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Cladribine to treat disease exacerbation after fingolimod discontinuation in progressive multiple sclerosis

机译:克拉屈滨治疗芬戈莫德停药后进行性多发性硬化症加重病情

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摘要

Rebound disease following cessation of disease modifying treatment (DMT) has been reported in people with both relapsing and progressive multiple sclerosis (pwRMS, pwPMS) questioning strict separation between these two phenotypes. While licensed DMT is available for pwRMS to counter rebound disease, no such option exists for pwPMS. We report on a pwPMS who developed rebound disease, with 45 Gadolinium‐enhancing lesions on T1 weighted MRI brain, within 6 months after fingolimod 0.5 mg/day was stopped. Treatment with a short course of subcutaneous cladribine 60 mg led to effective suppression of inflammatory activity and partial recovery with no short‐term safety issues or adverse events.
机译:在患有复发性和进行性多发性硬化症(pwRMS,pwPMS)的人中,有报道称在停止疾病改良治疗(DMT)后反弹的疾病质疑这两种表型之间的严格分离。尽管获得许可的DMT可用于pwRMS来对抗反弹疾病,但pwPMS没有这种选择。我们报道了在停用芬戈莫德0.5 mg /天后的6个月内,pwPMS发生了反弹性疾病,在T1加权MRI大脑上出现了45个Ga增强病灶。短期皮下注射克拉屈滨60 mg治疗可有效抑制炎症活动并部分恢复,没有短期安全性问题或不良事件。

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