Olokizumab reduces the risks of death in hospitalized patients with moderate and severe COVID-19
Q4 Social Sciences
E. V. Tavlueva, A. E. Markarov, M. Petrushin, A. Vizel’, G. Ignatova, V. Antonov, A. Agaf'ina, B. Bakirov, V.M. Mozgovaya, O. Filon, A. Zinkovskaya, A. Dolgorukova, M. Samsonov
求助PDF
{"title":"Olokizumab reduces the risks of death in hospitalized patients with moderate and severe COVID-19","authors":"E. V. Tavlueva, A. E. Markarov, M. Petrushin, A. Vizel’, G. Ignatova, V. Antonov, A. Agaf'ina, B. Bakirov, V.M. Mozgovaya, O. Filon, A. Zinkovskaya, A. Dolgorukova, M. Samsonov","doi":"10.33029/2305-3496-2022-11-4-8-18","DOIUrl":null,"url":null,"abstract":"Aim – to evaluate the efficacy and safety of olokizumab in hospitalized patients with moderate to severe coronavirus disease COVID-19. Material and methods. A multicenter non-interventional retrospective study of olokizumab treatment in hospitalized patients with COVID-19 was conducted. The initial population in this study included 2926 patients with COVID-19. Patients with moderate or severe disease who were taking corticosteroids as part of standard therapy were selected for this analysis. The final population was 1738 patients. A test group (standard therapy: corticosteroids, antiviral, pathogenetic or symptomatic therapy in combination with olokizumab) and a comparison group (standard therapy only) were formed. Each group included 869 patients. The primary end point was all-cause mortality from the start of anti-inflammatory therapy to the end of follow-up. We also analyzed the incidence of transfer and the length of stay of patients in the intensive care unit, the duration of hospitalization, as well as the change in C-reactive protein level. Results and discussion. It was found that olokizumab significantly reduces the all-cause mortality compared with standard therapy: 54 (6.21%) cases compared with 111 (12.77%) in the control arm, p<0.001, odds ratio (OR) 2.21 [1.57;3.1]. The results of factor analysis confirmed that olokizumab increases the odds of recovery, OR 2.41 (95% CI 1.64–3.54, p<0.001). In addition, patients in olokizumab group showed significantly lower plasma CRP levels compared with control group. Already on the 2nd day after the start of therapy the CRP level was almost 2 times lower in the olokizumab group than in the control group (the median was 13 [5.6;28.55] mg/l and 25 [15.3;79.25] mg/L in the olokizumab and comparison groups, respectively). Conclusion. The results of the study confirm the clinical data on the efficacy of olokizumab as therapy for COVID-19 patients. © 2022 Tomsk Polytechnic University, Publishing House. All rights reserved.","PeriodicalId":36113,"journal":{"name":"Infectious Diseases: News, Opinions, Training","volume":"1 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Infectious Diseases: News, Opinions, Training","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.33029/2305-3496-2022-11-4-8-18","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Social Sciences","Score":null,"Total":0}
引用次数: 0
引用
批量引用
Abstract
Aim – to evaluate the efficacy and safety of olokizumab in hospitalized patients with moderate to severe coronavirus disease COVID-19. Material and methods. A multicenter non-interventional retrospective study of olokizumab treatment in hospitalized patients with COVID-19 was conducted. The initial population in this study included 2926 patients with COVID-19. Patients with moderate or severe disease who were taking corticosteroids as part of standard therapy were selected for this analysis. The final population was 1738 patients. A test group (standard therapy: corticosteroids, antiviral, pathogenetic or symptomatic therapy in combination with olokizumab) and a comparison group (standard therapy only) were formed. Each group included 869 patients. The primary end point was all-cause mortality from the start of anti-inflammatory therapy to the end of follow-up. We also analyzed the incidence of transfer and the length of stay of patients in the intensive care unit, the duration of hospitalization, as well as the change in C-reactive protein level. Results and discussion. It was found that olokizumab significantly reduces the all-cause mortality compared with standard therapy: 54 (6.21%) cases compared with 111 (12.77%) in the control arm, p<0.001, odds ratio (OR) 2.21 [1.57;3.1]. The results of factor analysis confirmed that olokizumab increases the odds of recovery, OR 2.41 (95% CI 1.64–3.54, p<0.001). In addition, patients in olokizumab group showed significantly lower plasma CRP levels compared with control group. Already on the 2nd day after the start of therapy the CRP level was almost 2 times lower in the olokizumab group than in the control group (the median was 13 [5.6;28.55] mg/l and 25 [15.3;79.25] mg/L in the olokizumab and comparison groups, respectively). Conclusion. The results of the study confirm the clinical data on the efficacy of olokizumab as therapy for COVID-19 patients. © 2022 Tomsk Polytechnic University, Publishing House. All rights reserved.
Olokizumab可降低中重度COVID-19住院患者的死亡风险
目的:评价olokizumab治疗中重度冠状病毒病COVID-19住院患者的疗效和安全性。材料和方法。开展了一项多中心非介入性回顾性研究,探讨了olokizumab治疗COVID-19住院患者的疗效。本研究的初始人群包括2926例COVID-19患者。采用皮质类固醇作为标准治疗一部分的中度或重度疾病患者被选为本分析的对象。最终人群为1738名患者。实验组(标准治疗:皮质类固醇、抗病毒、致病或对症治疗联合olokizumab)和对照组(仅标准治疗)组成。每组869例。主要终点是从抗炎治疗开始到随访结束的全因死亡率。我们还分析了患者在重症监护室的转院发生率和住院时间、住院时间以及c反应蛋白水平的变化。结果和讨论。结果发现,与标准治疗相比,olokizumab显著降低了全因死亡率:54例(6.21%)与对照组111例(12.77%)相比,p<0.001,优势比(OR) 2.21[1.57;3.1]。因子分析结果证实,olokizumab增加了恢复的几率,OR为2.41 (95% CI 1.64-3.54, p<0.001)。此外,与对照组相比,olokizumab组患者血浆CRP水平显著降低。在治疗开始后的第2天,olokizumab组的CRP水平几乎比对照组低2倍(olokizumab组和对照组的中位数分别为13 [5.6;28.55]mg/l和25 [15.3;79.25]mg/l)。结论。该研究结果证实了olokizumab治疗COVID-19患者疗效的临床数据。©2022托木斯克理工大学出版社。版权所有。
本文章由计算机程序翻译,如有差异,请以英文原文为准。