Murakami Kosaku, Sekiguchi Masahiro, Hirata Shintaro, Fujii Takao, Matsui Kiyoshi, Morita Satoshi, Ohmura Koichiro, Kawahito Yutaka, Nishimoto Norihiro, Mimori Tsuneyo, Sano Hajime
a Department of Rheumatology and Clinical Immunology, Graduate School of Medicine , Kyoto University , Kyoto , Japan.
b Department of Internal Medicine, Division of Rheumatology, Hyogo College of Medicine , Nishinomiya , Japan.
Mod Rheumatol. 2019 May;29(3):406-412. doi: 10.1080/14397595.2018.1482609. Epub 2018 Jun 27.
To investigate the effect of abatacept (ABA) on preventing joint destruction in biological disease-modifying anti-rheumatic drug (bDMARD)-naïve rheumatoid arthritis (RA) patients in real-world clinical practice.
RA patients were collected from the ABROAD (ABatacept Research Outcomes as a First-line Biological Agent in the Real WorlD) study cohort. They had moderate or high disease activity and were treated with ABA as a first-line bDMARD. Radiographic change between baseline and 1 year after ABA treatment was assessed with the van der Heijde's modified Total Sharp Score (mTSS). Predictive factors for structural remission (St-REM), defined as ΔmTSS ≤0.5/year, were determined.
Among 118 patients, 81 (67.5%) achieved St-REM. Disease duration <3 years (odds ratio (OR) = 3.152, p = .007) and slower radiographic progression (shown as 'baseline mTSS/year <3', OR = 3.727, p = .004) were independently significant baseline predictive factors for St-REM irrespective of age and sex. St-REM prevalence increased significantly if clinical remission based on the Simplified Disease Activity Index was achieved at least once until 24 weeks after ABA treatment.
Shorter disease duration, smaller radiographic progression at baseline, and rapid clinical response were predictive factors for sustained St-REM after ABA therapy in bDMARD-naïve RA patients.
在真实世界临床实践中,研究阿巴西普(ABA)对初治生物改善病情抗风湿药(bDMARD)的类风湿关节炎(RA)患者预防关节破坏的效果。
从ABROAD(阿巴西普作为一线生物制剂在真实世界中的研究结果)研究队列中收集RA患者。他们具有中度或高度疾病活动度,并接受ABA作为一线bDMARD治疗。使用范德海伊德改良总 Sharp 评分(mTSS)评估ABA治疗基线至治疗1年后的影像学变化。确定结构缓解(St-REM,定义为ΔmTSS≤0.5/年)的预测因素。
118例患者中,81例(67.5%)实现了St-REM。疾病病程<3年(比值比(OR)=3.152,p=0.007)和影像学进展较慢(表现为“基线mTSS/年<3”,OR=3.727,p=0.004)是St-REM独立且显著的基线预测因素,与年龄和性别无关。如果在ABA治疗后24周内至少有一次基于简化疾病活动指数的临床缓解,则St-REM患病率显著增加。
较短的疾病病程、基线时较小的影像学进展以及快速的临床反应是初治bDMARD的RA患者接受ABA治疗后持续实现St-REM的预测因素。