van Rossum M A, Fiselier T J, Franssen M J, Zwinderman A H, ten Cate R, van Suijlekom-Smit L W, van Luijk W H, van Soesbergen R M, Wulffraat N M, Oostveen J C, Kuis W, Dijkstra P F, van Ede C F, Dijkmans B A
Leiden University Hospital, The Netherlands.
Arthritis Rheum. 1998 May;41(5):808-16. doi: 10.1002/1529-0131(199805)41:5<808::AID-ART6>3.0.CO;2-T.
To assess the efficacy, tolerability, and safety of sulfasalazine (SSZ) in the treatment of juvenile chronic arthritis (JCA).
We conducted a 24-week randomized, placebo-controlled, double-blind, multicenter study of patients with active JCA of both oligoarticular and polyarticular onset. Patients were treated with a dosage of 50 mg/kg/day of SSZ (maximum 2,000 mg/day) or placebo. The efficacy variables were joint scores, physician's, parents', and patient's overall assessments, and laboratory parameters of inflammation.
Of the 69 patients enrolled, 52 (75%) completed the trial. Six patients (18%) withdrew from the placebo group, and 11 (31%) withdrew from the SSZ group (P = 0.18). In the intention-to-treat analysis of end point efficacy, between-group differences were significant for the overall articular severity score (P = 0.02), all global assessments (P = 0.01), and the laboratory parameters (P < 0.001). Adverse events occurred more frequently in the SSZ group and were the main reason for withdrawal (P < 0.001), but in all instances, these events were transient or reversible upon cessation of treatment.
The results of this first placebo-controlled study show that SSZ is effective and safe in the treatment of children with oligoarticular- and polyarticular-onset JCA, although it was not well tolerated in one-third of the patients.
评估柳氮磺胺吡啶(SSZ)治疗青少年慢性关节炎(JCA)的疗效、耐受性及安全性。
我们对少关节型和多关节型起病的活动性JCA患者进行了一项为期24周的随机、安慰剂对照、双盲、多中心研究。患者接受50mg/kg/天的SSZ(最大剂量2000mg/天)或安慰剂治疗。疗效变量包括关节评分、医生、家长及患者的总体评估以及炎症实验室参数。
69名入组患者中,52名(75%)完成了试验。6名患者(18%)退出安慰剂组,11名患者(31%)退出SSZ组(P = 0.18)。在意向性分析的终点疗效方面,两组间在总体关节严重程度评分(P = 0.02)、所有总体评估(P = 0.01)及实验室参数(P < 0.001)上差异有统计学意义。不良事件在SSZ组发生更频繁,是退出试验的主要原因(P < 0.001),但在所有情况下,这些事件在停止治疗后均为短暂或可逆的。
这项首个安慰剂对照研究的结果表明,SSZ治疗少关节型和多关节型起病的JCA患儿有效且安全,尽管三分之一的患者耐受性不佳。