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Prognostic value of some inflammatory markers in patients with lymphoma

Background: Lymphoma is a group of blood cell tumors which develop from lymphocytes. The main forms of lymphoma are Hodgkin lymphoma (HL) and non-HL (NHL). Cytokines may contribute to lymphoma and they are related to risk NHL and HL. Aim: Assessment of the serum level of certain inflammatory markers...

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Autores principales: Hamed Anber, Nahla, EL-Sebaie, Ahmed H., Darwish, Noureldien H.E., Mousa, Shaker A., Shamaa, Sameh S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6422884/
https://www.ncbi.nlm.nih.gov/pubmed/30814315
http://dx.doi.org/10.1042/BSR20182174
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author Hamed Anber, Nahla
EL-Sebaie, Ahmed H.
Darwish, Noureldien H.E.
Mousa, Shaker A.
Shamaa, Sameh S.
author_facet Hamed Anber, Nahla
EL-Sebaie, Ahmed H.
Darwish, Noureldien H.E.
Mousa, Shaker A.
Shamaa, Sameh S.
author_sort Hamed Anber, Nahla
collection PubMed
description Background: Lymphoma is a group of blood cell tumors which develop from lymphocytes. The main forms of lymphoma are Hodgkin lymphoma (HL) and non-HL (NHL). Cytokines may contribute to lymphoma and they are related to risk NHL and HL. Aim: Assessment of the serum level of certain inflammatory markers as complementary indicators to confirm diagnosis of lymphoma patients that may be subjected to more invasive biopsy methods. Method: The serum levels of interleukin (IL)-1β (IL-1β), IL-6, IL-10, tumor necrosis factor-α (TNF-α), monocyte chemotactic protein-1 (MCP-1), granulocyte colony-stimulating factor (G-CSF), and eotaxin were assessed by Bio-Plex Pro assays in 81 lymphoma patients and 44 NHL and 37 HL patients before and after chemotherapy treatment as well as 20 healthy persons as a control group. Results: Lymphoma patients showed significantly raised marker levels before treatment and significantly reduced levels related to pre-treatment and controls of post-treatment for most of the markers. MCP-1 reported the highest diagnostic accuracy. G-CSF significantly raised pre-treatment and TNF-α. MCP-1 significantly increased in post treated HL compared with NHL. In order to distinguish HL from NHL, G-CSF reported the highest diagnostic accuracy. NHL patients reported complete remission (CR) and those who reported stable disease (SD) and progressive disease (PD) represented 25% and 38% respectively compared with 16% and 27% of HL patients, while partial remission (PR) of HL patients were 56% compared with 36% of NHL patients. Conclusion: Most of the markers were significantly increased in pre-treatment but significantly decreased post-treatment. However, it was not considerably enough to get better prognosis of the disease. Elevated serum levels of inflammatory markers correlate with disease severity and low benefit from treatment.
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spelling pubmed-64228842019-03-27 Prognostic value of some inflammatory markers in patients with lymphoma Hamed Anber, Nahla EL-Sebaie, Ahmed H. Darwish, Noureldien H.E. Mousa, Shaker A. Shamaa, Sameh S. Biosci Rep Research Articles Background: Lymphoma is a group of blood cell tumors which develop from lymphocytes. The main forms of lymphoma are Hodgkin lymphoma (HL) and non-HL (NHL). Cytokines may contribute to lymphoma and they are related to risk NHL and HL. Aim: Assessment of the serum level of certain inflammatory markers as complementary indicators to confirm diagnosis of lymphoma patients that may be subjected to more invasive biopsy methods. Method: The serum levels of interleukin (IL)-1β (IL-1β), IL-6, IL-10, tumor necrosis factor-α (TNF-α), monocyte chemotactic protein-1 (MCP-1), granulocyte colony-stimulating factor (G-CSF), and eotaxin were assessed by Bio-Plex Pro assays in 81 lymphoma patients and 44 NHL and 37 HL patients before and after chemotherapy treatment as well as 20 healthy persons as a control group. Results: Lymphoma patients showed significantly raised marker levels before treatment and significantly reduced levels related to pre-treatment and controls of post-treatment for most of the markers. MCP-1 reported the highest diagnostic accuracy. G-CSF significantly raised pre-treatment and TNF-α. MCP-1 significantly increased in post treated HL compared with NHL. In order to distinguish HL from NHL, G-CSF reported the highest diagnostic accuracy. NHL patients reported complete remission (CR) and those who reported stable disease (SD) and progressive disease (PD) represented 25% and 38% respectively compared with 16% and 27% of HL patients, while partial remission (PR) of HL patients were 56% compared with 36% of NHL patients. Conclusion: Most of the markers were significantly increased in pre-treatment but significantly decreased post-treatment. However, it was not considerably enough to get better prognosis of the disease. Elevated serum levels of inflammatory markers correlate with disease severity and low benefit from treatment. Portland Press Ltd. 2019-03-19 /pmc/articles/PMC6422884/ /pubmed/30814315 http://dx.doi.org/10.1042/BSR20182174 Text en © 2019 The Author(s). http://creativecommons.org/licenses/by/4.0/This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY) (http://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Articles
Hamed Anber, Nahla
EL-Sebaie, Ahmed H.
Darwish, Noureldien H.E.
Mousa, Shaker A.
Shamaa, Sameh S.
Prognostic value of some inflammatory markers in patients with lymphoma
title Prognostic value of some inflammatory markers in patients with lymphoma
title_full Prognostic value of some inflammatory markers in patients with lymphoma
title_fullStr Prognostic value of some inflammatory markers in patients with lymphoma
title_full_unstemmed Prognostic value of some inflammatory markers in patients with lymphoma
title_short Prognostic value of some inflammatory markers in patients with lymphoma
title_sort prognostic value of some inflammatory markers in patients with lymphoma
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6422884/
https://www.ncbi.nlm.nih.gov/pubmed/30814315
http://dx.doi.org/10.1042/BSR20182174
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