Concomitant prednisone may alleviate methotrexate side-effects in rheumatoid arthritis patients.

IF 2.1 Q3 RHEUMATOLOGY
Matthijs S van der Leeuw, Janneke Tekstra, Jacob M van Laar, Paco M J Welsing
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引用次数: 0

Abstract

Objectives: To evaluate whether addition of low-moderate dose prednisone to methotrexate (MTX) treatment can alleviate common MTX side-effects in rheumatoid arthritis (RA) patients.

Methods: We performed a post-hoc analysis of the CAMERA-II trial which randomized (1:1) 236 early DMARD and prednisone naive RA patients to treatment with MTX + prednisone 10 mg daily, or MTX monotherapy during two years. MTX dose was increased using a treat-to-target approach. We used Generalized Estimating Equations to model the occurrence of common MTX side-effects and of any adverse event over time, controlling for disease activity and MTX dose over time and other possible predictors of adverse events. To assess whether a possible effect was prednisone-specific, we performed the same analysis in the U-ACT-EARLY trial, in which the addition of tocilizumab (TCZ) to MTX was compared to MTX monotherapy in a comparable setting.

Results: MTX side-effects were reported at 5.9% of visits in the prednisone-MTX group, compared to 11.2% in the MTX monotherapy group. After controlling for MTX dose and disease activity over time, treatment duration, age, sex, and baseline transaminase levels, addition of prednisone significantly decreased the occurrence of MTX side-effects (OR: 0.54, CI: 0.38-0.77, p = 0.001). Specifically, the occurrence of nausea (OR 0.46, CI: 0.26-0.83,  p = 0.009)) and elevated ALT/AST (OR 0.29, CI: 0.17-0.49, p  < 0.001) was decreased. There was a trend towards fewer overall adverse events in the prednisone-MTX arm (OR: 0.89, CI: 0.72-1.11, p = 0.30). No difference in MTX side-effects was found between TCZ-MTX and MTX monotherapy in U-ACT-EARLY (OR 1.05, CI: 0.61-1.80, p  = 0.87).

Conclusion: Addition of 10 mg prednisone daily to MTX treatment in RA patients may ameliorate MTX side-effects, specifically nausea and elevated ALT/AST.

强的松合用可减轻类风湿关节炎患者甲氨蝶呤的副作用。
目的:评价在甲氨蝶呤(MTX)治疗中加入中低剂量强的松是否能减轻类风湿性关节炎(RA)患者常见的MTX副作用。方法:我们对CAMERA-II试验进行了事后分析,该试验随机(1:1)236例早期DMARD和强的松未发作的RA患者在两年内接受MTX +强的松10mg每日治疗或MTX单药治疗。使用从治疗到目标的方法增加MTX剂量。我们使用广义估计方程来模拟常见MTX副作用和任何不良事件随时间的发生,控制疾病活动性和MTX剂量随时间的变化以及其他可能的不良事件预测因子。为了评估是否可能产生强的松特异性的影响,我们在U-ACT-EARLY试验中进行了相同的分析,其中将tocilizumab (TCZ)加入MTX与在可比环境下的MTX单药治疗进行比较。结果:在强的松-MTX组中,5.9%的患者报告了MTX的副作用,而在MTX单药治疗组中,这一比例为11.2%。在控制MTX剂量和疾病活动性随时间、治疗持续时间、年龄、性别和基线转氨酶水平后,泼尼松的加入显著降低了MTX副作用的发生(OR: 0.54, CI: 0.38-0.77, p = 0.001)。特别是,恶心(OR 0.46, CI: 0.26-0.83, p = 0.009)和ALT/AST升高(OR 0.29, CI: 0.17-0.49, p)的发生。结论:RA患者在MTX治疗中每天添加10mg强的松可以改善MTX的副作用,特别是恶心和ALT/AST升高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMC Rheumatology
BMC Rheumatology Medicine-Rheumatology
CiteScore
3.80
自引率
0.00%
发文量
73
审稿时长
15 weeks
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