Systemic Inflammatory Markers in B-cell Neoplasm

NCT ID: NCT06847529

Last Updated: 2025-03-12

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

NOT_YET_RECRUITING

Total Enrollment

70 participants

Study Classification

OBSERVATIONAL

Study Start Date

2025-03-22

Study Completion Date

2025-12-30

Brief Summary

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This study was to evaluate the role of systemic inflammatory markers in predicting outcome for patients with B cell neoplasm

Detailed Description

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In malignant tumors, Inflammation plays a crucial role in the development, invasion, and metastasis of malignant tumors. Cancer is often described as a wound that does not heal, highlighting the significance of inflammation in cancer progression. Many tumors are heavily infiltrated by immune cells, including macrophages, neutrophils, and lymphocytes. Therefore, markers related to inflammation and the host immune response are pertinent as biological indicators of B-cell neoplasm progression. Inflammation contributes significantly to the initiation and advancement of B-cell neoplasms by providing nutrients to tumor cells, promoting cell growth, and disrupting immune homeostasis. Various composite indices based on circulating inflammatory cells have been developed as straightforward measures to assess systemic inflammation. Elevated serum inflammatory markers reflect the body's response to malignant tumors. Pro-inflammatory cytokines and inflammatory cells within the tumor microenvironment have been shown to promote tumor growth, induce DNA damage, facilitate angiogenesis, suppress the immune system, and correlate with poor patient survival outcomes. Targeting cytokine receptors or other components in inflammatory pathways involved in metastasis may offer therapeutic potential for malignant tumors. Given the pivotal role of inflammation in cancer biology, identifying novel immune markers is essential for predicting the prognosis of patients with Diffuse Large B-Cell Lymphoma (DLBCL). patients

Conditions

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B-cell Neoplasm

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* Individuals newly diagnosed with B-cell neoplasms, including:
* Burkitt's lymphoma (BL)
* Chronic lymphocytic leukemia (CLL)
* Diffuse large B-cell lymphoma (DLBCL)
* Follicular lymphoma (FL)
* Hairy cell leukemia (HCL)
* Splenic B-cell lymphoma/leukemia with prominent nucleoli (SBLPN)
* High-grade B-cell lymphoma (HGBL)
* Lymphoplasmacytic lymphoma (LPL)/Waldenström macroglobulinemia
* Mantle cell lymphoma (MCL)
* Splenic marginal zone lymphoma (MZL)
* Monoclonal B-cell lymphocytosis (MBL)
* Multiple myeloma (plasma cell myeloma)
* Monoclonal gammopathy of undetermined significance (MGUS)
* Age 18 years or older.

Exclusion Criteria

* Individuals previously diagnosed with B-cell neoplasms.
* Individuals younger than 18 years.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Assiut University

OTHER

Sponsor Role lead

Responsible Party

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Marline Wiliam Fayez Abdel-Shahid

Resident Doctor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Alaa El-Din Abdel Moneim El-Sayed, Doctor

Role: STUDY_CHAIR

Assiut University

Locations

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Assiut University

Asyut, , Egypt

Site Status

Countries

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Egypt

Central Contacts

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Marlien Wiliam Fayez, Resident doctor

Role: CONTACT

01156900472

Mai Mostafa Mohamed, Doctor

Role: CONTACT

01223971678

References

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Reference Type BACKGROUND
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Reference Type BACKGROUND
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Other Identifiers

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markers In B-cell tumors

Identifier Type: -

Identifier Source: org_study_id

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