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临床试验/NCT00182819
NCT00182819已完成3 期

Primary Chemotherapy With Temozolomide Versus Radiotherapy in Patients With Low Grade Gliomas After Stratification for Genetic 1p Loss: A Phase III Study

European Organisation for Research and Treatment of Cancer - EORTC89 个研究点 分布在 11 个国家目标入组 709 人开始时间: 2005年7月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
709
试验地点
89
主要终点
Progression-free survival

研究概览

简要总结

RATIONALE: Radiation therapy uses high-energy x-rays to kill tumor cells. Drugs used in chemotherapy, such as temozolomide, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. It is not yet known whether radiation therapy is more effective than temozolomide in treating gliomas.

PURPOSE: This randomized phase III trial is studying radiation therapy to see how well it works compared to temozolomide in treating patients with gliomas.

详细描述

OBJECTIVES:

Primary

  • Compare the progression-free survival of patients with low-grade gliomas treated with radiotherapy vs temozolomide.

Secondary

  • Compare the overall survival of patients treated with these regimens.
  • Determine whether the incidence of late toxicity can be decreased in patients who are randomized to receive temozolomide.
  • Compare the toxic effects of these regimens in these patients.
  • Compare the quality of life of patients treated with these regimens.

研究设计

研究类型
Interventional
分配方式
Randomized
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

radiotherapy

Other

Radiotherapy (control arm), 50.4 Gy, standard fractionation (28 x 1.8 Gy), conformal techniques

干预措施: radiation therapy (Radiation)

Temozolomide

Experimental

Temozolomide 75 mg/m2 daily x 21 days, q 28 days until progression or for max. 12 cycles (experimental arm)

干预措施: temozolomide (Drug)

结局指标

主要结局

Progression-free survival

时间窗: 5 years

次要结局

  • Overall survival(5 years)
  • Adverse events as measured by CTCAE v3.0(As indicated in the protocol)
  • Quality of life as measured by QLQ-C30 v3.0 and EORTC BN-20(every 3 months until progression, and then every 6 months until death)
  • Mini-Mental State Examination(every 3 months until progression, and then every 6 months until death)

研究者

申办方类型
Network
责任方
Sponsor

研究点 (89)

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