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Transarterial Chemoembolization Plus Lenvatinib and PD-1 Inhibitors for Hepatocellular Carcinoma with Main Trunk Portal Vein Tumor Thrombus: A Multicenter Retrospective Study

PURPOSE: In recent years, immune checkpoint inhibitors have been used in combination with tyrosine kinase inhibitors and local therapies, creating a new era in treating hepatocellular carcinoma (HCC) with portal vein tumor thrombus (PVTT). However, the benefits of this triple therapy remain unclear....

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Autores principales: Li, Shu-Qun, Wu, Jun-Yi, Wu, Jia-Yi, Xie, Huang, Li, Jin-Hai, Zeng, Zhen-Xin, Fu, Yang-Kai, Liu, De-Yi, Li, Han, Chen, Wei-Zhao, Huang, Jing-Yao, Yan, Mao-Lin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10577247/
https://www.ncbi.nlm.nih.gov/pubmed/37850080
http://dx.doi.org/10.2147/JHC.S428980
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author Li, Shu-Qun
Wu, Jun-Yi
Wu, Jia-Yi
Xie, Huang
Li, Jin-Hai
Zeng, Zhen-Xin
Fu, Yang-Kai
Liu, De-Yi
Li, Han
Chen, Wei-Zhao
Huang, Jing-Yao
Yan, Mao-Lin
author_facet Li, Shu-Qun
Wu, Jun-Yi
Wu, Jia-Yi
Xie, Huang
Li, Jin-Hai
Zeng, Zhen-Xin
Fu, Yang-Kai
Liu, De-Yi
Li, Han
Chen, Wei-Zhao
Huang, Jing-Yao
Yan, Mao-Lin
author_sort Li, Shu-Qun
collection PubMed
description PURPOSE: In recent years, immune checkpoint inhibitors have been used in combination with tyrosine kinase inhibitors and local therapies, creating a new era in treating hepatocellular carcinoma (HCC) with portal vein tumor thrombus (PVTT). However, the benefits of this triple therapy remain unclear. Thus, this study evaluated whether the combination of transarterial chemoembolization (TACE), lenvatinib, and programmed death-1 (PD-1) inhibitors (triple therapy) was effective and safe for unresectable HCC with main trunk portal vein tumor thrombus (Vp4). PATIENTS AND METHODS: This study enrolled patients receiving triple therapy at four institutions between August 2018 and April 2022. Patient characteristics and course of treatment were extracted from patient records. Tumors and tumor thrombus response were evaluated using an HCC-specific modified RECIST. Kaplan–Meier curve analysis demonstrated overall survival (OS) and progression-free survival (PFS). Adverse events (AEs) were evaluated according to the National Cancer Institute Common Terminology Criteria for Adverse Events, version 5.0. RESULTS: Median follow-up duration was 18 (4.0–26.3) months. Overall, 41 patients with HCC and Vp4 receiving first-line triple therapy were enrolled. The intrahepatic tumor objective response rate was 68.3%. The median OS was 21.7 (range, 2.8–30.5) months, whereas the median PFS was 14.5 (range, 1.3–27.6) months. Twelve patients received sequential resections. Resection was independently associated with favorable OS and PFS. Fever (31.7%), hypertension (26.8%), fatigue (24.4%), abnormal liver function (63.4%) and decreased appetite (21.9%) were the AEs frequently associated with treatment. No treatment-related mortality occurred. CONCLUSION: TACE plus lenvatinib and PD-1 inhibition was effective and tolerable for treating unresectable HCC with Vp4, with a high tumor response rate and favorable prognosis.
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spelling pubmed-105772472023-10-17 Transarterial Chemoembolization Plus Lenvatinib and PD-1 Inhibitors for Hepatocellular Carcinoma with Main Trunk Portal Vein Tumor Thrombus: A Multicenter Retrospective Study Li, Shu-Qun Wu, Jun-Yi Wu, Jia-Yi Xie, Huang Li, Jin-Hai Zeng, Zhen-Xin Fu, Yang-Kai Liu, De-Yi Li, Han Chen, Wei-Zhao Huang, Jing-Yao Yan, Mao-Lin J Hepatocell Carcinoma Original Research PURPOSE: In recent years, immune checkpoint inhibitors have been used in combination with tyrosine kinase inhibitors and local therapies, creating a new era in treating hepatocellular carcinoma (HCC) with portal vein tumor thrombus (PVTT). However, the benefits of this triple therapy remain unclear. Thus, this study evaluated whether the combination of transarterial chemoembolization (TACE), lenvatinib, and programmed death-1 (PD-1) inhibitors (triple therapy) was effective and safe for unresectable HCC with main trunk portal vein tumor thrombus (Vp4). PATIENTS AND METHODS: This study enrolled patients receiving triple therapy at four institutions between August 2018 and April 2022. Patient characteristics and course of treatment were extracted from patient records. Tumors and tumor thrombus response were evaluated using an HCC-specific modified RECIST. Kaplan–Meier curve analysis demonstrated overall survival (OS) and progression-free survival (PFS). Adverse events (AEs) were evaluated according to the National Cancer Institute Common Terminology Criteria for Adverse Events, version 5.0. RESULTS: Median follow-up duration was 18 (4.0–26.3) months. Overall, 41 patients with HCC and Vp4 receiving first-line triple therapy were enrolled. The intrahepatic tumor objective response rate was 68.3%. The median OS was 21.7 (range, 2.8–30.5) months, whereas the median PFS was 14.5 (range, 1.3–27.6) months. Twelve patients received sequential resections. Resection was independently associated with favorable OS and PFS. Fever (31.7%), hypertension (26.8%), fatigue (24.4%), abnormal liver function (63.4%) and decreased appetite (21.9%) were the AEs frequently associated with treatment. No treatment-related mortality occurred. CONCLUSION: TACE plus lenvatinib and PD-1 inhibition was effective and tolerable for treating unresectable HCC with Vp4, with a high tumor response rate and favorable prognosis. Dove 2023-10-11 /pmc/articles/PMC10577247/ /pubmed/37850080 http://dx.doi.org/10.2147/JHC.S428980 Text en © 2023 Li et al. https://creativecommons.org/licenses/by-nc/3.0/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/ (https://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. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Li, Shu-Qun
Wu, Jun-Yi
Wu, Jia-Yi
Xie, Huang
Li, Jin-Hai
Zeng, Zhen-Xin
Fu, Yang-Kai
Liu, De-Yi
Li, Han
Chen, Wei-Zhao
Huang, Jing-Yao
Yan, Mao-Lin
Transarterial Chemoembolization Plus Lenvatinib and PD-1 Inhibitors for Hepatocellular Carcinoma with Main Trunk Portal Vein Tumor Thrombus: A Multicenter Retrospective Study
title Transarterial Chemoembolization Plus Lenvatinib and PD-1 Inhibitors for Hepatocellular Carcinoma with Main Trunk Portal Vein Tumor Thrombus: A Multicenter Retrospective Study
title_full Transarterial Chemoembolization Plus Lenvatinib and PD-1 Inhibitors for Hepatocellular Carcinoma with Main Trunk Portal Vein Tumor Thrombus: A Multicenter Retrospective Study
title_fullStr Transarterial Chemoembolization Plus Lenvatinib and PD-1 Inhibitors for Hepatocellular Carcinoma with Main Trunk Portal Vein Tumor Thrombus: A Multicenter Retrospective Study
title_full_unstemmed Transarterial Chemoembolization Plus Lenvatinib and PD-1 Inhibitors for Hepatocellular Carcinoma with Main Trunk Portal Vein Tumor Thrombus: A Multicenter Retrospective Study
title_short Transarterial Chemoembolization Plus Lenvatinib and PD-1 Inhibitors for Hepatocellular Carcinoma with Main Trunk Portal Vein Tumor Thrombus: A Multicenter Retrospective Study
title_sort transarterial chemoembolization plus lenvatinib and pd-1 inhibitors for hepatocellular carcinoma with main trunk portal vein tumor thrombus: a multicenter retrospective study
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10577247/
https://www.ncbi.nlm.nih.gov/pubmed/37850080
http://dx.doi.org/10.2147/JHC.S428980
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