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Real-world treatment persistence of non-tumor necrosis factor inhibitors versus tumor necrosis factor inhibitors among patients with rheumatoid arthritis in South Korea

机译:韩国类风湿性关节炎患者的非肿瘤坏死因子抑制剂与肿瘤坏死因子抑制剂的实际治疗持久性

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Aims: We aimed to assess treatment persistence of tumor necrosis factor (TNF) inhibitors and non-TNF inhibitors in two groups of rheumatoid arthritis (RA) patients: biologic disease-modifying antirheumatic drug (bDMARD) initiators and switchers. Patients and methods: This retrospective cohort study utilized a national health insurance claims database. Patients aged >= 18 years initiating/switching bDMARD between 1 December 2013 and 31 December 2014, the index period, were followed for 12 months. Initiators who began treatment with a bDMARD during the index period were defined as having no bDMARD prescriptions for the previous year. Switchers who changed treatment from the previous bDMARD to the index bDMARD were defined as having different bDMARDs during the index period. Treatment persistence rates during the follow-up period were measured, and factors associated with non-persistence were assessed with the Cox proportional hazard model. Results: Of 2684 patients, treatment persistence rates were the highest for abatacept in initiators (69.3%) and tocilizumab in switchers (77.0%), while adalimumab showed the lowest persistence rates for both initiators and switchers (48.2%, 28.8%), followed by etanercept (51.3%, 41.0%). Adalimumab and etanercept were significantly more likely to show non-persistence (HR 1.58, 95% CI 1.27-1.96; HR 1.42, 95% CI 1.14-1.76) compared to infliximab for initiators, while tocilizumab was significantly more likely to show persistence (HR 0.411, 95% CI 0.206-0.819) in switchers. Conclusions: Non-TNF inhibitors showed higher persistence rates than TNF inhibitors in South Korean RA patients, and tocilizumab especially was associated with higher persistence in patients with inadequate response to TNF inhibitors. Good persistence with non-TNF inhibitors indicates the potential for long-term efficacy as first-line treatment.
机译:目的:我们旨在评估两组类风湿性关节炎(RA)患者的肿瘤坏死因子(TNF)抑制剂和非TNF抑制剂的治疗持久性:生物学疾病改性抗触发药物(BDMARD)引发剂和切换器。患者和方法:这种回顾性队列研究采用国家健康保险索赔数据库。年龄龄≥18岁2013年12月1日至12月3日期间的发起/交换BDMARD,遵循12个月的指数期。在指数期间与BDMARD进行治疗的启动人被定义为上一年的BDMARD处方。将处理从前一个BDMARD进行处理到索引BDMARD的切换器被定义为在索引期间具有不同的BDMARD。测量后续期间治疗持久性率,并评估与非持久性相关的因素与COX比例危害模型进行评估。结果:2684例患者,治疗持久性率最高,最高因素(69.3%)和切换器中的对照(77.0%)(77.0%),而Adalimumab展示了两个发起者和切换器的持久率(48.2%,28.8%),遵循通过Etanercept(51.3%,41.0%)。与IntiaImab的Ineliators相比,Adalimumab和依那西普有可能表现出非持久性(HR 1.58,95%CI 1.27-1.96),而Tocolizumab显着表现出持久性(HR切换器中0.411,95%CI 0.206-0.819)。结论:非TNF抑制剂表现出比韩国RA患者的TNF抑制剂更高的持久性率,特别是对TNF抑制剂反应不足患者的持久性尤其与持久性有关。与非TNF抑制剂的良好持久性表明了作为一线治疗的长期疗效的可能性。

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