Department of Internal Medicine, University of Arkansas for Medical Sciences Northwest, Fayetteville, Arkansas, USA.
Department of Family and Preventive Medicine, University of Arkansas for Medical Sciences Northwest, Fayetteville, Arkansas, USA.
Monoclon Antib Immunodiagn Immunother. 2022 Aug;41(4):210-213. doi: 10.1089/mab.2022.0008. Epub 2022 Aug 3.
Monoclonal antibody (mAb) therapy has emerged as one of the mainstay treatment options for SARS-CoV-2. To improve speed of delivery and decrease bedside nursing needs, subcutaneous (SC) delivery of mAbs has been explored as an alternative to standard intravenous (IV) administration. To date, data regarding the effectiveness of SC compared with IV mAb are lacking. This retrospective cohort analysis conducted between April 2021 and August 2021 compared hospitalization rates among patients receiving IV versus SC administration of casirivimab/imdevimab (Regen-COV) at a single institution in Arkansas. Casirivimab/imdevimab was a promising mAb therapy utilized during the height of the Delta variant surge of the SARS-CoV-2 pandemic. Before resistance developed by the Omicron variant, casirivimab/imdevimab was utilized for outpatient treatment of SARS-CoV-2 patients at risk of deterioration. Primary outcomes of this investigation were the 30-day post-treatment rate of hospitalization and intensive care unit (ICU) care during hospitalization. There was no increased risk of hospitalization or ICU care with SC administration compared with IV administration. As SARS-CoV-2 continues to mutate into variants such as Omicron and develop resistance to existing mAbs, these preliminary findings of noninferiority of SC versus IV warrant ongoing investigation into SC administration of other mAbs.
单克隆抗体 (mAb) 疗法已成为治疗 SARS-CoV-2 的主要选择之一。为了提高输送速度并减少床边护理需求,人们探索了皮下 (SC) 给药作为替代标准静脉内 (IV) 给药的方法。迄今为止,关于 SC 与 IV mAb 相比的有效性的数据尚缺乏。本回顾性队列分析于 2021 年 4 月至 2021 年 8 月在阿肯色州的一家机构进行,比较了接受 casirivimab/imdevimab(Regen-COV)IV 与 SC 给药的患者的住院率。Casirivimab/imdevimab 是一种在 SARS-CoV-2 大流行的 Delta 变体激增期间使用的很有前途的 mAb 疗法。在 Omicron 变体产生耐药性之前,casirivimab/imdevimab 被用于门诊治疗有恶化风险的 SARS-CoV-2 患者。本研究的主要结果是治疗后 30 天的住院率和住院期间的重症监护病房 (ICU) 护理。与 IV 给药相比,SC 给药并没有增加住院或 ICU 护理的风险。随着 SARS-CoV-2 继续变异为 Omicron 等变体并对现有 mAb 产生耐药性,这些关于 SC 与 IV 相比非劣效性的初步发现需要对其他 mAb 的 SC 给药进行持续研究。