Disease modification in rheumatoid arthritis with leflunomide.

P Emery
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引用次数: 9

Abstract

Rheumatoid arthritis (RA) is characterized by chronic inflammation and irreversible destruction of articular cartilage and bone. Disease progression as assessed by radiographic imaging of structural joint damage is a key outcome measure in RA. Joint damage is especially rapid during early phases of RA, thus the current trend of early aggressive therapy with disease-modifying antirheumatic drugs (DMARDs). Radiographic analysis of disease progression with the novel DMARD leflunomide was compared to methotrexate and sulfasalazine in two large, placebo-controlled, randomized Phase III studies (N = 580). The results as indicated by changes in x-ray scores indicate that leflunomide and both active comparators slow disease progression significantly better than placebo (P < or = 0.01). Slowing of disease progression with leflunomide was similar to sulfasalazine at 6 months but better than methotrexate (P < or = 0.049) at 12 months. These data verify the ability of leflunomide to slow disease progression and confirm its disease-modifying potential.

来氟米特治疗类风湿关节炎的疗效。
类风湿性关节炎(RA)的特点是慢性炎症和关节软骨和骨骼的不可逆破坏。通过结构关节损伤的x线影像学评估疾病进展是RA的关键预后指标。关节损伤在类风湿关节炎的早期阶段尤其迅速,因此目前的趋势是早期积极治疗疾病改善抗风湿药物(DMARDs)。在两项大型、安慰剂对照、随机III期研究(N = 580)中,将新型DMARD来氟米特与甲氨蝶呤和柳氮磺胺嘧啶的疾病进展放射学分析进行了比较。x线评分的变化表明,来氟米特和两种活性比较物延缓疾病进展的效果明显优于安慰剂(P <或= 0.01)。来氟米特在6个月时减缓疾病进展的效果与柳氮磺胺嘧啶相似,但在12个月时优于甲氨蝶呤(P < or = 0.049)。这些数据证实了来氟米特减缓疾病进展的能力,并证实了其改善疾病的潜力。
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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