van Dongen Henrike, van Aken Jill, Lard Leroy R, Visser Karen, Ronday H Karel, Hulsmans Harry M J, Speyer Irene, Westedt Marie-Louise, Peeters André J, Allaart Cornelia F, Toes René E M, Breedveld Ferdinand C, Huizinga Tom W J
Leiden University Medical Center, Leiden, The Netherlands.
Arthritis Rheum. 2007 May;56(5):1424-32. doi: 10.1002/art.22525.
To determine whether patients with undifferentiated arthritis (UA; inflammatory, nontraumatic arthritis that cannot be diagnosed using current classification criteria) benefit from treatment with methotrexate (MTX).
The PRObable rheumatoid arthritis: Methotrexate versus Placebo Treatment (PROMPT) study was a double-blind, placebo-controlled, randomized, multicenter trial involving 110 patients with UA who fulfilled the American College of Rheumatology (ACR) 1958 criteria for probable RA. Treatment started with MTX (15 mg/week) or placebo tablets, and every 3 months the dosage was increased if the Disease Activity Score was >2.4. After 12 months, the study medication was tapered and discontinued. Patients were followed up for 30 months. When a patient fulfilled the ACR criteria for RA (primary end point), the study medication was changed to MTX. Joint damage was scored on radiographs of the hands and feet.
In 22 of the 55 patients (40%) in the MTX group, UA progressed to RA compared with 29 of 55 patients (53%) in the placebo group. However, in the MTX group, patients fulfilled the ACR criteria for RA at a later time point than in the placebo group (P = 0.04), and fewer patients showed radiographic progression over 18 months (P = 0.046).
This study provides evidence for the efficacy of MTX treatment in postponing the diagnosis of RA, as defined by the ACR 1987 criteria, and retarding radiographic joint damage in UA patients.
确定未分化关节炎(UA;炎症性、非创伤性关节炎,无法使用当前分类标准进行诊断)患者是否能从甲氨蝶呤(MTX)治疗中获益。
“可能的类风湿关节炎:甲氨蝶呤与安慰剂治疗(PROMPT)”研究是一项双盲、安慰剂对照、随机、多中心试验,纳入了110例符合美国风湿病学会(ACR)1958年可能类风湿关节炎标准的UA患者。治疗起始采用MTX(15毫克/周)或安慰剂片,若疾病活动评分>2.4,则每3个月增加剂量。12个月后,逐渐减少并停用研究药物。对患者进行30个月的随访。当患者符合ACR类风湿关节炎标准(主要终点)时,将研究药物换为MTX。对手部和足部X线片的关节损伤进行评分。
MTX组55例患者中有22例(40%)UA进展为类风湿关节炎,而安慰剂组55例患者中有29例(53%)。然而,MTX组患者达到ACR类风湿关节炎标准的时间点晚于安慰剂组(P = 0.04),且在18个月内显示影像学进展的患者较少(P = 0.046)。
本研究为MTX治疗在推迟ACR 1987标准定义的类风湿关节炎诊断以及延缓UA患者影像学关节损伤方面的疗效提供了证据。