Tocilizumab for patients with severe COVID-19: a retrospective, multi-center study

Expert Rev Anti Infect Ther. 2021 Jan;19(1):93-100. doi: 10.1080/14787210.2020.1800453. Epub 2020 Aug 1.

Abstract

Background: Tocilizumab, an inhibitor of the interleukin-6 receptor, may decrease the inflammatory response and control the symptoms of severe coronavirus disease 2019 (COVID-19), but the evidence is scarce.

Methods: This retrospective study included patients with severe COVID-19 requiring oxygen therapy who received tocilizumab in seven centers across Poland. We assessed on-treatment changes in clinical status and inflammatory markers.

Results: Twenty-eight patients were included (19 male), with a mean age of 61.7 ± 12.4 years. The mean time from symptom onset to the first tocilizumab dose was 10.5 ± 5.7 days. Clinical status improved within 24 hours in 11 (39%) patients, within one week in 23 (82%) patients, and within two weeks in 25 (89%); one (4%) patient showed no change and two (7%) patients died. Sixteen patients (57%) no longer needed oxygen therapy within a week (p < 0.001). The serum concentrations of C-reactive protein, procalcitonin, and fibrinogen decreased significantly (p ≤ 0.001). Lung changes improved in 21 (84%) patients within two weeks of treatment; 19 had minimal or no changes upon final examination.

Conclusions: Tocilizumab can control the symptoms of severe COVID-19 by reducing the inflammatory response and rapidly improves the clinical status in most patients.

Keywords: COVID-19; SARS-CoV-2; interleukin-6; therapy; tocilizumab.

Publication types

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

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Antibodies, Monoclonal, Humanized / adverse effects
  • Antibodies, Monoclonal, Humanized / therapeutic use*
  • COVID-19 / diagnostic imaging
  • COVID-19 / immunology
  • COVID-19 Drug Treatment*
  • Female
  • Humans
  • Interleukin-6 / blood
  • Male
  • Middle Aged
  • Retrospective Studies
  • SARS-CoV-2*

Substances

  • Antibodies, Monoclonal, Humanized
  • Interleukin-6
  • tocilizumab

Grants and funding

This work was supported by Polish Association of Epidemiologists and Infectiologists; medical writing was supported by Roche Poland.