跳至主要内容
临床试验/NCT02299622
NCT02299622Unknown不适用

Establishment of Personalized Cancer Medicine Using Samsung Cancer Sequencing Platform in Lung Cancer/Mediastinal Tumor/ Head & Neck/Esophageal Cancer/Rare Cancer (PerSeq: Personalized Sequence)

Samsung Medical Center1 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2013年11月最近更新:
适应症

试验速览

阶段
不适用
入组人数
200
试验地点
1
主要终点
the spectrum of targetable genetic mutation in evaluated cancer specimens (for example, % of EGFR T790M mutation, BRAF mutation, or ALK mutation)

研究概览

简要总结

The next generation of personalized medical treatment according to the type of personal genetic information are evolving rapidly. The genome analysis needs systematic infra and database based on personal genetic information Therefore, a big data of genome-clinical information is important.

详细描述

To determine the feasibility of the use of tumor's molecular profiling and targeted therapies in the treatment of advanced cancer and to determine the clinical outcome(PFS, duration of response and overall survival) of patients with advanced cancer, the investigators are going to take a fresh tissue of patients and process molecular profiling.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

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

入选标准

  • metastatic, histologically confirmed NSCLC, head & Neck Cancer, Esophageal cancer

排除标准

  • 未提供

结局指标

主要结局

the spectrum of targetable genetic mutation in evaluated cancer specimens (for example, % of EGFR T790M mutation, BRAF mutation, or ALK mutation)

时间窗: 3 years

The pattern of the tumor's molecular profiling in advanced thoracic (lung, esophagus, or tthymic) cancer

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Keunchil Park

Professor

Samsung Medical Center

研究点 (1)

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