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Tocilizumab among patients with COVID-19 in the intensive care unit: a multicentre observational study

Authors :
Eric Hansen
Roman A Tuma
David S. Siegel
Aaron A Stein
Noa Biran
Valerie R.C. Allusson
Eric J Costanzo
Michael Marafelias
Lauren S Koniaris
Ronaldo C. Go
Vincent Vivona
George S Lin
Lisa Tank
Micky Simwenyi
Jaeil Ahn
Andre Goy
Andrew L. Pecora
Ihor S. Sawczuk
Joseph Reichman
William F Oser
Kim L Carpenter
Shivam Mathura
Louis Brusco
Urszula Bednarz
Stuart L. Goldberg
Brittany A Sinclaire
Shuqi Wang
Andrew Ip
Daniel W Varga
Source :
The Lancet Rheumatology
Publication Year :
2020
Publisher :
Elsevier BV, 2020.

Abstract

Summary Background Tocilizumab, a monoclonal antibody directed against the interleukin-6 receptor, has been proposed to mitigate the cytokine storm syndrome associated with severe COVID-19. We aimed to investigate the association between tocilizumab exposure and hospital-related mortality among patients requiring intensive care unit (ICU) support for COVID-19. Methods We did a retrospective observational cohort study at 13 hospitals within the Hackensack Meridian Health network (NJ, USA). We included patients (aged ≥18 years) with laboratory-confirmed COVID-19 who needed support in the ICU. We obtained data from a prospective observational database and compared outcomes in patients who received tocilizumab with those who did not. We applied a multivariable Cox model with propensity score matching to reduce confounding effects. The primary endpoint was hospital-related mortality. The prospective observational database is registered on ClinicalTrials.gov , NCT04347993 . Findings Between March 1 and April 22, 2020, 764 patients with COVID-19 required support in the ICU, of whom 210 (27%) received tocilizumab. Factors associated with receiving tocilizumab were patients' age, gender, renal function, and treatment location. 630 patients were included in the propensity score-matched population, of whom 210 received tocilizumab and 420 did not receive tocilizumab. 358 (57%) of 630 patients died, 102 (49%) who received tocilizumab and 256 (61%) who did not receive tocilizumab. Overall median survival from time of admission was not reached (95% CI 23 days–not reached) among patients receiving tocilizumab and was 19 days (16–26) for those who did not receive tocilizumab (hazard ratio [HR] 0·71, 95% CI 0·56–0·89; p=0·0027). In the primary multivariable Cox regression analysis with propensity matching, an association was noted between receiving tocilizumab and decreased hospital-related mortality (HR 0·64, 95% CI 0·47–0·87; p=0·0040). Similar associations with tocilizumab were noted among subgroups requiring mechanical ventilatory support and with baseline C-reactive protein of 15 mg/dL or higher. Interpretation In this observational study, patients with COVID-19 requiring ICU support who received tocilizumab had reduced mortality. Results of ongoing randomised controlled trials are awaited. Funding None.

Details

Language :
English
ISSN :
26659913
Database :
OpenAIRE
Journal :
The Lancet Rheumatology
Accession number :
edsair.doi.dedup.....6b45a8ce6c8f0574e260475f6ffd3fdd
Full Text :
https://doi.org/10.1016/s2665-9913(20)30277-0