Brigham and Women's Hospital, Boston, Massachusetts.
Genentech, South San Francisco, California.
Arthritis Rheumatol. 2017 Jun;69(6):1154-1164. doi: 10.1002/art.40084. Epub 2017 Apr 28.
While tocilizumab (TCZ) is known to increase low-density lipoprotein (LDL) cholesterol levels, it is unclear whether TCZ increases cardiovascular risk in patients with rheumatoid arthritis (RA). This study was undertaken to compare the cardiovascular risk associated with receiving TCZ versus tumor necrosis factor inhibitors (TNFi).
To examine comparative cardiovascular safety, we conducted a cohort study of RA patients who newly started TCZ or TNFi using claims data from Medicare, IMS PharMetrics, and MarketScan. All patients were required to have previously used a different TNFi, abatacept, or tofacitinib. The primary outcome measure was a composite cardiovascular end point of hospitalization for myocardial infarction or stroke. TCZ initiators were propensity score matched to TNFi initiators with a variable ratio of 1:3 within each database, controlling for >65 baseline characteristics. A fixed-effects model combined database-specific hazard ratios (HRs).
We included 9,218 TCZ initiators propensity score matched to 18,810 TNFi initiators across all 3 databases. The mean age was 72 years in Medicare, 51 in PharMetrics, and 53 in MarketScan. Cardiovascular disease was present at baseline in 14.3% of TCZ initiators and 13.5% of TNFi initiators. During the study period (mean ± SD 0.9 ± 0.7 years; maximum 4.5 years), 125 composite cardiovascular events occurred, resulting in an incidence rate of 0.52 per 100 person-years for TCZ initiators and 0.59 per 100 person-years for TNFi initiators. The risk of cardiovascular events associated with TCZ use versus TNFi use was similar across all 3 databases, with a combined HR of 0.84 (95% confidence interval 0.56-1.26).
This multi-database population-based cohort study showed no evidence of an increased cardiovascular risk among RA patients who switched from a different biologic drug or tofacitinib to TCZ versus to a TNFi.
虽然托珠单抗(TCZ)已知会增加低密度脂蛋白(LDL)胆固醇水平,但尚不清楚 TCZ 是否会增加类风湿关节炎(RA)患者的心血管风险。本研究旨在比较接受 TCZ 与肿瘤坏死因子抑制剂(TNFi)治疗相关的心血管风险。
为了研究比较心血管安全性,我们使用来自 Medicare、IMS PharMetrics 和 MarketScan 的索赔数据,对新开始接受 TCZ 或 TNFi 的 RA 患者进行了队列研究。所有患者均需先前使用过不同的 TNFi、阿巴西普或托法替尼。主要结局指标为心肌梗死或卒中住院的复合心血管终点。TCZ 起始者与 TNFi 起始者按每个数据库中 1:3 的变量比例进行倾向评分匹配,控制了超过 65 个基线特征。固定效应模型合并了数据库特异性风险比(HRs)。
我们纳入了来自所有 3 个数据库的 9218 名 TCZ 起始者和 18810 名 TNFi 起始者进行倾向评分匹配。在 Medicare 中,平均年龄为 72 岁,在 PharMetrics 中为 51 岁,在 MarketScan 中为 53 岁。心血管疾病在 TCZ 起始者中为 14.3%,在 TNFi 起始者中为 13.5%。在研究期间(平均±标准差 0.9±0.7 年;最长 4.5 年),共发生 125 例复合心血管事件,TCZ 起始者的发生率为 0.52/100 人年,TNFi 起始者为 0.59/100 人年。TCZ 与 TNFi 相比,使用 TCZ 与使用 TNFi 相关的心血管事件风险在所有 3 个数据库中相似,合并 HR 为 0.84(95%置信区间 0.56-1.26)。
这项多数据库基于人群的队列研究未发现 RA 患者从另一种生物药物或托法替尼转换为 TCZ 与转换为 TNFi 相比,心血管风险增加的证据。