跳至主要内容
临床试验/NCT02517892
NCT02517892已完成不适用

A Prospective Trial to Study the Evolution of Clonal Architecture of Tumors From Patients Treated With Molecular Targeted Agents

Gustave Roussy, Cancer Campus, Grand Paris2 个研究点 分布在 1 个国家目标入组 1,500 人开始时间: 2014年12月18日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
1,500
试验地点
2
主要终点
Type and frequency of molecular alterations in resistant tumors using whole exome sequencing

研究概览

简要总结

This is a prospective study to identify molecular mechanisms of acquired resistance to targeted therapies in patients with unresectable or metastatic cancer.

This is a protocol to study clinical characteristics and biopsy tissue of patients with oncogene-driven cancer who have had previous clinical response to targeted therapy and subsequently experience progression of disease. The tissues and other specimens will be used to carry out laboratory studies to explore the molecular basis of acquired resistance to targeted therapies.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Other
盲法
None

入排标准

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

入选标准

  • Patients diagnosed with confirmed cancer and who fulfill the following eligibility criteria will be considered eligible for this study:
  • Patient affiliated to a social security regimen
  • Patients scheduled to receive anticancer agents or currently receiving anticancer agents
  • Tumor lesion accessible to core biopsies (malignant effusions can represent an alternative)
  • Patient who is fully informed, able to comply with the protocol and who signed the informed consent.
  • Availability of initial tumor material (ideally frozen, or non-Bouin fixed paraffin embedded material) acquired before exposure to the targeted therapy Note: Patients may have received other treatments since treatment with targeted therapies including radiation or chemotherapy, before undergoing the study biopsy.

排除标准

  • Coagulation abnormality prohibiting a biopsy

结局指标

主要结局

Type and frequency of molecular alterations in resistant tumors using whole exome sequencing

时间窗: 30 days after inclusion

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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