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静脉注射环磷酰胺对视神经脊髓炎谱系障碍相关视神经炎急性期皮质类固醇难治性患者的治疗效果

Remedial Effect of Intravenous Cyclophosphamide in Corticosteroid-Refractory Patients in the Acute Phase of Neuromyelitis Optica Spectrum Disorder-Related Optic Neuritis.

作者信息

Wang Ling, Liu Kaiqun, Tan Xiao, Zhou Lin, Zhang Yuxin, Liu Xiaoning, Fu Yue, Qiu Wei, Yang Hui

机构信息

State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou, China.

Department of Neurology, Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.

出版信息

Front Neurol. 2021 Jan 15;11:612097. doi: 10.3389/fneur.2020.612097. eCollection 2020.

Abstract

To investigate the remedial efficacy and safety of intravenous cyclophosphamide (CP) in the acute phase in patients with neuromyelitis optica spectrum disorder-related optic neuritis (NMOSD-ON) who are refractory to intravenous methylprednisolone (MP) treatment. This study was a single-center, retrospective, observational case-control cohort study. Thirty-six patients who had acute NMOSD-ON attacks and were refractory to MP treatment were included. Patents were divided into two groups: the remedial CP group, and the MP group. The best-corrected visual acuity (BCVA), mean deviation (MD) of the visual field (VF), visual evoked potential amplitude (VEP-A), visual evoked potential latency (VEP-T), and average thickness of the retinal nerve fiber layer (RNFL) at onset, 1 month (m), 3 m, and 6 m after the attack were analyzed. Routine blood test results, liver and kidney function, routine urinalysis results and general condition were analyzed for safety issues at each follow-up. Fisher's exact test, the Mann-Whitney U test, the Kruskal-Wallis test and the Wilcoxon rank-sum test were used for statistical analysis. The remedial CP group showed significant improvement over 6 m with regard to BCVA and MD ( < 0.05),whereas MP group only showed significant improvement in MD ( < 0.05). Regarding remedial CP intervention time window, the CP ≤ 30 days group showed significant improvement over 6 m with regard to BCVA ( = 0.002), MD ( = 0.003), and VEP-A ( = 0.036), while those CP > 30 days group did not. Both two subgroups showed significantly RNFL thickness reduction, however, BCVA, MD, VEP-A, VEP-T, and RNFL thickness showed no significant differences between the two subgroups at any follow-up point ( > 0.05). CP within 30 days of attack onset is safe and might have a beneficial degree of therapeutic efficacy for acute-phase treatment of NMOSD-ON that is refractory to MP treatment alone.

摘要

探讨静脉注射环磷酰胺(CP)对甲基强的松龙(MP)治疗无效的视神经脊髓炎谱系障碍相关性视神经炎(NMOSD-ON)急性期患者的补救疗效及安全性。本研究为单中心、回顾性、观察性病例对照队列研究。纳入36例急性NMOSD-ON发作且对MP治疗无效的患者。将患者分为两组:CP补救治疗组和MP组。分析发作时、发作后1个月、3个月和6个月的最佳矫正视力(BCVA)、视野平均偏差(MD)、视觉诱发电位振幅(VEP-A)、视觉诱发电位潜伏期(VEP-T)以及视网膜神经纤维层(RNFL)平均厚度。每次随访时分析血常规结果、肝肾功能、尿常规结果及一般状况以评估安全性问题。采用Fisher精确检验、Mann-Whitney U检验、Kruskal-Wallis检验和Wilcoxon秩和检验进行统计分析。CP补救治疗组在6个月时BCVA和MD有显著改善(P<0.05),而MP组仅MD有显著改善(P<0.05)。关于CP补救干预时间窗,CP≤30天组在6个月时BCVA(P=0.002)、MD(P=0.003)和VEP-A(P=0.036)有显著改善,而CP>30天组无改善。两个亚组RNFL厚度均显著降低,然而,在任何随访时间点,两个亚组的BCVA、MD、VEP-A、VEP-T和RNFL厚度均无显著差异(P>0.05)。发作后30天内使用CP是安全的,对于单独使用MP治疗无效的NMOSD-ON急性期治疗可能具有有益的治疗效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d37/7874161/13d045e37af6/fneur-11-612097-g0001.jpg

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