State Key Laboratory of Pathogen and Biosecurity, Academy of Military Medical Science, Beijing, China; School of Public Health, Shandong First Medical University and Shandong Academy of Medical Sciences, Jinan, China.
The 154th Hospital, Xinyang, China.
J Infect. 2024 Jul;89(1):106181. doi: 10.1016/j.jinf.2024.106181. Epub 2024 May 12.
Severe fever with thrombocytopenia syndrome (SFTS) is an emerging viral hemorrhagic fever with high fatality rates. The blockade of pro-inflammatory cytokines presents a promising therapeutic strategy.
We conducted a randomized clinical trial at the 154th hospital, Xinyang, Henan Province. Eligible patients with severe SFTS disease were randomly assigned in a 1:2 ratio to receive either a single intravenous infusion of tocilizumab plus usual care; or usual care only. The primary outcome was the clinical status of death/survival at day 14, while secondary outcomes included improvement from baseline in liver and kidney damage and time required for hospital discharge. The efficacy of tocilizumab plus corticosteroid was compared to those receiving corticosteroid alone. The trial is registered with the Chinese Clinical Trial Registry website (ChiCTR2300076317).
63 eligible patients were assigned to the tocilizumab group and 126 to the control group. The addition of tocilizumab to usual care was associated with a reduced death rate (9.5%) compared to those received only usual care (23.0%), with an adjusted hazard ratio (aHR) of 0.37 (95% confidence interval [CI], 0.15 to 0.91, P = 0.029). Combination therapy of tocilizumab and corticosteroids was associated with a significantly reduced fatality (aHR, 0.21; 95% CI, 0.08 to 0.56; P = 0.002) compared to those receiving corticosteroids alone.
A significant benefit of reducing fatality in severe SFTS patients was observed by using tocilizumab. A combined therapy of tocilizumab plus corticosteroids was recommended for the therapy of severe SFTS.
严重发热伴血小板减少综合征(SFTS)是一种新兴的病毒性出血热,死亡率较高。阻断促炎细胞因子是一种很有前途的治疗策略。
我们在河南省信阳市第 154 医院进行了一项随机临床试验。符合条件的重症 SFTS 患者按 1:2 的比例随机分为托珠单抗单药静脉输注联合常规治疗组或仅常规治疗组。主要终点为第 14 天的临床死亡/存活状态,次要终点包括肝肾功能从基线改善情况和出院所需时间。比较了托珠单抗联合皮质类固醇与单独使用皮质类固醇的疗效。该试验在中国临床试验注册网站(ChiCTR2300076317)注册。
共有 63 名符合条件的患者被分配到托珠单抗组,126 名患者被分配到对照组。与仅接受常规治疗的患者相比,托珠单抗联合常规治疗组的死亡率(9.5%)降低,调整后的危险比(aHR)为 0.37(95%置信区间[CI],0.15 至 0.91,P=0.029)。与单独使用皮质类固醇相比,托珠单抗联合皮质类固醇的联合治疗显著降低了死亡率(aHR,0.21;95%CI,0.08 至 0.56;P=0.002)。
托珠单抗可显著降低重症 SFTS 患者的死亡率。建议联合使用托珠单抗加皮质类固醇治疗重症 SFTS。