Razonable Raymund R, Pawlowski Colin, O'Horo John C, Arndt Lori L, Arndt Richard, Bierle Dennis M, Borgen Molly Destro, Hanson Sara N, Hedin Michelle C, Lenehan Patrick, Puranik Arjun, Seville Maria T, Speicher Leigh L, Tulledge-Scheitel Sidna M, Venkatakrishnan A J, Wilker Caroline G, Badley Andrew D, Ganesh Ravindra
Mayo Clinic, Rochester, MN, United States.
nFerence, Cambridge, MA, United States.
EClinicalMedicine. 2021 Oct;40:101102. doi: 10.1016/j.eclinm.2021.101102. Epub 2021 Aug 30.
Real-world clinical data to support the use of casirivimab-imdevimab for the treatment of outpatients with mild to moderate coronavirus disease-19 (COVID-19) is needed. This study aimed to assess the outcomes of casirivimab-imdevimab treatment of mild to moderate COVID-19.
A retrospective cohort of 696 patients who received casirivimab-imdevimab between December 4, 2020 and April 9, 2021 was compared to a propensity-matched control of 696 untreated patients with mild to moderate COVID-19 at Mayo Clinic sites in Arizona, Florida, Minnesota, and Wisconsin. Primary outcome was rate of hospitalization at days 14, 21 and 28 after infusion.
The median age of the antibody-treated cohort was 63 years (interquartile range, 52-71); 45·5% were ≥65 years old; 51.4% were female. High-risk characteristics were hypertension (52.4%), body mass index ≥35 (31.0%), diabetes mellitus (24.6%), chronic lung disease (22.1%), chronic renal disease (11.4%), congestive heart failure (6.6%), and compromised immune function (6.7%). Compared to the propensity-matched untreated control, patients who received casirivimab-imdevimab had significantly lower all-cause hospitalization rates at day 14 (1.3% vs 3.3%; Absolute Difference: 2.0%; 95% confidence interval (CI): 0.5-3.7%), day 21 (1.3% vs 4.2%; Absolute Difference: 2.9%; 95% CI: 1.2-4.7%), and day 28 (1.6% vs 4.8%; Absolute Difference: 3.2%; 95% CI: 1.4-5.1%). Rates of intensive care unit admission and mortality at days 14, 21 and 28 were similarly low for antibody-treated and untreated groups.
Among high-risk patients with mild to moderate COVID-19, casirivimab-imdevimab treatment was associated with a significantly lower rate of hospitalization.
Mayo Clinic.
需要真实世界的临床数据来支持使用卡西瑞维单抗-英夫利昔单抗治疗轻度至中度冠状病毒病(COVID-19)门诊患者。本研究旨在评估卡西瑞维单抗-英夫利昔单抗治疗轻度至中度COVID-19的疗效。
对2020年12月4日至2021年4月9日期间接受卡西瑞维单抗-英夫利昔单抗治疗的696例患者进行回顾性队列研究,并与亚利桑那州、佛罗里达州、明尼苏达州和威斯康星州梅奥诊所的696例未治疗的轻度至中度COVID-19患者进行倾向匹配对照。主要结局是输注后第14、21和28天的住院率。
接受抗体治疗队列的中位年龄为63岁(四分位间距,52-71岁);45.5%的患者年龄≥65岁;51.4%为女性。高危特征包括高血压(52.4%)、体重指数≥35(31.0%)、糖尿病(24.6%)、慢性肺病(22.1%)、慢性肾病(11.4%)、充血性心力衰竭(6.6%)和免疫功能受损(6.7%)。与倾向匹配的未治疗对照组相比,接受卡西瑞维单抗-英夫利昔单抗治疗的患者在第14天(1.3%对3.3%;绝对差异:2.0%;95%置信区间(CI):0.5-3.7%)、第21天(1.3%对4.2%;绝对差异:2.9%;95%CI:1.2-4.7%)和第28天(1.6%对4.8%;绝对差异:3.2%;95%CI:1.4-5.1%)的全因住院率显著降低。抗体治疗组和未治疗组在第14、21和28天的重症监护病房入住率和死亡率同样较低。
在轻度至中度COVID-19的高危患者中,卡西瑞维单抗-英夫利昔单抗治疗与显著较低的住院率相关。
梅奥诊所。