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Early clinical outcomes with tocilizumab for severe COVID-19: a two-centre retrospective study

Severe COVID-19 (coronavirus disease 2019) is associated with elevated inflammatory markers, consistent with cytokine release syndrome (CRS). Tocilizumab is an interleukin-6 (IL-6) inhibitor effective in treating CRS secondary to chimeric antigen receptor T-cell (CAR T-cell) therapy. The efficacy of...

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Autores principales: Smoke, Steven M., Raja, Karan, Hilden, Patrick, Daniel, Nicole M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Ltd and International Society of Antimicrobial Chemotherapy. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7834231/
https://www.ncbi.nlm.nih.gov/pubmed/33338559
http://dx.doi.org/10.1016/j.ijantimicag.2020.106265
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author Smoke, Steven M.
Raja, Karan
Hilden, Patrick
Daniel, Nicole M.
author_facet Smoke, Steven M.
Raja, Karan
Hilden, Patrick
Daniel, Nicole M.
author_sort Smoke, Steven M.
collection PubMed
description Severe COVID-19 (coronavirus disease 2019) is associated with elevated inflammatory markers, consistent with cytokine release syndrome (CRS). Tocilizumab is an interleukin-6 (IL-6) inhibitor effective in treating CRS secondary to chimeric antigen receptor T-cell (CAR T-cell) therapy. The efficacy of tocilizumab in treating COVID-19 is unknown. This was a retrospective cohort study conducted at two hospitals in northern New Jersey (USA). All patients treated with tocilizumab for confirmed or suspected COVID-19 between 10 March 2020 and 9 April 2020 at the study sites were included. The primary endpoint was clinical improvement on Day 7 after treatment as assessed by respiratory status. Univariate analysis compared data between those who improved and those who did not. A total of 45 severe and critically ill patients treated with tocilizumab for COVID-19 were evaluated. Of the 45 patients, 11 (24.4%), 22 (48.9%) and 12 (26.7%) patients improved, had no change or worsened by Day 7 after treatment, respectively. Lower white blood cell count and lactate dehydrogenase at the time of drug administration as well as shorter time from supplemental oxygen initiation to dosing were significantly associated with clinical improvement in the univariate analysis. In conclusion, tocilizumab administration was associated with a low rate of clinical improvement within 7 days in this cohort of severe and critically ill patients with COVID-19.
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spelling pubmed-78342312021-01-26 Early clinical outcomes with tocilizumab for severe COVID-19: a two-centre retrospective study Smoke, Steven M. Raja, Karan Hilden, Patrick Daniel, Nicole M. Int J Antimicrob Agents Article Severe COVID-19 (coronavirus disease 2019) is associated with elevated inflammatory markers, consistent with cytokine release syndrome (CRS). Tocilizumab is an interleukin-6 (IL-6) inhibitor effective in treating CRS secondary to chimeric antigen receptor T-cell (CAR T-cell) therapy. The efficacy of tocilizumab in treating COVID-19 is unknown. This was a retrospective cohort study conducted at two hospitals in northern New Jersey (USA). All patients treated with tocilizumab for confirmed or suspected COVID-19 between 10 March 2020 and 9 April 2020 at the study sites were included. The primary endpoint was clinical improvement on Day 7 after treatment as assessed by respiratory status. Univariate analysis compared data between those who improved and those who did not. A total of 45 severe and critically ill patients treated with tocilizumab for COVID-19 were evaluated. Of the 45 patients, 11 (24.4%), 22 (48.9%) and 12 (26.7%) patients improved, had no change or worsened by Day 7 after treatment, respectively. Lower white blood cell count and lactate dehydrogenase at the time of drug administration as well as shorter time from supplemental oxygen initiation to dosing were significantly associated with clinical improvement in the univariate analysis. In conclusion, tocilizumab administration was associated with a low rate of clinical improvement within 7 days in this cohort of severe and critically ill patients with COVID-19. Elsevier Ltd and International Society of Antimicrobial Chemotherapy. 2021-02 2020-12-15 /pmc/articles/PMC7834231/ /pubmed/33338559 http://dx.doi.org/10.1016/j.ijantimicag.2020.106265 Text en © 2020 Elsevier Ltd and International Society of Antimicrobial Chemotherapy. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Smoke, Steven M.
Raja, Karan
Hilden, Patrick
Daniel, Nicole M.
Early clinical outcomes with tocilizumab for severe COVID-19: a two-centre retrospective study
title Early clinical outcomes with tocilizumab for severe COVID-19: a two-centre retrospective study
title_full Early clinical outcomes with tocilizumab for severe COVID-19: a two-centre retrospective study
title_fullStr Early clinical outcomes with tocilizumab for severe COVID-19: a two-centre retrospective study
title_full_unstemmed Early clinical outcomes with tocilizumab for severe COVID-19: a two-centre retrospective study
title_short Early clinical outcomes with tocilizumab for severe COVID-19: a two-centre retrospective study
title_sort early clinical outcomes with tocilizumab for severe covid-19: a two-centre retrospective study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7834231/
https://www.ncbi.nlm.nih.gov/pubmed/33338559
http://dx.doi.org/10.1016/j.ijantimicag.2020.106265
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