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Drug-induced liver injury following the use of tocilizumab or sarilumab in patients with coronavirus disease 2019

BACKGROUNDS: Interleukin-6 (IL-6) blockers including tocilizumab and sarilumab were approved by the U.S. Food and Drug Administration (FDA) in June 2021 for the treatment of patients with moderate to severe COVID-19. The use of sarilumab or tocilizumab in COVID-19 patients has been related to a redu...

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Autores principales: Gao, Qian, Yin, Xuedong, Tan, Boyu, Wang, Junshi, Chen, Jiayan, Zhao, Bin, Yang, Qiaoling, Li, Zhiling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9742033/
https://www.ncbi.nlm.nih.gov/pubmed/36503381
http://dx.doi.org/10.1186/s12879-022-07896-0
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author Gao, Qian
Yin, Xuedong
Tan, Boyu
Wang, Junshi
Chen, Jiayan
Zhao, Bin
Yang, Qiaoling
Li, Zhiling
author_facet Gao, Qian
Yin, Xuedong
Tan, Boyu
Wang, Junshi
Chen, Jiayan
Zhao, Bin
Yang, Qiaoling
Li, Zhiling
author_sort Gao, Qian
collection PubMed
description BACKGROUNDS: Interleukin-6 (IL-6) blockers including tocilizumab and sarilumab were approved by the U.S. Food and Drug Administration (FDA) in June 2021 for the treatment of patients with moderate to severe COVID-19. The use of sarilumab or tocilizumab in COVID-19 patients has been related to a reduction in mortality compared to standard care. Recent evidence has emerged concerning drug-induced liver injury (DILI) after sarilumab or tocilizumab applications in COVID-19 patients. AIMS: The study aimed to estimate DILI associated with sarilumab or tocilizumab in treating moderate to severe patients infected with SARS-Cov-2. METHODS: We conducted a retrospective pharmacovigilance study by data mining of the FDA’s adverse event reporting systems (FAERS) database from the first quarter of 2004 to the fourth quarter of 2021 in confirmed COVID-19 patients. We analyzed DILI cases associated with tocilizumab or sarilumab in treating COVID-19 patients from the FAERS during this period. Disproportionality analysis and Bayesian analysis of COVID-19 patients were utilized for case analysis, and we also next compared the onset time and fatality rates of DILI following tocilizumab or sarilumab. RESULTS: A total of 275 cases of TCZ or SAR-related DILI reports were extracted. A total of 192 AEs cases were related to tocilizumab (TCZ), and 83 were related to sarilumab (SAR). In patients treated with TCZ, most were < 75 years old (51.57%), with more male than female (46.35% vs. 13.02%). The correlation between IL-6 receptor antagonists and DILI was stronger in SAR (ROR = 12.94; 95%CI 9.6–17.44) than in TCZ (ROR = 1.33; 95%CI 1.14–1.55). The onset time of DILI was different between TCZ and SAR, and a significant difference was observed in TCZ than SAR (P < 0.0001). A significant difference was observed in the mortality rate of TCZ and SAR (P = 0.0009). DILI associated with COVID-19 patients treated with TCZ appeared to have earlier onset-time (1(0–46) day) VS. SAR (3.5(0–27) day). CONCLUSION: This study shows strict monitor ought to be paid for TCZ or SAR when used for COVID-19 patients with poor liver function. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12879-022-07896-0.
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spelling pubmed-97420332022-12-12 Drug-induced liver injury following the use of tocilizumab or sarilumab in patients with coronavirus disease 2019 Gao, Qian Yin, Xuedong Tan, Boyu Wang, Junshi Chen, Jiayan Zhao, Bin Yang, Qiaoling Li, Zhiling BMC Infect Dis Research BACKGROUNDS: Interleukin-6 (IL-6) blockers including tocilizumab and sarilumab were approved by the U.S. Food and Drug Administration (FDA) in June 2021 for the treatment of patients with moderate to severe COVID-19. The use of sarilumab or tocilizumab in COVID-19 patients has been related to a reduction in mortality compared to standard care. Recent evidence has emerged concerning drug-induced liver injury (DILI) after sarilumab or tocilizumab applications in COVID-19 patients. AIMS: The study aimed to estimate DILI associated with sarilumab or tocilizumab in treating moderate to severe patients infected with SARS-Cov-2. METHODS: We conducted a retrospective pharmacovigilance study by data mining of the FDA’s adverse event reporting systems (FAERS) database from the first quarter of 2004 to the fourth quarter of 2021 in confirmed COVID-19 patients. We analyzed DILI cases associated with tocilizumab or sarilumab in treating COVID-19 patients from the FAERS during this period. Disproportionality analysis and Bayesian analysis of COVID-19 patients were utilized for case analysis, and we also next compared the onset time and fatality rates of DILI following tocilizumab or sarilumab. RESULTS: A total of 275 cases of TCZ or SAR-related DILI reports were extracted. A total of 192 AEs cases were related to tocilizumab (TCZ), and 83 were related to sarilumab (SAR). In patients treated with TCZ, most were < 75 years old (51.57%), with more male than female (46.35% vs. 13.02%). The correlation between IL-6 receptor antagonists and DILI was stronger in SAR (ROR = 12.94; 95%CI 9.6–17.44) than in TCZ (ROR = 1.33; 95%CI 1.14–1.55). The onset time of DILI was different between TCZ and SAR, and a significant difference was observed in TCZ than SAR (P < 0.0001). A significant difference was observed in the mortality rate of TCZ and SAR (P = 0.0009). DILI associated with COVID-19 patients treated with TCZ appeared to have earlier onset-time (1(0–46) day) VS. SAR (3.5(0–27) day). CONCLUSION: This study shows strict monitor ought to be paid for TCZ or SAR when used for COVID-19 patients with poor liver function. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12879-022-07896-0. BioMed Central 2022-12-12 /pmc/articles/PMC9742033/ /pubmed/36503381 http://dx.doi.org/10.1186/s12879-022-07896-0 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
Gao, Qian
Yin, Xuedong
Tan, Boyu
Wang, Junshi
Chen, Jiayan
Zhao, Bin
Yang, Qiaoling
Li, Zhiling
Drug-induced liver injury following the use of tocilizumab or sarilumab in patients with coronavirus disease 2019
title Drug-induced liver injury following the use of tocilizumab or sarilumab in patients with coronavirus disease 2019
title_full Drug-induced liver injury following the use of tocilizumab or sarilumab in patients with coronavirus disease 2019
title_fullStr Drug-induced liver injury following the use of tocilizumab or sarilumab in patients with coronavirus disease 2019
title_full_unstemmed Drug-induced liver injury following the use of tocilizumab or sarilumab in patients with coronavirus disease 2019
title_short Drug-induced liver injury following the use of tocilizumab or sarilumab in patients with coronavirus disease 2019
title_sort drug-induced liver injury following the use of tocilizumab or sarilumab in patients with coronavirus disease 2019
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9742033/
https://www.ncbi.nlm.nih.gov/pubmed/36503381
http://dx.doi.org/10.1186/s12879-022-07896-0
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