Department of Respiratory Medicine, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, North 15 West 7, Kita-ku, Sapporo 060-8638, Japan.
Department of Mycobacterium Reference and Research, The Research Institute of Tuberculosis, Japan Anti-Tuberculosis Association, 3-1-24, Matsuyama Kiyose, Tokyo 101-0061, Japan.
Medicina (Kaunas). 2022 Apr 4;58(4):513. doi: 10.3390/medicina58040513.
Tocilizumab and baricitinib have been observed to improve the outcomes of patients with coronavirus disease 2019 (COVID-19). However, a comparative evaluation of these drugs has not been performed. A retrospective, single-center study was conducted using the data of COVID-19 patients admitted to Hokkaido University hospital between April 2020 and September 2021, who were treated with tocilizumab or baricitinib. The clinical characteristics of the patients who received tocilizumab were compared to those of patients who received baricitinib. Univariate and multivariate logistic regression analyses of the outcomes of all-cause mortality and improvement in respiratory status were performed. The development of secondary infection events was analyzed using the Kaplan-Meier method and the log-rank test. Of the 459 patients hospitalized with COVID-19 during the study, 64 received tocilizumab treatment and 34 baricitinib treatment, and those 98 patients were included in the study. Most patients were treated with concomitant steroids and exhibited the same severity level at the initiation of drug treatment. When compared to each other, neither tocilizumab nor baricitinib use were associated with all-cause mortality or improvement in respiratory status within 28 days from drug administration. Age, chronic renal disease and early administration of TCZ or BRT from the onset of COVID-19 were independent prognostic factors for all-cause mortality, whereas anti-viral drug use and the severity of COVID-19 at baseline were associated with an improvement in respiratory status. Secondary infection-free survival rates of patients treated with tocilizumab and those treated with baricitinib did not significantly differ. The results suggest that both tocilizumab and baricitinib could be clinically equivalent agents of choice in treatment of COVID-19.
托珠单抗和巴瑞替尼已被观察到可改善 2019 年冠状病毒病(COVID-19)患者的结局。然而,尚未对这些药物进行比较评估。
本研究采用回顾性单中心研究方法,使用了 2020 年 4 月至 2021 年 9 月北海道大学医院收治的 COVID-19 患者的数据,这些患者接受了托珠单抗或巴瑞替尼治疗。比较了接受托珠单抗治疗的患者与接受巴瑞替尼治疗的患者的临床特征。对所有原因死亡率和呼吸状态改善的结局进行了单变量和多变量逻辑回归分析。使用 Kaplan-Meier 方法和对数秩检验分析继发感染事件的发生情况。
在研究期间,住院的 459 例 COVID-19 患者中,64 例接受了托珠单抗治疗,34 例接受了巴瑞替尼治疗,这 98 例患者被纳入研究。大多数患者同时接受皮质类固醇治疗,在开始药物治疗时具有相同的严重程度。相互比较时,托珠单抗和巴瑞替尼的使用均与给药后 28 天内的全因死亡率或呼吸状态改善无关。
年龄、慢性肾脏病以及 COVID-19 发病早期使用 TCZ 或 BRT 是全因死亡率的独立预后因素,而抗病毒药物的使用和基线 COVID-19 的严重程度与呼吸状态的改善相关。接受托珠单抗和巴瑞替尼治疗的患者的继发感染无事件生存率无显著差异。这些结果表明,托珠单抗和巴瑞替尼均可作为 COVID-19 治疗的临床等效选择药物。