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临床试验/NCT00561873
NCT00561873已完成不适用

Phase-II-Study of Efficacy of OSAG 101 (Theraloc®) for Adolscent Patients With Recurrent High Grade Glioma

Oncoscience AG1 个研究点 分布在 1 个国家目标入组 45 人开始时间: 2004年6月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
45
试验地点
1
主要终点
Response rate according to RECIST criteria

研究概览

简要总结

Determination of efficiency of nimotuzumab in children with high grade glioma.

详细描述

High grade malignant gliomas are tumors grade III and IV according to WHO classification, that originate from oligodendroglia and astrocytes, where the latter are also known as anaplastic astrocytoma(WHO grade III) and glioblastoma(WHO grade IV). This also includes intrinsic pontine gliomas of adolescents, which are usually not documented histologically due to their localisation, but they have a similar clinical progress when compared to high grade malignant astrocytic tumors. Among various molecular alterations, malignant gliomas overexpress EGFR (epidermal growth factor) in nearly 50% of cases, which is particularly pronounced in glioblastoma.(Schlegel 2003) Standard therapy consists of radical surgery as extensive as medically responsible followed by radiotherapy dose of 60 Gy, which is aimed at the area with a safety margin. The long-term efficacy of additional chemotherapy has been a subject for controversy for several decades. The combination of all three treatment modalities in grade III tumors can lead to median survival times of 3-5 years in adults.

For this treatment group reports of 5 year recurrence free periods in 33-50% of cases have been reported in children and adolescents.

For glioblastoma(WHO grade IV) 5year recurrence free periods are 3% in elderly patients and 10-20% for adolescents.(Schlegel 2003) In German speaking territories chemotherapy with Cisplatin, Etoposid and Ifosfamid is used as a postoperative treatment option for adolescents and this disease.(Wolff HIT-GBM) In case of recurrence therapy choices are even more limited, thus if medically feasible the enrolment in clinical trials is an option.

In this study the aim is to use an antibody directed against the EGF-receptor to effect the proliferation of the tumor cells negatively. Pilot studies conducted in adults indicate that the median survival time for patients with malignant glioma can be prolonged by the antibody treatment.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Prospective

入排标准

年龄范围
3 Years 至 20 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Histologically confirmed diagnosis of high grade glioma (WHO III und IV) [not needed for intrinsic pontine glioma]
  • Progressive patients under primary therapy or first and second radiologically confirmed recurrence(MRI not older than 2 weeks) of high grade gliomas between the age of > 3 years < 20 years
  • Lack of curative standard therapy which is currently under investigation in a national GPOH-therapy optimization study
  • Sufficient haematological, renal and hepatic function (CTC Grad ≤ 2)
  • Disease measurable radiologicaly in at least one dimension
  • Life expectancy > 4 Weeks
  • Written declaration of consent of the parents/legal guardians and if possible of the child after prior information

排除标准

  • Curative therapy with an alternative method after diagnosis of progression and during this study
  • Prior administration of human or murine antibody
  • Pregnancy in girls of child-bearing age

结局指标

主要结局

Response rate according to RECIST criteria

时间窗: week 8, week 21

次要结局

  • Progress free interval, Toxicity according to CTC criteria, Symptom control(week 8, week 21)

研究者

申办方类型
Industry

研究点 (1)

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