Acute-phase reactants during tocilizumab therapy for severe COVID-19 pneumonia

Clin Exp Rheumatol. 2020 Nov-Dec;38(6):1215-1222. Epub 2020 Dec 3.

Abstract

Objectives: To identify predictors of clinical improvement and intubation/death in tocilizumab-treated severe COVID19, focusing on IL6 and CRP longitudinal monitoring.

Methods: 173 consecutive patients with severe COVID-19 pneumonia receiving tocilizumab in Reggio Emilia province Hospitals between 11 March and 3 June 2020 were enrolled in a prospective cohort study. Clinical improvement was defined as status improvement on a six-category ordinal scale or discharge from the hospital, whichever came first. A composite outcome of intubation/death was also evaluated. CRP and IL-6 levels were determined before TCZ administration (T0) and after 3 (T3), and 7 (T7) days.

Results: At multivariate analysis T0 and T3 CRP levels were negatively associated with clinical improvement (OR 0.13, CI 0.03-0.55 and OR 0.11, CI 0.0-0.46) (p=0.006 and p=0.003) and positively associated with intubation/death (OR 17.66, CI 2.47-126.14 and OR 5.34, CI: 1.49-19.12) (p=0.01 and p=0.004). No significant associations with IL-6 values were observed. General linear model analyses for repeated measures showed significantly different trends for CRP from day 3 to day 7 between patients who improved and those who did not, and between patients who were intubated or died and those who were not (p<0.0001 for both). ROC analysis identified a baseline CRP level of 15.8 mg/dl as the best cut-off to predict intubation/death (AUC = 0.711, sensitivity = 0.67, specificity = 0.71).

Conclusions: CRP serial measurements in the first week of TCZ therapy are useful in identifying patients developing poor outcomes.

MeSH terms

  • Acute-Phase Proteins
  • Antibodies, Monoclonal, Humanized
  • Betacoronavirus*
  • COVID-19 Drug Treatment*
  • Coronavirus Infections*
  • Humans
  • Pandemics
  • Pneumonia, Viral*
  • Prospective Studies
  • SARS-CoV-2

Substances

  • Acute-Phase Proteins
  • Antibodies, Monoclonal, Humanized
  • tocilizumab