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临床试验/NCT00476541
NCT00476541已完成3 期

NOPHO-AML 2004 Study for Children With Acute Myeloid Leukemia

University of Aarhus2 个研究点 分布在 1 个国家目标入组 250 人开始时间: 2004年1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
250
试验地点
2
主要终点
Event free survival

研究概览

简要总结

The overall objective is to improve the cure rate of children with newly diagnosed acute myeloid leukemia (AML) who undergo risk-adapted therapy.

Stem cell transplantation (SCT) is reserved to high-risk patients defined by cytogenetics and response to chemotherapy. The efficacy and toxicity of Gemtuzumab ozogamicin (GO, Mylotarg) will be evaluated.

详细描述

The overall objective is to improve the cure rate of pediatric patients with newly diagnosed acute myeloid leukemia (AML). The specific aims are as follows:

1.1 Therapeutic aims

To improve the event-free survival (EFS) of AML patients who undergo risk-adapted therapy.

To improve the overall survival (OS) by reserving stem cell transplantation (SCT) to high-risk patients based on cytogenetics and response to induction therapy.

To compare the outcome of SCT using HLA-matched sibling donor (MSD) or HLA-matched unrelated donor (MUD).

研究设计

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

入排标准

年龄范围
1 Day 至 18 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • AML as defined by the diagnostic criteria,
  • Age < 19 years at time of study entry,
  • Written informed consent

排除标准

  • Previous chemo- or radiotherapy,
  • AML secondary to previous bone marrow failure syndrome,
  • Down syndrome (DS),
  • Acute promyelocytic leukemia (APL),
  • Juvenile myelomonocytic leukemia (JMML),
  • Myelodysplastic syndrome (MDS),
  • Fanconi anemia,
  • Positive pregnancy test

研究组 & 干预措施

1

Experimental

Gemtuzumab 5 mg / m2 two courses with three week interval

干预措施: Gemtuzumab ozogamicin (Drug)

结局指标

主要结局

Event free survival

时间窗: 5 years

次要结局

  • Overall survival(5 years)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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