Department of Rare Diseases Research, Institute of Medical Science, St. Marianna University School of Medicine, Kawasaki 216-8512, Japan.
Division of Neurology, Department of Internal Medicine, St. Marianna University School of Medicine, Kawasaki 216-8511, Japan.
Viruses. 2022 Jan 12;14(1):136. doi: 10.3390/v14010136.
Corticosteroids are most commonly used to treat HTLV-1-associated myelopathy (HAM); however, their clinical efficacy has not been tested in randomized clinical trials. This randomized controlled trial included 8 and 30 HAM patients with rapidly and slowly progressing walking disabilities, respectively. Rapid progressors were assigned (1:1) to receive or not receive a 3-day course of intravenous methylprednisolone in addition to oral prednisolone therapy. Meanwhile, slow progressors were assigned (1:1) to receive oral prednisolone or placebo. The primary outcomes were a composite of ≥1-grade improvement in the Osame Motor Disability Score or ≥30% improvement in the 10 m walking time (10 mWT) at week 2 for rapid progressors and changes from baseline in 10 mWT at week 24 for slow progressors. In the rapid progressor trial, all four patients with but only one of four without intravenous methylprednisolone achieved the primary outcome ( = 0.14). In the slow progressor trial, the median changes in 10 mWT were -13.8% (95% CI: -20.1--7.1; < 0.001) and -6.0% (95% CI: -12.8-1.3; = 0.10) with prednisolone and placebo, respectively ( for between-group difference = 0.12). Whereas statistical significance was not reached for the primary endpoints, the overall data indicated the benefit of corticosteroid therapy. (Registration number: UMIN000023798, UMIN000024085).
皮质类固醇最常用于治疗 HTLV-1 相关脊髓病(HAM);然而,它们的临床疗效尚未在随机临床试验中得到检验。这项随机对照试验纳入了分别具有快速和缓慢进展性步行障碍的 8 名和 30 名 HAM 患者。快速进展者按 1:1 被分配接受或不接受 3 天的静脉甲基强的松龙治疗,同时加用口服泼尼松龙治疗。而缓慢进展者按 1:1 被分配接受口服泼尼松龙或安慰剂。主要结局是在第 2 周时,快速进展者的 Osame 运动功能障碍评分至少改善 1 级或 10 米步行时间(10 mWT)至少改善 30%,以及在第 24 周时缓慢进展者的 10 mWT 从基线的变化。在快速进展者试验中,所有 4 名接受静脉甲基强的松龙治疗的患者均达到了主要结局,而仅 4 名未接受静脉甲基强的松龙治疗的患者中有 1 名达到了主要结局( = 0.14)。在缓慢进展者试验中,泼尼松龙和安慰剂组的 10 mWT 中位数变化分别为-13.8%(95%CI:-20.1--7.1; < 0.001)和-6.0%(95%CI:-12.8-1.3; = 0.10)( = 0.12)。尽管主要终点未达到统计学意义,但总体数据表明皮质类固醇治疗有益。(注册号:UMIN000023798,UMIN000024085)。