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Urokinase-type Plasminogen Activator Receptor and Gastroesophageal Cancer

Urokinase-type Plasminogen Activator Receptor and Gastroesophageal Adenocarcinomas

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04669951
Enrollment
100
Registered
2020-12-17
Start date
2019-11-18
Completion date
2020-11-30
Last updated
2021-06-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Esophagus Cancer, Adenocarcinoma

Keywords

urokinase plasminogen activator receptor, uPAR, Cardia, Adenocarcinoma, Immunohistochemistry

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.

Interventions

OTHERuPAR immunohistochemistry

Resected esophageal cancer will be qualitatively and semi-quantitatively analyzed for uPAR expression

Sponsors

Michael Patrick Achiam
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Intervention model description

The patients will be drawn from the existing clinical biobank. The biobank is located at the department of pathology, Rigshospitalet. From this clinical biobank, a new temporary research biobank will be made. Supplementary sections from formalin-fixed paraffin embedded (FFPE) blocks containing tumor tissue will be cut and Haematoxylin and eosin (HE) and immunohistochemical (IHC) staining will be performed.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
uPAR microexpressionUp to 6 monthsOur 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 monthsA pathology staining will determine the uPAR in the tumor compared with the healthy cells.

Secondary

MeasureTime frameDescription
uPAR in patient groupsUp to 6 monthsBaseline statistical analysis of patient groups and their expression of uPAR in their resected tumor tissues will be made.

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026