Groupe d'analyse, Ltée, Montreal, Quebec, Canada.
Value, Evidence & Outcomes, GSK Collegeville, Collegeville, Pennsylvania, USA
Lupus Sci Med. 2024 Apr 3;11(1):e001111. doi: 10.1136/lupus-2023-001111.
To investigate the real-world impact of intravenous belimumab treatment among patients with SLE using rheumatoid arthritis-derived disease activity measures and SLE-related laboratory values.
This retrospective cohort study used US electronic medical record data from the United Rheumatology Normalised Integrated Community Evidence (UR-NICE) database. Adult patients with SLE who initiated intravenous belimumab between 1 January 2012 and 3 December 2019 (index), had 12 months of pre-index and 24 months of post-index clinical activity, and had ≥6 infusions of belimumab during the 24 months post-index were included. The primary outcome measure was time to first improvement of minimally important difference (MID) for Routine Assessment of Patient Index Data 3 (RAPID3), Patient Pain Index (PPI), swollen joint count, tender joint count (TJC), complement C3 and C4 and anti-double-stranded DNA antibodies during the on-treatment follow-up period of up to 24 months. The secondary outcome measure evaluated the trajectories of these outcome measures for up to 24 months of belimumab treatment.
Of 495 patients included, between 21.0% and 52.1% had ≥1 record for each of the disease activity measures or laboratory values in the pre-index and post-index periods and were included in analyses for that measure. The proportion of patients achieving MID for each measure increased rapidly within 3 months, with continued gradual improvement throughout the remaining on-treatment period, up to 24 months. After 6 months, 52.3% and 55.3% of patients had achieved MID in RAPID3 and PPI, respectively. Outcome measure trajectories indicated improved disease activity with belimumab treatment, particularly in RAPID3, TJC and laboratory values.
In this real-world effectiveness study, belimumab therapy for SLE resulted in clinically meaningful improvements in rheumatoid arthritis-derived disease activity measures within 3 months of treatment, with patients who remained on belimumab therapy experiencing improvement even up to 24 months of observation.
使用源自类风湿关节炎的疾病活动指标和与系统性红斑狼疮相关的实验室值,研究静脉注射贝利尤单抗治疗系统性红斑狼疮患者的真实世界影响。
这项回顾性队列研究使用了美国联合风湿病规范化综合社区证据 (UR-NICE) 数据库中的电子病历数据。纳入的系统性红斑狼疮成年患者在 2012 年 1 月 1 日至 2019 年 12 月 3 日期间首次接受静脉注射贝利尤单抗(索引),在索引前有 12 个月的临床活动期,在索引后有 24 个月的临床活动期,并且在索引后 24 个月内至少接受了 6 次贝利尤单抗输注。主要结局指标是达到常规评估患者指数数据 3(RAPID3)、患者疼痛指数(PPI)、肿胀关节计数、压痛关节计数(TJC)、补体 C3 和 C4 以及抗双链 DNA 抗体最小有意义差异(MID)改善的时间,在治疗随访期内最长可达 24 个月。次要结局指标评估了在接受贝利尤单抗治疗的 24 个月内这些结局指标的变化轨迹。
在 495 名纳入的患者中,在索引前和索引后期间,有 21.0%至 52.1%的患者至少有一次疾病活动指标或实验室值的记录,且纳入了该指标的分析。在 3 个月内,每个指标的 MID 达标率迅速增加,在整个治疗期间持续逐渐改善,最长可达 24 个月。在 6 个月时,分别有 52.3%和 55.3%的患者在 RAPID3 和 PPI 中达到了 MID。结局指标变化轨迹表明,随着贝利尤单抗治疗,疾病活动得到改善,尤其是在 RAPID3、TJC 和实验室值方面。
在这项真实世界的有效性研究中,在治疗开始后的 3 个月内,系统性红斑狼疮患者接受贝利尤单抗治疗后,与类风湿关节炎相关的疾病活动指标出现了有临床意义的改善,而继续接受贝利尤单抗治疗的患者在观察的 24 个月内仍有改善。