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奥法妥木单抗用于对利妥昔单抗过敏的系统性红斑狼疮患者的B细胞清除。

Ofatumumab for B cell depletion in patients with systemic lupus erythematosus who are allergic to rituximab.

作者信息

Masoud Sherry, McAdoo Stephen P, Bedi Rachna, Cairns Thomas D, Lightstone Liz

机构信息

Imperial College Lupus Centre, Imperial College Healthcare NHS Trust, Imperial College London, London, UK.

Renal and Vascular Inflammation Section, Department of Medicine, Imperial College London, London, UK.

出版信息

Rheumatology (Oxford). 2018 Jul 1;57(7):1156-1161. doi: 10.1093/rheumatology/key042.

Abstract

OBJECTIVE

B cell depletion, most commonly with rituximab, is an evolving therapeutic approach in SLE. Infusion reactions after rituximab are common, and may prevent re-treatment in patients who previously demonstrated beneficial response. We have used ofatumumab, a fully humanized anti-CD20 mAb, as an alternative B cell-depleting agent in patients with SLE who are rituximab-intolerant due to severe infusion reactions.

METHODS

A single-centre retrospective case series of 16 patients were treated with ofatumumab for SLE between 2012 and 2015.

RESULTS

Ofatumumab infusion was well tolerated in 14/16 patients, in whom the median age was 34 (range 19-55) and the median duration of SLE 9.2 years (0.6-28.5). The cohort was heavily pre-treated, with 50% having prior CYC exposure, and a median cumulative dose of prior rituximab 4 g (1-6). Twelve patients were treated for LN, one for extra-renal flare and one for remission maintenance. B cell-depletion was achieved in 12/14 patients, with comparable reconstitution kinetics to a previous cohort treated with rituximab at our centre, and was associated with improvements in serological markers of disease activity, including ANA, anti-dsDNA antibody and complement levels. Half of the patients with LN achieved renal remission by 6 months. Progressive disease that was unresponsive to augmented immunosuppression with CYC was seen in five patients. During long-term follow-up (median 28 months), five grade III infections were reported, and there were no malignancies or deaths.

CONCLUSION

In this pre-treated cohort with long-standing SLE, ofatumumab was a well-tolerated, safe and effective alternative to rituximab for B cell-depletion therapy.

摘要

目的

B细胞耗竭,最常用利妥昔单抗,是系统性红斑狼疮(SLE)中一种不断发展的治疗方法。利妥昔单抗治疗后的输注反应很常见,可能会阻止先前显示出有益反应的患者再次接受治疗。我们使用奥法木单抗,一种完全人源化的抗CD20单克隆抗体,作为因严重输注反应而不耐受利妥昔单抗的SLE患者的替代B细胞耗竭剂。

方法

对2012年至2015年间接受奥法木单抗治疗SLE的16例患者进行单中心回顾性病例系列研究。

结果

16例患者中有14例对奥法木单抗输注耐受性良好,其中位年龄为34岁(范围19 - 55岁),SLE中位病程为9.2年(0.6 - 28.5年)。该队列患者接受过大量预处理,50%曾接受过环磷酰胺(CYC)治疗,先前利妥昔单抗的中位累积剂量为4g(1 - 6g)。12例患者因狼疮性肾炎(LN)接受治疗,1例因肾外疾病发作接受治疗,1例因维持缓解接受治疗。14例患者中有12例实现了B细胞耗竭,其重建动力学与我们中心先前接受利妥昔单抗治疗的队列相当,并且与疾病活动的血清学标志物改善相关,包括抗核抗体(ANA)、抗双链DNA抗体和补体水平。一半的LN患者在6个月时实现了肾脏缓解。5例患者出现对CYC强化免疫抑制无反应的进行性疾病。在长期随访(中位28个月)期间,报告了5例3级感染,未发生恶性肿瘤或死亡。

结论

在这个患有长期SLE的预处理队列中,奥法木单抗是一种耐受性良好、安全有效的替代利妥昔单抗的B细胞耗竭疗法。

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