Wang Haiting, Zhao Liling, Yang Shaoying, Ding Huihua, Wu Wanlong, Yu Liqin, Jin Jiajia, Shen Nan, Fu Qiong, Ye Shuang
Department of Rheumatology, Renji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Immune Regulation Unit, National Institute of Dental and Craniofacial Research (NIDCR), National Institutes of Health (NIH), Bethesda, MD, United States.
Front Immunol. 2025 Jun 20;16:1599473. doi: 10.3389/fimmu.2025.1599473. eCollection 2025.
Rituximab (RTX) has been commonly used for the treatment of patients with severe or refractory systemic lupus erythematosus (SLE), yet real-world data concerning RTX as the first-line treatment in newly diagnosed moderate-to-severe SLE patients is lacking.
We conducted a retrospective cohort study using a newly diagnosed (<3 months) hospitalized Systemic Lupus Inception Cohort (hSLIC) at our center between April 1, 2013 and September 1, 2022. All patients were followed up for at least 12 months or until death. The cohort included patients on RTX ( = 104) as the first-line treatment and those on conventional immunosuppressants (IS) ( = 154) as comparators. Propensity-score-based inverse probability of treatment weighting (IPTW) was used to minimize possible confounding factors. The primary outcome analyses included attainment of modified lupus low disease activity state (mLLDAS) and remission by 12 months. The secondary outcomes focused on mortality, major flare rates, and the incidence of adverse events of interest, i.e., major infections.
After IPTW, 76.0%/50.5% of RTX-treated patients achieved mLLDAS/remission versus 45.8%/9.7% in the conventional IS group during 12 months of follow-up, respectively ( = 0.005 and < 0.001). The sensitivity analyses with renal or neuropsychiatric lupus removal and timeline breakout (pre- versus post-November 2019) confirmed the robustness of RTX's efficacy in achieving mLLDAS and remission outcomes. Additionally, the incidence of major infections was similar between the two groups (12.5% vs. 8.4%, = 0.288).
In patients with newly diagnosed moderate-to-severe SLE, upfront treatment with RTX was associated with improved clinical outcomes compared to conventional immunosuppressive therapy in terms of achieving low disease activity or remission by 12 months.
利妥昔单抗(RTX)已普遍用于治疗重症或难治性系统性红斑狼疮(SLE)患者,但缺乏关于RTX作为新诊断的中重度SLE患者一线治疗的真实世界数据。
我们进行了一项回顾性队列研究,使用了2013年4月1日至2022年9月1日期间在我们中心新诊断(<3个月)的住院系统性狼疮起始队列(hSLIC)。所有患者均随访至少12个月或直至死亡。该队列包括接受RTX(n = 104)作为一线治疗的患者和接受传统免疫抑制剂(IS)(n = 154)作为对照的患者。使用基于倾向评分的治疗加权逆概率(IPTW)来最小化可能的混杂因素。主要结局分析包括在12个月时达到改良狼疮低疾病活动状态(mLLDAS)和缓解。次要结局集中在死亡率、严重复发率以及感兴趣的不良事件发生率,即严重感染。
经过IPTW后,在12个月的随访期间,接受RTX治疗的患者分别有76.0%/50.5%达到mLLDAS/缓解,而传统IS组为45.8%/9.7%(P = 0.005和P < 0.001)。去除肾性或神经精神性狼疮以及时间线分组(2019年11月之前与之后)的敏感性分析证实了RTX在实现mLLDAS和缓解结局方面疗效的稳健性。此外,两组之间严重感染的发生率相似(12.5%对8.4%,P = 0.288)。
在新诊断的中重度SLE患者中,与传统免疫抑制治疗相比,早期使用RTX治疗在12个月时实现低疾病活动或缓解方面与改善的临床结局相关。