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Survival and effectiveness of leflunomide compared with methotrexate and sulfasalazine in rheumatoid arthritis: a matched observational study

机译:来氟米特与甲氨蝶呤和柳氮磺胺吡啶在类风湿关节炎中的存活率和有效性:一项匹配的观察性研究

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摘要

>Objective: To determine the survival and clinical effectiveness of leflunomide (LEF) compared with methotrexate (MTX) and sulfasalazine (SSZ) for RA in an observational study. >Methods: An observational database of 1088 patients and 5141 patient years of DMARD treatment (2680 courses) from two academic hospitals was filtered for treatment with LEF, MTX, and SSZ. LEF treatment groups were matched for patients' age, baseline ESR, number of previous DMARDs, and hospital cohort with MTX and SSZ treatment groups. For these treatments, Kaplan-Meier analyses of time until the drug was discontinued (drug "survival"), and the effectiveness and safety of continuation of treatment, were performed. The change in disease activity markers (CRP, ESR) was compared between the groups. >Results: The median dose during the study increased from 10 to 15 mg MTX/week and from 1.5 to 2.0 g SSZ/day. Matched survival analysis showed better retention rates for MTX (mean (SEM) survival 28 (1) months) than for LEF (20 (1) months; p=0.001), whereas retention rates of SSZ (23 (1) months) were similar to those of LEF (p=NS). Treatments were stopped earlier because of adverse events (AEs, 3 months) than because of ineffectiveness (IE, 10 months; p<0.001). LEF and MTX were less likely to be stopped because of AEs than SSZ. LEF courses were stopped earlier for AEs (p<0.001) than MTX. >Conclusions: Current dosing strategies should be re-evaluated, and coping strategies for common AEs should be investigated. This will be necessary to achieve better drug retention of LEF. At present, MTX continues to be the most effective drug in clinical practice.
机译:>目的:在一项观察性研究中,确定来氟米特(LEF)与甲氨蝶呤(MTX)和柳氮磺胺吡啶(SSZ)相比在RA中的存活率和临床有效性。 >方法:筛选了两个学术医院的1088例患者和5141例患者的DMARD治疗(2680个疗程)的观察数据库,以进行LEF,MTX和SSZ治疗。 LEF治疗组的患者年龄,基线ESR,既往DMARD的数量以及与MTX和SSZ治疗组的医院队列相匹配。对于这些治疗,进行了Kaplan-Meier药物停药前的时间(药物“存活”)的分析,以及继续治疗的有效性和安全性。比较两组之间疾病活动标志物(CRP,ESR)的变化。 >结果:研究期间的中位剂量从每周10毫克MTX增加到15毫克MTX /天,从每天SSG的中位数剂量增加至2.0克/天。配对生存分析显示,MTX(平均(SEM)生存28(1)个月)比LEF(20(1)个月; p = 0.001)更好的保留率,而SSZ(23(1)个月)的保留率相似到LEF(p = NS)。与不良事件(IE,10个月; p <0.001)相比,由于不良事件(AE,3个月)而停止治疗的时间更早。与SSZ相比,LEF和MTX因AE而停药的可能性较小。 AE的LEF课程比MTX提前终止(p <0.001)。 >结论:应重新评估当前的给药策略,并应调查常见不良事件的应对策略。这对于实现LEF更好的药物保留是必要的。目前,MTX仍然是临床实践中最有效的药物。

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