Stanford University Medical Center, Palo Alto, California, USA.
Leiden University Medical Centre, Leiden, The Netherlands.
RMD Open. 2019 Aug 1;5(2):e000887. doi: 10.1136/rmdopen-2018-000887. eCollection 2019.
In MOBILITY (NCT01061736), sarilumab significantly reduced disease activity, improved physical function and inhibited radiographic progression at week 52 versus placebo in patients with rheumatoid arthritis (RA) and an inadequate response to methotrexate. We report 5-year safety, efficacy and radiographic outcomes of sarilumab from NCT01061736 and the open-label extension (EXTEND; NCT01146652), in which patients received sarilumab 200 mg every 2 weeks (q2w) + methotrexate.
Patients (n=1197) with moderately to severely active RA were initially randomised to placebo, sarilumab 150 mg or sarilumab 200 mg subcutaneously q2w plus weekly methotrexate for 52 weeks. Completers were eligible to enrol in the open-label extension and receive sarilumab 200 mg q2w + methotrexate.
Overall, 901 patients entered the open-label extension. The safety profile remained stable over 5-year follow-up and consistent with interleukin-6 receptor blockade. Absolute neutrophil count <1000 cells/mm was observed but not associated with increased infection rate. Initial treatment with sarilumab 200 mg + methotrexate was associated with reduced radiographic progression over 5 years versus sarilumab 150 mg + methotrexate or placebo + methotrexate (mean±SE change from baseline in van der Heijde-modified Total Sharp Score: 1.46±0.27, 2.35±0.28 and 3.68±0.27, respectively (p<0.001 for each sarilumab dose versus placebo)). Clinical efficacy was sustained through 5 years according to Disease Activity Score (28-joint count) using C reactive protein, Clinical Disease Activity Index (CDAI) and Health Assessment Questionnaire-Disability Index. The number of patients achieving CDAI ≤2.8 at 5 years was similar among initial randomisation groups (placebo, 76/398 (19%); sarilumab 150 mg, 68/400 (17%); sarilumab 200 mg, 84/399 (21%)).
Clinical efficacy, including inhibition of radiographic progression, reduction in disease activity and improvement in physical function, was sustained with sarilumab + methotrexate over 5 years. Safety appeared stable over the 5-year period.
在 MOBILITY(NCT01061736)中,与安慰剂相比,在对甲氨蝶呤应答不足的类风湿关节炎(RA)患者中,sarilumab 显著降低疾病活动度,改善身体功能并抑制影像学进展,在第 52 周。我们报告了来自 NCT01061736 和开放标签扩展(EXTEND;NCT01146652)的 sarilumab 的 5 年安全性、疗效和影像学结果,其中患者接受了 sarilumab 200mg 每 2 周(q2w)+甲氨蝶呤。
最初有 1197 名中度至重度活跃性 RA 患者被随机分配至安慰剂、sarilumab 150mg 或 sarilumab 200mg 皮下注射 q2w 加每周甲氨蝶呤治疗 52 周。完成者有资格参加开放标签扩展并接受 sarilumab 200mg q2w+甲氨蝶呤。
总体而言,有 901 名患者进入了开放标签扩展。5 年随访期间安全性状况保持稳定,与白细胞介素-6 受体阻滞剂一致。观察到绝对中性粒细胞计数<1000 个/毫米,但与感染率增加无关。与 sarilumab 150mg+甲氨蝶呤或安慰剂+甲氨蝶呤相比,初始接受 sarilumab 200mg+甲氨蝶呤治疗与 5 年内降低影像学进展相关(van der Heijde 改良总 Sharp 评分的基线变化平均值±SE:1.46±0.27、2.35±0.28 和 3.68±0.27,分别为(p<0.001 对于每个 sarilumab 剂量与安慰剂))。根据 C 反应蛋白、临床疾病活动指数(CDAI)和健康评估问卷残疾指数,5 年内疾病活动评分(28 关节计数)持续显示临床疗效。5 年内达到 CDAI≤2.8 的患者比例在初始随机分组中相似(安慰剂,76/398(19%);sarilumab 150mg,68/400(17%);sarilumab 200mg,84/399(21%))。
在 5 年期间,sarilumab+甲氨蝶呤的临床疗效,包括抑制影像学进展、降低疾病活动度和改善身体功能,持续存在。安全性在 5 年期间似乎稳定。