跳至主要内容
临床试验/NCT04762862
NCT04762862Enrolling By Invitation不适用

QUANTACT : Impact of Pangenomic QUANTitative Alterations in Cancer Therapy

Centre Hospitalier Universitaire de Nice1 个研究点 分布在 1 个国家目标入组 1,200 人开始时间: 2021年2月1日最近更新:
适应症

试验速览

阶段
不适用
状态
Enrolling By Invitation
入组人数
1,200
试验地点
1
主要终点
Number of targeted molecular alterations

研究概览

简要总结

"Precision medicine and targeted therapies have played a crucial role over the past ten years in the personalized care of cancer patients. In this retrospective and observational study, we focused on patients for which no standard or curative treatment was available and for which the management was discussed in a Molecular Tumor Board (MTB).

The role of the MTB is to decide the most appropriate therapeutic options for patients according to the potential identification of molecular targets.

Among the analyses carried out, we focused on a quantitative genome-wide analysis: the CGH/SNP-array (Comparative Genomic Hybridization / Single Nucleotide Polymorphism on array). The objective was to evaluate the impact of CGH/SNP-array analyses in the identification of targeted molecular alterations.

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研究设计

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

入排标准

性别
All
接受健康志愿者

入选标准

  • Histologically or cytologically confirmed solid tumor malignancy that is advanced or metastatic ;
  • no standard or curative treatment available;
  • non-opposition of the patient collected.

排除标准

  • multiple cancer patient;
  • ECOG Scale of Performance Status (PS) ≥2

结局指标

主要结局

Number of targeted molecular alterations

时间窗: at day 0

Number of targeted molecular alterations

次要结局

  • Number of patients eligible for targeted therapy (clinical trials or "off-label" drug)(at day 0)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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