Risk of Reactivation of Hepatitis B Virus (HBV) and Tuberculosis (TB) and Complications of Hepatitis C Virus (HCV) Following Tocilizumab Therapy: A Systematic Review to Inform Risk Assessment in the COVID-19 Era

被引:28
作者
Campbell, Cori [1 ]
Andersson, Monique I. [2 ,3 ]
Ansari, M. Azim [1 ,4 ]
Moswela, Olivia [5 ]
Misbah, Siraj A. [6 ]
Klenerman, Paul [1 ,2 ]
Matthews, Philippa C. [1 ,2 ]
机构
[1] Univ Oxford, Nuffield Dept Med, Medawar Bldg Pathogen Res, Oxford, England
[2] Oxford Univ Hosp NHS Fdn Trust, John Radcliffe Hosp, Dept Infect Dis & Microbiol, Oxford, England
[3] Univ Oxford, Nuffield Dept Clin Lab Sci, Oxford, England
[4] Univ Oxford, Wellcome Ctr Human Genet, Oxford, England
[5] Oxford Univ Hosp NHS Fdn Trust, John Radcliffe Hosp, Dept Pharm, Oxford, England
[6] Oxford Univ Hosp NHS Fdn Trust, John Radcliffe Hosp, Dept Clin Immunol, Oxford, England
基金
英国惠康基金;
关键词
tocilizumab; biologic; SARS-CoV-2; COVID-19; infection; reactivation; hepatitis B virus; tuberculosis; IL-6; INTERLEUKIN-6; SUSCEPTIBILITY; INFECTIONS;
D O I
10.3389/fmed.2021.706482
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives: Tocilizumab (TCZ), an IL-6 receptor antagonist, is used in the treatment of severe COVID-19 caused by infection with SARS-CoV-2. However, unintended consequences of TCZ therapy include reactivation of tuberculosis (TB) or hepatitis B virus (HBV), and worsening of hepatitis C virus (HCV). We set out to assimilate existing data for these complications, in order to help inform evidence-based risk assessments for the use of TCZ, and thus to reduce the risk of serious but preventable complications.</p> & nbsp;</p> Methods: We searched the global WHO database of Individual Case Safety Reports (ICSRs) and adverse drug reactions (ADRs) ( "VigiBase ") and undertook a systematic literature review, in accordance with PRISMA guidelines. We generated mean cumulative incidence estimates for infection complications.</p> & nbsp;</p> Results: Mean cumulative incidence of HBV and TB were 3.3 and 4.3%, respectively, in patients receiving TCZ. Insufficient data were available to generate estimates for HCV. These estimates derive from heterogeneous studies pre-dating SARS-CoV-2, with differing epidemiology and varied approaches to screening and prophylaxis, so formal meta-analysis was not possible.</p> & nbsp;</p> Conclusions: We underline the need for careful individual risk assessment prior to TCZ prescription, and present an algorithm to guide clinical stratification. There is an urgent need for ongoing collation of safety data as TCZ therapy is used in COVID.</p>
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页数:13
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