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Coexpression of CD5 and CD43 predicts worse prognosis in diffuse large B‐cell lymphoma
Both CD5 and CD43 are expressed on the surface of B lymphocytes of definite phase and associated with the adverse outcome in diffuse large B‐cell lymphoma (DLBCL). However, the relationship between CD5 and CD43 expression and the prognostic value of CD5/CD43 coexpression in DLBCL are unknown. We her...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6144247/ https://www.ncbi.nlm.nih.gov/pubmed/30019388 http://dx.doi.org/10.1002/cam4.1674 |
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author | Ma, Xiao‐bo Zhong, Yan‐ping Zheng, Yan Jiang, Jing Wang, Yin‐ping |
author_facet | Ma, Xiao‐bo Zhong, Yan‐ping Zheng, Yan Jiang, Jing Wang, Yin‐ping |
author_sort | Ma, Xiao‐bo |
collection | PubMed |
description | Both CD5 and CD43 are expressed on the surface of B lymphocytes of definite phase and associated with the adverse outcome in diffuse large B‐cell lymphoma (DLBCL). However, the relationship between CD5 and CD43 expression and the prognostic value of CD5/CD43 coexpression in DLBCL are unknown. We herein determined the correlation between CD5 and CD43 expression, as separate factors or in combination, with the clinicopathological features and survival of 200 patients with DLBCL receiving standard chemotherapy with or without rituximab. Among these DLBCL patients, CD5 expression, CD43 expression, and CD5/CD43 coexpression were detected in 18 (9%), 57 (27%), and 10 (5%) patients, respectively, and all were positively correlated with advanced age and nongerminal cell type. CD5‐positive and CD43‐positive DLBCL patients had poorer event‐free survival (EFS, P < 0.001) and overall survival (OS, P < 0.001) than CD5‐negative and CD43‐negative patients, respectively. CD5/CD43 coexpression was correlated with a significantly worse prognosis than CD5 or CD43 expression alone. Univariate analysis showed that CD5 expression, CD43 expression, and CD5/CD43 coexpression were all adverse prognostic factors for DLBCL patient survival, and CD5/CD43 coexpression was associated with a greater relative risk for recurrence and death than either CD5 or CD43 expression alone. Multivariate analysis demonstrated that CD5/CD43 coexpression was an independent prognostic factor for EFS (P < 0.001) and OS (P < 0.001) in DLBCL. In conclusion, our data indicate that DLBCL patients with CD5/CD43 coexpression represent a specific subgroup with a significantly worse prognosis than those expressing either marker alone. |
format | Online Article Text |
id | pubmed-6144247 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-61442472018-09-24 Coexpression of CD5 and CD43 predicts worse prognosis in diffuse large B‐cell lymphoma Ma, Xiao‐bo Zhong, Yan‐ping Zheng, Yan Jiang, Jing Wang, Yin‐ping Cancer Med Clinical Cancer Research Both CD5 and CD43 are expressed on the surface of B lymphocytes of definite phase and associated with the adverse outcome in diffuse large B‐cell lymphoma (DLBCL). However, the relationship between CD5 and CD43 expression and the prognostic value of CD5/CD43 coexpression in DLBCL are unknown. We herein determined the correlation between CD5 and CD43 expression, as separate factors or in combination, with the clinicopathological features and survival of 200 patients with DLBCL receiving standard chemotherapy with or without rituximab. Among these DLBCL patients, CD5 expression, CD43 expression, and CD5/CD43 coexpression were detected in 18 (9%), 57 (27%), and 10 (5%) patients, respectively, and all were positively correlated with advanced age and nongerminal cell type. CD5‐positive and CD43‐positive DLBCL patients had poorer event‐free survival (EFS, P < 0.001) and overall survival (OS, P < 0.001) than CD5‐negative and CD43‐negative patients, respectively. CD5/CD43 coexpression was correlated with a significantly worse prognosis than CD5 or CD43 expression alone. Univariate analysis showed that CD5 expression, CD43 expression, and CD5/CD43 coexpression were all adverse prognostic factors for DLBCL patient survival, and CD5/CD43 coexpression was associated with a greater relative risk for recurrence and death than either CD5 or CD43 expression alone. Multivariate analysis demonstrated that CD5/CD43 coexpression was an independent prognostic factor for EFS (P < 0.001) and OS (P < 0.001) in DLBCL. In conclusion, our data indicate that DLBCL patients with CD5/CD43 coexpression represent a specific subgroup with a significantly worse prognosis than those expressing either marker alone. John Wiley and Sons Inc. 2018-07-17 /pmc/articles/PMC6144247/ /pubmed/30019388 http://dx.doi.org/10.1002/cam4.1674 Text en © 2018 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Clinical Cancer Research Ma, Xiao‐bo Zhong, Yan‐ping Zheng, Yan Jiang, Jing Wang, Yin‐ping Coexpression of CD5 and CD43 predicts worse prognosis in diffuse large B‐cell lymphoma |
title | Coexpression of CD5 and CD43 predicts worse prognosis in diffuse large B‐cell lymphoma |
title_full | Coexpression of CD5 and CD43 predicts worse prognosis in diffuse large B‐cell lymphoma |
title_fullStr | Coexpression of CD5 and CD43 predicts worse prognosis in diffuse large B‐cell lymphoma |
title_full_unstemmed | Coexpression of CD5 and CD43 predicts worse prognosis in diffuse large B‐cell lymphoma |
title_short | Coexpression of CD5 and CD43 predicts worse prognosis in diffuse large B‐cell lymphoma |
title_sort | coexpression of cd5 and cd43 predicts worse prognosis in diffuse large b‐cell lymphoma |
topic | Clinical Cancer Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6144247/ https://www.ncbi.nlm.nih.gov/pubmed/30019388 http://dx.doi.org/10.1002/cam4.1674 |
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