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Regorafenib combined with transarterial chemoembolization for unresectable hepatocellular carcinoma: a real-world study
BACKGROUND: The benefits and tolerability of transarterial chemoembolization (TACE) combined with regorafenib as a second-line therapy has not been reported for unresectable hepatocellular carcinoma (HCC). This study aimed to explore the benefits and tolerability of TACE combined with second-line re...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8529854/ https://www.ncbi.nlm.nih.gov/pubmed/34670512 http://dx.doi.org/10.1186/s12876-021-01967-3 |
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author | Han, Yue Cao, Guang Sun, Bin Wang, Jian Yan, Dong Xu, Haifeng Shi, Qinsheng Liu, Zechuan Zhi, Weihua Xu, Liang Liu, Bojun Zou, Yinghua |
author_facet | Han, Yue Cao, Guang Sun, Bin Wang, Jian Yan, Dong Xu, Haifeng Shi, Qinsheng Liu, Zechuan Zhi, Weihua Xu, Liang Liu, Bojun Zou, Yinghua |
author_sort | Han, Yue |
collection | PubMed |
description | BACKGROUND: The benefits and tolerability of transarterial chemoembolization (TACE) combined with regorafenib as a second-line therapy has not been reported for unresectable hepatocellular carcinoma (HCC). This study aimed to explore the benefits and tolerability of TACE combined with second-line regorafenib in patients with unresectable advanced HCC and failure to first-line treatment. METHODS: This was a multicenter retrospective study of patients with progression after first-line sorafenib and/or lenvatinib between 01/2019 and 04/2020 at four tertiary hospitals in China. The patients were treated with TACE. Then, 5–7 days after the first TACE, the patients started taking regorafenib for 3 weeks every 4-week cycle. The overall survival (OS), time to progression (TTP), progression-free survival (PFS), and adverse events (AEs) were observed. RESULTS: The median follow-up was 5.6 (range 0.7, 17.0) months. The median age was 60 (range 35, 79) years. There were 32 (84.2%) males. The patients underwent a median of three TACE sessions (range 1–13). The initial doses of regorafenib were 20 mg/d (n = 1, 2.6%), 80 mg/d (n = 10, 26.3%), 120 mg/d (n = 15, 39.5%), and 160 mg/d (n = 11, 28.9%). The incidence of grade 3/4 AEs was 15.8%. Two patients stopped regorafenib due to AEs. The median OS was 14.3 months. The median PFS and TTP were 9.1 (95% CI 4.0, 14.2) and 9.1 (95% CI 5.5, 12.8) months, respectively. CONCLUSIONS: The present study provides real-world evidence indicating that regorafenib combined with TACE was beneficial and tolerable in patients with unresectable HCC. Additional prospective large-scale studies are required for confirmation. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12876-021-01967-3. |
format | Online Article Text |
id | pubmed-8529854 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-85298542021-10-25 Regorafenib combined with transarterial chemoembolization for unresectable hepatocellular carcinoma: a real-world study Han, Yue Cao, Guang Sun, Bin Wang, Jian Yan, Dong Xu, Haifeng Shi, Qinsheng Liu, Zechuan Zhi, Weihua Xu, Liang Liu, Bojun Zou, Yinghua BMC Gastroenterol Research BACKGROUND: The benefits and tolerability of transarterial chemoembolization (TACE) combined with regorafenib as a second-line therapy has not been reported for unresectable hepatocellular carcinoma (HCC). This study aimed to explore the benefits and tolerability of TACE combined with second-line regorafenib in patients with unresectable advanced HCC and failure to first-line treatment. METHODS: This was a multicenter retrospective study of patients with progression after first-line sorafenib and/or lenvatinib between 01/2019 and 04/2020 at four tertiary hospitals in China. The patients were treated with TACE. Then, 5–7 days after the first TACE, the patients started taking regorafenib for 3 weeks every 4-week cycle. The overall survival (OS), time to progression (TTP), progression-free survival (PFS), and adverse events (AEs) were observed. RESULTS: The median follow-up was 5.6 (range 0.7, 17.0) months. The median age was 60 (range 35, 79) years. There were 32 (84.2%) males. The patients underwent a median of three TACE sessions (range 1–13). The initial doses of regorafenib were 20 mg/d (n = 1, 2.6%), 80 mg/d (n = 10, 26.3%), 120 mg/d (n = 15, 39.5%), and 160 mg/d (n = 11, 28.9%). The incidence of grade 3/4 AEs was 15.8%. Two patients stopped regorafenib due to AEs. The median OS was 14.3 months. The median PFS and TTP were 9.1 (95% CI 4.0, 14.2) and 9.1 (95% CI 5.5, 12.8) months, respectively. CONCLUSIONS: The present study provides real-world evidence indicating that regorafenib combined with TACE was beneficial and tolerable in patients with unresectable HCC. Additional prospective large-scale studies are required for confirmation. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12876-021-01967-3. BioMed Central 2021-10-20 /pmc/articles/PMC8529854/ /pubmed/34670512 http://dx.doi.org/10.1186/s12876-021-01967-3 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Han, Yue Cao, Guang Sun, Bin Wang, Jian Yan, Dong Xu, Haifeng Shi, Qinsheng Liu, Zechuan Zhi, Weihua Xu, Liang Liu, Bojun Zou, Yinghua Regorafenib combined with transarterial chemoembolization for unresectable hepatocellular carcinoma: a real-world study |
title | Regorafenib combined with transarterial chemoembolization for unresectable hepatocellular carcinoma: a real-world study |
title_full | Regorafenib combined with transarterial chemoembolization for unresectable hepatocellular carcinoma: a real-world study |
title_fullStr | Regorafenib combined with transarterial chemoembolization for unresectable hepatocellular carcinoma: a real-world study |
title_full_unstemmed | Regorafenib combined with transarterial chemoembolization for unresectable hepatocellular carcinoma: a real-world study |
title_short | Regorafenib combined with transarterial chemoembolization for unresectable hepatocellular carcinoma: a real-world study |
title_sort | regorafenib combined with transarterial chemoembolization for unresectable hepatocellular carcinoma: a real-world study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8529854/ https://www.ncbi.nlm.nih.gov/pubmed/34670512 http://dx.doi.org/10.1186/s12876-021-01967-3 |
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