Favorable outcomes for patients with refractory systemic lupus erythematosus treated with rituximab as evidenced with a follow-up of ≥ 10 years: a real-world evidence study.

IF 3.2 3区 医学 Q2 RHEUMATOLOGY
Chrysanthi Staveri, Chrysa Lykoura, Konstantinos Melissaropoulos, Stamatis-Nick C Liossis
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引用次数: 0

Abstract

Treatment of Systemic Lupus Erythematosus (SLE) remains challenging. The aim of this real-world evidence study of patients with refractory SLE treated with rituximab (RTX) was to explore for any potential long-term effect(s) of this particular B cell depletion approach. This study included patients with SLE who had i) received at least 1 cycle of RTX and had ii) an at least 10 yr of follow-up after their first RTX infusion. Outcomes were assessed at 1 year and at their latest evaluation that was ≥ 10 yr after RTX treatment initiation. In cases where the SLE Disease Activity Index 2000 (cSLEDAI-2 k) was employed, a response was defined as a cSLEDAI-2 k of less than 4 in cases where the cSLEDAI-2 k was ≥ 4. In cases where the cSLEDAI-2 k was 2-4 at baseline, a response was defined as a cSLEDAI-2 k of 0. RTX was administered in 62 patients with SLE. For this real-world evidence study 23 patients (25 cases) with SLE (all Caucasian female, age range: 14-72 yr, mean: 31 yr) with active or relapsing disease, fulfilling inclusion criteria were enrolled. RTX treatment was associated with a response rate of 68.75% after 1 yr and 75% after ≥ 10 yr. The median cSLEDAI-2 K score decreased from 5.83 ± 3.70 at baseline to 1.95 ± 2.40 (p < 0.001) at 1 yr and to 2.37 ± 3.00 (p < 0.001) at the ≥ 10 yr time-point of follow-up. Our data suggest that RTX may indeed represent an alternative therapeutic option in patients with SLE refractory to standard treatment with an acceptable safety profile.

利妥昔单抗治疗难治性系统性红斑狼疮患者的有利结果,随访≥10年:一项真实世界证据研究。
系统性红斑狼疮(SLE)的治疗仍然具有挑战性。这项对难治性SLE患者进行利妥昔单抗(RTX)治疗的真实世界证据研究的目的是探索这种特殊的B细胞消耗方法的任何潜在的长期影响。本研究纳入了1)接受至少1个周期RTX治疗的SLE患者,2)首次RTX输注后随访至少10年。结果在RTX治疗开始后1年和最近一次评估≥10年进行评估。在采用SLE疾病活动指数2000 (cSLEDAI-2 k)的病例中,在cSLEDAI-2 k≥4的病例中,应答定义为cSLEDAI-2 k小于4。如果基线时cSLEDAI-2 k为2-4,则应答定义为cSLEDAI-2 k为0。62例SLE患者接受RTX治疗。在这项真实世界证据研究中,23例(25例)SLE患者(均为白人女性,年龄范围:14-72岁,平均:31岁)符合纳入标准,患有活动性或复发性疾病。RTX治疗1年后的有效率为68.75%,≥10年后的有效率为75%。中位cSLEDAI-2 K评分从基线时的5.83±3.70降至1.95±2.40 (p < 0.05)
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来源期刊
Rheumatology International
Rheumatology International 医学-风湿病学
CiteScore
7.30
自引率
5.00%
发文量
191
审稿时长
16. months
期刊介绍: RHEUMATOLOGY INTERNATIONAL is an independent journal reflecting world-wide progress in the research, diagnosis and treatment of the various rheumatic diseases. It is designed to serve researchers and clinicians in the field of rheumatology. RHEUMATOLOGY INTERNATIONAL will cover all modern trends in clinical research as well as in the management of rheumatic diseases. Special emphasis will be given to public health issues related to rheumatic diseases, applying rheumatology research to clinical practice, epidemiology of rheumatic diseases, diagnostic tests for rheumatic diseases, patient reported outcomes (PROs) in rheumatology and evidence on education of rheumatology. Contributions to these topics will appear in the form of original publications, short communications, editorials, and reviews. "Letters to the editor" will be welcome as an enhancement to discussion. Basic science research, including in vitro or animal studies, is discouraged to submit, as we will only review studies on humans with an epidemological or clinical perspective. Case reports without a proper review of the literatura (Case-based Reviews) will not be published. Every effort will be made to ensure speed of publication while maintaining a high standard of contents and production. Manuscripts submitted for publication must contain a statement to the effect that all human studies have been reviewed by the appropriate ethics committee and have therefore been performed in accordance with the ethical standards laid down in an appropriate version of the 1964 Declaration of Helsinki. It should also be stated clearly in the text that all persons gave their informed consent prior to their inclusion in the study. Details that might disclose the identity of the subjects under study should be omitted.
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