Veeken Lara D, Opdam Merel A A, Verhoef Lise M, Popa Calin, van Crevel Reinout, den Broeder Alfons A
Department of Rheumatology, Sint Maartenskliniek, Nijmegen, The Netherlands.
Radboud University Medical Center, Radboud Institute for Health Sciences, Nijmegen, The Netherlands.
Rheumatology (Oxford). 2024 May 2;63(5):1246-1250. doi: 10.1093/rheumatology/kead328.
Rituximab (RTX) is a safe and effective treatment for RA. However, there are some concerns about infection risk and preliminary data suggest dose and time dependency. This study aims to determine the infection incidence in a large real-life population of RA patients using RTX, with special focus on (ultra-)low dosing and time since last infusion.
RA patients treated with 1000, 500 or 200 mg RTX per cycle between 2012 and 2021 at the Sint Maartenskliniek were included in a retrospective cohort study. Patient-, disease-, treatment- and infection characteristics were retrieved from electronic health records. Infection incidence rates, dose and time relations with RTX infusion were analysed using mixed-effects Poisson regression.
Among 490 patients, we identified 819 infections in 1254 patient years. Most infections were mild and respiratory tract infections were most common. Infection incidence rates were 41, 54 and 71 per 100 patient years for doses of 200, 500 and 1000 mg. Incidence rate ratio (IRR) was significantly lower for 200 mg compared with 1000 mg (adjusted IRR 0.35, 95% CI 0.17, 0.72, P = 0.004). In patients receiving 1000 or 500 mg RTX, infections seemed to occur more frequently within the first two months after infusion compared with later on in the treatment cycle, suggesting an association with peak concentration.
Ultra-low dosing (200 mg) of RTX is associated with a lower risk of infections in RA. Future interventions focusing on ultra-low dosing and slow release of RTX (e.g. by subcutaneous administration) may lower infection risk.
利妥昔单抗(RTX)是一种治疗类风湿关节炎(RA)安全有效的药物。然而,人们对感染风险存在一些担忧,初步数据表明存在剂量和时间依赖性。本研究旨在确定大量使用RTX的RA患者真实人群中的感染发生率,特别关注(超)低剂量以及末次输注后的时间。
2012年至2021年在圣马丁诊所接受每周期1000、500或200mg RTX治疗的RA患者纳入一项回顾性队列研究。从电子健康记录中获取患者、疾病、治疗和感染特征。使用混合效应泊松回归分析感染发生率、剂量以及与RTX输注的时间关系。
在490例患者中,我们在1254患者年中识别出819例感染。大多数感染为轻度,呼吸道感染最为常见。200、500和1000mg剂量的感染发生率分别为每100患者年41、54和71例。200mg与1000mg相比,发病率比(IRR)显著更低(调整后IRR 0.35,95%CI 0.17,0.72,P = 0.004)。在接受1000或500mg RTX的患者中,与治疗周期后期相比,感染似乎在输注后的前两个月更频繁发生,这表明与峰值浓度有关。
超低剂量(200mg)的RTX与RA患者较低的感染风险相关。未来针对RTX超低剂量和缓释(例如通过皮下给药)的干预措施可能会降低感染风险。