Lupus Clinic, Division of Rheumatology, Department of Internal Clinical Sciences, Anaesthesiologic and Cardiovascular Sciences, Sapienza University of Rome, Italy.
Clin Exp Rheumatol. 2024 Jul;42(7):1491-1494. doi: 10.55563/clinexprheumatol/l5976o. Epub 2024 May 28.
To assess the efficacy of subcutaneous (sc) belimumab (BLM) by the application of SLE-DAS in a monocentric SLE cohort.
We evaluated SLE patients treated with sc BLM from March 2019. Disease activity has been assessed by SLEDAI-2k, SLE-DAS and PGA (Physician Global Assessment) in all the established time-points [baseline (T0), after 1 (T1), 3 (T3), 6 (T6) and 12 (T12) months]. Furthermore, we applied and compared the achievement of remission according to SLE-DAS values (SLEDAS ≤2.08 + PDN ≤5mg/daily) and DORIS definition (clinical SLEDAI- 2k=0 + PGA<0.5 + antimalarial treatment, PDN≤5mg/daily, stable immunosuppressive treatment).
We enrolled 86 patients [M/F 5/81, median age 48 years (IQR 17.5), median disease duration 166 months (IQR 216)]. At baseline, median values of SLEDA-2k and SLE-DAS were 6 (IQR 4) and 5.77 (IQR 4.33), respectively, and they significantly correlated (r=0.719, CI 95% 0.586-0.815, p<0.0001). Median duration of treatment was 14 months (IQR 20). We found a significant reduction of SLEDAI-2k and SLE-DAS already at T1, maintained in the subsequent time-points (p<0.0001). At T12, a remission state was achieved by 60.4% of patients according to SLE-DAS definition and by 62.3% according to the DORIS definition. Both definitions of remission have demonstrated an agreement of 84%, with a Cohen's kappa equal to 0.6.
In this study we applied SLE-DAS to assess the efficacy of sc BLM, by analysing its over-time changes and by comparing its performance with SLEDAI-2k. Indeed, our results suggest the usefulness of this new activity index in a real-life setting.
通过在单中心 SLE 队列中应用 SLE-DAS 评估皮下(sc)贝利尤单抗(BLM)的疗效。
我们评估了 2019 年 3 月以来接受 sc BLM 治疗的 SLE 患者。在所有既定时间点(基线(T0)、治疗后 1 个月(T1)、3 个月(T3)、6 个月(T6)和 12 个月(T12)),通过 SLEDAI-2k、SLE-DAS 和 PGA(医生总体评估)评估疾病活动。此外,我们根据 SLE-DAS 值(SLEDAS≤2.08+PDN≤5mg/天)和 DORIS 定义(临床 SLEDAI-2k=0+PGA<0.5+抗疟治疗,PDN≤5mg/天,稳定免疫抑制治疗)应用和比较了缓解的达标情况。
我们纳入了 86 例患者[M/F 5/81,中位年龄 48 岁(IQR 17.5),中位疾病病程 166 个月(IQR 216)]。基线时,SLEDAI-2k 和 SLE-DAS 的中位数分别为 6(IQR 4)和 5.77(IQR 4.33),且两者显著相关(r=0.719,95%CI 0.586-0.815,p<0.0001)。中位治疗时间为 14 个月(IQR 20)。我们发现 T1 时 SLEDAI-2k 和 SLE-DAS 显著降低,并在后续时间点保持降低(p<0.0001)。在 T12,根据 SLE-DAS 定义,60.4%的患者达到缓解状态,根据 DORIS 定义,62.3%的患者达到缓解状态。两种缓解定义之间的一致性为 84%,Cohen's kappa 值为 0.6。
在这项研究中,我们通过分析 SLE-DAS 的时间变化并将其与 SLEDAI-2k 进行比较,应用 SLE-DAS 评估了 sc BLM 的疗效。事实上,我们的结果表明,在真实环境中,这种新的活动指数具有一定的实用性。