Lancet Neurol. 2009 Feb;8(2):158-64. doi: 10.1016/S1474-4422(08)70299-0. Epub 2009 Jan 10.
Chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) responds to treatment with corticosteroids, intravenous immunoglobulin, and plasma exchange. We aimed to test whether the standard immunosuppressive drug methotrexate was of use in treatment of CIDP.
In a pilot, multicentre, randomised, double-blind, controlled trial we compared oral methotrexate 7.5 mg weekly for 4 weeks, then 10 mg weekly for 4 weeks, and finally 15 mg weekly for 32 weeks (40 weeks' total treatment) with placebo in patients with CIDP requiring intravenous immunoglobulin or corticosteroids. After about 16 weeks, the dose of corticosteroids or intravenous immunoglobulin was decreased by 20% every 4 weeks if participants did not deteriorate. Primary outcome was a greater than 20% reduction in mean weekly dose in the last 4 weeks of the trial compared with the first 4 weeks. Secondary outcomes analysed separately at the mid-trial and final visits measured activity limitations and strength. Analyses were done by intention to treat. This study is registered as an International Standard Randomised Controlled Trial, number ISRCTN73774524.
59 of the 60 enrolled participants completed the trial. 14 (52%) of 27 taking methotrexate and 14 (44%) of 32 taking placebo had a greater than 20% reduction in mean weekly dose of corticosteroids or intravenous immunoglobulin (adjusted odds ratio 1.21, 95% CI 0.40-3.70). There were no clinically and statistically significant differences in secondary outcomes. The one serious adverse event in the placebo group and the three in the methotrexate group were not thought to be related to treatment.
Oral methotrexate 15 mg weekly showed no significant benefit, but limitations in the trial design and the high rate of response in the placebo group meant that a treatment effect could not be excluded. This study can inform design of future trials in CIDP.
The GBS/CIDP Foundation International.
慢性炎性脱髓鞘性多发性神经根神经病(CIDP)对皮质类固醇、静脉注射免疫球蛋白及血浆置换治疗有效。我们旨在测试标准免疫抑制药物甲氨蝶呤是否可用于CIDP的治疗。
在一项先导性、多中心、随机、双盲、对照试验中,我们将需要静脉注射免疫球蛋白或皮质类固醇的CIDP患者分为两组,一组每周口服甲氨蝶呤7.5毫克,共4周,然后每周10毫克,共4周,最后每周15毫克,共32周(总计治疗40周),另一组服用安慰剂。约16周后,如果参与者病情未恶化,皮质类固醇或静脉注射免疫球蛋白的剂量每4周减少20%。主要结局是与试验前4周相比,试验最后4周平均每周剂量降低超过20%。在试验中期和最终访视时分别分析的次要结局指标为活动受限情况和肌力。分析采用意向性分析。本研究已注册为国际标准随机对照试验,注册号为ISRCTN73774524。
60名入组参与者中有59名完成了试验。服用甲氨蝶呤的27名参与者中有14名(52%),服用安慰剂的32名参与者中有14名(44%)皮质类固醇或静脉注射免疫球蛋白的平均每周剂量降低超过20%(校正比值比1.21,95%可信区间0.40 - 3.70)。次要结局在临床和统计学上均无显著差异。安慰剂组的1例严重不良事件和甲氨蝶呤组的3例严重不良事件被认为与治疗无关。
每周口服15毫克甲氨蝶呤未显示出显著益处,但试验设计的局限性以及安慰剂组的高缓解率意味着不能排除治疗效果。本研究可为未来CIDP试验的设计提供参考。
国际格林巴利综合征/慢性炎性脱髓鞘性多发性神经根神经病基金会。