Pfizer Inc, Ann Arbor, Michigan, USA.
Ann Rheum Dis. 2010 Feb;69(2):413-6. doi: 10.1136/ard.2009.108159. Epub 2009 Jul 8.
To determine the efficacy of CP-690,550 in improving pain, function and health status in patients with moderate to severe active rheumatoid arthritis (RA) and an inadequate response to methotrexate or a tumour necrosis factor alpha inhibitor.
Patients were randomised equally to placebo, CP-690,550 5, 15 or 30 mg twice daily for 6 weeks, with 6 weeks' follow-up. The patient's assessment of arthritis pain (pain), patient's assessment of disease activity, Health Assessment Questionnaire-Disability Index (HAQ-DI) and Short Form-36 (SF-36) were recorded.
At week 6, significantly more patients in the CP-690,550 5, 15 and 30 mg twice-daily groups experienced a 50% improvement in pain compared with placebo (44%, 66%, 78% and 14%, respectively), clinically meaningful reductions in HAQ-DI (> or =0.3 units) (57%, 75%, 76% and 36%, respectively) and clinically meaningful improvements in SF-36 domains and physical and mental components.
CP-690,550 was efficacious in improving the pain, function and health status of patients with RA, from week 1 to week 6.
评估 CP-690,550 改善中度至重度活动性类风湿关节炎(RA)患者疼痛、功能和健康状况的疗效,这些患者对甲氨蝶呤或肿瘤坏死因子α抑制剂反应不足。
患者被随机均分为安慰剂组、CP-690,550 5mg、15mg 或 30mg 每日 2 次组,共治疗 6 周,随后随访 6 周。记录患者关节炎疼痛评估(疼痛)、患者疾病活动评估、健康评估问卷残疾指数(HAQ-DI)和健康调查简表 36(SF-36)。
第 6 周时,CP-690,550 5mg、15mg 和 30mg 每日 2 次组中,与安慰剂组相比,更多患者疼痛改善达 50%(分别为 44%、66%、78%和 14%),HAQ-DI 显著降低(≥0.3 单位)(分别为 57%、75%、76%和 36%),SF-36 各领域以及躯体和精神成分评分显著改善。
CP-690,550 能有效改善 RA 患者的疼痛、功能和健康状况,从第 1 周到第 6 周均如此。