跳至主要内容
临床试验/NCT01585376
NCT01585376已完成不适用

Study Recurrency Testing of Mutations Identified in WGS of Pediatric Rhabdomyosarcoma

Children's Oncology Group0 个研究点目标入组 58 人开始时间: 2012年4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
58
主要终点
Frequency of particular genetic lesions

研究概览

简要总结

RATIONALE: Studying samples of blood and tissue from patients with cancer in the laboratory may help doctors learn more about changes that occur in DNA and find biomarkers related to cancer. It may also help doctors find better ways to treat cancer.

PURPOSE: This research trial studies genes in samples from younger patients with rhabdomyosarcoma.

详细描述

OBJECTIVES:

  • To obtain a larger cohort of rhabdomyosarcoma samples (alveolar and embryonal) to establish a more accurate estimate of the frequency of particular genetic lesions.
  • To provide the statistical power to establish an unambiguous connection between focal genetic lesions, histological subtype, and outcome for patients with rhabdomyosarcoma.

OUTLINE: DNA samples are analyzed in solid and liquid phase for exons of all genes mutated from previous discovery. DNA is then eluted and sequenced by illumina platform.

研究设计

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

入排标准

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

Frequency of particular genetic lesions

Identification of mutations that occur in at least 5% of rhabdomyosarcomas as a whole

次要结局

未报告次要终点

研究者

申办方类型
Network
责任方
Sponsor

相似试验

Studying Genes in Samples From Younger Patients With... | 临床试验