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大剂量依托泊苷及自体骨髓移植后的周围神经病变

Peripheral neuropathy following high-dose etoposide and autologous bone marrow transplantation.

作者信息

Imrie K R, Couture F, Turner C C, Sutcliffe S B, Keating A

机构信息

University of Toronto Autologous Bone Marrow Transplant Program, Toronto Hospital, Canada.

出版信息

Bone Marrow Transplant. 1994 Jan;13(1):77-9.

PMID:8019457
Abstract

We investigated the incidence of peripheral neuropathy in 142 consecutive patients receiving high-dose etoposide between August 1988 and December 1991. A retrospective chart review was conducted. Six patients with hematologic malignancies presented with a new sensory polyneuropathy after receiving an intensive therapy regimen consisting of etoposide 60 mg/kg i.v. and melphalan 140-160 mg/m2 i.v. followed by autologous bone marrow transplantation. Neurologic symptoms began 2-8 weeks after transplant, were grade 2-3 in severity and pursued a chronic course with slow improvement over months. Electromyographic studies in three of the patients tested confirmed distal sensory polyneuropathy. All 6 patients had previously received vincristine 1-60 months prior to autotransplant. We conclude that peripheral neuropathy of moderate severity is a potential complication of high-dose etoposide therapy but appears to be self-limited.

摘要

我们调查了1988年8月至1991年12月期间连续接受高剂量依托泊苷治疗的142例患者周围神经病变的发生率。进行了一项回顾性病历审查。6例血液系统恶性肿瘤患者在接受由静脉注射60mg/kg依托泊苷和静脉注射140 - 160mg/m²美法仑组成的强化治疗方案后,继以自体骨髓移植,出现了新的感觉性多发性神经病变。神经症状在移植后2 - 8周开始出现,严重程度为2 - 3级,呈慢性病程,数月内缓慢改善。对其中3例患者进行的肌电图研究证实为远端感觉性多发性神经病变。所有6例患者在自体移植前1 - 60个月均曾接受过长春新碱治疗。我们得出结论,中度严重程度的周围神经病变是高剂量依托泊苷治疗的一种潜在并发症,但似乎是自限性的。

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