Wang Ling, Liu Kaiqun, Tan Xiao, Zhou Lin, Zhang Yuxin, Liu Xiaoning, Fu Yue, Qiu Wei, Yang Hui
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.
Front Neurol. 2021 Jan 15;11:612097. doi: 10.3389/fneur.2020.612097. eCollection 2020.
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.
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。