Courvoisier D S, Alpizar-Rodriguez D, Gottenberg J E, Hernandez M V, Iannone F, Lie E, Santos M J, Pavelka K, Turesson C, Mariette X, Choquette D, Hetland M L, Finckh A
University Hospitals Geneva, Switzerland.
University Hospitals Geneva, Switzerland.
EBioMedicine. 2016 Sep;11:302-306. doi: 10.1016/j.ebiom.2016.08.024. Epub 2016 Aug 18.
Response to disease modifying antirheumatic drugs (DMARDs) in rheumatoid arthritis (RA) is often heterogeneous. We aimed to identify types of disease activity trajectories following the initiation of a new biologic DMARD (bDMARD).
Pooled analysis of nine national registries of patients with diagnosis of RA, who initiated Abatacept and had at least two measures of disease activity (DAS28). We used growth mixture models to identify groups of patients with similar courses of treatment response, and examined these patients' characteristics and effectiveness outcomes.
We identified three types of treatment response trajectories: 'gradual responders' (GR; 3576 patients, 91·7%) had a baseline mean DAS28 of 4·1 and progressive improvement over time; 'rapid responders' (RR; 219 patients, 5·6%) had higher baseline DAS28 and rapid improvement in disease activity; 'inadequate responders' (IR; 103 patients, 2·6%) had high DAS28 at baseline (5·1) and progressive worsening in disease activity. They were similar in baseline characteristics. Drug discontinuation for ineffectiveness was shorter among inadequate responders (p=0.03), and EULAR good or moderate responses at 1year was much higher among 'rapid responders' (p<0.001).
Clinical information and baseline clinical characteristics do not allow a reliable prediction of which trajectory the patients will follow after bDMARD initiation.
类风湿关节炎(RA)患者对改善病情抗风湿药物(DMARDs)的反应通常存在异质性。我们旨在确定开始使用新型生物DMARD(bDMARD)后疾病活动轨迹的类型。
对九个国家注册的诊断为RA且开始使用阿巴西普并至少有两项疾病活动度测量值(DAS28)的患者进行汇总分析。我们使用生长混合模型来识别治疗反应过程相似的患者组,并检查这些患者的特征和疗效结果。
我们确定了三种治疗反应轨迹:“逐渐反应者”(GR;3576例患者,91.7%)基线平均DAS28为4.1,且随时间逐渐改善;“快速反应者”(RR;219例患者,5.6%)基线DAS28较高,疾病活动度快速改善;“反应不足者”(IR;103例患者,2.6%)基线时DAS28较高(5.1),疾病活动度逐渐恶化。他们在基线特征方面相似。反应不足者因无效而停药的时间较短(p = 0.03),“快速反应者”在1年时达到欧洲抗风湿病联盟(EULAR)良好或中等反应的比例要高得多(p < 0.001)。
临床信息和基线临床特征无法可靠预测患者在开始使用bDMARD后会遵循哪种轨迹。