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Clinical features and prognostic factors of primary bone marrow lymphoma
BACKGROUND: Primary bone marrow lymphoma (PBML) is a very uncommon neoplasm originally arising in the bone marrow system, and the most common pathological type is diffuse large B-cell lymphoma. PATIENTS AND METHODS: To describe the clinical characteristics of PBML and evaluate the risk factors relat...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6446986/ https://www.ncbi.nlm.nih.gov/pubmed/31015766 http://dx.doi.org/10.2147/CMAR.S187522 |
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author | Wang, Gangjian Chang, Yu Wu, Xiaolong Li, Xin Li, Ling Zhang, Lei Fu, Xiaorui Sun, Zhenchang Zhang, Xudong Zhang, Mingzh |
author_facet | Wang, Gangjian Chang, Yu Wu, Xiaolong Li, Xin Li, Ling Zhang, Lei Fu, Xiaorui Sun, Zhenchang Zhang, Xudong Zhang, Mingzh |
author_sort | Wang, Gangjian |
collection | PubMed |
description | BACKGROUND: Primary bone marrow lymphoma (PBML) is a very uncommon neoplasm originally arising in the bone marrow system, and the most common pathological type is diffuse large B-cell lymphoma. PATIENTS AND METHODS: To describe the clinical characteristics of PBML and evaluate the risk factors related to prognosis, we recruited and studied 66 patients from our center and the current published literature. Various symptoms are present at the onset of PBML, the most important of which is cytopenia, followed by fever. Forty-seven of these patients were included in our analysis. RESULTS: Univariate analysis suggested that B symptoms (P=0.024), a low serum platelet level (<75×10(9)/L; P=0.032), an elevated serum LDH level (P=0.039), and not achieving a complete response (CR) following initial therapy (P=0.007) are associated with worse outcomes. Multivariate analysis showed that only a low serum platelet level (<75×10(9)/L), B symptoms, and not achieving a CR following initial therapy are independent factors for prognosis. In addition, intensive regimens appear to be beneficial for prognosis. CONCLUSION: PBML is a lymphoma with special clinical features, and its recognition is important for establishing a definitive prognosis model and searching for appropriate therapy. |
format | Online Article Text |
id | pubmed-6446986 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-64469862019-04-23 Clinical features and prognostic factors of primary bone marrow lymphoma Wang, Gangjian Chang, Yu Wu, Xiaolong Li, Xin Li, Ling Zhang, Lei Fu, Xiaorui Sun, Zhenchang Zhang, Xudong Zhang, Mingzh Cancer Manag Res Original Research BACKGROUND: Primary bone marrow lymphoma (PBML) is a very uncommon neoplasm originally arising in the bone marrow system, and the most common pathological type is diffuse large B-cell lymphoma. PATIENTS AND METHODS: To describe the clinical characteristics of PBML and evaluate the risk factors related to prognosis, we recruited and studied 66 patients from our center and the current published literature. Various symptoms are present at the onset of PBML, the most important of which is cytopenia, followed by fever. Forty-seven of these patients were included in our analysis. RESULTS: Univariate analysis suggested that B symptoms (P=0.024), a low serum platelet level (<75×10(9)/L; P=0.032), an elevated serum LDH level (P=0.039), and not achieving a complete response (CR) following initial therapy (P=0.007) are associated with worse outcomes. Multivariate analysis showed that only a low serum platelet level (<75×10(9)/L), B symptoms, and not achieving a CR following initial therapy are independent factors for prognosis. In addition, intensive regimens appear to be beneficial for prognosis. CONCLUSION: PBML is a lymphoma with special clinical features, and its recognition is important for establishing a definitive prognosis model and searching for appropriate therapy. Dove Medical Press 2019-03-29 /pmc/articles/PMC6446986/ /pubmed/31015766 http://dx.doi.org/10.2147/CMAR.S187522 Text en © 2019 Wang et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Wang, Gangjian Chang, Yu Wu, Xiaolong Li, Xin Li, Ling Zhang, Lei Fu, Xiaorui Sun, Zhenchang Zhang, Xudong Zhang, Mingzh Clinical features and prognostic factors of primary bone marrow lymphoma |
title | Clinical features and prognostic factors of primary bone marrow lymphoma |
title_full | Clinical features and prognostic factors of primary bone marrow lymphoma |
title_fullStr | Clinical features and prognostic factors of primary bone marrow lymphoma |
title_full_unstemmed | Clinical features and prognostic factors of primary bone marrow lymphoma |
title_short | Clinical features and prognostic factors of primary bone marrow lymphoma |
title_sort | clinical features and prognostic factors of primary bone marrow lymphoma |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6446986/ https://www.ncbi.nlm.nih.gov/pubmed/31015766 http://dx.doi.org/10.2147/CMAR.S187522 |
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