Effectiveness and safety of intravenous tocilizumab to treat COVID-19-associated hyperinflammatory syndrome: Covizumab-6 observational cohort

Clin Immunol. 2021 Feb:223:108631. doi: 10.1016/j.clim.2020.108631. Epub 2020 Nov 12.

Abstract

Although the starting event in COVID-19 is a viral infection some patients present with an over-exuberant inflammatory response, leading to acute lung injury (ALI) and adult respiratory distress syndrome (ARDS). Since IL-6 plays a critical role in the inflammatory response, we assessed the efficacy and safety of tocilizumab (TCZ) in this single-centre, observational study in all Covid-19 in-patient with a proven SARS-CoV-2 rapidly progressing infection to prevent ALI and ARDS. 104 patients with COVID-19 treated with TCZ had a lower mortality rate (5·8%) compared with the regional mortality rate (11%), hospitalized patient's mortality (10%), and slightly lower than hospitalized patients treated with our standard of care alone (6%). We found that TCZ rapidly decreased acute phase reactants, ferritin and liver release of proteins. D-Dimer decreased slowly. We did not observe specific safety concerns. Early administration of IL6-R antagonists in COVID-19 patients with impending hyperinflammatory response, may be safe and effective treatment to prevent, ICU admission and further complications.

Keywords: COVID-19; Cytokine release syndrome; IL-6R antagonist; SARS-CoV-2; Tocilizumab; Treatment.

Publication types

  • Observational Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Lung Injury / drug therapy*
  • Acute Lung Injury / mortality
  • Aged
  • Antibodies, Monoclonal, Humanized / therapeutic use*
  • COVID-19 / mortality
  • COVID-19 Drug Treatment*
  • Cohort Studies
  • Cytokine Release Syndrome / drug therapy*
  • Cytokine Release Syndrome / mortality
  • Female
  • Ferritins / metabolism
  • Fibrin Fibrinogen Degradation Products / metabolism
  • Humans
  • Inflammation / drug therapy*
  • Inflammation / mortality
  • Male
  • Middle Aged
  • Receptors, Interleukin-6 / immunology
  • Respiratory Distress Syndrome / drug therapy*
  • Respiratory Distress Syndrome / mortality
  • SARS-CoV-2 / physiology*
  • Survival Analysis

Substances

  • Antibodies, Monoclonal, Humanized
  • Fibrin Fibrinogen Degradation Products
  • Receptors, Interleukin-6
  • fibrin fragment D
  • Ferritins
  • tocilizumab