Clinical characteristics and predictors of survival in adults with coronavirus disease 2019 receiving tocilizumab

J Autoimmun. 2020 Nov:114:102512. doi: 10.1016/j.jaut.2020.102512. Epub 2020 Jul 3.

Abstract

Coronavirus disease 2019 (COVID-19) can progress to cytokine storm that is associated with organ dysfunction and death. The purpose of the present study is to determine clinical characteristics associated with 28 day in-hospital survival in patients with coronavirus disease 2019 (COVID-19) that received tocilizumab. This was a retrospective observational cohort study conducted at a five hospital health system in Michigan, United States. Adult patients with confirmed COVID-19 that were admitted to the hospital and received tocilizumab for cytokine storm from March 1, 2020 through April 3, 2020 were included. Patients were grouped into survivors and non-survivors based on 28 day in-hospital mortality. Study day 0 was defined as the day tocilizumab was administered. Factors independently associated with in-hospital survival at 28 days after tocilizumab administration were assessed. Epidemiologic, demographic, laboratory, prognostic scores, treatment, and outcome data were collected and analyzed. Clinical response was collected and defined as a decline of two levels on a six-point ordinal scale of clinical status or discharged alive from the hospital. Of the 81 patients included, the median age was 64 (58-71) years and 56 (69.1%) were male. The 28 day in-hospital mortality was 43.2%. There were 46 (56.8%) patients in the survivors and 35 (43.2%) in the non-survivors group. On study day 0 no differences were noted in demographics, clinical characteristics, severity of illness scores, or treatments received between survivors and non-survivors. C-reactive protein was significantly higher in the non-survivors compared to survivors. Compared to non-survivors, recipients of tocilizumab within 12 days of symptom onset was independently associated with survival (adjusted OR: 0.296, 95% CI: 0.098-0.889). SOFA score ≥8 on day 0 was independently associated with mortality (adjusted OR: 2.842, 95% CI: 1.042-7.753). Clinical response occurred more commonly in survivors than non-survivors (80.4% vs. 5.7%; p < 0.001). Improvements in the six-point ordinal scale and SOFA score were observed in survivors after tocilizumab. Early receipt of tocilizumab in patients with severe COVID-19 was an independent predictor for in-hospital survival at 28 days.

Keywords: COVID-19; Critical illness; Cytokine release syndrome; Interleukin-6; Severe acute respiratory syndrome coronavirus 2; Tocilizumab.

Publication types

  • Multicenter Study
  • Observational Study

MeSH terms

  • Adult
  • Aged
  • Antibodies, Monoclonal, Humanized / administration & dosage*
  • Betacoronavirus / immunology
  • C-Reactive Protein / analysis*
  • COVID-19
  • COVID-19 Drug Treatment
  • Coronavirus Infections / blood
  • Coronavirus Infections / drug therapy*
  • Coronavirus Infections / immunology
  • Coronavirus Infections / mortality
  • Cytokine Release Syndrome / blood
  • Cytokine Release Syndrome / drug therapy*
  • Cytokine Release Syndrome / immunology
  • Cytokine Release Syndrome / mortality
  • Female
  • Hospital Mortality
  • Humans
  • Infusions, Intravenous
  • Interleukin-6 / immunology
  • Interleukin-6 / metabolism
  • Male
  • Michigan / epidemiology
  • Middle Aged
  • Organ Dysfunction Scores
  • Pandemics
  • Pneumonia, Viral / blood
  • Pneumonia, Viral / drug therapy*
  • Pneumonia, Viral / immunology
  • Pneumonia, Viral / mortality
  • Prognosis
  • Receptors, Interleukin-6 / antagonists & inhibitors
  • Receptors, Interleukin-6 / metabolism
  • Retrospective Studies
  • SARS-CoV-2
  • Survival Analysis
  • Time Factors
  • Time-to-Treatment
  • Treatment Outcome

Substances

  • Antibodies, Monoclonal, Humanized
  • IL6 protein, human
  • IL6R protein, human
  • Interleukin-6
  • Receptors, Interleukin-6
  • C-Reactive Protein
  • tocilizumab