Frontiers in Immunology (Apr 2023)

Randomized phase II clinical trial of ruxolitinib plus simvastatin in COVID19 clinical outcome and cytokine evolution

  • Jesus Garcia-Donas,
  • Diego Martínez-Urbistondo,
  • Kyra Velázquez Kennedy,
  • Paula Villares,
  • Arántzazu Barquin,
  • Andrea Dominguez,
  • Juan Francisco Rodriguez-Moreno,
  • Elena Caro,
  • Rafael Suarez del Villar,
  • Estanislao Nistal-Villan,
  • Estanislao Nistal-Villan,
  • Monica Yagüe,
  • Maria Ortiz,
  • Maria Barba,
  • Sergio Ruiz-Llorente,
  • Miguel Quiralte,
  • Massimiliano Zanin,
  • Cristina Rodríguez,
  • Paloma Navarro,
  • Pedro Berraondo,
  • Pedro Berraondo,
  • Pedro Berraondo,
  • Rodrigo Madurga

DOI
https://doi.org/10.3389/fimmu.2023.1156603
Journal volume & issue
Vol. 14

Abstract

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BackgroundManaging the inflammatory response to SARS-Cov-2 could prevent respiratory insufficiency. Cytokine profiles could identify cases at risk of severe disease.MethodsWe designed a randomized phase II clinical trial to determine whether the combination of ruxolitinib (5 mg twice a day for 7 days followed by 10 mg BID for 7 days) plus simvastatin (40 mg once a day for 14 days), could reduce the incidence of respiratory insufficiency in COVID-19. 48 cytokines were correlated with clinical outcome.ParticipantsPatients admitted due to COVID-19 infection with mild disease.ResultsUp to 92 were included. Mean age was 64 ± 17, and 28 (30%) were female. 11 (22%) patients in the control arm and 6 (12%) in the experimental arm reached an OSCI grade of 5 or higher (p = 0.29). Unsupervised analysis of cytokines detected two clusters (CL-1 and CL-2). CL-1 presented a higher risk of clinical deterioration vs CL-2 (13 [33%] vs 2 [6%] cases, p = 0.009) and death (5 [11%] vs 0 cases, p = 0.059). Supervised Machine Learning (ML) analysis led to a model that predicted patient deterioration 48h before occurrence with a 85% accuracy.ConclusionsRuxolitinib plus simvastatin did not impact the outcome of COVID-19. Cytokine profiling identified patients at risk of severe COVID-19 and predicted clinical deterioration.Trial registrationhttps://clinicaltrials.gov/, identifier NCT04348695.

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