Rituximab as an effective add-on maintenance therapy for disease activities in childhood-onset systemic lupus erythematosus.

IF 3.7 2区 医学 Q1 RHEUMATOLOGY Lupus Science & Medicine Pub Date : 2024-01-19 DOI:10.1136/lupus-2023-000987
Ting-Wei Lin, Yu-Tsan Lin, Ya-Chiao Hu, Hsin-Hui Yu, Bor-Luen Chiang
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Abstract

Objectives: Systemic lupus erythematosus (SLE) is a chronic inflammatory autoimmune disease that can result in high morbidity if not treated. This retrospective study aimed to evaluate the outcomes of rituximab treatment in a paediatric SLE cohort in Taiwan.

Methods: The medical records of paediatric patients diagnosed with SLE at the National Taiwan University Hospital between January 1992 and August 2022 who received rituximab as maintenance therapy between January 2015 and August 2022 were retrospectively reviewed. To enhance our analysis, we included a contemporary comparison group, matching in case number and demographic characteristics. This study aimed to describe the indications, efficacy and safety of rituximab in the treatment of paediatric SLE and to analyse the factors associated with disease outcomes.

Results: The study included 40 rituximab-treated patients with a median age of 14.3 years at the time of disease diagnosis. In the rituximab-treated cohort, the median score on the Systemic Lupus Erythematosus Disease Activity Index 2000 decreased from 8 before rituximab administration to 4 after 2 years. The levels of C3 and C4 increased and anti-double stranded DNA (anti-dsDNA) levels decreased significantly within 6 months. The equivalent oral prednisolone dose halved after 6 months. Finally, 8 (20%) patients achieved disease control and 35 (87.5%) patients had no flare-ups during the follow-up period (median, 2 years). Those patients who achieved disease control had a significantly shorter interval between diagnosis and rituximab administration. In terms of adverse effects, only one patient developed hypogammaglobulinaemia that required intravenous immunoglobulin (IVIG) replacement. Compared with the comparison group (n=53), the rituximab-treated cohort exhibited superior disease outcomes and a reduced incidence of flare-ups.

Conclusions: This study provides real-world data and illuminates rituximab's role in maintaining disease stability among patients with paediatric-onset SLE who are serologically active without major clinical deterioration. Most importantly, no mortality or development of end-stage renal disease was observed in the rituximab-treated cohort.

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利妥昔单抗是治疗儿童期系统性红斑狼疮疾病活动的有效附加维持疗法。
目的:系统性红斑狼疮(SLE)是一种慢性炎症性自身免疫性疾病,如不及时治疗可导致高发病率。这项回顾性研究旨在评估利妥昔单抗在台湾儿科系统性红斑狼疮队列中的治疗效果:方法:我们回顾性分析了1992年1月至2022年8月期间在台湾大学医院确诊为系统性红斑狼疮的儿科患者的病历,这些患者在2015年1月至2022年8月期间接受了利妥昔单抗作为维持治疗。为了加强分析,我们还纳入了一个与病例数和人口统计学特征相匹配的当代对比组。本研究旨在描述利妥昔单抗治疗儿童系统性红斑狼疮的适应症、疗效和安全性,并分析与疾病结局相关的因素:研究共纳入了40名利妥昔单抗治疗患者,患者确诊时的中位年龄为14.3岁。在接受利妥昔单抗治疗的人群中,2000年系统性红斑狼疮疾病活动指数的中位数从使用利妥昔单抗前的8分降至2年后的4分。6个月内,C3和C4水平上升,抗双链DNA(anti-dsDNA)水平显著下降。6 个月后,口服泼尼松龙的等效剂量减半。最后,8 名(20%)患者的病情得到控制,35 名(87.5%)患者在随访期间(中位数为 2 年)没有复发。病情得到控制的患者从确诊到使用利妥昔单抗的时间间隔明显较短。在不良反应方面,只有一名患者出现了低丙种球蛋白血症,需要静脉补充免疫球蛋白(IVIG)。与对比组(53 人)相比,利妥昔单抗治疗组的疾病疗效更好,复发率更低:这项研究提供了真实世界的数据,揭示了利妥昔单抗在维持血清学活跃的儿科系统性红斑狼疮患者病情稳定方面的作用,且无重大临床恶化。最重要的是,在接受利妥昔单抗治疗的队列中没有观察到死亡或终末期肾病的发生。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Lupus Science & Medicine
Lupus Science & Medicine RHEUMATOLOGY-
CiteScore
5.30
自引率
7.70%
发文量
88
审稿时长
15 weeks
期刊介绍: Lupus Science & Medicine is a global, peer reviewed, open access online journal that provides a central point for publication of basic, clinical, translational, and epidemiological studies of all aspects of lupus and related diseases. It is the first lupus-specific open access journal in the world and was developed in response to the need for a barrier-free forum for publication of groundbreaking studies in lupus. The journal publishes research on lupus from fields including, but not limited to: rheumatology, dermatology, nephrology, immunology, pediatrics, cardiology, hepatology, pulmonology, obstetrics and gynecology, and psychiatry.
期刊最新文献
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