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严重难治性 CIDP:10 例硼替佐米治疗的病例系列

Severe refractory CIDP: a case series of 10 patients treated with bortezomib.

机构信息

Department of Neurology, St. Josef-Hospital, Ruhr University, Gudrunstr. 56, 44791, Bochum, Germany.

Department of Hematology and Oncology, St. Josef Hospital, Ruhr University, Bochum, Germany.

出版信息

J Neurol. 2017 Sep;264(9):2010-2020. doi: 10.1007/s00415-017-8599-4. Epub 2017 Aug 23.

DOI:10.1007/s00415-017-8599-4
PMID:28836002
Abstract

Treatment options for patients with aggressive chronic inflammatory demyelinating neuropathy are limited and include the anti-CD20 antibody rituximab and the immunosuppressive regime cyclophosphamide. We aimed to investigate retrospectively the efficacy of bortezomib, a proteasome inhibitor tackling highly metabolically active cell types such as plasma cells, in a case series of 10 treatment refractory CIDP patients. All patients reported showed a deterioration of the clinical CIDP scores under first-line treatment or escalating treatment with cyclophosphamide or rituximab. One or two cycles of bortezomib treatment (each cycle with 1.3 mg/m administered s.c. on days 1, 4, 8, and 11) stabilized the majority of the patients (n = 6) during treatment and even improved clinical and electrophysiological parameters of four patients up to 1 year later. No relevant side-effects were reported. Two patients received autologous peripheral blood stem cell transplantation after bortezomib, which led to fatal infections. We conclude that bortezomib could be an attractive escalating treatment option with a good side-effect profile for patients with treatment refractory CIDP.

摘要

治疗侵袭性慢性炎症性脱髓鞘性多发性神经病的选择有限,包括抗 CD20 抗体利妥昔单抗和免疫抑制方案环磷酰胺。我们旨在回顾性研究蛋白酶体抑制剂硼替佐米在 10 例治疗抵抗性 CIDP 患者中的疗效,该药物针对浆细胞等代谢活跃的细胞类型。所有报告的患者在一线治疗或环磷酰胺或利妥昔单抗递增治疗下,CIDP 临床评分均恶化。硼替佐米治疗 1 或 2 个周期(每个周期皮下给予 1.3mg/m2,第 1、4、8 和 11 天)稳定了大多数患者(n=6)的病情,甚至在 1 年后,4 名患者的临床和电生理参数得到改善。没有报告相关的副作用。两名患者在硼替佐米治疗后接受了自体外周血干细胞移植,导致致命感染。我们的结论是,硼替佐米可能是一种具有良好副作用特征的治疗抵抗性 CIDP 的有吸引力的递增治疗选择。

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