Vasculogenic Mimicry in Urothelial Carcinoma

Sponsor
Assiut University (Other)
Overall Status
Unknown status
CT.gov ID
NCT04295967
Collaborator
(none)
70
24

Study Details

Study Description

Brief Summary

In this study, the investigators aim at:
  1. Evaluate the presence of vasculogenic mimicry in urothelial carcinomas by CD31-PAS double staining.

  2. Correlate the presence of vasculogenic mimicry with the clinicopathologic features as age, sex, TNM stage, pathological grade, recurrence, carcinoma in situ, lymphovascular emboli, lymph node metastasis, necrosis, surgical margin, multifocality and tumor size in urothelial carcinoma.

Condition or Disease Intervention/Treatment Phase
  • Other: formalin fixed paraffin embedded blocks

Detailed Description

Bladder cancer is the ninth most common cancer worldwide which seriously affects human health. In Egypt, it is the third common malignant tumor.

Urothelial carcinoma (UC) is considered the most common histologic type of bladder cancer.

It is well recognized that the biological behavior of several cancers is closely related to their blood supply. Tumor progression and metastasis have been long associated with tumor angiogenesis. However, several studies demonstrated that vascular targeting drugs which induce endothelial cell apoptosis have a little effect. So, it has been suggested that novel tumor microcirculation patterns may exist in these neoplasms.

Vasculogenic mimicry (VM), is a novel tumor microcirculation system. Maniotis et al initially discovered VM in melanoma and defined these channels to be composed of tumor basement membrane lined externally by tumor cells, lacking blood vessel endothelium and containing plasma and red blood cells. So VM can be distinguished using immunohistochemical (IHC) staining and histochemical double staining. VM is CD31- or CD34-negative (endothelial markers) and periodic acid-Schiff (PAS) positive.

Vasculogenic mimicry was detected in several malignant tumors. Several studies reported that VM can promote tumor progression and metastasis and it is positively associated with pathological grade, stage, recurrence and drug resistance. Previous studies which evaluate, the role of VM in urothelial carcinoma yield controversial results. So, the value of VM in urothelial carcinomas and its relation to the clinicopathologic parameters remains to be elucidated.

Study Design

Study Type:
Observational
Anticipated Enrollment :
70 participants
Observational Model:
Other
Time Perspective:
Cross-Sectional
Official Title:
Vasculogenic Mimicry in Urothelial Carcinoma and Its Association With Clinicopathologic Features
Anticipated Study Start Date :
May 1, 2020
Anticipated Primary Completion Date :
May 1, 2021
Anticipated Study Completion Date :
May 1, 2022

Arms and Interventions

Arm Intervention/Treatment
1

presence of recurrence of urothelial carcinoma

Other: formalin fixed paraffin embedded blocks
The study will be conducted using formalin fixed paraffin embedded blocks of seventy cases of urothelial carcinomas .CD31-PAS dual-staining will be performed to confirm the presence of VM.

2

absence of recurrence of urothelial carcinoma

Other: formalin fixed paraffin embedded blocks
The study will be conducted using formalin fixed paraffin embedded blocks of seventy cases of urothelial carcinomas .CD31-PAS dual-staining will be performed to confirm the presence of VM.

Outcome Measures

Primary Outcome Measures

  1. Evaluate the presence of vasculogenic mimicry in urothelial carcinomas by CD31-PAS double staining [baseline]

Secondary Outcome Measures

  1. Correlate the presence of vasculogenic mimicry with the clinicopathologic features in urothelial carcinoma. [baseline]

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Inclusion Criteria:
    • Specimens of urothelial carcinoma.
Exclusion Criteria:
    • Any criteria that not fulfill the inclusion criteria such as resected urinary bladder tumors other than urothelial carcinoma.

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Assiut University

Investigators

  • Principal Investigator: Abeer R Mohamed, professor, Assiut University

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Ereny Kamal Louis, administrator, Assiut University
ClinicalTrials.gov Identifier:
NCT04295967
Other Study ID Numbers:
  • VM in urothelial carcinoma
First Posted:
Mar 5, 2020
Last Update Posted:
Mar 5, 2020
Last Verified:
Mar 1, 2020
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 5, 2020