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异环磷酰胺脑病:重新评估

Ifosfamide encephalopathy: a reappraisal.

作者信息

Watkin S W, Husband D J, Green J A, Warenius H M

机构信息

University of Liverpool, Department of Radiation Oncology, U.K.

出版信息

Eur J Cancer Clin Oncol. 1989 Sep;25(9):1303-10. doi: 10.1016/0277-5379(89)90077-1.

DOI:10.1016/0277-5379(89)90077-1
PMID:2806353
Abstract

Eighteen consecutive cases of encephalopathy occurring after ifosfamide/mesna chemotherapy were prospectively assessed. No relationship was found with tumour type or chemotherapy response. Onset was from 12 to 146 (mean 46) h after the start of the infusion and median duration was 3 days (range 1-12). In two patients recovery was incomplete. A confusional state and agitation were the major clinical features. Plasma potassium fell from a mean of 4.12 mmol/l before chemotherapy to 2.94 mmol/l at the onset of encephalopathy (P less than 0.001) with plasma potassium less than 3.0 mmol/l in 10 patients. Duration of hypokalaemia was not related to duration of encephalopathy. Median survival following encephalopathy was 25 days. The incidence of encephalopathy in 82 patients treated on two protocols was 11% and the sensitivity of a published nomogram was 18%. It is concluded that ifosfamide/mesna encephalopathy is a serious complication which may be irreversible and remains difficult to predict.

摘要

对18例异环磷酰胺/美司钠化疗后发生脑病的连续病例进行了前瞻性评估。未发现与肿瘤类型或化疗反应有关。发病时间为输注开始后12至146小时(平均46小时),中位持续时间为3天(范围1至12天)。两名患者恢复不完全。意识模糊状态和躁动是主要临床特征。血浆钾从化疗前的平均4.12 mmol/L降至脑病发作时的2.94 mmol/L(P<0.001),10例患者血浆钾低于3.0 mmol/L。低钾血症的持续时间与脑病的持续时间无关。脑病后的中位生存期为25天。在两个方案治疗的82例患者中,脑病的发生率为11%,已发表的列线图的敏感性为18%。结论是,异环磷酰胺/美司钠脑病是一种严重并发症,可能不可逆转,且仍然难以预测。

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Ifosfamide encephalopathy: a reappraisal.异环磷酰胺脑病:重新评估
Eur J Cancer Clin Oncol. 1989 Sep;25(9):1303-10. doi: 10.1016/0277-5379(89)90077-1.
2
Prediction of ifosfamide/mesna associated encephalopathy.异环磷酰胺/美司钠相关性脑病的预测
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Irreversible encephalopathy with ifosfamide/mesna.异环磷酰胺/美司钠所致不可逆性脑病
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Ifosfamide, mesna, and encephalopathy.异环磷酰胺、美司钠与脑病
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2
Phase I study of docetaxel plus ifosfamide in patients with advanced cancer.多西他赛联合异环磷酰胺治疗晚期癌症患者的I期研究。
Br J Cancer. 2002 Oct 7;87(8):846-9. doi: 10.1038/sj.bjc.6600542.
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Gender difference in ifosfamide metabolism by human liver microsomes.
人肝微粒体对异环磷酰胺代谢的性别差异。
Eur J Drug Metab Pharmacokinet. 2001 Jul-Sep;26(3):193-200. doi: 10.1007/BF03190396.
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Clinical pharmacokinetics and pharmacodynamics of ifosfamide and its metabolites.异环磷酰胺及其代谢产物的临床药代动力学和药效学
Clin Pharmacokinet. 2001 Jan;40(1):41-62. doi: 10.2165/00003088-200140010-00004.
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Clinical and preclinical modulation of chemotherapy-induced toxicity in patients with cancer.癌症患者化疗诱导毒性的临床及临床前调节
Drugs. 1999 Feb;57(2):133-55. doi: 10.2165/00003495-199957020-00002.
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Determination of the urinary excretion of ifosfamide and its phosphorated metabolites by phosphorus-31 nuclear magnetic resonance spectroscopy.
Cancer Chemother Pharmacol. 1993;31(5):387-94. doi: 10.1007/BF00686153.
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Ifosfamide clinical pharmacokinetics.异环磷酰胺的临床药代动力学。
Clin Pharmacokinet. 1994 Jun;26(6):439-56. doi: 10.2165/00003088-199426060-00003.
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Urinary excretion of the enantiomers of ifosfamide and its inactive metabolites in children.
Cancer Chemother Pharmacol. 1991;28(6):455-60. doi: 10.1007/BF00685822.
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Dosing and side-effects of ifosfamide plus mesna.异环磷酰胺加美司钠的剂量及副作用
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