From the Novartis Pharmaceuticals Corporation (R.S.), East Hanover, NJ; Novartis Pharma AG (A.K., T.H., V.D.), Basel, Switzerland; Department of Neurology, Technical University of Munich, and Munich Cluster for Systems Neurology (SyNergy) (B.H.), Germany; Weill Institute for Neurosciences (B.A.C.C.), Department of Neurology, University of California San Francisco, CA; Department of Neurology (B.M.G.), University of Texas Southwestern, Dallas, TX; Novartis Healthcare Pvt. Ltd. (U.K.), Hyderabad, India; Department of Medicine (B.J.W.), Division of Experimental Medicine, Research Institute of the McGill University Health Centre, Montreal, Canada; and Department of Neurology (J.B.), Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
Neurol Neuroimmunol Neuroinflamm. 2021 Nov 30;9(1). doi: 10.1212/NXI.0000000000001092. Print 2021 Nov.
A descriptive analysis of COVID-19 infection in patients with multiple sclerosis (MS) receiving fingolimod or siponimod.
We reviewed the cases of COVID-19 from postmarketing or ongoing clinical trials reported to Novartis through December 27, 2020.
As of December 27, 2020, 283 cases had been reported in fingolimod-treated patients. The mean age was 44 years (from n = 224; range 11-69 years), and 190 were women. Of 161 cases with available information, 138 were asymptomatic (6), mild (100), or moderate (32); 50 cases required hospitalization. At the last follow-up, 140 patients were reported as recovered/recovering, condition was unchanged in 22, and deteriorated in 3 patients; 4 patients had a fatal outcome. Information was not available for 114 patients. Of the 54 cases of COVID-19 reported in siponimod-treated patients, 45 were from the postmarketing setting and 9 from an ongoing open-label clinical trial. The mean age was 54 years (from n = 45; range 31-70), and 30 were women. Of 28 cases with available information, 24 were asymptomatic (2), mild (17), or moderate (5); 9 cases required hospitalization. At the last follow-up, 27 patients were reported as recovered/recovering, condition remained unchanged for 1, and 3 patients had a fatal outcome. Information was not available for 23 patients.
Based on a review of available information, the risk of more severe COVID-19 in patients receiving fingolimod or siponimod seems to be similar to that reported in the general population and the MS population with COVID-19. However, limitations of spontaneous reporting, especially missing data, should be considered in the interpretation of these observations.
对接受芬戈莫德或西尼莫德治疗的多发性硬化症 (MS) 患者 COVID-19 感染情况进行描述性分析。
我们回顾了截至 2020 年 12 月 27 日诺华公司通过上市后或正在进行的临床试验报告的 COVID-19 病例。
截至 2020 年 12 月 27 日,在接受芬戈莫德治疗的患者中报告了 283 例病例。平均年龄为 44 岁(n = 224;年龄范围为 11-69 岁),其中 190 例为女性。在可获得信息的 161 例病例中,138 例为无症状(6)、轻症(100)或中度(32);50 例需要住院治疗。在最后一次随访时,报告 140 例患者已康复/正在康复,22 例病情未变,3 例病情恶化;4 例患者死亡。114 例患者的信息不可用。在接受西尼莫德治疗的 54 例 COVID-19 病例中,45 例来自上市后环境,9 例来自正在进行的开放标签临床试验。平均年龄为 54 岁(n = 45;年龄范围为 31-70 岁),其中 30 例为女性。在可获得信息的 28 例病例中,24 例为无症状(2)、轻症(17)或中度(5);9 例需要住院治疗。在最后一次随访时,报告 27 例患者已康复/正在康复,1 例病情未变,3 例患者死亡。23 例患者的信息不可用。
基于对可用信息的审查,接受芬戈莫德或西尼莫德治疗的患者发生更严重 COVID-19 的风险似乎与普通人群和 COVID-19 多发性硬化症患者报告的风险相似。然而,在解释这些观察结果时,应考虑到自发报告的局限性,尤其是数据缺失。