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Effects of the oral Janus kinase inhibitor tofacitinib on patient-reported outcomes in patients with active rheumatoid arthritis: results of two Phase 2 randomised controlled trials

机译:口服Janus激酶抑制剂tofacitinib对活动性类风湿关节炎患者报告的结局的影响:两项2期随机对照试验的结果

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OBJECTIVES: Tofacitinib is an oral Janus kinase inhibitor for the treatment of rheumatoid arthritis (RA). Here we investigated the effects of tofacitinib on patient-reported outcomes (PRO) in patients with active RA. METHODS: Two, 6-month, double-blind, placebo-controlled Phase 2b studies were performed. The combination study evaluated patients with inadequate response to methotrexate who received tofacitinib 1-15 mg twice daily (BID), 20 mg once daily or placebo, on background methotrexate. In the monotherapy study, patients with inadequate response to disease-modifying anti-rheumatic drugs received tofacitinib 1-15 mg BID, adalimumab 40 mg once every other week or placebo. PROs measured were: Patienta€?s Assessment of Arthritis Pain (PAAP), Patienta€?s Assessment of Disease Activity, HAQ-DI, FACIT-F and SF-36. RESULTS: In the combination study (n=507), significant improvements (p
机译:目的:Tofacitinib是口服类Janus激酶抑制剂,用于治疗类风湿关节炎(RA)。在这里,我们调查了托法替尼对活动性RA患者的患者报告结局(PRO)的影响。方法:进行了两个为期六个月,双盲,安慰剂对照的2b期研究。联合研究评估了对甲氨蝶呤反应不充分的患者,他们在背景甲氨蝶呤上接受托法替尼每天两次1-15 mg(BID),每天一次20 mg或安慰剂一次。在单药治疗研究中,对改变疾病的抗风湿药反应不足的患者每两周一次接受托法替尼1-15 mg BID,阿达木单抗40 mg或安慰剂。所测量的PRO是:病人对关节炎疼痛的评估(PAAP),病人对疾病活动性的评估,HAQ-DI,FACIT-F和SF-36。结果:在组合研究中(n = 507),显着改善(p

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