Department of Hematologic Oncology, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Sun Yat-sen University Cancer Center, Guangzhou, China.
State Key Laboratory of Respiratory Disease, Guangzhou Institute of Respiratory Health, First Affiliated Hospital of Guangzhou Medical University, Guangzhou, Guangdong Province, China.
Leukemia. 2021 Sep;35(9):2616-2620. doi: 10.1038/s41375-021-01266-6. Epub 2021 May 14.
We analyzed reports on safety and efficacy of JAK-inhibitors in patients with coronavirus infectious disease-2019 (COVID-19) published between January 1st and March 6th 2021 using the Newcastle-Ottawa and Jadad scales for quality assessment. We used disease severity as a proxy for time when JAK-inhibitor therapy was started. We identified 6 cohort studies and 5 clinical trials involving 2367 subjects treated with ruxolitinib (N = 3) or baricitinib 45 (N = 8). Use of JAK-inhibitors decreased use of invasive mechanical ventilation (RR = 0.63; [95% Confidence Interval (CI), 0.47, 0.84]; P = 0.002) and had borderline impact on rates of intensive care unit (ICU) admission (RR = 0.24 [0.06, 1.02]; P = 0.05) and acute respiratory distress syndrome (ARDS; RR = 0.50 [0.19, 1.33]; P = 0.16). JAK-inhibitors did not decrease length of hospitalization (mean difference (MD) -0.18 [-4.54, 4.18]; P = 0.94). Relative risks of death for both drugs were 0.42 [0.30, 0.59] (P < 0.001), for ruxolitinib, RR = 0.33 (0.13, 0.88; P = 0.03) and for baricitinib RR = 0.44 (0.31, 0.63; P < 0.001). Timing of JAK-inhibitor treatment during the course of COVID-19 treatment may be important in determining impact on outcome. However, these data are not consistently reported.
我们使用纽卡斯尔-渥太华量表和 Jadad 量表对 2021 年 1 月 1 日至 3 月 6 日期间发表的关于 JAK 抑制剂在冠状病毒感染疾病 2019(COVID-19)患者中的安全性和疗效的报告进行了分析,以评估质量。我们使用疾病严重程度作为开始 JAK 抑制剂治疗时间的替代指标。我们确定了 6 项队列研究和 5 项临床试验,涉及 2367 名接受鲁索替尼(N=3)或巴瑞替尼治疗的患者(N=8)。使用 JAK 抑制剂可降低使用有创机械通气的比率(RR=0.63;[95%置信区间(CI),0.47,0.84];P=0.002),且对 ICU 入院率有边缘影响(RR=0.24[0.06,1.02];P=0.05)和急性呼吸窘迫综合征(ARDS;RR=0.50[0.19,1.33];P=0.16)。JAK 抑制剂并未降低住院时间(平均差异(MD)-0.18[-4.54,4.18];P=0.94)。两种药物的死亡相对风险均为 0.42[0.30,0.59](P<0.001),鲁索替尼的 RR=0.33(0.13,0.88;P=0.03),巴瑞替尼的 RR=0.44(0.31,0.63;P<0.001)。在 COVID-19 治疗过程中,JAK 抑制剂治疗的时间可能对结局的影响很重要,但这些数据并未得到一致报告。