TY - JOUR
T1 - Interleukin-6 receptor antagonists in critically ill patients with covid-19
AU - The REMAP-CAP Investigators
AU - Gordon, Anthony C.
AU - Mouncey, Paul R.
AU - Al-Beidh, Farah
AU - Rowan, Kathryn M.
AU - Nichol, Alistair D.
AU - Arabi, Yaseen M.
AU - Annane, Djillali
AU - Beane, Abi
AU - van Bentum-Puijk, Wilma
AU - Berry, Lindsay R.
AU - Bhimani, Zahra
AU - Bonten, Marc J.M.
AU - Bradbury, Charlotte A.
AU - Brunkhorst, Frank M.
AU - Buzgau, Adrian
AU - Cheng, Allen C.
AU - Detry, Michelle A.
AU - Duffy, Eamon J.
AU - Estcourt, Lise J.
AU - Fitzgerald, Mark
AU - Goossens, Herman
AU - Haniffa, Rashan
AU - Higgins, Alisa M.
AU - Hills, Thomas E.
AU - Horvat, Christopher M.
AU - Lamontagne, Francois
AU - Lawler, Patrick R.
AU - Leavis, Helen L.
AU - Linstrum, Kelsey M.
AU - Litton, Edward
AU - Lorenzi, Elizabeth
AU - Marshall, John C.
AU - Mayr, Florian B.
AU - McAuley, Daniel F.
AU - McGlothlin, Anna
AU - McGuinness, Shay P.
AU - McVerry, Bryan J.
AU - Montgomery, Stephanie K.
AU - Morpeth, Susan C.
AU - Murthy, Srinivas
AU - Orr, Katrina
AU - Parke, Rachael L.
AU - Parker, Jane C.
AU - Patanwala, Asad E.
AU - Pettilä, Ville
AU - Rademaker, Emma
AU - Santos, Marlene S.
AU - Saunders, Christina T.
AU - Seymour, Christopher W.
AU - Shankar-Hari, Manu
AU - Sligl, Wendy I.
AU - Turgeon, Alexis F.
AU - Turner, Anne M.
AU - van de Veerdonk, Frank L.
AU - Zarychanski, Ryan
AU - Green, Cameron
AU - Lewis, Roger J.
AU - Angus, Derek C.
AU - McArthur, Colin J.
AU - Berry, Scott
AU - Webb, Steve A.
AU - Derde, Lennie P.G.
N1 - Funding Information:
Supported by the European Union — through FP7-HEALTH-2013-INNOVATION: the Platform for European Preparedness Against (Re-)emerging Epidemics (PREPARE) consortium (602525); and the Horizon 2020 research and innovation program: the Rapid European Covid-19 Emergency Research response (RECOVER) consortium (101003589) — and by the Australian National Health and Medical Research Council (APP1101719), the Health Research Council of New Zealand (16/631), a Canadian Institutes of Health Research Strategy for Patient-Oriented Research Innovative Clinical Trials Program Grant (158584), the U.K. NIHR and the NIHR Imperial Biomedical Research Centre, the Health Research Board of Ireland (CTN 2014-012), the UPMC Learning While Doing Program, the Breast Cancer Research Foundation, the French Ministry of Health (PHRC-20-0147), the Minderoo Foundation, Amgen, Eisai, the Global Coalition for Adaptive Research, and the Wellcome Trust Innovations Project (215522). Dr. Gordon is funded by an NIHR Research Professorship (RP-2015-06-18), and Dr. Shankar-Hari by an NIHR Clinician Scientist Fellowship (CS-2016-16-011).
Publisher Copyright:
© 2021 Massachusetts Medical Society.
PY - 2021/4/22
Y1 - 2021/4/22
N2 - BACKGROUND: The efficacy of interleukin-6 receptor antagonists in critically ill patients with coronavirus disease 2019 (Covid-19) is unclear. METHODS We evaluated tocilizumab and sarilumab in an ongoing international, multifactorial, adaptive platform trial. Adult patients with Covid-19, within 24 hours after starting organ support in the intensive care unit (ICU), were randomly assigned to receive tocilizumab (8 mg per kilogram of body weight), sarilumab (400 mg), or standard care (control). The primary outcome was respiratory and cardiovascular organ support-free days, on an ordinal scale combining in-hospital death (assigned a value of −1) and days free of organ support to day 21. The trial uses a Bayesian statistical model with predefined criteria for superiority, efficacy, equivalence, or futility. An odds ratio greater than 1 represented improved survival, more organ support-free days, or both. RESULTS Both tocilizumab and sarilumab met the predefined criteria for efficacy. At that time, 353 patients had been assigned to tocilizumab, 48 to sarilumab, and 402 to control. The median number of organ support-free days was 10 (interquartile range, −1 to 16) in the tocilizumab group, 11 (interquartile range, 0 to 16) in the sarilumab group, and 0 (interquartile range, −1 to 15) in the control group. The median adjusted cumulative odds ratios were 1.64 (95% credible interval, 1.25 to 2.14) for tocilizumab and 1.76 (95% credible interval, 1.17 to 2.91) for sarilumab as compared with control, yielding posterior probabilities of superiority to control of more than 99.9% and of 99.5%, respectively. An analysis of 90-day survival showed improved survival in the pooled interleukin-6 receptor antagonist groups, yielding a hazard ratio for the comparison with the control group of 1.61 (95% credible interval, 1.25 to 2.08) and a posterior probability of superiority of more than 99.9%. All secondary analyses supported efficacy of these interleukin-6 receptor antagonists. CONCLUSIONS In critically ill patients with Covid-19 receiving organ support in ICUs, treatment with the interleukin-6 receptor antagonists tocilizumab and sarilumab improved outcomes, including survival.
AB - BACKGROUND: The efficacy of interleukin-6 receptor antagonists in critically ill patients with coronavirus disease 2019 (Covid-19) is unclear. METHODS We evaluated tocilizumab and sarilumab in an ongoing international, multifactorial, adaptive platform trial. Adult patients with Covid-19, within 24 hours after starting organ support in the intensive care unit (ICU), were randomly assigned to receive tocilizumab (8 mg per kilogram of body weight), sarilumab (400 mg), or standard care (control). The primary outcome was respiratory and cardiovascular organ support-free days, on an ordinal scale combining in-hospital death (assigned a value of −1) and days free of organ support to day 21. The trial uses a Bayesian statistical model with predefined criteria for superiority, efficacy, equivalence, or futility. An odds ratio greater than 1 represented improved survival, more organ support-free days, or both. RESULTS Both tocilizumab and sarilumab met the predefined criteria for efficacy. At that time, 353 patients had been assigned to tocilizumab, 48 to sarilumab, and 402 to control. The median number of organ support-free days was 10 (interquartile range, −1 to 16) in the tocilizumab group, 11 (interquartile range, 0 to 16) in the sarilumab group, and 0 (interquartile range, −1 to 15) in the control group. The median adjusted cumulative odds ratios were 1.64 (95% credible interval, 1.25 to 2.14) for tocilizumab and 1.76 (95% credible interval, 1.17 to 2.91) for sarilumab as compared with control, yielding posterior probabilities of superiority to control of more than 99.9% and of 99.5%, respectively. An analysis of 90-day survival showed improved survival in the pooled interleukin-6 receptor antagonist groups, yielding a hazard ratio for the comparison with the control group of 1.61 (95% credible interval, 1.25 to 2.08) and a posterior probability of superiority of more than 99.9%. All secondary analyses supported efficacy of these interleukin-6 receptor antagonists. CONCLUSIONS In critically ill patients with Covid-19 receiving organ support in ICUs, treatment with the interleukin-6 receptor antagonists tocilizumab and sarilumab improved outcomes, including survival.
UR - http://www.scopus.com/inward/record.url?scp=85104689064&partnerID=8YFLogxK
U2 - 10.1056/NEJMoa2100433
DO - 10.1056/NEJMoa2100433
M3 - Article
C2 - 33631065
AN - SCOPUS:85104689064
SN - 0028-4793
VL - 384
SP - 1491
EP - 1502
JO - New England Journal of Medicine
JF - New England Journal of Medicine
IS - 16
ER -