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The association between antibiotic use and outcomes of HCC patients treated with immune checkpoint inhibitors

OBJECTIVE: Recently, immune checkpoint inhibitor (ICI) treatment has shown encouraging performance in improving the prognosis of hepatocellular carcinoma (HCC) patients. The gut microbiome plays a vital role in altering the efficacy of ICIs, which may be impacted by antibiotics. The aim of the meta-...

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Autores principales: Zhang, Lilong, Chen, Chen, Chai, Dongqi, Li, Chunlei, Guan, Yongjun, Liu, Li, Kuang, Tianrui, Deng, Wenhong, Wang, Weixing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9429218/
https://www.ncbi.nlm.nih.gov/pubmed/36059512
http://dx.doi.org/10.3389/fimmu.2022.956533
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author Zhang, Lilong
Chen, Chen
Chai, Dongqi
Li, Chunlei
Guan, Yongjun
Liu, Li
Kuang, Tianrui
Deng, Wenhong
Wang, Weixing
author_facet Zhang, Lilong
Chen, Chen
Chai, Dongqi
Li, Chunlei
Guan, Yongjun
Liu, Li
Kuang, Tianrui
Deng, Wenhong
Wang, Weixing
author_sort Zhang, Lilong
collection PubMed
description OBJECTIVE: Recently, immune checkpoint inhibitor (ICI) treatment has shown encouraging performance in improving the prognosis of hepatocellular carcinoma (HCC) patients. The gut microbiome plays a vital role in altering the efficacy of ICIs, which may be impacted by antibiotics. The aim of the meta-analysis is to estimate the influence of antibiotic use on the survival of HCC patients treated with ICIs. METHODS: The literature review was conducted using databases like PubMed, EMBASE, Cochrane Library, CNKI, WANFANG DATA, VIP, Google Scholar, and ClinicalTrials.gov before May 15, 2022. The primary endpoints were overall survival (OS), progression-free survival (PFS), objective response rate (ORR), and disease control rate (DCR). RESULTS: A total of six retrospective studies met the inclusion criteria. 1056 patients were included in the study, of which 352 (33.33%) received antibiotic treatment. The meta-analysis results revealed antibiotic use did not affect the OS (HR: 1.41, 95% CI: 0.96-2.08, P = 0.088) and PFS (HR: 1.21, 95% CI: 0.73-2.00, P = 0.459) in HCC patients treated with ICIs. Besides, the use of antibiotics did not reduce the ORR (OR: 1.06, 95% CI: 0.69-1.64, P = 0.784) and DCR (OR: 0.42, 95% CI: 0.09-2.06, P = 0.286) in HCC patients treated with ICIs. CONCLUSION: Current evidence reveals that antibiotic use does alter the therapeutic efficacy of ICIs in HCC patients. SYSTEMATIC REVIEW REGISTRATION: https://www.crd.york.ac.uk/, identifier CRD42022311948.
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spelling pubmed-94292182022-09-01 The association between antibiotic use and outcomes of HCC patients treated with immune checkpoint inhibitors Zhang, Lilong Chen, Chen Chai, Dongqi Li, Chunlei Guan, Yongjun Liu, Li Kuang, Tianrui Deng, Wenhong Wang, Weixing Front Immunol Immunology OBJECTIVE: Recently, immune checkpoint inhibitor (ICI) treatment has shown encouraging performance in improving the prognosis of hepatocellular carcinoma (HCC) patients. The gut microbiome plays a vital role in altering the efficacy of ICIs, which may be impacted by antibiotics. The aim of the meta-analysis is to estimate the influence of antibiotic use on the survival of HCC patients treated with ICIs. METHODS: The literature review was conducted using databases like PubMed, EMBASE, Cochrane Library, CNKI, WANFANG DATA, VIP, Google Scholar, and ClinicalTrials.gov before May 15, 2022. The primary endpoints were overall survival (OS), progression-free survival (PFS), objective response rate (ORR), and disease control rate (DCR). RESULTS: A total of six retrospective studies met the inclusion criteria. 1056 patients were included in the study, of which 352 (33.33%) received antibiotic treatment. The meta-analysis results revealed antibiotic use did not affect the OS (HR: 1.41, 95% CI: 0.96-2.08, P = 0.088) and PFS (HR: 1.21, 95% CI: 0.73-2.00, P = 0.459) in HCC patients treated with ICIs. Besides, the use of antibiotics did not reduce the ORR (OR: 1.06, 95% CI: 0.69-1.64, P = 0.784) and DCR (OR: 0.42, 95% CI: 0.09-2.06, P = 0.286) in HCC patients treated with ICIs. CONCLUSION: Current evidence reveals that antibiotic use does alter the therapeutic efficacy of ICIs in HCC patients. SYSTEMATIC REVIEW REGISTRATION: https://www.crd.york.ac.uk/, identifier CRD42022311948. Frontiers Media S.A. 2022-08-17 /pmc/articles/PMC9429218/ /pubmed/36059512 http://dx.doi.org/10.3389/fimmu.2022.956533 Text en Copyright © 2022 Zhang, Chen, Chai, Li, Guan, Liu, Kuang, Deng 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 Immunology
Zhang, Lilong
Chen, Chen
Chai, Dongqi
Li, Chunlei
Guan, Yongjun
Liu, Li
Kuang, Tianrui
Deng, Wenhong
Wang, Weixing
The association between antibiotic use and outcomes of HCC patients treated with immune checkpoint inhibitors
title The association between antibiotic use and outcomes of HCC patients treated with immune checkpoint inhibitors
title_full The association between antibiotic use and outcomes of HCC patients treated with immune checkpoint inhibitors
title_fullStr The association between antibiotic use and outcomes of HCC patients treated with immune checkpoint inhibitors
title_full_unstemmed The association between antibiotic use and outcomes of HCC patients treated with immune checkpoint inhibitors
title_short The association between antibiotic use and outcomes of HCC patients treated with immune checkpoint inhibitors
title_sort association between antibiotic use and outcomes of hcc patients treated with immune checkpoint inhibitors
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9429218/
https://www.ncbi.nlm.nih.gov/pubmed/36059512
http://dx.doi.org/10.3389/fimmu.2022.956533
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