Department of Neurological Surgery, University of Virginia Health System, Charlottesville, Virginia, USA.
J Neurosurg. 2011 Jun;114(6):1617-21. doi: 10.3171/2010.12.JNS101602. Epub 2011 Jan 14.
Seizures occur in approximately 80% of patients with low-grade gliomas (LGGs). The majority of patients are treated with anticonvulsant monotherapy; however, many patients require multidrug therapy, or their seizures are refractory to antiepileptic drugs altogether. The oral alkylating agent temozolomide has emerged as a potential initial treatment option for LGG. A few reports suggest an association between temozolomide and reduced seizure frequency in patients with intractable epilepsy.
Using their clinical database, the authors identified adult patients whose LGGs were treated using temozolomide as the initial antineoplastic therapy at the University of Virginia Health System. As a control group, the authors assessed patients whose LGGs were under observation. All patients had seizure disorders that were treated with anticonvulsants. Seizure frequency in patients with intractable epilepsy was analyzed before and after treatment with temozolomide. Age at diagnosis, sex, antiepileptic drugs, pathological subtype, surgical treatment, and follow-up until progression were also assessed. Interval seizure frequency was meticulously analyzed at each neurooncology clinic visit. A meaningful difference in seizures was defined as a reduction in seizure frequency of greater than 50% per month.
Thirty-nine patients were identified in the temozolomide cohort and 30 patients in the control cohort. The median age at diagnosis was 46 years for the former cohort and 41.5 years for the latter. The median length of follow-up was 39 months for the temozolomide group and 37 months for the control group. There was a significant difference in reduced seizure frequency between patients receiving temozolomide (59%) and those who did not receive temozolomide (13%, p < 0.001). Seven patients (18%) in the temozolomide group displayed this improvement independent of antiepileptic drug adjustment compared with no patient in the control group (p < 0.001).
The authors' data suggest that a subset of patients with LGGs experience improvement in seizure frequency during treatment with temozolomide independent of antiepileptic drug adjustment. This decrease in seizure frequency appears independent of the natural history of seizures in patients whose tumors are under observation. Consequently, seizures in patients with LGGs may be better controlled with the combination of AEDs and temozolomide.
约 80%的低级别胶质瘤(LGG)患者会出现癫痫发作。大多数患者接受抗癫痫药物单药治疗;然而,许多患者需要多药治疗,或他们的癫痫发作完全对抗癫痫药物耐药。口服烷化剂替莫唑胺已成为 LGG 的潜在初始治疗选择。少数报告表明替莫唑胺与难治性癫痫患者的癫痫发作频率降低之间存在关联。
作者使用他们的临床数据库,在弗吉尼亚大学健康系统中确定了接受替莫唑胺作为初始抗肿瘤治疗的 LGG 成年患者。作为对照组,作者评估了其 LGG 处于观察状态的患者。所有患者均患有接受抗癫痫药物治疗的癫痫发作障碍。分析了难治性癫痫患者在接受替莫唑胺治疗前后的癫痫发作频率。还评估了诊断时的年龄、性别、抗癫痫药物、病理亚型、手术治疗以及进展前的随访情况。在每次神经肿瘤学就诊时都仔细分析了间隔性癫痫发作频率。定义有意义的癫痫发作改善为每月癫痫发作频率降低大于 50%。
替莫唑胺组中确定了 39 例患者,对照组中确定了 30 例患者。前者的中位诊断年龄为 46 岁,后者为 41.5 岁。替莫唑胺组的中位随访时间为 39 个月,对照组为 37 个月。接受替莫唑胺治疗的患者(59%)与未接受替莫唑胺治疗的患者(13%)的癫痫发作频率降低有显著差异(p < 0.001)。与对照组无患者相比,替莫唑胺组有 7 例(18%)患者独立于抗癫痫药物调整而显示出这种改善(p < 0.001)。
作者的数据表明,接受替莫唑胺治疗的 LGG 患者中,有一部分患者的癫痫发作频率得到改善,而与抗癫痫药物调整无关。这种癫痫发作频率的降低似乎与肿瘤处于观察状态的患者的癫痫发作自然史无关。因此,LGG 患者的癫痫发作可能可以通过 AEDs 和替莫唑胺联合治疗得到更好的控制。