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本文引用的文献

1
Comparative pharmacokinetics of oral and intravenous ifosfamide/mesna/methylene blue therapy.口服与静脉注射异环磷酰胺/美司钠/亚甲蓝疗法的比较药代动力学
Drug Metab Dispos. 1998 Sep;26(9):883-90.
2
Inhibition of (mono)amine oxidase activity and prevention of ifosfamide encephalopathy by methylene blue.亚甲蓝对(单)胺氧化酶活性的抑制作用及对异环磷酰胺脑病的预防作用
Drug Metab Dispos. 1996 Dec;24(12):1336-9.
3
[Methylene blue in ifosfamide-induced encephalopathy].[亚甲蓝治疗异环磷酰胺所致脑病]
Dtsch Med Wochenschr. 1996 Sep 27;121(39):1210.
4
Ifosfamide encephalopathy and methylene-blue: a case report.异环磷酰胺脑病与亚甲蓝:一例报告
Ann Oncol. 1996 Aug;7(6):643-4. doi: 10.1093/oxfordjournals.annonc.a010686.
5
Methylene blue and the neurotoxic mechanisms of ifosfamide encephalopathy.亚甲蓝与异环磷酰胺脑病的神经毒性机制
Eur J Clin Pharmacol. 1996;50(4):249-52. doi: 10.1007/s002280050102.
6
[Successful treatment with methylene blue of ifosfamide-induced central nervous system effects].[亚甲蓝成功治疗异环磷酰胺引起的中枢神经系统效应]
Dtsch Med Wochenschr. 1996 Apr 26;121(17):575.
7
Hallucinations and ifosfamide-induced neurotoxicity.幻觉与异环磷酰胺诱导的神经毒性。
Cancer. 1994 Mar 1;73(5):1509-14. doi: 10.1002/1097-0142(19940301)73:5<1509::aid-cncr2820730531>3.0.co;2-g.
8
Ifosfamide metabolism and pharmacokinetics (review).异环磷酰胺的代谢与药代动力学(综述)
Anticancer Res. 1994 Mar-Apr;14(2A):517-31.
9
Methylene blue for ifosfamide-associated encephalopathy.亚甲蓝用于治疗异环磷酰胺相关性脑病。
N Engl J Med. 1995 May 4;332(18):1239-40. doi: 10.1056/NEJM199505043321817.
10
[Treatment of ifosfamide induced encephalopathy with methylene-blue].[亚甲蓝治疗异环磷酰胺诱发的脑病]
Bull Cancer. 1995 Jul;82(7):598-9.

亚甲蓝治疗和预防异环磷酰胺所致脑病:12例报告及文献复习

Methylene blue in the treatment and prevention of ifosfamide-induced encephalopathy: report of 12 cases and a review of the literature.

作者信息

Pelgrims J, De Vos F, Van den Brande J, Schrijvers D, Prové A, Vermorken J B

机构信息

Department of Medical Oncology, University Hospital Antwerp, Edegem, Belgium.

出版信息

Br J Cancer. 2000 Jan;82(2):291-4. doi: 10.1054/bjoc.1999.0917.

DOI:10.1054/bjoc.1999.0917
PMID:10646879
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2363270/
Abstract

Ifosfamide is an alkylating agent used in the treatment of a variety of solid tumours. Ten to 15% of patients treated with ifosfamide develop an encephalopathy. Methylene blue (MB) may be used in the treatment of this encephalopathy. The purpose of this study was to evaluate the neuroprotective effect of MB in these patients and to review the literature. Between 1993 and 1997, 52 patients (age 16-77 years) with solid tumours were treated with ifosfamide in dosages ranging from 3 to 5 g m(-2) q3w when given in combination schedules and up to 12 g m(-2) q4w when given as a single agent. Twelve patients developed central nervous system (CNS) depression, defined as National Cancer Institute Common Toxicity Criteria (NCI-CTC) neurocortical toxicity grade 2 or higher. Eight were treated with MB at a dose of 6 x 50 mg day(-1) intravenously (i.v.). Four recovered fully within 24 h, two recovered partially after 24 h and completely after 48 h while two recovered only after 72 h. Four patients did not receive MB and all recovered only after 48 h. Three patients received prophylaxis with MB at a dose of 4 x 50 mg day(-1) i.v. for the subsequent chemotherapy cycles. Two developed milder encephalopathy; one had no CNS depression at all. We conclude that MB is an effective treatment for ifosfamide-induced encephalopathy. Our findings suggest that it may also be used as a prophylactic agent.

摘要

异环磷酰胺是一种用于治疗多种实体瘤的烷化剂。接受异环磷酰胺治疗的患者中有10%至15%会发生脑病。亚甲蓝(MB)可用于治疗这种脑病。本研究的目的是评估MB对这些患者的神经保护作用并回顾相关文献。1993年至1997年期间,52例(年龄16 - 77岁)实体瘤患者接受了异环磷酰胺治疗,联合用药时剂量为3至5 g m(-2) 每3周一次,单用时剂量高达12 g m(-2) 每4周一次。12例患者出现中枢神经系统(CNS)抑制,定义为美国国立癌症研究所通用毒性标准(NCI - CTC)神经皮质毒性2级或更高。8例患者接受了剂量为6×50 mg day(-1) 的静脉注射(i.v.)MB治疗。4例在24小时内完全恢复,2例在24小时后部分恢复并在48小时后完全恢复,而2例仅在72小时后恢复。4例患者未接受MB治疗,均仅在48小时后恢复。3例患者在随后的化疗周期中接受了剂量为4×50 mg day(-1) 的静脉注射MB预防性治疗。2例发生较轻的脑病;1例根本没有CNS抑制。我们得出结论,MB是治疗异环磷酰胺诱导的脑病的有效药物。我们的研究结果表明,它也可作为一种预防药物使用。