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Drug-related adverse events potentially predict the efficacy of apatinib on advanced hepatocellular carcinoma

BACKGROUND: Hepatocellular carcinoma (HCC) is the fourth leading cause of cancer-related deaths worldwide every year, and most HCC patients are diagnosed with advanced disease and can only receive systemic treatment. TKIs are the most important components of the systemic treatment of HCC and have bo...

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Autores principales: Gu, Xiaoying, Zhang, Su, Yang, Xuejiao, Guan, Tao, Hou, Zhenyu, Cao, Manqing, Li, Huikai, Zhang, Ti
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9620633/
https://www.ncbi.nlm.nih.gov/pubmed/36316630
http://dx.doi.org/10.1186/s12876-022-02542-0
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author Gu, Xiaoying
Zhang, Su
Yang, Xuejiao
Guan, Tao
Hou, Zhenyu
Cao, Manqing
Li, Huikai
Zhang, Ti
author_facet Gu, Xiaoying
Zhang, Su
Yang, Xuejiao
Guan, Tao
Hou, Zhenyu
Cao, Manqing
Li, Huikai
Zhang, Ti
author_sort Gu, Xiaoying
collection PubMed
description BACKGROUND: Hepatocellular carcinoma (HCC) is the fourth leading cause of cancer-related deaths worldwide every year, and most HCC patients are diagnosed with advanced disease and can only receive systemic treatment. TKIs are the most important components of the systemic treatment of HCC and have both good efficacy and adverse events (AEs).  METHODS: This analysis included 207 patients with locally advanced unresectable or metastatic HCC who received oral treatment with apatinib. We analyzed the overall survival (OS) and progression-free survival (PFS) of patients with or without corresponding AEs to evaluate which AEs can predict the efficacy of apatinib. RESULTS: Patients with hand-foot syndrome (HFS; p = 0.005), proteinuria (p = 0.006) and diarrhea (p < 0.001) had significantly better OS than those without corresponding AEs, and the appearance of HFS (p = 0.006) and proteinuria (p = 0.004) was associated with longer PFS. CONCLUSION: Among all the AEs induced by apatinib in the treatment of advanced HCC, proteinuria could potentially predict PFS, and diarrhea was a potential predictor of OS. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12876-022-02542-0.
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spelling pubmed-96206332022-11-01 Drug-related adverse events potentially predict the efficacy of apatinib on advanced hepatocellular carcinoma Gu, Xiaoying Zhang, Su Yang, Xuejiao Guan, Tao Hou, Zhenyu Cao, Manqing Li, Huikai Zhang, Ti BMC Gastroenterol Research Article BACKGROUND: Hepatocellular carcinoma (HCC) is the fourth leading cause of cancer-related deaths worldwide every year, and most HCC patients are diagnosed with advanced disease and can only receive systemic treatment. TKIs are the most important components of the systemic treatment of HCC and have both good efficacy and adverse events (AEs).  METHODS: This analysis included 207 patients with locally advanced unresectable or metastatic HCC who received oral treatment with apatinib. We analyzed the overall survival (OS) and progression-free survival (PFS) of patients with or without corresponding AEs to evaluate which AEs can predict the efficacy of apatinib. RESULTS: Patients with hand-foot syndrome (HFS; p = 0.005), proteinuria (p = 0.006) and diarrhea (p < 0.001) had significantly better OS than those without corresponding AEs, and the appearance of HFS (p = 0.006) and proteinuria (p = 0.004) was associated with longer PFS. CONCLUSION: Among all the AEs induced by apatinib in the treatment of advanced HCC, proteinuria could potentially predict PFS, and diarrhea was a potential predictor of OS. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12876-022-02542-0. BioMed Central 2022-10-31 /pmc/articles/PMC9620633/ /pubmed/36316630 http://dx.doi.org/10.1186/s12876-022-02542-0 Text en © The Author(s) 2022 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 Article
Gu, Xiaoying
Zhang, Su
Yang, Xuejiao
Guan, Tao
Hou, Zhenyu
Cao, Manqing
Li, Huikai
Zhang, Ti
Drug-related adverse events potentially predict the efficacy of apatinib on advanced hepatocellular carcinoma
title Drug-related adverse events potentially predict the efficacy of apatinib on advanced hepatocellular carcinoma
title_full Drug-related adverse events potentially predict the efficacy of apatinib on advanced hepatocellular carcinoma
title_fullStr Drug-related adverse events potentially predict the efficacy of apatinib on advanced hepatocellular carcinoma
title_full_unstemmed Drug-related adverse events potentially predict the efficacy of apatinib on advanced hepatocellular carcinoma
title_short Drug-related adverse events potentially predict the efficacy of apatinib on advanced hepatocellular carcinoma
title_sort drug-related adverse events potentially predict the efficacy of apatinib on advanced hepatocellular carcinoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9620633/
https://www.ncbi.nlm.nih.gov/pubmed/36316630
http://dx.doi.org/10.1186/s12876-022-02542-0
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