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spelling pubmed-94344012022-09-02 Evaluation of D-TACE combined with endovascular brachytherapy for HCC with MPVTT Huang, Wei Gong, Ju Wang, Qingbing Wang, Ziyin Liu, Qin Liu, Jingjing Gu, Junwei Ding, Xiaoyi Wu, Zhiyuan Front Oncol Oncology BACKGROUND: Hepatocellular carcinoma (HCC) patients with main portal vein tumor thrombus (MPVTT) may be able to have TACE through stent implantation into the portal vein with thrombosis to recover portal blood flow. PURPOSE: The goal of this study was to compare clinical results of conventional transcatheter arterial chemoembolization (C-TACE) and doxorubicin-eluting bead transcatheter arterial chemoembolization (D-TACE) combined with endovascular brachytherapy in HCC patients with MPVTT. METHODS: This study was a retrospective controlled study with follow-up dates spanning from Mar 2015 to Feb 2020. Patients with both HCC and MPVTT were divided into two groups. Portal vein stents with iodine-125 seed strands were implanted first; then, C-TACE or D-TACE was administered to all patients. Objective response rates were assessed. RESULTS: A total of 26 patients were enrolled, with 13 in each group. During follow-up, the portal stent patency times were 112.3 ± 98.2 days in the C-TACE group and 101.7 ± 90.4 days in the D-TACE group. The time to disease progression was 42 days in the C-TACE group and 120 days in the D-TACE group (p=0.03). The overall survival time from the first intervention procedure was 216 days in the C-TACE group and 239 days in the D-TACE group (p=0.047). The D-TACE group was superior to the C-TACE group in terms of progression-free survival (PFS) and overall survival (OS) times. CONCLUSION: Endovascular implantation of brachytherapy combined with TACE is safe and effective in HCC patients with MPVTT. This combination therapy may be helpful for survival benefits to patients with stage BCLC-C HCC. Frontiers Media S.A. 2022-08-18 /pmc/articles/PMC9434401/ /pubmed/36059634 http://dx.doi.org/10.3389/fonc.2022.973357 Text en Copyright © 2022 Huang, Gong, Wang, Wang, Liu, Liu, Gu, Ding and Wu https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Huang, Wei
Gong, Ju
Wang, Qingbing
Wang, Ziyin
Liu, Qin
Liu, Jingjing
Gu, Junwei
Ding, Xiaoyi
Wu, Zhiyuan
Evaluation of D-TACE combined with endovascular brachytherapy for HCC with MPVTT
title Evaluation of D-TACE combined with endovascular brachytherapy for HCC with MPVTT
title_full Evaluation of D-TACE combined with endovascular brachytherapy for HCC with MPVTT
title_fullStr Evaluation of D-TACE combined with endovascular brachytherapy for HCC with MPVTT
title_full_unstemmed Evaluation of D-TACE combined with endovascular brachytherapy for HCC with MPVTT
title_short Evaluation of D-TACE combined with endovascular brachytherapy for HCC with MPVTT
title_sort evaluation of d-tace combined with endovascular brachytherapy for hcc with mpvtt
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9434401/
https://www.ncbi.nlm.nih.gov/pubmed/36059634
http://dx.doi.org/10.3389/fonc.2022.973357
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