Aberrant Expression of CD56 in Patients With Hematologic Malignancies.

Sponsor
Asmaa Hassan mohamed Abdel Mawjoud (Other)
Overall Status
Recruiting
CT.gov ID
NCT04546945
Collaborator
(none)
38
2
53.4
19
0.4

Study Details

Study Description

Brief Summary

CD56(cluster of differentiation 56) was found to be ectopically expressed in multiple myeloma . A met analysis indicated that CD56 over expression may be an adverse prognostic factor in AML. To the best of our knowledge, no available data the expression pattern of CD56 in other Hematologic malignancies. This work is designed to evaluate the expression pattern of CD56 in hematologic malignancies.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: CD56

Detailed Description

CD56 is the archetypal phenotypic marker of natural killer cells but can actually be expressed by many more immune cells, including alpha, beta T cells, gamma, delta T cells, dendritic cells, and monocytes. Common to all these CD56 expressing cell types have strong immunostimulatory effector functions, including T helper 1 cytokine production and an efficient cytotoxic capacity. Interestingly, both numerical , functional deficiencies and phenotypic alterations of the CD56 immune cell fraction have been reported in patients with various infectious, autoimmune, or malignant diseases.CD56 is also known as neural cell adhesion molecule (NCAM).

Hematologic malignancies are a heterogeneous group of diseases of diverse incidence, prognosis and etiology that arise from malignant transformation of cells from the bone marrow or the lymphatic system.There are two major groups of Hematologic malignancies according to their cell lineage: Myeloid and lymphoid. Lymphoid neoplasms are a varied group that includes non-Hodgkin lymphoma (NHL), Hodgkin lymphoma (HL), leukemia and multiple myeloma (MM).myeloid neoplasms and acute leukaemia include: Myeloproliferative neoplasms (MPN), Myelodysplastic/myeloproliferative neoplasms (MDS/MPN), Myelodysplastic syndromes (MDS), Acute myeloid leukaemia (AML), Acute leukemias of ambiguous lineage, B-lymphoblastic leukaemia/lymphoma, T-lymphoblastic leukaemia/lymphoma.The exact causes of Hematologic malignancies are still unknown although multiple epidemiological studies have reported an association between the development of Hematologic malignancies and several risk factors. Some factors are well documented to increase the risk of some types of leukaemia such as benzene exposure and ionizing radiation.However, many other factors were observed to have an association with Hematologic malignancies such as age, gender, tobacco smoking , obesity , hepatitis C virus (HCV) infection , family history , and environmental exposure to pesticides but with no clear evidence.

CD56 was found to be ectopically expressed in multiple myeloma. A met analysis indicated that CD56 over expression may be an adverse prognostic factor in AML. To the best of our knowledge, no available data the expression pattern of CD56 in other Hematologic malignancies. This work is designed to evaluate the expression pattern of CD56 in hematologic malignancies.

Study Design

Study Type:
Observational [Patient Registry]
Anticipated Enrollment :
38 participants
Observational Model:
Case-Control
Time Perspective:
Cross-Sectional
Official Title:
Resident Doctor at Clinical Pathology Department
Actual Study Start Date :
Jul 20, 2020
Anticipated Primary Completion Date :
Dec 30, 2024
Anticipated Study Completion Date :
Dec 30, 2024

Arms and Interventions

Arm Intervention/Treatment
control cases

normal healthy person

Diagnostic Test: CD56
detection of CD56 by flow cytometry

Patients

Patients with hematologic malignancies. Newly diagnosed.

Diagnostic Test: CD56
detection of CD56 by flow cytometry

Outcome Measures

Primary Outcome Measures

  1. To identify the Pattern of expression of CD56 in hematologic malignancies. [1 years]

    Expression of aberrant CD56 in hematologic malignancies by flowcytometry. To explore incidence of Expression of aberrant CD56 in hematologic malignancies . Correlation between this expression and outcome of the patient.

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Patients with hematologic malignancies.

  • Newly diagnosed

Exclusion Criteria:
  • Patients with hematologic disorders other than hematologic malignancies.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Assiut University Assiut Egypt
2 Assiut university Assiut Egypt

Sponsors and Collaborators

  • Asmaa Hassan mohamed Abdel Mawjoud

Investigators

  • Study Director: Maged S Mahmoud, prof, Assiut University

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

None provided.
Responsible Party:
Asmaa Hassan mohamed Abdel Mawjoud, resident doctor clinical pathology, Assiut University
ClinicalTrials.gov Identifier:
NCT04546945
Other Study ID Numbers:
  • Asmaa Hassan
First Posted:
Sep 14, 2020
Last Update Posted:
Jul 22, 2022
Last Verified:
Jul 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
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 Jul 22, 2022