Systematic review and meta-analysis of tocilizumab in persons with coronavirus disease-2019 (COVID-19)

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作者
Chong-xiang Chen
Fang Hu
Jin Wei
Le-tao Yuan
Tian-meng Wen
Robert Peter Gale
Yang Liang
机构
[1] Sun Yat-sen University Cancer Center,Department of Hematologic Oncology, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine
[2] First Affiliated Hospital of Guangzhou Medical University,State Key Laboratory of Respiratory Disease, Guangzhou Institute of Respiratory Health
[3] Sun Yat-sen University Cancer Center,Department of ICU, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine
[4] Affiliated Hospital of North Sichuan Medical College,Department of Hematology
[5] Sun Yat-sen University,School of Public Health
[6] Imperial College London,Department of Immunology and Inflammation, Haematology Research Centre
来源
Leukemia | 2021年 / 35卷
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摘要
We performed a meta-analysis to determine safety and efficacy of tocilizumab in persons with coronavirus disease-2019 (COVID-19). We searched PubMed, Web of Science and Medline using Boolean operators for studies with the terms coronavirus OR COVID-19 OR 2019-nCoV OR SARS-CoV-2 AND tocilizumab. Review Manager 5.4 was used to analyze data and the modified Newcastle–Ottawa and Jadad scales for quality assessment. We identified 32 studies in 11,487 subjects including three randomized trials and 29 cohort studies with a comparator cohort, including historical controls (N = 5), a matched cohort (N = 12), or concurrent controls (N = 12). Overall, tocilizumab decreased risk of death (Relative Risk [RR] = 0.74; 95% confidence interval [CI], 0.59, 0.93; P = 0.008; I2 = 80%) but not of surrogate endpoints including ICU admission (RR = 1.40 [0.64,3.06]; P = 0.4; I2 = 88%), invasive mechanical ventilation (RR = 0.83 [0.57,1.22]; P = 0.34; I2 = 65%) or secondary infections (RR = 1.30 [0.97,1.74]; P = 0.08; I2 = 65%) and increased interval of hospitalization of subjects discharged alive(mean difference [MD] = 2 days [<1, 4 days]; P = 0.006; I2 = 0). RRs of death in studies with historical controls (RR = 0.28 [0.16,0.49; P < 0.001]; I2 = 62%) or a matched cohort (RR = 0.68 [0.53, 0.87]; P = 0.002; I2 = 42%) were decreased. In contrast, RRs of death in studies with a concurrent control (RR = 1.10 [0.77, 1.56]; P = 0.60; I2 = 85%) or randomized (RR = 1.18 [0.57,2.44]; P = 0.66; I2 = 0) were not decreased. A reduced risk of death was not confirmed in our analyses which questions safety and efficacy of tocilizumab in persons with COVID-19.
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页码:1661 / 1670
页数:9
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