Mapi Group, Stockholm, Sweden.
Center for Observational and Real-World Evidence (CORE), Merck & Co., Inc., Kenilworth, NJ, USA.
Rheumatol Int. 2017 Dec;37(12):2049-2058. doi: 10.1007/s00296-017-3825-z. Epub 2017 Oct 3.
The objective of this study was to describe treatment persistence with second-line subcutaneous tumor necrosis factor-alpha inhibitors (SC-TNFis) in patients with immune-mediated rheumatic diseases (IMRDs) in Sweden, and the impact of non-persistence on healthcare costs. This retrospective observational study was based on Swedish national health register data. Adults were identified through filled prescriptions for adalimumab (ADA), etanercept (ETA), certolizumab pegol (CZP) and golimumab (GLM). Persistence was estimated over 3 years for propensity score-matched (PSM) cohorts using non-parametric survival analysis. Unadjusted comparisons of costs comprised specialized outpatient care, inpatient care, and medication. In total, N = 845 patients were identified and three PSM cohorts were generated (GLM vs. ADA, ETA, and CZP, respectively). GLM exhibited higher persistence than ADA over the study period (p = 0.040), and numerically higher persistence than ETA and CZP for 36 and 30 months, respectively. Persistent and non-persistent patients had similar mean total cost at 12 month pre-treatment ($5185 vs. $5064, p = 0.750). During the 12 month post-treatment initiation, persistent patients had lower mean total costs ($4377 vs. $6605), corresponding to a cost difference of $2228 (p < 0.001). In second-line treatment with SC-TNFis for IMRDs in Sweden, GLM exhibited significantly higher persistence than ADA over the course of the study. Similarly, GLM showed numerically higher persistence than ETA and CZP, which is concurrent with results observed in first-line SC-TNFi treatment. Considering the lower healthcare costs for persistent patients, the choice of second-line SC-TNFi among eligible patients may merit careful consideration given its impact on patients and payers.
本研究的目的是描述瑞典免疫介导性风湿病(IMRDs)患者二线皮下肿瘤坏死因子-α抑制剂(SC-TNFis)的治疗持续性,并评估非持续性对医疗成本的影响。这项回顾性观察性研究基于瑞典国家健康登记数据。通过阿达木单抗(ADA)、依那西普(ETA)、培塞利珠单抗(CZP)和戈利木单抗(GLM)的处方确定成年人。使用非参数生存分析对倾向评分匹配(PSM)队列进行了 3 年的持续性估计。未调整的成本比较包括专科门诊护理、住院护理和药物治疗。共确定了 845 名患者,并生成了三个 PSM 队列(分别为 GLM 与 ADA、ETA 和 CZP)。在研究期间,GLM 的持续性高于 ADA(p=0.040),且在 36 和 30 个月时,GLM 的持续性也高于 ETA 和 CZP,数值上更高。在治疗前 12 个月,持续性和非持续性患者的总平均费用相似(5185 美元与 5064 美元,p=0.750)。在治疗后 12 个月,持续性患者的总平均费用较低(4377 美元与 6605 美元),差异为 2228 美元(p<0.001)。在瑞典,IMRDs 二线使用 SC-TNFis 治疗中,GLM 的持续性明显高于 ADA。同样,GLM 与 ETA 和 CZP 相比,持续性数值更高,这与一线 SC-TNFi 治疗中观察到的结果一致。考虑到持续性患者的医疗成本较低,在符合条件的患者中选择二线 SC-TNFi 可能需要仔细考虑,因为这对患者和支付方都有影响。