脑肿瘤相关性癫痫的抗惊厥治疗

W. Fröscher, T. Kirschstein, J. Rösche
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引用次数: 4

摘要

背景脑肿瘤患者发生局灶性癫痫发作的终生风险为10-100%;风险取决于不同的组织学。脑肿瘤相关癫痫的药物治疗的具体指导方针尚未建立。目的综述抗癫痫药物(AED)治疗脑肿瘤相关性癫痫的特点。方法对截至2015年12月的文献进行分析。结果根据目前的证据,肿瘤相关癫痫发作的治疗与其他病因癫痫发作的治疗没有本质上的不同。因此,AED的选择首先是基于耐受性和与化疗药物的药代动力学相互作用。许多作者推荐左乙拉西坦作为脑肿瘤相关癫痫的一线治疗药物。由于可能存在相互作用,通常不推荐将酶诱导抗癫痫药与化疗药物联合使用。目前没有证据表明对没有癫痫发作的脑肿瘤患者预防性开长期抗癫痫药是合理的。然而,由于复发的高风险,在单一的脑肿瘤相关癫痫发作后,应强烈考虑使用AED治疗。停用aed的决定必须仔细考虑癫痫复发的风险。结论目前左乙拉西坦是治疗脑肿瘤相关性癫痫的首选药物,特别是在需要避免药物相互作用的情况下。在未来,我们希望通过揭示其发病机制来获得更多针对这种疾病的靶向药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Anticonvulsant therapy in brain-tumor related epilepsy
Summary Background The lifetime risk of patients with brain tumors to have focal epileptic seizures is 10–100%; the risk depends on different histology. Specific guidelines for drug treatment of brain tumor-related seizures have not yet been established. Aim This review addresses the special aspects of antiepileptic drug (AED) therapy in brain tumor-related epilepsy. Methods We analyzed the literature up to December 2015. Results Based on current evidence the management of tumor-related seizures does not differ substantially from that applied to epilepsies from other etiologies. Therefore, the choice of an AED is based, above all, on tolerability and pharmacokinetic interactions with chemotherapeutic drugs. Levetiracetam is recommended by many authors as first-line therapy in brain tumor-related epilepsy. Due to the possibility of interactions, the combination of enzyme-inducing AEDs and chemotherapeutic drugs, is usually not recommended as a first choice. Currently there is no evidence that prophylactic prescription of long-term AEDs in brain tumor-patients who did not present with seizures is justified. Because of the high risk of recurrence, however, AED treatment should be strongly considered after a single brain tumor-related seizure. The decision to withdraw AEDs must carefully consider the risk of seizure recurrence. Conclusion At present levetiracetam is the preferred drug in brain tumor-related epilepsy, especially when drug interactions need to be avoided. In the future we hope to acquire more targeted drugs against this disorder by uncovering its pathogenesis.
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