医学
重症肌无力
养生
血浆置换术
倾向得分匹配
泼尼松龙
甲基强的松龙
内科学
钙调神经磷酸酶
对数秩检验
生存分析
免疫学
抗体
移植
作者
Akiyuki Uzawa,Shigeaki Suzuki,Satoshi Kuwabara,Hiroyuki Akamine,Yosuke Onishi,Manato Yasuda,Yukiko Ozawa,Naoki Kawaguchi,Tomoya Kubota,Masanori Takahashi,Yasushi Suzuki,Genya Watanabe,Takashi Kimura,Takamichi Sugimoto,Makoto Samukawa,Naoya Minami,Masayuki Masuda,Shingo Konno,Yuriko Nagane,Kimiaki Utsugisawa
标识
DOI:10.1136/jnnp-2022-330519
摘要
Early fast-acting treatment (EFT) is the aggressive use of fast-acting therapies such as plasmapheresis, intravenous immunoglobulin and/or intravenous high-dose methylprednisolone (IVMP) from the early phases of treatment. EFT is reportedly beneficial for early achievement of minimal manifestations (MM) or better status with ≤5 mg/day prednisolone (MM5mg), a practical therapeutic target for myasthenia gravis (MG).The current study aimed to clarify which specific EFT regimen is efficacious and the patient characteristics that confer sensitivity to EFT.We recruited a total of 1710 consecutive patients with MG who enrolled in the Japan MG Registry for this large-cohort study. Among them, 1066 with generalised MG who had received immunotherapy were analysed. Prognostic background factors were matched in a 1:1 ratio using propensity score matching analysis between patients treated with EFT (n=350) and those treated without EFT (n=350). The clinical course and time to first achieve MM5mg after starting immunotherapy was analysed in relation to treatment combinations and patient characteristics.Kaplan-Meier analyses showed that EFT had a significant effect on the achievement of MM5mg (p<0.0001, log-rank test; HR 1.82, p<0.0001). Notably, EFT was efficacious for any type of MG, and the inclusion of IVMP resulted in earlier and more frequent achievement of MM5mg (p=0.0352, log-rank test; HR 1.46, p=0.0380). In addition, early administration of calcineurin inhibitors also promoted MM5mg achievement.Early cycles of intervention with EFT and early use of calcineurin inhibitors provides long-term benefits in terms of achieving therapeutic targets for generalised MG, regardless of clinical subtype.
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