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利妥昔单抗诱导哥伦比亚严重和难治性系统性红斑狼疮患者快速和持续缓解。

Rituximab induces a rapid and sustained remission in Colombian patients with severe and refractory systemic lupus erythematosus.

机构信息

Internal Medicine, Rheumatology, Hospital Pablo Tobón Uribe, Universidad Pontificia Bolivariana, Medellín, Colombia.

出版信息

Lupus. 2011 Oct;20(11):1219-26. doi: 10.1177/0961203311409273. Epub 2011 Jul 22.

Abstract

Despite aggressive treatment for systemic lupus erythematosus (SLE) with high-dose glucocorticoids and immunosuppressive agents, a significant proportion of patients persist with activity or relapse. Although the results from randomized studies showed no beneficial effects of rituximab (RTX) in SLE, this treatment has proven promising results in open label trials including patients with severe and refractory disease. We report a prospective cohort of 42 Colombian patients with severe and refractory SLE treated with RTX after failure response to glucocorticoids and, at least, another immunosuppressive drug. We observed a reduction in steroid requirement [47.4 mg/day at 24 months (p < 0.001)]. Since the first three-month follow-up, 28% and 36% of the patients fulfilled criteria of complete or partial remission according to proteinuria, and 12.5% and 33% according to creatinine clearance, respectively. These response criteria remained at 12 months. Both neuropsychiatric and hematological sub-groups had a favorable clinical response. The median reinfusion-free survival time was 44 months (95% confidence interval: 10.1-50.1) and 80% of the patients did not require RTX reinfusion. Eleven adverse events were reported in 28 subjects. Most of these occurred during the first three-month follow-up, time during which patients were exposed to high-dose glucocorticoids.

摘要

尽管对系统性红斑狼疮 (SLE) 患者进行了大剂量糖皮质激素和免疫抑制剂的积极治疗,但仍有相当一部分患者存在疾病活动或复发。尽管随机研究的结果显示利妥昔单抗 (RTX) 对 SLE 没有有益效果,但在包括严重和难治性疾病患者在内的开放性试验中,这种治疗方法已被证明有良好的效果。我们报告了一项前瞻性队列研究,该研究纳入了 42 名来自哥伦比亚的严重和难治性 SLE 患者,他们在对糖皮质激素和至少另一种免疫抑制剂治疗反应不佳后接受了 RTX 治疗。我们观察到类固醇需求减少[24 个月时为 47.4 mg/天(p<0.001)]。自首次随访的第三个月起,根据蛋白尿标准,28%和 36%的患者达到完全或部分缓解标准,根据肌酐清除率标准,分别有 12.5%和 33%的患者达到缓解标准。这些缓解标准在 12 个月时仍然存在。神经精神和血液学亚组均有良好的临床反应。无再输注的中位生存时间为 44 个月(95%置信区间:10.1-50.1),80%的患者无需再输注 RTX。28 名受试者中有 11 名报告了 11 项不良事件。大多数不良事件发生在首次随访的前 3 个月,在此期间患者接受了大剂量糖皮质激素治疗。

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