Centre for Clinical Research, Epidemiology, Modelling and Evaluation (CREME), Institute for Global Health, UCL, London, UK.
Centre for Clinical Research, Epidemiology, Modelling and Evaluation (CREME), Institute for Global Health, UCL, London, UK.
Clin Microbiol Infect. 2022 Mar;28(3):371-374. doi: 10.1016/j.cmi.2021.10.018. Epub 2021 Nov 9.
Most treatment guidelines for coronavirus disease 2019 (COVID-19) currently recommend tocilizumab in combination with dexamethasone in critically ill patients who are exhibiting rapid respiratory decompensation.
To produce a critical review and summary of the pathway which led to the repurposing of tocilizumab for COVID-19 treatment, from in vitro observations to guidelines recommendations.
All studies evaluating the effectiveness of tocilizumab to treat COVID-19 disease published between July 2020 and July 2021.
Two large and methodologically well conducted observational studies, the TESEO and the STOP COVID cohorts, showed a reduction in the risk of invasive mechanical ventilation or death in patients treated with tocilizumab as compared to standard of care in 2020. Concomitantly, and up to February 2021, a number of randomized trials (RCTs) with small sample sizes were showing discrepant results. These RCTs had a number of issues: small sample size, various designs and inclusion criteria, and different dosages of tocilizumab used. The confidence interval of the meta-analytic estimate for the RCT results was consistent with the hypothesis of no efficacy of tocilizumab. In our opinion, this was mainly because the meta-analysis included small and heterogeneous studies. These results led to a delay in the inclusion of tocilizumab in guidelines which occurred only in the summer of 2021.
Although observational studies are unable to control for unmeasured confounding, they can be put together quickly during a pandemic and promptly provide important information. The large sample size allows us to investigate effect measure modifiers and to better target interventions. It is key that the effect size is somewhat large (RR > 2), all sources of bias are properly accounted for, and the direct evidence is weighted against these factors. It appears to us that for tocilizumab, not having dismissed the results of carefully designed and analysed observational studies in 2020 could have prevented many deaths over those months.
大多数关于 2019 年冠状病毒病(COVID-19)的治疗指南目前建议在出现快速呼吸失代偿的重症患者中,将托珠单抗与地塞米松联合使用。
对托珠单抗用于 COVID-19 治疗的途径进行批判性回顾和总结,从体外观察到指南推荐。
所有评估托珠单抗治疗 COVID-19 疾病有效性的研究均发表于 2020 年 7 月至 2021 年 7 月之间。
两项大型、方法学上精心设计的观察性研究——TESEO 和 STOP COVID 队列研究表明,与 2020 年的标准治疗相比,托珠单抗治疗可降低患者接受有创机械通气或死亡的风险。同时,截至 2021 年 2 月,多项样本量较小的随机对照试验(RCT)显示出不一致的结果。这些 RCT 存在一些问题:样本量小、设计和纳入标准不同以及使用的托珠单抗剂量不同。RCT 结果的荟萃分析估计的置信区间与托珠单抗无效的假设一致。在我们看来,这主要是因为荟萃分析纳入了小型和异质性研究。这些结果导致托珠单抗纳入指南的时间延迟,直到 2021 年夏季才被纳入。
虽然观察性研究无法控制未测量的混杂因素,但在大流行期间可以迅速进行组合,并及时提供重要信息。大样本量使我们能够研究效应量修饰剂,并更好地针对干预措施。关键是效应大小要大一些(RR>2),所有偏倚来源都要得到妥善考虑,并且直接证据要与这些因素相权衡。在我们看来,对于托珠单抗,如果在 2020 年没有忽视精心设计和分析的观察性研究的结果,可能会在这几个月内避免许多死亡。