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Urokinase-type Plasminogen Activator Receptor and Gastroesophageal Cancer

Not Applicable
Completed
Conditions
Esophagus Cancer, Adenocarcinoma
Interventions
Other: uPAR immunohistochemistry
Registration Number
NCT04669951
Lead Sponsor
Michael Patrick Achiam
Brief Summary

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.

Detailed Description

* 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.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
100
Inclusion Criteria
  • Age ≥18 years old.
  • Patients who underwent curatively intended surgery for gastroesophageal cancer
  • Patients who underwent surgery after 01-01-2016.
Exclusion Criteria
  • Patients who applied for an exception from medical research at the "National Registry of Tissue Use."
  • Patients with other histological subtypes than adenocarcinoma.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
uPAR expressionuPAR immunohistochemistryImmunohistochemistry
Primary Outcome Measures
NameTimeMethod
uPAR microexpressionUp 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 ratioUp to 6 months

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

Secondary Outcome Measures
NameTimeMethod
uPAR in patient groupsUp to 6 months

Baseline statistical analysis of patient groups and their expression of uPAR in their resected tumor tissues will be made.

Trial Locations

Locations (1)

Rigshospitalet

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Copenhagen, Region Hovedstaden, Denmark

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