The First Department of Internal Medicine, University of Occupational and Environmental Health, Kitakyushu, Japan.
Department of Orthopedics, Matsubara Mayflower Hospital, Hyogo, Japan.
Mod Rheumatol. 2022 Apr 18;32(3):500-507. doi: 10.1093/mr/roab029.
The objective of this study is to evaluate efficacy and safety of abatacept in biologic-naïve, anti-citrullinated protein antibody (ACPA)-positive Japanese patients with active rheumatoid arthritis (RA) by background methotrexate (MTX) dose.
In this post hoc analysis of a randomized, double-blind, placebo-controlled phase 4 study (NCT01758198), patients received intravenous abatacept (∼10 mg/kg) or placebo both with MTX (≥6 mg/week). Efficacy (Disease Activity Score 28 using C-reactive protein [DAS28 (CRP)] and Health Assessment Questionnaire-Disability Index [HAQ-DI]) was assessed by baseline MTX dosage (≤8 and >8 mg/week) to week 16; safety was assessed by MTX dosage ≤8 and >8 mg/week. Change from baseline in DAS28 (CRP) and HAQ-DI was assessed using longitudinal repeated measures analysis.
Overall, 101 and 102 patients received abatacept + MTX ≤8 and >8 mg/week, while 96 and 106 patients received placebo + MTX ≤8 and >8 mg/week, respectively. Regardless of baseline MTX dose received, mean changes from baseline in DAS28 (CRP) and HAQ-DI in abatacept groups were similar; repeated measures analysis showed similar trends in changes from baseline in DAS28 (CRP) and HAQ-DI. Abatacept safety profile was consistent with previous observations.
Post hoc analysis demonstrated similar efficacy and safety of abatacept in biologic-naïve ACPA-positive Japanese patients with RA regardless of baseline MTX dose.
本研究旨在评估背景甲氨蝶呤(MTX)剂量下,生物初治、抗瓜氨酸化蛋白抗体(ACPA)阳性的日本活动性类风湿关节炎(RA)患者使用阿巴西普的疗效和安全性。
在这项随机、双盲、安慰剂对照的 4 期研究(NCT01758198)的事后分析中,患者接受阿巴西普(约 10mg/kg)或安慰剂联合 MTX(≥6mg/周)治疗。通过基线 MTX 剂量(≤8mg/周和>8mg/周)评估疗效(基于 C 反应蛋白的 28 关节疾病活动度评分[DAS28(CRP)]和健康评估问卷残疾指数[HAQ-DI]),并于第 16 周进行评估;安全性评估根据 MTX 剂量≤8mg/周和>8mg/周进行。采用纵向重复测量分析评估从基线到 DAS28(CRP)和 HAQ-DI 的变化。
总体而言,101 例和 102 例患者接受阿巴西普+MTX≤8mg/周和>8mg/周治疗,96 例和 106 例患者接受安慰剂+MTX≤8mg/周和>8mg/周治疗。无论基线 MTX 剂量如何,阿巴西普组的 DAS28(CRP)和 HAQ-DI 从基线的平均变化相似;重复测量分析显示,DAS28(CRP)和 HAQ-DI 从基线的变化趋势相似。阿巴西普的安全性特征与既往观察结果一致。
事后分析表明,生物初治、ACPA 阳性的日本 RA 患者无论基线 MTX 剂量如何,阿巴西普的疗效和安全性相似。