Cyclophosphamide for severe acute forms of central nervous system inflammatory disorders

被引:2
作者
Osen, Allison [1 ]
Stefoski, Dusan [1 ]
Shoemaker, Thomas [1 ]
Kaplan, Tyler [1 ]
Morales, Fabian Sierra [1 ,2 ]
机构
[1] Rush Univ, Dept Neurol, Div Multiple Sclerosis, Med Ctr, 1625 W Harrison St, Chicago, IL 60612 USA
[2] Rush Univ, Multiple Sclerosis Ctr, Dept Neurol Sci, Med Ctr, 1725 W Harrison St, Chicago, IL 60612 USA
关键词
Cyclophosphamide; Multiple sclerosis; Neuroinflammatory disorders; Encephalitis; Vasculitis; MULTIPLE-SCLEROSIS; PLASMA-EXCHANGE; FOLLOW-UP; VASCULITIS;
D O I
10.1016/j.jns.2023.120693
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Cyclophosphamide (CYC) may be an effective treatment in patients who fail first line therapy for severe central nervous system (CNS) inflammatory disorders including CNS vasculitis, neuromyelitis optica, autoimmune encephalitis, tumefactive and aggressive multiple sclerosis (MS). We performed a retrospective analysis of 46 patients treated with CYC after failing first line therapy for severe CNS inflammatory conditions. Primary outcomes included modified Rankin Scale (mRS) for patients classified into a non-MS group, Expanded Disability Status Score (EDSS) for MS patients, and Targeted Neurological Deficit score (TND) for all patients. Secondary outcome included neuroimaging studies following CYC treatment. By the second follow up period (average of 7 months) mRS in the non-MS group improved from 3.7 to 2.2 and EDSS in the MS group improved from 5.6 to 3.8. Average TND score at 7 months was 2.8 (mild-marked improvement). At first follow up (average 5.6 months), 76.2% (32/ 42) patients had either stable or improving imaging, and 83.3% (30/36) patients had stable or improving imaging at second follow up (average 13.6 months). Adverse events were reported by 31.9% of patients with most common being nausea and vomiting, headache, alopecia, and hyponatremia. Treatment with CYC can result in disease stabilization of severe CNS inflammatory diseases and is generally well tolerated.
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