van Dooren-Greebe R J, Kuijpers A L, Termorshuizen F, van de Kerkhof P C
Department of Dermatology, University Hospital Nijmegen, The Netherlands.
Acta Derm Venereol. 1995 Sep;75(5):393-6. doi: 10.2340/0001555575393396.
The effects of interval treatment were evaluated in 10 psoriatic patients on long-term treatment with low-dose oral methotrexate (MTX). In all patients, the dosage of MTX had already been tapered off as much as possible. After interruption of MTX treatment, the clinical course and changes in laboratory parameters were evaluated. The mean MTX-free period was 17 weeks, and the mean reduction in cumulative MTX dose was 76 mg (p = 0.05). However, only 3 patients preferred interval treatment to a continuous schedule. During the first 3 weeks of discontinuation, a significant decrease in the serum transaminases was observed, indicating a direct toxic influence of MTX on the liver parenchym. We conclude that interruption of long-term MTX treatment leads to a substantial reduction of the cumulative MTX dose and reduces the hepatotoxic load of MTX. It is necessary to motivate patients on long-term MTX treatment for regular treatment interruptions to establish a further reduction in their cumulative MTX dose.
对10例接受低剂量口服甲氨蝶呤(MTX)长期治疗的银屑病患者进行了间歇治疗效果评估。所有患者的MTX剂量已尽可能逐渐减少。在中断MTX治疗后,评估临床病程和实验室参数变化。无MTX的平均疗程为17周,累积MTX剂量平均减少76mg(p = 0.05)。然而,只有3例患者更喜欢间歇治疗而非持续治疗方案。在停药的前3周,观察到血清转氨酶显著下降,表明MTX对肝实质有直接毒性影响。我们得出结论,长期MTX治疗的中断导致累积MTX剂量大幅减少,并降低了MTX的肝毒性负荷。有必要鼓励接受长期MTX治疗的患者定期中断治疗,以进一步减少其累积MTX剂量。