COVID-19 in ocrelizumab-treated people with multiple sclerosis

被引:65
作者
Hughes, Richard [1 ]
Whitley, Louise [2 ]
Fitovski, Kocho [1 ]
Schneble, Hans-Martin [1 ]
Muros, Erwan [1 ]
Sauter, Annette [1 ]
Craveiro, Licinio [1 ]
Dillon, Paul [1 ]
Bonati, Ulrike [1 ]
Jessop, Nikki [1 ]
Pedotti, Rosetta [1 ]
Koendgen, Harold [1 ]
机构
[1] F Hoffmann La Roche Ltd, Grenzacherstr 124, CH-4070 Basel, Switzerland
[2] TranScrip Partners LLP, Wokingham, England
关键词
COVID-19; multiple sclerosis; ocrelizumab; disease-modifying therapy; anti-CD20;
D O I
10.1016/j.msard.2020.102725
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: There are limited data on the impact of coronavirus disease 2019 (COVID-19) caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) on people with multiple sclerosis (MS). Objective: To better understand SARS-CoV-2 infection in ocrelizumab-treated people with MS. Methods: Internal Roche/Genentech data sources: Cases of COVID-19 from ongoing Roche/Genentech clinical trials and from post-marketing use of ocrelizumab until July 31, 2020 were identified and assessed using descriptive statistics. External real-world data (RWD) source: An MS COVID-19 cohort and an ocrelizumab-treated MS COVID-19 cohort were identified and assessed from the OPTUM (R) de-identified COVID-19 electronic health record (EHR) database. Results: Roche/Genentech clinical trial data: There were 51 (1.3%) suspected or confirmed cases of COVID-19 identified from 4,000 patients ongoing in 10 Roche/Genentech clinical trials. Of these, 26 (51%) were confirmed COVID-19 and 25 (49%) were suspected COVID-19. Sixteen (31.4%) patients were hospitalized. COVID-19 severity was mild to moderate in most patients (35, 68.6%). Ten (19.6%) patients had severe disease and there were three (5.9%) fatal cases. Most patients (43, 84.3%) recovered or were recovering. There was no association apparent between duration of exposure to ocrelizumab and COVID-19. Among COVID-19 patients with previous serum immunoglobulin status (27/51, 52.9%), all (27/27, 100%) had IgG levels within the normal range. Roche/Genentech post-marketing safety database data: There were 307 post-marketing cases of COVID-19 in the Roche/Genentech global safety database. Of these, 263 (85.7%) were confirmed and 44 (14.3%) were suspected COVID-19. 100 (32.6%) patients were hospitalized. COVID-19 was asymptomatic, mild or moderate in 143 (46.6%) patients, severe in 52 (16.9%) patients, and critical in 15 (4.9%) patients. There were 17 (5.5%) fatal cases. Information on severity was not reported in 80 (26.1%) cases. Most patients (211, 68.7%) recovered or were recovering at the time of the report. External RWD data source: As of July 13, 2020, the OPTUM (R) database included EHRs for almost 1.2 million patients with suspected COVID-19, 130,500 of whom met the criteria for confirmed/clinically diagnosed COVID-19. A total of 357 patients with MS with confirmed COVID-19 were identified. Forty-eight (13.4%) were treated with ocrelizumab, of whom 12 (25.0%) were hospitalized and one died (2.1%). Similar rates of hospitalization, invasive ventilation, and death were observed in the ocrelizumab-treated and non-ocrelizumab-treated MS cohorts.
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页数:13
相关论文
共 70 条
[1]   SARS-CoV-2 and Multiple Sclerosis: Not All Immune Depleting DMTs are Equal or Bad [J].
Amor, Sandra ;
Baker, David ;
Khoury, Samia J. ;
Schmierer, Klaus ;
Giovanonni, Gavin .
ANNALS OF NEUROLOGY, 2020, 87 (06) :794-797
[2]   COVID-19 vaccine-readiness for anti-CD20-depleting therapy in autoimmune diseases [J].
Baker, D. ;
Roberts, C. A. K. ;
Pryce, G. ;
Kang, A. S. ;
Marta, M. ;
Reyes, S. ;
Schmierer, K. ;
Giovannoni, G. ;
Amor, S. .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2020, 202 (02) :149-161
[3]   The underpinning biology relating to multiple sclerosis disease modifying treatments during the COVID-19 pandemic [J].
Baker, David ;
Amor, Sandra ;
Kang, Angray S. ;
Schmierer, Klaus ;
Giovannoni, Gavin .
MULTIPLE SCLEROSIS AND RELATED DISORDERS, 2020, 43
[4]   Effect of ocrelizumab on vaccine responses in patients with multiple sclerosis The VELOCE study [J].
Bar-Or, Amit ;
Calkwood, Jonathan C. ;
Chognot, Cathy ;
Evershed, Joanna ;
Fox, Edward J. ;
Herman, Ann ;
Manfrini, Marianna ;
McNamara, John ;
Robertson, Derrick S. ;
Stokmaier, Daniela ;
Wendt, Jeanette K. ;
Winthrop, Kevin L. ;
Traboulsee, Anthony .
NEUROLOGY, 2020, 95 (14) :E1999-E2008
[5]   Treating multiple sclerosis and neuromyelitis optica spectrum disorder during the COVID-19 pandemic [J].
Brownlee, Wallace ;
Bourdette, Dennis ;
Broadley, Simon ;
Killestein, Joep ;
Ciccarelli, Olga .
NEUROLOGY, 2020, 94 (22) :949-952
[6]  
CDC, 2020, ASS RISK FACT SEV CO
[7]  
Chawla D., 2020, MEDRXIV, V2020, DOI [10.1101/2020.07.17.20156265, DOI 10.1101/2020.07.17.20156265]
[8]   The immunobiology of SARS [J].
Chen, Jun ;
Subbarao, Kanta .
ANNUAL REVIEW OF IMMUNOLOGY, 2007, 25 :443-472
[9]   Global, regional, and national estimates of the population at increased risk of severe COVID-19 due to underlying health conditions in 2020: a modelling study [J].
Clark, Andrew ;
Jit, Mark ;
Warren-Gash, Charlotte ;
Guthrie, Bruce ;
Wang, Harry H. X. ;
Mercer, Stewart W. ;
Sanderson, Colin ;
McKee, Martin ;
Troeger, Christopher ;
Ong, Kanyin L. ;
Checchi, Francesco ;
Perel, Pablo ;
Joseph, Sarah ;
Gibbs, Hamish P. ;
Banerjee, Amitava ;
Eggo, Rosalind M. .
LANCET GLOBAL HEALTH, 2020, 8 (08) :1003-1017
[10]   Attenuation of antibody response to SARS-CoV-2 in a patient on ocrelizumab with hypogammaglobulinemia [J].
Conte, William L. .
MULTIPLE SCLEROSIS AND RELATED DISORDERS, 2020, 44