Fraser A D, van Kuijk A W R, Westhovens R, Karim Z, Wakefield R, Gerards A H, Landewé R, Steinfeld S D, Emery P, Dijkmans B A C, Veale D J
Rheumatology and Rehabilitation Research Unit, Old Nurses Home, Great Georges Street, Leeds, West Yorkshire LS1 3EX, UK.
Ann Rheum Dis. 2005 Jun;64(6):859-64. doi: 10.1136/ard.2004.024463. Epub 2004 Nov 4.
To evaluate the safety and efficacy of adding ciclosporin A (CSA) to the treatment of patients with psoriatic arthritis (PsA) demonstrating an incomplete response to methotrexate (MTX) monotherapy.
In a 12 month, randomised, double blind, placebo controlled trial at five centres in three countries, 72 patients with active PsA with an incomplete response to MTX were randomised to receive either CSA (n = 38) or placebo (n = 34). Patients underwent full clinical and radiological assessment and, in addition, high resolution ultrasound (HRUS) was performed at one centre. An intention to treat (last observation carried forward) analysis was employed.
Some significant improvements were noted at 12 months in both groups. However, in the active but not the placebo arm there were significant improvements in swollen joint count, mean (SD), from 11.7 (9.7) to 6.7 (6.5) (p<0.001) and C reactive protein, from 17.4 (14.5) to 12.7 (14.3) mg/l (p<0.05) as compared with baseline. The Psoriasis Area and Severity Index (PASI) score improved in the active group (2 (2.3) to 0.8 (1.3)) as compared with placebo (2.2 (2.7) to 1.9 (2.8)), p<0.001, and synovitis detected by HRUS (33 patients, 285 joints) was reduced by 33% in the active group compared with 6% in the placebo group (p<0.05). No improvement in Health Assessment Questionnaire or pain scores was detected.
Synovitis detected by HRUS was significantly reduced. Combining CSA and MTX treatment in patients with active PsA, and a partial response to MTX, significantly improves the signs of inflammation but not pain or quality of life.
评估在对甲氨蝶呤(MTX)单药治疗反应不完全的银屑病关节炎(PsA)患者的治疗中添加环孢素A(CSA)的安全性和有效性。
在三个国家五个中心进行的一项为期12个月的随机、双盲、安慰剂对照试验中,72例对MTX反应不完全的活动性PsA患者被随机分为接受CSA组(n = 38)或安慰剂组(n = 34)。患者接受了全面的临床和放射学评估,此外,在一个中心进行了高分辨率超声(HRUS)检查。采用意向性治疗(末次观察结转)分析。
两组在12个月时均有一些显著改善。然而,与基线相比,在活性药物组而非安慰剂组中,肿胀关节计数均值(标准差)从11.7(9.7)显著改善至6.7(6.5)(p<0.001),C反应蛋白从17.4(14.5)降至12.7(14.3)mg/l(p<0.05)。与安慰剂组(2.2(2.7)至1.9(2.8))相比,活性药物组的银屑病面积和严重程度指数(PASI)评分有所改善(从2(2.3)至0.8(1.3)),p<0.001,且活性药物组通过HRUS检测到的滑膜炎(33例患者,285个关节)减少了33%,而安慰剂组减少了6%(p<0.05)。未检测到健康评估问卷或疼痛评分的改善。
HRUS检测到的滑膜炎显著减少。在活动性PsA且对MTX有部分反应的患者中联合使用CSA和MTX治疗可显著改善炎症体征,但不能改善疼痛或生活质量。