跳至主要内容
临床试验/NCT01334008
NCT01334008已完成不适用

Development and Validation of a Circulating Tumor DNA Detection Technique in Patients With Metastatic Choroidal Melanoma

Institut Curie1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2011年4月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
40
试验地点
1
主要终点
Assessment and development of circulating tumor DNA detection techniques

研究概览

简要总结

Circulating tumor DNA detection and quantification in patients with metastatic choroidal melanoma.

详细描述

Technique development: In first step, the different available techniques will be evaluated for specificity and sensibility using serial dilutions of cell lines with or without GNAQ mutation.

Validation: The tumor DNA detection rate will be estimated from metastatic uveal patient's blood. The investigators will study 40 patients to obtain at least 15 patients bearing a GNAQ mutation in the primitive tumor or in metastasis. With those 15 patients, the investigators will determinate the most sensitive technique and the best cost/efficiency ratio.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Diagnostic
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

  • Age > or = 18 years.
  • Patient with a metastatic choroidal melanoma.
  • Patient with tumor or metastasis available for GNAQ (Guanine nucleotide blinding protein) status characterization.
  • Patient able to stand a blood collection.
  • Signed written informed consent approved by competent authority and ethic committee.

排除标准

  • Patient without social protection/insurance.
  • Current pregnancy and lactation.
  • All social, medical, psychological, situations making the study impossible.
  • Person deprived of liberty.

研究组 & 干预措施

Blood sampling

Other

干预措施: Blood sampling (Biological)

结局指标

主要结局

Assessment and development of circulating tumor DNA detection techniques

时间窗: 2 years

Quantification of circulating tumor DNA in blood samples. Results expressed in number of samples where circulating DNA is present.

次要结局

  • Detection technique comparison (PAP (pyrophosphorolysis activated polymerisation), BEAMing, NGS(next sequencing generation)) in terms of feasibility, robustness, sensitivity and cost.(2 years)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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