Sunny Subin, Tran Ami, Lee Jennifer, Abdallah Marie, Chaudhry Nimra, Quale John
Division of Infectious Diseases, Department of Medicine, NYC Health + Hospitals/Kings County, Brooklyn, New York, USA.
Department of Pharmacy, NYC Health + Hospitals/Queens, Queens, New York, USA.
Open Forum Infect Dis. 2023 Aug 9;10(8):ofad426. doi: 10.1093/ofid/ofad426. eCollection 2023 Aug.
Tocilizumab and baricitinib are immunomodulators that have been repurposed for the treatment of coronavirus disease 2019 (COVID-19). Whether one medication should be preferred over the other has not been established.
This multicenter retrospective cohort study comprised hospitalized patients with COVID-19 who received either tocilizumab or baricitinib. The primary outcome was improvement in respiratory status (at least 1-point reduction on the respiratory ordinal scale) at day 7 and up to day 28. Secondary outcomes included mortality, disposition, deep vein thrombosis, pulmonary embolism, or positive blood culture. Outcomes were stratified by baseline respiratory status and variant-predominating periods. Results were reported for the overall and propensity-matched cohorts.
A total of 921 patients received tocilizumab and 638 received baricitinib. The propensity-matched cohort included 597 patients in each group. At day 7 in the overall and propensity-matched cohorts, significantly more patients had improvement in respiratory status in the baricitinib group. These improvements were seen in patients requiring supplemental oxygen and noninvasive ventilation/high-flow oxygen but not in patients requiring mechanical ventilation. Favorable outcomes with baricitinib were observed during the Alpha and Omicron periods. By day 28, there were no differences in the changes of respiratory status for the treatment groups in either cohort. Also, no differences were seen in mortality, disposition, development of deep vein thrombosis/pulmonary embolism, or bloodstream infections.
Baricitinib treatment was associated with more favorable respiratory improvement at day 7 when compared with tocilizumab, but no differences were observed up to day 28.
托珠单抗和巴瑞替尼是已被重新用于治疗2019冠状病毒病(COVID-19)的免疫调节剂。尚未确定一种药物是否应优于另一种药物。
这项多中心回顾性队列研究纳入了接受托珠单抗或巴瑞替尼治疗的COVID-19住院患者。主要结局是第7天至第28天呼吸状况的改善(呼吸序贯量表至少降低1分)。次要结局包括死亡率、出院情况、深静脉血栓形成、肺栓塞或血培养阳性。结局按基线呼吸状况和变异株主导期进行分层。报告了总体队列和倾向匹配队列的结果。
共有921例患者接受托珠单抗治疗,638例接受巴瑞替尼治疗。倾向匹配队列每组包括597例患者。在总体队列和倾向匹配队列的第7天,巴瑞替尼组呼吸状况改善的患者明显更多。这些改善在需要补充氧气和无创通气/高流量氧气的患者中可见,但在需要机械通气的患者中未见。在阿尔法和奥密克戎时期观察到巴瑞替尼的良好结局。到第28天,两个队列中治疗组的呼吸状况变化没有差异。此外,在死亡率、出院情况、深静脉血栓形成/肺栓塞的发生或血流感染方面也没有差异。
与托珠单抗相比,巴瑞替尼治疗在第7天与更有利的呼吸改善相关,但到第28天未观察到差异。