Short-term celecoxib (celebrex) adjuvant therapy: a clinical trial study on COVID-19 patients

Inflammopharmacology. 2022 Oct;30(5):1645-1657. doi: 10.1007/s10787-022-01029-4. Epub 2022 Jul 14.

Abstract

Background: It is known that severe acute respiratory coronavirus 2 (SARS-CoV-2) is the viral strain responsible for the recent coronavirus disease 2019 (COVID-19) pandemic. Current documents have demonstrated that the virus causes a PGE2 storm in a substantial proportion of patients via upregulating cyclooxygenase-2 (COX-2) and downregulating prostaglandin E2 (PGE2)-degrading enzymes within the host cell.

Aim: Herein, we aimed to study how short-term treatment with celecoxib (Celebrex), a selective COX-2 inhibitor, affects demographic features, early symptoms, O2 saturation, and hematological indices of cases with COVID-19.

Methods: A total of 67 confirmed COVID-19 cases with a mild or moderate disease, who had been referred to an institutional hospital in south-eastern Iran from October 2020 to September 2021, were enrolled. Demographic characteristics, symptoms, and hematological indices of the patients were recorded within different time periods. One-way ANOVA or Kruskal-Wallis tests were used to determine differences between data sets based on normal data distribution.

Results: O2 saturation was statistically different between the control group and patients receiving celecoxib (p = 0.039). There was no marked difference between the groups in terms of the symptoms they experienced (p > 0.05). On the first days following Celebrex therapy, analysis of complete blood counts showed that white blood cell (WBC) counts were markedly lower in patients treated with a high dose of celecoxib (0.4 g/day) than in controls (p = 0.026). However, mean lymphocyte levels in patients receiving a high dose of celecoxib (0.4 g/day) were markedly higher than in patients receiving celecoxib with half of the dose (0.2 g/day) for one week or the untreated subjects (p = 0.004). Changes in platelet count also followed the WBC alteration pattern.

Conclusion: Celecoxib is a relatively safe, inexpensive, and widely available drug with non-steroidal anti-inflammatory properties. The therapeutic efficacy of celecoxib depends on the administrated dose. Celecoxib might improve disease-free survival in patients with COVID-19.

Keywords: Adjuvant therapy; COVID-19; Celecoxib (Celebrex); Cyclooxygenase-2 (COX-2); NSAID.

MeSH terms

  • Anti-Inflammatory Agents, Non-Steroidal / adverse effects
  • COVID-19 Drug Treatment*
  • Celecoxib / therapeutic use
  • Cyclooxygenase 2
  • Cyclooxygenase 2 Inhibitors* / pharmacology
  • Cyclooxygenase 2 Inhibitors* / therapeutic use
  • Dinoprostone
  • Humans
  • Pyrazoles / adverse effects
  • SARS-CoV-2
  • Sulfonamides / pharmacology
  • Sulfonamides / therapeutic use

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Cyclooxygenase 2 Inhibitors
  • Pyrazoles
  • Sulfonamides
  • Cyclooxygenase 2
  • Celecoxib
  • Dinoprostone