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评估 COVID-19 细胞因子风暴综合征患者中使用英夫利昔单抗/托珠单抗与托珠单抗的效果。

Evaluation of infliximab/tocilizumab versus tocilizumab among COVID-19 patients with cytokine storm syndrome.

机构信息

Clinical Pharmacy Department, Faculty of Pharmacy, Misr International University, Cairo, Egypt.

Clinical Pharmacy Department, Faculty of Pharmacy, October 6 University, Giza, 12585, Egypt.

出版信息

Sci Rep. 2023 Apr 20;13(1):6456. doi: 10.1038/s41598-023-33484-6.

DOI:10.1038/s41598-023-33484-6
PMID:37081046
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10116445/
Abstract

Coronavirus Disease 2019 (COVID-19) continues to spread rapidly. Monoclonal antibodies as well as anti-tumor necrosis factor are considered promising treatments for COVID-19. A prospective cohort study in which patients are divided into three groups. Group 1: moderate and severe COVID-19 patients received standard treatment; Group 2: moderate and severe COVID-19 patients received tocilizumab; Group 3: moderate and severe COVID-19 patients received treatment with infliximab and tocilizumab. 153 patients were recruited in the study. 40 received standard treatment alone, 70 received tocilizumab with standard treatment, and 43 received tocilizumab/infliximab with standard treatment. There was a significant difference in length of hospital stay (10.3, 8.9, and 7.6 days respectively P = 0.03), need for a non-invasive mechanical ventilator (4, 5, and one patient; P = 1.2E-8), intensive care admission (32, 45, and 16 patients; P = 2.5E-5), the occurrence of sepsis (18, 12, and 10 patients; P = 0.005) and in death (42.5%, 14.2%, and 7%; P = 0.0008) which were significantly lower in tocilizumab/infliximab group compared to tocilizumab and standard of care groups. Our study showed that tocilizumab/ infliximab in addition to standard of care was considered a promising treatment for moderate and severe COVID-19 patients.Trial registration number: ClinicalTrials.gov NCT04734678; date of registration: 02/02/2021.

摘要

新型冠状病毒病(COVID-19)仍在迅速传播。单克隆抗体和抗肿瘤坏死因子被认为是 COVID-19 的有前途的治疗方法。一项前瞻性队列研究,将患者分为三组。第 1 组:中重度 COVID-19 患者接受标准治疗;第 2 组:中重度 COVID-19 患者接受托珠单抗治疗;第 3 组:中重度 COVID-19 患者接受英夫利昔单抗和托珠单抗治疗。本研究共纳入 153 例患者。40 例患者单独接受标准治疗,70 例患者接受托珠单抗联合标准治疗,43 例患者接受托珠单抗/英夫利昔单抗联合标准治疗。三组患者的住院时间(分别为 10.3、8.9 和 7.6 天;P=0.03)、需要无创机械通气(4、5 和 1 例患者;P=1.2E-8)、重症监护病房入住(32、45 和 16 例患者;P=2.5E-5)、发生脓毒症(18、12 和 10 例患者;P=0.005)和死亡率(42.5%、14.2%和 7%;P=0.0008)差异有统计学意义,托珠单抗/英夫利昔单抗组显著低于托珠单抗组和标准治疗组。我们的研究表明,托珠单抗/英夫利昔单抗联合标准治疗被认为是中重度 COVID-19 患者的一种有前途的治疗方法。试验注册编号:ClinicalTrials.gov NCT04734678;登记日期:2021 年 2 月 2 日。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/530a/10119078/5959e89f9a29/41598_2023_33484_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/530a/10119078/5959e89f9a29/41598_2023_33484_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/530a/10119078/5959e89f9a29/41598_2023_33484_Fig1_HTML.jpg

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