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临床试验/NCT01016379
NCT01016379已完成不适用

Genome-Wide Interrogations in Childhood Acute Lymphoblastic Leukemia (ALL)

Children's Oncology Group0 个研究点目标入组 1,000 人开始时间: 2009年11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
1,000
主要终点
Data resource, that can be linked with additional tumor cell information, to better characterize the biology and subtypes of childhood ALL

研究概览

简要总结

RATIONALE: 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.

PURPOSE: This research study is looking at DNA in blood and bone marrow samples from young patients with acute lymphoblastic leukemia.

详细描述

OBJECTIVES:

  • To manage and oversee determination of genome-wide genotypes using common laboratory methodologies for young patients with newly diagnosed acute lymphoblastic leukemia (ALL).
  • To provide a mechanism for storing, distributing, and tracking usage of blast and germline genomic information for approved projects.
  • To facilitate research for childhood ALL using genome-wide germline and blast data to identify genetic variations associated with important phenotypes: treatment response (e.g., relapse risk, minimal residual disease status), adverse effects (e.g., osteonecrosis, infection risk, neurotoxicity), risk of ALL, and risk of ALL subtypes (e.g., TEL/AML1, BCR/ABL, T-cell).
  • To provide a data resource, that can be linked with additional tumor cell information, to better characterize the biology and subtypes of childhood ALL.

OUTLINE: This is a multicenter study.

DNA from previously collected and banked blood and bone marrow samples is utilized for genome-wide genotyping.

Genotype data is only used to examine specific questions related to the epidemiology and etiology of leukemia, response of leukemia to treatment, risk of recurrence, risk for development of side effects, and complications related to treatment.

研究设计

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

入排标准

年龄范围
1 Year 至 30 Years(Child, 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

结局指标

主要结局

Data resource, that can be linked with additional tumor cell information, to better characterize the biology and subtypes of childhood ALL

Mechanism for storing, distributing, and tracking usage of blast and germline genomic information

Determination of genome-wide genotypes

Identification of genetic variations associated with important phenotypes (treatment response, adverse effects, risk of acute lymphoblastic leukemia [ALL], and risk of ALL subtypes)

次要结局

未报告次要终点

研究者

申办方类型
Network
责任方
Sponsor

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