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抗癫痫药物与化疗药物之间的相互作用。

Interactions between antiepileptic and chemotherapeutic drugs.

作者信息

Vecht Charles J, Wagner G Louis, Wilms Erik B

机构信息

Department of Neurology, Medical Centre Haaglanden, The Hague, Netherlands.

出版信息

Lancet Neurol. 2003 Jul;2(7):404-9. doi: 10.1016/s1474-4422(03)00435-6.

Abstract

Cancer and epilepsy commonly co-occur, and concomitant administration of antiepileptic (AEDS) and chemotherapeutic drugs (CTDs) is necessary in many cases. Many drugs are metabolised by the hepatic cytochrome P450 (CYP) isoenzyme system, and coadministration of AEDs and CTDs can lead to clinically relevant interactions by induction or inhibition of enzymes in shared metabolic pathways. These interactions can cause insufficient tumour and seizure control or lead to unforeseen toxicity. Enzyme-inducing AEDs reduce the effects of taxanes, vinca alkaloids, methotrexate, teniposide, and camptothecin analogues. Inhibition of the metabolism of nitrosoureas or etoposide by valproic acid can lead to CTD toxicity. Poor seizure control may result from the combinations of phenytoin with cisplatin or corticosteroids, and valproic acid with methotrexate. Increased toxicity of AEDs can occur when phenytoin is combined with 5-fluorouracil. Use of enzyme-inducing AEDs should be avoided in patients with cancer, particularly in association with chemotherapy. Generally, valproic acid-although not free from interactions-would be the agent of first choice. Some of the newer AEDs not metabolised by the P450 system may prove to be good alternatives.

摘要

癌症和癫痫常常同时出现,在许多情况下有必要同时使用抗癫痫药物(AEDs)和化疗药物(CTDs)。许多药物由肝脏细胞色素P450(CYP)同工酶系统代谢,同时使用AEDs和CTDs可通过诱导或抑制共同代谢途径中的酶而导致具有临床意义的相互作用。这些相互作用可导致肿瘤控制不佳和癫痫发作控制不佳,或导致不可预见的毒性。诱导酶的AEDs可降低紫杉烷类、长春花生物碱、甲氨蝶呤、替尼泊苷和喜树碱类似物的疗效。丙戊酸抑制亚硝基脲类或依托泊苷的代谢可导致CTD毒性。苯妥英与顺铂或皮质类固醇联合使用,以及丙戊酸与甲氨蝶呤联合使用,可能导致癫痫发作控制不佳。苯妥英与5-氟尿嘧啶联合使用时,AEDs的毒性可能增加。癌症患者应避免使用诱导酶的AEDs,尤其是在接受化疗时。一般来说,丙戊酸——尽管并非没有相互作用——将是首选药物。一些不由P450系统代谢的新型AEDs可能被证明是很好的替代品。

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