Department of Rheumatology, Hiroshima City Hiroshima Citizens Hospital, Hiroshima, Japan.
Department of Clinical Immunology and Rheumatology, Hiroshima University Hospital, Hiroshima, Japan.
Lupus. 2024 Apr;33(5):502-510. doi: 10.1177/09612033241238055. Epub 2024 Mar 12.
In addition to various immunosuppressive agents, belimumab and anifrolumab became available in Japan. We aimed to investigate glucocorticoid-free clinical remission in a single-centre retrospective cohort in October 2023.
Our cohort included patients with SLE who needed to start or increase glucocorticoids for disease activity and were followed up for more than 1 year. We investigated the rate of achievement of clinical remission off corticosteroids (CR off C), defined as no clinical score on the SLEDAI-2K without glucocorticoids, baseline predictors of CR off C, medications used when CR off C was achieved, and flare rates following CR off C.
Out of the 60 patients followed for an average of 5.4 (±2.6) years, 17 (28.3%) achieved CR off C in 3.6 (±1.2) years after enrolment. Use of belimumab and anifrolumab accounted for eight (47.1%) of the achievers. Among the baseline data, male sex, recent enrolment, high glucocorticoid dose, and detection of immune complex (IC) significantly predicted CR off C, while lupus nephritis (LN) and a low C3 level tended to predict it. In the multivariate analysis, IC detection was the only predictor of CR off C. Clinical flares were observed in 5.9% of the achievers during a median 1.2 years after achievement of CR off C.
In the era of biologics, CR off C was achieved in 28.3% of the patient cohort requiring the start or increase of glucocorticoids for disease activity, with a relatively low rate of flares, suggesting that glucocorticoid-free clinical remission is an achievable target in SLE. IC disease, represented by male sex or nephritis, is likely to benefit from currently available medications.
除了各种免疫抑制剂外,贝利尤单抗和阿尼鲁单抗在日本也已上市。我们旨在 2023 年 10 月调查单中心回顾性队列中糖皮质激素停药的临床缓解率。
我们的队列包括因疾病活动需要开始或增加糖皮质激素治疗且随访时间超过 1 年的 SLE 患者。我们调查了无皮质类固醇(SLEDAI-2K 无皮质类固醇)下达到临床缓解的患者比例,定义为无临床评分的患者,无皮质类固醇的预测因子,达到无皮质类固醇缓解时使用的药物以及达到无皮质类固醇缓解后的复发率。
在平均随访 5.4(±2.6)年的 60 例患者中,有 17 例(28.3%)在入组后 3.6(±1.2)年内达到无皮质类固醇缓解。使用贝利尤单抗和阿尼鲁单抗的患者中,有 8 例(47.1%)达到了缓解。在基线数据中,男性、近期入组、高剂量糖皮质激素和免疫复合物(IC)检测显著预测无皮质类固醇缓解,而狼疮肾炎(LN)和低 C3 水平则倾向于预测无皮质类固醇缓解。在多变量分析中,IC 检测是无皮质类固醇缓解的唯一预测因素。在达到无皮质类固醇缓解后的中位 1.2 年内,有 5.9%的缓解者出现临床复发。
在生物制剂时代,需要开始或增加糖皮质激素治疗以控制疾病活动的患者中,有 28.3%达到无皮质类固醇缓解,复发率相对较低,这表明无皮质类固醇的临床缓解是 SLE 可以实现的目标。以男性或肾炎为代表的 IC 疾病可能受益于目前可用的药物。