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Identifying optimal therapies in patients with advanced hepatocellular carcinoma: a systematic review and network meta-analysis

BACKGROUND: Recently, increasing literature has been reported on optimal therapies in patients with advanced hepatocellular carcinoma (HCC) and many therapeutic modalities have been proposed to improve the survival rate. However, the results are not consistent due to different research protocols, sm...

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Autores principales: Yang, Zhenyu, Tong, Yao, Yang, Lin, He, Xianli, Bao, Guoqiang, Du, Xilin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9468989/
https://www.ncbi.nlm.nih.gov/pubmed/36300147
http://dx.doi.org/10.21037/tgh-20-318
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author Yang, Zhenyu
Tong, Yao
Yang, Lin
He, Xianli
Bao, Guoqiang
Du, Xilin
author_facet Yang, Zhenyu
Tong, Yao
Yang, Lin
He, Xianli
Bao, Guoqiang
Du, Xilin
author_sort Yang, Zhenyu
collection PubMed
description BACKGROUND: Recently, increasing literature has been reported on optimal therapies in patients with advanced hepatocellular carcinoma (HCC) and many therapeutic modalities have been proposed to improve the survival rate. However, the results are not consistent due to different research protocols, small sample sizes and different study endpoints and there is no standard treatment protocol has been defined. Therefore, it is very important to explore the optimal bonding mode and to evaluate the efficacy and safety of the optimal sequential therapy for those patients. METHODS: We searched available databases through January 2020 for relevant studies. The main outcome measure was 1-year overall survival (OS) and overall response rate (ORR); the secondary outcome measure was a composite of toxic effects retrieved grade 3 or 4 adverse events (AEs) from all included studies. Statistical analyses were conducted using STATA version 15 and GeMTC package in the R statistical software. RESULTS: After a detailed review, 8 randomized controlled trials (RCTs) and 20 retrospective studies involving 3,675 advanced HCC patients were included for network meta-analysis. Indirect comparisons showed that hepatic arterial infusion chemotherapy (HAIC) plus radiofrequency ablation (RFA) was highest probability of obtaining the best OS rate of 1 year [surface under the cumulative ranking (SUCRA), 0.95] and ORR (SUCRA, 0.86) when compared with other potential optimal therapies and which had ranked the first in all treatment regimens, followed by HAIC (SUCRA, 0.75). Direct and indirect comparison of 1-year OS and ORR with all treatment regimens each other showed that for all treatment regimens, patients showed significant clinical benefit when compared with transcatheter arterial chemoembolization (TACE) or sorafenib alone. However, the incidence of treatment-related AEs of grade 3 or 4 occurred in patients who have received targeted drug sorafenib therapy (SUCRA, 0.51) compared with other interesting regimens. CONCLUSIONS: HAIC may be a valuable therapeutic strategy for advanced HCC patients to prevent recurrence and metastasis after RFA, as well as in improving patient prognosis and quality of life. Meanwhile, HAIC combined with RFA is a safe and effective treatment in patients with advanced HCC, and this combination therapy can significantly prolong 1-year survival rate when compared with other optimal sequential therapies. TRIAL REGISTRATION: This study is registered with PROSPERO, number CRD42020176149.
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spelling pubmed-94689892022-10-25 Identifying optimal therapies in patients with advanced hepatocellular carcinoma: a systematic review and network meta-analysis Yang, Zhenyu Tong, Yao Yang, Lin He, Xianli Bao, Guoqiang Du, Xilin Transl Gastroenterol Hepatol Original Article BACKGROUND: Recently, increasing literature has been reported on optimal therapies in patients with advanced hepatocellular carcinoma (HCC) and many therapeutic modalities have been proposed to improve the survival rate. However, the results are not consistent due to different research protocols, small sample sizes and different study endpoints and there is no standard treatment protocol has been defined. Therefore, it is very important to explore the optimal bonding mode and to evaluate the efficacy and safety of the optimal sequential therapy for those patients. METHODS: We searched available databases through January 2020 for relevant studies. The main outcome measure was 1-year overall survival (OS) and overall response rate (ORR); the secondary outcome measure was a composite of toxic effects retrieved grade 3 or 4 adverse events (AEs) from all included studies. Statistical analyses were conducted using STATA version 15 and GeMTC package in the R statistical software. RESULTS: After a detailed review, 8 randomized controlled trials (RCTs) and 20 retrospective studies involving 3,675 advanced HCC patients were included for network meta-analysis. Indirect comparisons showed that hepatic arterial infusion chemotherapy (HAIC) plus radiofrequency ablation (RFA) was highest probability of obtaining the best OS rate of 1 year [surface under the cumulative ranking (SUCRA), 0.95] and ORR (SUCRA, 0.86) when compared with other potential optimal therapies and which had ranked the first in all treatment regimens, followed by HAIC (SUCRA, 0.75). Direct and indirect comparison of 1-year OS and ORR with all treatment regimens each other showed that for all treatment regimens, patients showed significant clinical benefit when compared with transcatheter arterial chemoembolization (TACE) or sorafenib alone. However, the incidence of treatment-related AEs of grade 3 or 4 occurred in patients who have received targeted drug sorafenib therapy (SUCRA, 0.51) compared with other interesting regimens. CONCLUSIONS: HAIC may be a valuable therapeutic strategy for advanced HCC patients to prevent recurrence and metastasis after RFA, as well as in improving patient prognosis and quality of life. Meanwhile, HAIC combined with RFA is a safe and effective treatment in patients with advanced HCC, and this combination therapy can significantly prolong 1-year survival rate when compared with other optimal sequential therapies. TRIAL REGISTRATION: This study is registered with PROSPERO, number CRD42020176149. AME Publishing Company 2022-10-25 /pmc/articles/PMC9468989/ /pubmed/36300147 http://dx.doi.org/10.21037/tgh-20-318 Text en 2022 Translational Gastroenterology and Hepatology. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Original Article
Yang, Zhenyu
Tong, Yao
Yang, Lin
He, Xianli
Bao, Guoqiang
Du, Xilin
Identifying optimal therapies in patients with advanced hepatocellular carcinoma: a systematic review and network meta-analysis
title Identifying optimal therapies in patients with advanced hepatocellular carcinoma: a systematic review and network meta-analysis
title_full Identifying optimal therapies in patients with advanced hepatocellular carcinoma: a systematic review and network meta-analysis
title_fullStr Identifying optimal therapies in patients with advanced hepatocellular carcinoma: a systematic review and network meta-analysis
title_full_unstemmed Identifying optimal therapies in patients with advanced hepatocellular carcinoma: a systematic review and network meta-analysis
title_short Identifying optimal therapies in patients with advanced hepatocellular carcinoma: a systematic review and network meta-analysis
title_sort identifying optimal therapies in patients with advanced hepatocellular carcinoma: a systematic review and network meta-analysis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9468989/
https://www.ncbi.nlm.nih.gov/pubmed/36300147
http://dx.doi.org/10.21037/tgh-20-318
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