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临床试验/NCT00526175
NCT00526175已完成4 期

LAL-BR/2001: Study Treatment to Low Risk ALL

PETHEMA Foundation27 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2001年6月1日最近更新:
适应症
相关药物

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
150
试验地点
27
主要终点
To evaluate the efficacy of treatment in order to response rate, relapse free survival and global survival

研究概览

简要总结

The purpose of this study is increase the efficacy of consolidation (C1) after an intensification phase with high dose of methotrexate, applying analysis of minimal residual disease

详细描述

REMISION INDUCTION

Systemic chemotherapy:

Prednisolone (PDN):

  • 60 mg/m2 day, i.v. or p.o., days 1 to 27
  • 30 mg/m2 day, i.v. or p.o., days 28 to 35

Vincristine (VCR): 1,5 mg/m2 i.v., days 8, 15, 22 and 28. Daunorubicin (DNR): 30 mg/m2, i.v., days 8 and 15. L-asparaginase (L-ASA): 10.000 UI/m2, i.m. or i.v., days 9 to 11, 16 to 18 and 23 to 25.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
— 至 15 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Diagnoses of low risk acute lymphoblastic leukemia in children no treated previously

排除标准

  • Mature B-ALL (FABL3) or with cytogenetic ALL "Burkitt-like" alterations (t[8;14], t[2;8], t[8;22])
  • Mixed forms of ALL
  • Acute Leukemia no differentiate
  • Patients with coronary disorders, valvular or hypertensive cardiopathy
  • Patients with chronic liver disorders
  • Chronic pulmonary disorders
  • Renal insufficiency
  • Neurologic disfunctions
  • ECOG 3 and 4
  • No signed consent form

结局指标

主要结局

To evaluate the efficacy of treatment in order to response rate, relapse free survival and global survival

时间窗: 2 years

次要结局

未报告次要终点

研究者

发起方
PETHEMA Foundation
申办方类型
Other
责任方
Sponsor

研究点 (27)

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