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临床试验/NCT01024127
NCT01024127已完成不适用

Genetic Predictors of AML Treatment Response

Children's Oncology Group1 个研究点 分布在 1 个国家目标入组 2,500 人开始时间: 2009年12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
2,500
试验地点
1
主要终点
Incidence of first acute myeloid leukemia relapse

研究概览

简要总结

This research trial studies deoxyribonucleic acid (DNA) in blood or bone marrow samples from younger patients with acute myeloid leukemia. Studying samples of blood and bone marrow from patients with cancer in the laboratory may help doctors learn more about changes that occur in DNA and identify biomarkers related to cancer. It may also help doctors predict how well patients will respond to treatment.

详细描述

PRIMARY OBJECTIVES:

l. Perform a genome-wide scan to test for loci associated with acute myeloid leukemia (AML) relapse and infection risk.

II. Validate positive associations seen in the genome-wide scan with a fine mapping approach.

III. Perform simulated clinical trials using germline genetic variation data to test the feasibility of using genetic data to inform the clinical care of pediatric patients with AML.

OUTLINE:

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Cross Sectional

入排标准

年龄范围
— 至 30 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Diagnosis of AML
  • In remission
  • Adequate DNA from peripheral blood or bone marrow samples
  • Concurrent enrollment on CCG-2961, COG-AAML03P1, COG-AAML0531, AML-93, AML-97, AML-04,AML-09, or Canada AML Infection clinical trial required

排除标准

  • 未提供

结局指标

主要结局

Incidence of first acute myeloid leukemia relapse

时间窗: Up to 2 years

Rate of invasive bacterial infections defined as the number of invasive infection episodes divided by the days at risk

时间窗: From study entry date to completion of therapy date provided on the final Reporting Period case reporting form, assessed up to 2 years

次要结局

未报告次要终点

研究者

申办方类型
Network
责任方
Sponsor

研究点 (1)

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