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Efficacy of Tocilizumab in Patients Hospitalized with Covid-19

Authors :
Sebastian Unizony
Zsofia D. Drobni
Cory A. Perugino
Deborah S. Collier
Janeth Yinh
Chana A. Sacks
Brian C. Healy
John H. Stone
Ana D. Fernandes
Michael Dougan
Allison K. Scherer
Kathryn Bowman
Harry M Schrager
Crystal M. North
Michael K. Mansour
Nina Lin
Eric A. Meyerowitz
Sarah Nikiforow
Amna Zafar
Rachel Wallwork
Mark Matza
Yuan Di C. Halvorsen
Jorge Fleisher
Jonathan Dau
Michael D. Pincus
Arthur Y. Kim
Matthew J. Frigault
Brittany Weber
David S. Huckins
Ana Maria Bensaci
Liam Harvey
Ruta Shah
Megan Lockwood
Tara K. Thurber
Pritha Sen
Manish Sagar
Andrea S. Foulkes
Tomas G. Neilan
Zeina Dagher
Nora Horick
Ann E. Woolley
Minna J. Kohler
Naomi Serling-Boyd
Sara R. Schoenfeld
Matthew Axelrod
Caroline Cubbison
Marcy B. Bolster
Kristin M. D’Silva
Source :
New England Journal of Medicine
Publication Year :
2020
Publisher :
Massachusetts Medical Society, 2020.

Abstract

BACKGROUND: The efficacy of interleukin-6 receptor blockade in hospitalized patients with coronavirus disease 2019 (Covid-19) who are not receiving mechanical ventilation is unclear. METHODS: We performed a randomized, double-blind, placebo-controlled trial involving patients with confirmed severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection, hyperinflammatory states, and at least two of the following signs: fever (body temperature >38°C), pulmonary infiltrates, or the need for supplemental oxygen in order to maintain an oxygen saturation greater than 92%. Patients were randomly assigned in a 2:1 ratio to receive standard care plus a single dose of either tocilizumab (8 mg per kilogram of body weight) or placebo. The primary outcome was intubation or death, assessed in a time-to-event analysis. The secondary efficacy outcomes were clinical worsening and discontinuation of supplemental oxygen among patients who had been receiving it at baseline, both assessed in time-to-event analyses. RESULTS: We enrolled 243 patients; 141 (58%) were men, and 102 (42%) were women. The median age was 59.8 years (range, 21.7 to 85.4), and 45% of the patients were Hispanic or Latino. The hazard ratio for intubation or death in the tocilizumab group as compared with the placebo group was 0.83 (95% confidence interval [CI], 0.38 to 1.81; P = 0.64), and the hazard ratio for disease worsening was 1.11 (95% CI, 0.59 to 2.10; P = 0.73). At 14 days, 18.0% of the patients in the tocilizumab group and 14.9% of the patients in the placebo group had had worsening of disease. The median time to discontinuation of supplemental oxygen was 5.0 days (95% CI, 3.8 to 7.6) in the tocilizumab group and 4.9 days (95% CI, 3.8 to 7.8) in the placebo group (P = 0.69). At 14 days, 24.6% of the patients in the tocilizumab group and 21.2% of the patients in the placebo group were still receiving supplemental oxygen. Patients who received tocilizumab had fewer serious infections than patients who received placebo. CONCLUSIONS: Tocilizumab was not effective for preventing intubation or death in moderately ill hospitalized patients with Covid-19. Some benefit or harm cannot be ruled out, however, because the confidence intervals for efficacy comparisons were wide. (Funded by Genentech; ClinicalTrials.gov number, NCT04356937.).

Details

ISSN :
15334406 and 00284793
Volume :
383
Database :
OpenAIRE
Journal :
New England Journal of Medicine
Accession number :
edsair.doi.dedup.....a795b175647af45180304c4251ff459f
Full Text :
https://doi.org/10.1056/nejmoa2028836