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临床试验/NCT04669951
NCT04669951已完成不适用

Urokinase-type Plasminogen Activator Receptor and Gastroesophageal Adenocarcinomas

Michael Patrick Achiam2 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2019年11月18日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
100
试验地点
2
主要终点
uPAR microexpression

研究概览

简要总结

The aim of this study is to investigate urokinase Plasminogen Activator Receptor (uPAR) microexpression in gastroesophageal cancer (adenocarcinomas) both qualitatively and semi-quantitatively and to evaluate if it offers a possibility for future imagining purposes.

详细描述

  • Sections of the tumor tissue will be HE stained.
  • Sections of the tumor tissue will be stained with an uPAR antibody for immunohistochemistry.
  • Immunohistochemical staining against cytokeratin which colors cancer cells will be made to assist the observer in the evaluation of uPAR microexpression pattern.
  • A semiqualitative scale corresponding to the level of uPAR expression will be made.
  • Quantitative polymerase chain reaction will be used to validate the immunohistochemistry uPAR expression pattern.
  • An electronic scoring system (digital pathology) will be trained to access the expression of uPAR in both tumor- and normal tissue.

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

  • Age ≥18 years old.
  • Patients who underwent curatively intended surgery for gastroesophageal cancer
  • Patients who underwent surgery after 01-01-2016.

排除标准

  • Patients who applied for an exception from medical research at the "National Registry of Tissue Use."
  • Patients with other histological subtypes than adenocarcinoma.

结局指标

主要结局

uPAR microexpression

时间窗: Up to 6 months

Our primary objective is to investigate uPAR microexpression in gastroesophageal adenocarcinomas both qualitatively and semi-quantitatively. This will be done by a pathology analysis of gastroesophageal cancer resections.

Tumor-to-background ratio

时间窗: Up to 6 months

A pathology staining will determine the uPAR in the tumor compared with the healthy cells.

次要结局

  • uPAR in patient groups(Up to 6 months)

研究者

发起方
Michael Patrick Achiam
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Michael Patrick Achiam

Consultant, MD, DMSci, Ph.D., FEBS-OG, Ass. Professor

Rigshospitalet, Denmark

研究点 (2)

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