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Ruxolitinib and the Mitigation of Severe COVID-19: A Systematic Review and Meta-analysis

BACKGROUND: The cause of end-organ damage and acute respiratory distress syndrome (ARDS) in coronavirus disease 2019 (COVID-19) patients is postulated to be connected to the uncontrolled increase of pro-inflammatory cytokines. The upregulation of many cytokines is dependent on signaling through the...

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Autores principales: Quiros, Jorge R., Ross-Comptis, Jennifer, Hathaway, Donald, Sarfraz, Azza, Sarfraz, Zouina, Grigoryan, Zhanna, Romero, Kimberly Anne, Gapizov, Abubakar, Príncipe-Meneses, Fortunato S, Somagutta, Manoj Reddy, Riva-Moscoso, Adrian, Kapasi, Abdulhusein
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Infectious Diseases; Korean Society for Antimicrobial Therapy; The Korean Society for AIDS 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8511368/
https://www.ncbi.nlm.nih.gov/pubmed/34623777
http://dx.doi.org/10.3947/ic.2020.0126
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author Quiros, Jorge R.
Ross-Comptis, Jennifer
Hathaway, Donald
Sarfraz, Azza
Sarfraz, Zouina
Grigoryan, Zhanna
Romero, Kimberly Anne
Gapizov, Abubakar
Príncipe-Meneses, Fortunato S
Somagutta, Manoj Reddy
Riva-Moscoso, Adrian
Kapasi, Abdulhusein
author_facet Quiros, Jorge R.
Ross-Comptis, Jennifer
Hathaway, Donald
Sarfraz, Azza
Sarfraz, Zouina
Grigoryan, Zhanna
Romero, Kimberly Anne
Gapizov, Abubakar
Príncipe-Meneses, Fortunato S
Somagutta, Manoj Reddy
Riva-Moscoso, Adrian
Kapasi, Abdulhusein
author_sort Quiros, Jorge R.
collection PubMed
description BACKGROUND: The cause of end-organ damage and acute respiratory distress syndrome (ARDS) in coronavirus disease 2019 (COVID-19) patients is postulated to be connected to the uncontrolled increase of pro-inflammatory cytokines. The upregulation of many cytokines is dependent on signaling through the Janus kinase 1 (JAK-1) and JAK-2 pathways. Ruxolitinib, a JAK-1 and JAK-2 inhibitor, is documented to have potent anti-inflammatory activity by targeting several cytokines and growth factors with proposed efficacy in the cytokine storm observed in severe COVID-19 patients; therefore, this study examines the efficacy and tolerability of ruxolitinib for adult COVID-19 patients. MATERIALS AND METHODS: This review was conducted using preferred reporting items for aystematic reviews and meta-analyses (PRISMA) methodology. Six reviewers analyzed 1,120 results. Seven studies were selected and validated. A quantitative meta-analysis was further performed to evaluate clinical improvement at day 28, mortality at day 28, and oxygen requirements comparing treatment and standard of care groups. RESULTS: 168 individuals were involved in the studies selected: 122 in cohort studies, 4 in case reports, and 41 in randomized controlled studies. The ruxolitinib group had a higher likelihood of clinical improvement by the 28th day of treatment when assessed with the standard of care (SOC) group (odds ratio [OR]: 1.48; 95% confidence interval [CI]: 0.53 - 4.16; P = 0.45; I(2) = 0%). The SOC group was at a higher risk of experiencing serious adverse events (OR: 0.17; 95% CI: 0.03 - 1.13; P = 0.07). Notably the SOC group had a higher likelihood of death (OR: 0.51; 95% CI: 0.11-2.29; P = 0.07; I(2) = 0%). CONCLUSION: Prior studies on ruxolitinib have demonstrated it is able to decrease inflammatory markers. In recent studies on COVID-19, treatment with ruxolitinib decreased the time on mechanical ventilation, hospitalization time, and the need for vasopressor support. Additionally, ruxolitinib showed decreased mortality and demonstrated improvement in lung congestion as evidenced by computerized tomography imaging. These findings warrant further clinical investigation into Ruxolitinib as a potential treatment approach for severe COVID-19.
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spelling pubmed-85113682021-10-25 Ruxolitinib and the Mitigation of Severe COVID-19: A Systematic Review and Meta-analysis Quiros, Jorge R. Ross-Comptis, Jennifer Hathaway, Donald Sarfraz, Azza Sarfraz, Zouina Grigoryan, Zhanna Romero, Kimberly Anne Gapizov, Abubakar Príncipe-Meneses, Fortunato S Somagutta, Manoj Reddy Riva-Moscoso, Adrian Kapasi, Abdulhusein Infect Chemother Original Article BACKGROUND: The cause of end-organ damage and acute respiratory distress syndrome (ARDS) in coronavirus disease 2019 (COVID-19) patients is postulated to be connected to the uncontrolled increase of pro-inflammatory cytokines. The upregulation of many cytokines is dependent on signaling through the Janus kinase 1 (JAK-1) and JAK-2 pathways. Ruxolitinib, a JAK-1 and JAK-2 inhibitor, is documented to have potent anti-inflammatory activity by targeting several cytokines and growth factors with proposed efficacy in the cytokine storm observed in severe COVID-19 patients; therefore, this study examines the efficacy and tolerability of ruxolitinib for adult COVID-19 patients. MATERIALS AND METHODS: This review was conducted using preferred reporting items for aystematic reviews and meta-analyses (PRISMA) methodology. Six reviewers analyzed 1,120 results. Seven studies were selected and validated. A quantitative meta-analysis was further performed to evaluate clinical improvement at day 28, mortality at day 28, and oxygen requirements comparing treatment and standard of care groups. RESULTS: 168 individuals were involved in the studies selected: 122 in cohort studies, 4 in case reports, and 41 in randomized controlled studies. The ruxolitinib group had a higher likelihood of clinical improvement by the 28th day of treatment when assessed with the standard of care (SOC) group (odds ratio [OR]: 1.48; 95% confidence interval [CI]: 0.53 - 4.16; P = 0.45; I(2) = 0%). The SOC group was at a higher risk of experiencing serious adverse events (OR: 0.17; 95% CI: 0.03 - 1.13; P = 0.07). Notably the SOC group had a higher likelihood of death (OR: 0.51; 95% CI: 0.11-2.29; P = 0.07; I(2) = 0%). CONCLUSION: Prior studies on ruxolitinib have demonstrated it is able to decrease inflammatory markers. In recent studies on COVID-19, treatment with ruxolitinib decreased the time on mechanical ventilation, hospitalization time, and the need for vasopressor support. Additionally, ruxolitinib showed decreased mortality and demonstrated improvement in lung congestion as evidenced by computerized tomography imaging. These findings warrant further clinical investigation into Ruxolitinib as a potential treatment approach for severe COVID-19. The Korean Society of Infectious Diseases; Korean Society for Antimicrobial Therapy; The Korean Society for AIDS 2021-09 2021-09-25 /pmc/articles/PMC8511368/ /pubmed/34623777 http://dx.doi.org/10.3947/ic.2020.0126 Text en Copyright © 2021 by The Korean Society of Infectious Diseases, Korean Society for Antimicrobial Therapy, and The Korean Society for AIDS https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Quiros, Jorge R.
Ross-Comptis, Jennifer
Hathaway, Donald
Sarfraz, Azza
Sarfraz, Zouina
Grigoryan, Zhanna
Romero, Kimberly Anne
Gapizov, Abubakar
Príncipe-Meneses, Fortunato S
Somagutta, Manoj Reddy
Riva-Moscoso, Adrian
Kapasi, Abdulhusein
Ruxolitinib and the Mitigation of Severe COVID-19: A Systematic Review and Meta-analysis
title Ruxolitinib and the Mitigation of Severe COVID-19: A Systematic Review and Meta-analysis
title_full Ruxolitinib and the Mitigation of Severe COVID-19: A Systematic Review and Meta-analysis
title_fullStr Ruxolitinib and the Mitigation of Severe COVID-19: A Systematic Review and Meta-analysis
title_full_unstemmed Ruxolitinib and the Mitigation of Severe COVID-19: A Systematic Review and Meta-analysis
title_short Ruxolitinib and the Mitigation of Severe COVID-19: A Systematic Review and Meta-analysis
title_sort ruxolitinib and the mitigation of severe covid-19: a systematic review and meta-analysis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8511368/
https://www.ncbi.nlm.nih.gov/pubmed/34623777
http://dx.doi.org/10.3947/ic.2020.0126
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