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Effects of adjuvant huaier granule therapy on survival rate of patients with hepatocellular carcinoma

Objective: Clinical trials have reported that Huaier granule inhibits the recurrence of hepatocellular carcinoma (HCC) after resection. However, its efficacy in patients at different clinical stages of HCC remains unknown. We investigated the effects of Huaier granule on the 3-year overall survival...

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Autores principales: Shi, Ke, Bi, Yufei, Zeng, Xuanwei, Wang, Xianbo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10213905/
https://www.ncbi.nlm.nih.gov/pubmed/37251326
http://dx.doi.org/10.3389/fphar.2023.1163304
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author Shi, Ke
Bi, Yufei
Zeng, Xuanwei
Wang, Xianbo
author_facet Shi, Ke
Bi, Yufei
Zeng, Xuanwei
Wang, Xianbo
author_sort Shi, Ke
collection PubMed
description Objective: Clinical trials have reported that Huaier granule inhibits the recurrence of hepatocellular carcinoma (HCC) after resection. However, its efficacy in patients at different clinical stages of HCC remains unknown. We investigated the effects of Huaier granule on the 3-year overall survival (OS) rate of patients at different clinical stages. Design: This cohort study included 826 patients with HCC, screened between January 2015 and December 2019. The patients were divided into Huaier (n = 174) and control groups (n = 652), and the 3-year OS rates were compared between the two groups. To eliminate bias caused by confounding factors, propensity score matching (PSM) was performed. We used the Kaplan-Meier method to estimate OS rate and tested the difference using the log-rank test. Results: Multivariable regression analysis revealed that Huaier therapy was an independent protective factor for 3-year survival rate. After PSM (1:2), the Huaier and control groups comprised 170 and 340 patients, respectively. The 3-year OS rate was remarkably higher in the Huaier group than in the control group (adjusted hazard ratio [aHR]: 0.36; 95% confidence interval: 0.26–0.49; p < 0.001). The aHR for Huaier use for 3–12, 12–24, and >24 months was 0.48, 0.23, and 0.16, respectively, indicating a dose-response pattern. For the 3–12-, 12–24-, and >24-month groups, the 3-year OS rate was 54.1%, 68.6%, and 90.4%, respectively. Multivariate stratified analysis confirmed that the mortality risk in Huaier users was lower than that in non-Huaier users in most subgroups. Conclusion: Adjuvant Huaier therapy improved the OS rate in patients with HCC. However, these findings require further verification through prospective clinical studies.
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spelling pubmed-102139052023-05-27 Effects of adjuvant huaier granule therapy on survival rate of patients with hepatocellular carcinoma Shi, Ke Bi, Yufei Zeng, Xuanwei Wang, Xianbo Front Pharmacol Pharmacology Objective: Clinical trials have reported that Huaier granule inhibits the recurrence of hepatocellular carcinoma (HCC) after resection. However, its efficacy in patients at different clinical stages of HCC remains unknown. We investigated the effects of Huaier granule on the 3-year overall survival (OS) rate of patients at different clinical stages. Design: This cohort study included 826 patients with HCC, screened between January 2015 and December 2019. The patients were divided into Huaier (n = 174) and control groups (n = 652), and the 3-year OS rates were compared between the two groups. To eliminate bias caused by confounding factors, propensity score matching (PSM) was performed. We used the Kaplan-Meier method to estimate OS rate and tested the difference using the log-rank test. Results: Multivariable regression analysis revealed that Huaier therapy was an independent protective factor for 3-year survival rate. After PSM (1:2), the Huaier and control groups comprised 170 and 340 patients, respectively. The 3-year OS rate was remarkably higher in the Huaier group than in the control group (adjusted hazard ratio [aHR]: 0.36; 95% confidence interval: 0.26–0.49; p < 0.001). The aHR for Huaier use for 3–12, 12–24, and >24 months was 0.48, 0.23, and 0.16, respectively, indicating a dose-response pattern. For the 3–12-, 12–24-, and >24-month groups, the 3-year OS rate was 54.1%, 68.6%, and 90.4%, respectively. Multivariate stratified analysis confirmed that the mortality risk in Huaier users was lower than that in non-Huaier users in most subgroups. Conclusion: Adjuvant Huaier therapy improved the OS rate in patients with HCC. However, these findings require further verification through prospective clinical studies. Frontiers Media S.A. 2023-05-11 /pmc/articles/PMC10213905/ /pubmed/37251326 http://dx.doi.org/10.3389/fphar.2023.1163304 Text en Copyright © 2023 Shi, Bi, Zeng and Wang. 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 Pharmacology
Shi, Ke
Bi, Yufei
Zeng, Xuanwei
Wang, Xianbo
Effects of adjuvant huaier granule therapy on survival rate of patients with hepatocellular carcinoma
title Effects of adjuvant huaier granule therapy on survival rate of patients with hepatocellular carcinoma
title_full Effects of adjuvant huaier granule therapy on survival rate of patients with hepatocellular carcinoma
title_fullStr Effects of adjuvant huaier granule therapy on survival rate of patients with hepatocellular carcinoma
title_full_unstemmed Effects of adjuvant huaier granule therapy on survival rate of patients with hepatocellular carcinoma
title_short Effects of adjuvant huaier granule therapy on survival rate of patients with hepatocellular carcinoma
title_sort effects of adjuvant huaier granule therapy on survival rate of patients with hepatocellular carcinoma
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10213905/
https://www.ncbi.nlm.nih.gov/pubmed/37251326
http://dx.doi.org/10.3389/fphar.2023.1163304
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