Immunotherapy in Intractable Cryptogenic Epilepsy Patients With Autoimmune Antibody
试验速览
- 阶段
- 4 期
- 入组人数
- 40
- 试验地点
- 1
- 主要终点
- Percent seizure reduction
研究概览
简要总结
The purpose of the study is to investigate effect of immunotherapy in intractable cryptogenic epilepsy patients with autoimmune antibody.
详细描述
Cryptogenic epilepsy is an epilepsy of presumed symptomatic nature but the cause has not been identified. It account for at least 40% of adult-onset epilepsy. Autoimmune encephalitis including classic paraneoplastic syndrome and autoimmune synaptic encephalitis is a new category of immune-mediated disorders which often has favorable outcome. Recent studies reported that immunotherapy improves seizure outcome in medically intractable epilepsy patients with clinical and serological evidence of an autoimmune basis. Neural autoantibodies were detected in 22% of epilepsy due to unknown cause in a study, mostly from the antiepileptic drug(AED)-resistant epilepsy group. Of the patients who received immunotherapy, 75% archived >50% reduction in seizure frequency.
Many patients with cryptogenic epilepsy are refractory to AED and significant percent of cryptogenic epilepsy harbor neural autoantibody. In those cases, immunotherapy is suggestive based on favorable outcome of immunotherapy in autoimmune encephalitis and autoimmune epilepsy. Investigators aim to investigate the response to immunotherapy in intractable cryptogenic epilepsy patients with neural autoantibodies.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 85 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •A diagnosis of cryptogenic epilepsy according to the International League Against Epilepsy's Classification of Epilepsy.
- •Intractable epilepsy: Complete seizure control is not achieved with trials of two appropriate antiepileptic drugs
- •At least 1 seizure within the past 8 weeks
- •Presence of autoimmune antibody (NMDAR, LGI1, CASPR2, AMPA1, AMPA2, GABAB-R, anti-Hu, -Yo, -Ri, -Ma2, -CV2/CRMP5, -amphiphysin, GAD) in serum or cerebrospinal fluid
- •Written informed consent signed by the subject or legal guardian prior to entering the study
排除标准
- •Clinical evidence of autoimmune encephalitis such as autoimmune limbic encephalitis
- •History of severe head trauma
- •Presence of structural abnormality which is thought to be epileptogenic in brain MRI
- •Epilepsy of predominantly genetic or presumed genetic origin
- •An active CNS infection, demyelinating disease, degenerative neurologic disease or any CNS disease deemed to be progressive during the course of the study that may confound the interpretation of the study results History of immunotherapy
- •A history of nonepileptic or psychogenic seizures within past 1 year
- •Any clinically significant laboratory abnormality that in the opinion of the Investigator would exclude the subject from the study
- •Any clinically significant psychiatric illness, psychological, or behavioral problems that, in the opinion of the Investigator, would interfere with the subject's ability to participate in the study
- •Recent (within 4 weeks) change or dose adjustment of anti-epileptic drug (1 to 2 doses of rescue benzodiazepine is permitted)
- •Refuse to participate in the study
研究组 & 干预措施
Immunotherapy
Intravenous immunoglobulin (IVIG) and oral prednisolone. IVIG and oral prednisolone are administered simultaneously: IVIG (400mg/kg/day for 5 days) with oral prednisolone (60mg for 5days, than decrease by 10 mg every 2 day).
干预措施: IVIG (Other)
Immunotherapy
Intravenous immunoglobulin (IVIG) and oral prednisolone. IVIG and oral prednisolone are administered simultaneously: IVIG (400mg/kg/day for 5 days) with oral prednisolone (60mg for 5days, than decrease by 10 mg every 2 day).
干预措施: Prednisolone (Drug)
结局指标
主要结局
Percent seizure reduction
时间窗: 3 months
次要结局
- Seizure free rate(3 months)
- Responder rate(3 months)
- Quality of life scores as measured by QOLIE-31(3 months)
- Quality of life scores as measured by BDI-2(3 months)
- Cognition scores as measured by K-MMSE(3 months)
- Amount of epileptiform discharge measured by EEG(3 months)
- Treatment failure rate(3 months)
研究者
Sang Kun Lee
Professor
Seoul National University Hospital