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间歇性环磷酰胺和泼尼松治疗意义未明的单克隆丙种球蛋白病相关多发性神经病。

Intermittent cyclophosphamide and prednisone treatment of polyneuropathy associated with monoclonal gammopathy of undetermined significance.

作者信息

Notermans N C, Lokhorst H M, Franssen H, Van der Graaf Y, Teunissen L L, Jennekens F G, Van den Berg L H, Wokke J H

机构信息

Rudolph Magnus Institute of Neurosciences, Department of Neurology, Utrecht, The Netherlands.

出版信息

Neurology. 1996 Nov;47(5):1227-33. doi: 10.1212/wnl.47.5.1227.

Abstract

In an open prospective study, we analyzed the effect of cyclophosphamide (300 mg/m2 body surface daily for 4 days) combined with prednisone (40 mg/m2 body surface daily for 5 days) at 4-week intervals during 6 months in 16 patients with polyneuropathy associated with monoclonal gammopathy of undetermined significance (MGUS). Eleven patients had an IgM-MGUS and five an IgG-MGUS. During a follow-up period of 3 years, eight patients had improvement and six patients stabilized, based on quantitative neurologic examination, the Rankin disability scale, and electrophysiologic studies. These 14 patients had neuropathy with demyelinating and axonal features. One patient with a purely axonal neuropathy had deterioration despite therapy. One other patients developed severe leukopenia as side effect of cyclophosphamide, necessitating withdrawal of treatment. A difference in response was not present in patient with IgM- or IgG-MGUS, nor in patients with or without autoantibodies against myelin-associated glycoprotein. Nine patients had a bone marrow biopsy before and 1 year after treatment. In eight patients, the monoclonal lymphoid IgM or plasma cell IgG infiltration decreased, while in four the monoclonality disappeared after treatment. In the patient who had neurologic deterioration, repeated bone marrow biopsy showed deposits of amyloid. In conclusion, short-term treatment with intermittent cyclophosphamide and prednisone may have a long-term favorable effect in patients with demyelinating polyneuropathy associated with MGUS.

摘要

在一项开放性前瞻性研究中,我们分析了环磷酰胺(每日300mg/m²体表面积,共4天)联合泼尼松(每日40mg/m²体表面积,共5天),每4周一次,连续6个月对16例意义未明的单克隆丙种球蛋白病(MGUS)相关多发性神经病患者的疗效。11例患者为IgM-MGUS,5例为IgG-MGUS。在3年的随访期内,根据定量神经学检查、Rankin残疾量表和电生理研究,8例患者病情改善,6例患者病情稳定。这14例患者的神经病具有脱髓鞘和轴突特征。1例纯轴索性神经病患者尽管接受了治疗仍病情恶化。另1例患者出现严重白细胞减少作为环磷酰胺的副作用,需要停止治疗。IgM-或IgG-MGUS患者之间,以及有无抗髓鞘相关糖蛋白自身抗体的患者之间,在反应上没有差异。9例患者在治疗前和治疗1年后进行了骨髓活检。8例患者单克隆淋巴IgM或浆细胞IgG浸润减少,4例患者治疗后单克隆性消失。在病情恶化的患者中,重复骨髓活检显示有淀粉样蛋白沉积。总之,间歇性环磷酰胺和泼尼松短期治疗可能对MGUS相关脱髓鞘性多发性神经病患者有长期的有益效果。

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