Vascularity Impact on the Treatment Outcome in Malignant Pleural Mesothelioma(VITMPM)

NCT ID: NCT02603315

Last Updated: 2016-06-01

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

50 participants

Study Classification

OBSERVATIONAL

Study Start Date

2015-10-31

Study Completion Date

2016-05-31

Brief Summary

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The purpose of this study is to To assess the correlation between the predictive factor of vascularity (CD74) in malignant pleural mesothelioma and treatment results (response rate, and overall survival) .

Detailed Description

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This is a randomized controlled retrospective study through Examination of paraffin blocks of the patient selected to be included in the study for assessment of the selected vascularity marker of malignant pleural mesothelioma of both types . The CD74 (LN2) antibody is intended for qualified laboratories to qualitatively identify by light microscopy the presence of associated antigens in sections of formalin-fixed paraffin-embedded tissue sections using Immunohistochemistry test methods.

Conditions

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Malignant Pleural Mesotheliomas

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Interventions

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marker CD74 and vascular endothelial growth factor VEGF

correlate the result of vascularity test done on paraffin blocks on both types of malignant pleural mesothelioma patients diagnosed and receive treatment and evaluated after treatment

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Histopathological confirmation of malignant pleural mesothelioma .
* Full clinical data.
* Availability for follow up: Personal communication will be attempted in order to collect missing information.

3-The files of all patients will be reviewed to analyze the following :
* Operative data if done .
* Pathological review and immunohistochemistry.
* Laboratory investigations: (routine investigations: complete blood picture,liver and renal function test)
* Radiological investigations:( CXR and CT-chest, Abdominal and pelvic U\\S and MRI ).
* Treatment protocols applied: Radiotherapy and Chemotherapy.
* Response and survival after treatment .

Exclusion Criteria

* cases not receive chemotherapy ,on available of evaluation after treatment
Minimum Eligible Age

39 Years

Maximum Eligible Age

84 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Ain Shams University

OTHER

Sponsor Role lead

Responsible Party

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Muna Sami Jassim

Doctor in clinical oncology and nuclear medicine department

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Amr S Saad, MD

Role: STUDY_DIRECTOR

Ain Shams University

Mahmoud Ellithy, MD

Role: STUDY_CHAIR

Ain Shams University

Doaa Atef, MD

Role: STUDY_DIRECTOR

Ain Shams University

Hoda Abougabal, MD

Role: STUDY_DIRECTOR

Ain Shams University

Locations

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Ain Shams University Hospital

Cairo, , Egypt

Site Status

Countries

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Egypt

Other Identifiers

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DR-81

Identifier Type: -

Identifier Source: org_study_id

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