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临床试验/NCT04581109
NCT04581109终止不适用

Detection of Viable CTCs Using the EPIDROP Technology in Metastatic Prostate Cancer

University Hospital, Montpellier4 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2021年5月27日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
终止
入组人数
100
试验地点
4
主要终点
EPIDROP technique sensitivity versus CellSearch system sensitivity

研究概览

简要总结

The use of liquid biopsy could be the key for precision medicine. Circulating tumor cells (CTCs) are the most studied circulating biomarkers used to assess the metastatic process and they have shown their clinical validity and utility in cancer patients. However, their detection and capture are still a challenge as they are very rare in the bloodstream. In this clinical trial named "EPIDROP", the investigators will use an innovative device called EPIDROP (for EPIspot in a DROP) in metastatic prostate cancer. EPIDROP is a completely new technology answering to biological and clinical questions by proposing a procedure detecting the functional subset of prostatic CTCs at the single cell level. The investigators will stain cells in the sample for EpCAM, PSMA, CD45 before to encapsulate them one by one in microdroplets and measure the PSA secretion by only the viable CTCs. This study aims to demonstrate the non-inferiority of the EPIDROP compared to the CellSearch system.

详细描述

Methods :

One hundred patients with a metastatic prostate cancer will be recruited plus 50 healthy donors. Twenty ml of blood will be drawn : 10 ml of blood will be drawn on CellSave tubes (fixed cells) for CTC detection using the FDA-cleared CellSearch system (gold standard) and 10 ml of blood will be drawn on EDTA tubes (viable cells) for the detection of functional CTCs using the EPIDROP. Patients will be followed for 18 months.

Samples from fifty control subjects will be provided by the Etablissement Français du Sang.

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
Male
接受健康志愿者

入选标准

  • To be male, over 18 years old
  • Metastatic prostate cancer naive to any treatment or metastatic prostate cancer in biological recurrence (PSA increase) and/or clinical recurrence after hormone suppression (mCRPC)

排除标准

  • Non-metastatic prostate cancer in biological and/or clinical recurrence after hormone-suppression (nmCRPC)
  • Other active or treated cancer less than 5 years old
  • Be protected by law (guardianship or curatorship)
  • Be deprived of liberty by administrative decision
  • Not being affiliated to a social security scheme, or not being a beneficiary of such a plan
  • Being in a period of exclusion from another protocol
  • Inability to understand and/or respond to questionnaires
  • Inability to understand the nature, purpose and methodology of the study
  • Refusal to sign informed consent

研究组 & 干预措施

Patients with metastatic prostate cancer

Experimental

干预措施: Blood sample (Biological)

结局指标

主要结局

EPIDROP technique sensitivity versus CellSearch system sensitivity

时间窗: At 18 months

Proportion of true positive and false negative patients with a confidence interval

EPIDROP technique specificity versus CellSearch system specificity

时间窗: At 18 months

Proportion of true negative and false positive healthy controls with a confidence interval

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 (4)

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