Division of Rheumatology, Department of Medicine, Northwell Health, Great Neck, NY; Donald and Barbara Zucker School of Medicine at Hofstra/Northwell Health, Hempstead, NY.
Biostatistics Unit, The Feinstein Institutes for Medical Research, Northwell Health, Manhasset, NY; Institute of Health Innovations and Outcomes Research, The Feinstein Institutes for Medical Research, Northwell Health, Manhasset, NY.
Chest. 2021 Mar;159(3):933-948. doi: 10.1016/j.chest.2020.09.275. Epub 2020 Oct 17.
Cytokine storm is a marker of coronavirus disease 2019 (COVID-19) illness severity and increased mortality. Immunomodulatory treatments have been repurposed to improve mortality outcomes.
Do immunomodulatory therapies improve survival in patients with COVID-19 cytokine storm (CCS)?
We conducted a retrospective analysis of electronic health records across the Northwell Health system. COVID-19 patients hospitalized between March 1, 2020, and April 24, 2020, were included. CCS was defined by inflammatory markers: ferritin, > 700 ng/mL; C-reactive protein (CRP), > 30 mg/dL; or lactate dehydrogenase (LDH), > 300 U/L. Patients were subdivided into six groups: no immunomodulatory treatment (standard of care) and five groups that received either corticosteroids, anti-IL-6 antibody (tocilizumab), or anti-IL-1 therapy (anakinra) alone or in combination with corticosteroids. The primary outcome was hospital mortality.
Five thousand seven hundred seventy-six patients met the inclusion criteria. The most common comorbidities were hypertension (44%-59%), diabetes (32%-46%), and cardiovascular disease (5%-14%). Patients most frequently met criteria with high LDH (76.2%) alone or in combination, followed by ferritin (63.2%) and CRP (8.4%). More than 80% of patients showed an elevated D-dimer. Patients treated with corticosteroids and tocilizumab combination showed lower mortality compared with patients receiving standard-of-care (SoC) treatment (hazard ratio [HR], 0.44; 95% CI, 0.35-0.55; P < .0001) and with patients treated with corticosteroids alone (HR, 0.66; 95% CI, 0.53-0.83; P = .004) or in combination with anakinra (HR, 0.64; 95% CI, 0.50-0.81; P = .003). Corticosteroids when administered alone (HR, 0.66; 95% CI, 0.57-0.76; P < .0001) or in combination with tocilizumab (HR, 0.43; 95% CI, 0.35-0.55; P < .0001) or anakinra (HR, 0.68; 95% CI, 0.57-0.81; P < .0001) improved hospital survival compared with SoC treatment.
The combination of corticosteroids with tocilizumab showed superior survival outcome when compared with SoC treatment as well as treatment with corticosteroids alone or in combination with anakinra. Furthermore, corticosteroid use either alone or in combination with tocilizumab or anakinra was associated with reduced hospital mortality for patients with CCS compared with patients receiving SoC treatment.
细胞因子风暴是 2019 年冠状病毒病(COVID-19)疾病严重程度和死亡率增加的标志。免疫调节治疗已被重新用于改善死亡率结局。
免疫调节疗法是否能改善 COVID-19 细胞因子风暴(CCS)患者的生存率?
我们对 Northwell Health 系统内的电子健康记录进行了回顾性分析。纳入 2020 年 3 月 1 日至 2020 年 4 月 24 日期间住院的 COVID-19 患者。CCS 通过炎症标志物定义:铁蛋白>700ng/ml;C 反应蛋白(CRP)>30mg/dL;或乳酸脱氢酶(LDH)>300U/L。患者分为六组:无免疫调节治疗(标准治疗)和五组,分别单独或联合使用皮质类固醇、抗 IL-6 抗体(托珠单抗)或抗 IL-1 治疗。主要结局是住院死亡率。
符合纳入标准的患者有 5776 名。最常见的合并症是高血压(44%-59%)、糖尿病(32%-46%)和心血管疾病(5%-14%)。患者最常因高 LDH(76.2%)单独或联合出现标准,其次是铁蛋白(63.2%)和 CRP(8.4%)。超过 80%的患者出现 D-二聚体升高。与接受标准治疗(SoC)的患者(危险比[HR],0.44;95%CI,0.35-0.55;P<0.0001)和接受皮质类固醇单药治疗(HR,0.66;95%CI,0.53-0.83;P=0.004)或联合使用阿那白滞素(HR,0.64;95%CI,0.50-0.81;P=0.003)的患者相比,接受皮质类固醇和托珠单抗联合治疗的患者死亡率较低。皮质类固醇单独治疗(HR,0.66;95%CI,0.57-0.76;P<0.0001)或与托珠单抗(HR,0.43;95%CI,0.35-0.55;P<0.0001)或阿那白滞素(HR,0.68;95%CI,0.57-0.81;P<0.0001)联合治疗与 SoC 治疗相比,可改善住院生存率。
与 SoC 治疗以及皮质类固醇单药治疗或联合阿那白滞素治疗相比,皮质类固醇联合托珠单抗治疗显示出更好的生存结果。此外,与接受 SoC 治疗的患者相比,单独使用皮质类固醇或联合使用托珠单抗或阿那白滞素可降低 CCS 患者的住院死亡率。