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

Authors :
Biran N
Ip A
Ahn J
Go RC
Wang S
Mathura S
Sinclaire BA
Bednarz U
Marafelias M
Hansen E
Siegel DS
Goy AH
Pecora AL
Sawczuk IS
Koniaris LS
Simwenyi M
Varga DW
Tank LK
Stein AA
Allusson V
Lin GS
Oser WF
Tuma RA
Reichman J
Brusco L Jr
Carpenter KL
Costanzo EJ
Vivona V
Goldberg SL
Source :
The Lancet. Rheumatology [Lancet Rheumatol] 2020 Oct; Vol. 2 (10), pp. e603-e612. Date of Electronic Publication: 2020 Aug 14.
Publication Year :
2020

Abstract

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.<br />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.<br />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.<br />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.<br />Funding: None.<br /> (© 2020 Elsevier Ltd. All rights reserved.)

Details

Language :
English
ISSN :
2665-9913
Volume :
2
Issue :
10
Database :
MEDLINE
Journal :
The Lancet. Rheumatology
Publication Type :
Academic Journal
Accession number :
32838323
Full Text :
https://doi.org/10.1016/S2665-9913(20)30277-0