College of Medicine, Drexel University, Philadelphia, PA, USA.
AbbVie Inc., 26525 N Riverwoods Blvd., Mettawa, North Chicago, IL, 60045, USA.
Adv Ther. 2023 Oct;40(10):4493-4503. doi: 10.1007/s12325-023-02619-6. Epub 2023 Aug 5.
This study evaluated 12 months adherence and persistence among Janus kinase inhibitors (upadacitinib, baricitinib, tofacitinib) and adalimumab, a tumor necrosis factor inhibitor (TNFi), in patients with rheumatoid arthritis (RA).
This retrospective analysis used administrative claims data from the Merative™ MarketScan Research Databases (2018-2022). Eligible adults had ≥ 1 RA diagnosis before the index date, ≥ 1 pharmacy claim for index medication, and ≥ 12 months of continuous insurance enrollment pre- and post-index. Adherence to treatment [defined as proportion of days covered (PDC) ≥ 80%], risk of treatment discontinuation, and mean time to discontinuation were assessed during the 12 months follow-up. Adjusted odds ratios (aOR), adjusted hazard ratios (aHR), and 95% confidence intervals (CI) were reported.
In total, 6317 patients were included (683 upadacitinib, 3732 adalimumab, 132 baricitinib, 1770 tofacitinib). Compared with upadacitinib, patients initiating adalimumab [aOR (95% CI): 0.82 (0.69, 0.96)], baricitinib [0.46 (0.31, 0.68)], and tofacitinib [0.74 (0.62, 0.88)] were significantly less likely to achieve PDC ≥ 80%. Risk of treatment discontinuation was significantly higher in patients treated with adalimumab [aHR (95% CI): 1.14 (1.01, 1.29)], baricitinib [1.48 (1.16, 1.90)], and tofacitinib [1.22 (1.07, 1.38)] compared with upadacitinib. Mean time to discontinuation was 256 (upadacitinib), 249 (adalimumab), 221 (baricitinib), and 239 (tofacitinib) days. Similar results were observed in patients with prior TNFi use.
Patients with RA, regardless of recent TNFi experience, initiating upadacitinib were significantly more likely to be adherent and less likely to discontinue therapy compared to adalimumab, baricitinib, and tofacitinib in the first 12 months of treatment.
本研究评估了在类风湿关节炎(RA)患者中,12 个月时接受 Janus 激酶抑制剂(乌帕替尼、巴瑞替尼、托法替尼)和肿瘤坏死因子抑制剂(TNFi)阿达木单抗的依从性和持久性。
本回顾性分析使用了 MerativeTM MarketScan 研究数据库(2018-2022 年)中的行政索赔数据。符合条件的成年人在指数日期前有≥1 次 RA 诊断,指数药物有≥1 次药房配药,且在指数前和指数后至少有 12 个月的连续保险参保。在 12 个月的随访期间,评估了治疗的依从性(定义为比例覆盖天数(PDC)≥80%)、停药风险和平均停药时间。报告了调整后的优势比(aOR)、调整后的危险比(aHR)和 95%置信区间(CI)。
共有 6317 名患者入组(683 名乌帕替尼、3732 名阿达木单抗、132 名巴瑞替尼、1770 名托法替尼)。与乌帕替尼相比,起始接受阿达木单抗[aOR(95%CI):0.82(0.69,0.96)]、巴瑞替尼[0.46(0.31,0.68)]和托法替尼[0.74(0.62,0.88)]的患者达到 PDC≥80%的可能性显著降低。与乌帕替尼相比,接受阿达木单抗[aHR(95%CI):1.14(1.01,1.29)]、巴瑞替尼[1.48(1.16,1.90)]和托法替尼[1.22(1.07,1.38)]治疗的患者停药风险显著增加。与乌帕替尼相比,停药的平均时间为 256(乌帕替尼)、249(阿达木单抗)、221(巴瑞替尼)和 239(托法替尼)天。在有既往 TNFi 治疗史的患者中也观察到了类似的结果。
在开始治疗的前 12 个月内,无论近期是否使用过 TNFi,RA 患者起始接受乌帕替尼治疗的患者与阿达木单抗、巴瑞替尼和托法替尼相比,其依从性更高,停药可能性更小。