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The clinical features and prognosis of 100 AIDS-related lymphoma cases
To improve outcomes and risk assessment, we systematically analyzed the clinical features of patients with acquired immunodeficiency syndrome (AIDS)-related lymphoma (ARL) and identified survival-associated factors. Data were collected from 100 patients diagnosed with ARL at the Henan Provincial Inf...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6441082/ https://www.ncbi.nlm.nih.gov/pubmed/30926889 http://dx.doi.org/10.1038/s41598-019-41869-9 |
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author | Wu, Dedong Chen, Chen Zhang, Mingzhi Li, Zhaoming Wang, Suqian Shi, Jijing Zhang, Yu Yao, Dingzhu Hu, Shuang |
author_facet | Wu, Dedong Chen, Chen Zhang, Mingzhi Li, Zhaoming Wang, Suqian Shi, Jijing Zhang, Yu Yao, Dingzhu Hu, Shuang |
author_sort | Wu, Dedong |
collection | PubMed |
description | To improve outcomes and risk assessment, we systematically analyzed the clinical features of patients with acquired immunodeficiency syndrome (AIDS)-related lymphoma (ARL) and identified survival-associated factors. Data were collected from 100 patients diagnosed with ARL at the Henan Provincial Infectious Disease Hospital in China. The progression-free survival (PFS) duration and 2-year overall survival (OS) rate were determined. A multivariate analysis was used to evaluate the associations between survival and the following variables: sex, age, histological subtype, Ann Arbor stage, lactate dehydrogenase (LDH) level, primary site, baseline CD4(+) count, use of chemotherapy, and age-adjusted international prognostic index IPI (aaIPI). The timing of combined antiretroviral therapy (cART) relative to chemotherapy was also assessed. The PFS duration and 2-year OS rate were significantly higher in the chemotherapy vs. the non-chemotherapy group (P < 0.001), but did not differ significantly between patients who received chemotherapy before vs. simultaneously as cART (P > 0.05). Age, aaIPI, chemotherapy, LDH level, and the Burkitt/Burkitt-like lymphoma subtype were significant prognostic factors for 2-year OS; the other factors were not associated with prognosis. Our results show that cART plus chemotherapy significantly improves the survival of patients with ARL and identifies several prognostic factors. |
format | Online Article Text |
id | pubmed-6441082 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64410822019-04-04 The clinical features and prognosis of 100 AIDS-related lymphoma cases Wu, Dedong Chen, Chen Zhang, Mingzhi Li, Zhaoming Wang, Suqian Shi, Jijing Zhang, Yu Yao, Dingzhu Hu, Shuang Sci Rep Article To improve outcomes and risk assessment, we systematically analyzed the clinical features of patients with acquired immunodeficiency syndrome (AIDS)-related lymphoma (ARL) and identified survival-associated factors. Data were collected from 100 patients diagnosed with ARL at the Henan Provincial Infectious Disease Hospital in China. The progression-free survival (PFS) duration and 2-year overall survival (OS) rate were determined. A multivariate analysis was used to evaluate the associations between survival and the following variables: sex, age, histological subtype, Ann Arbor stage, lactate dehydrogenase (LDH) level, primary site, baseline CD4(+) count, use of chemotherapy, and age-adjusted international prognostic index IPI (aaIPI). The timing of combined antiretroviral therapy (cART) relative to chemotherapy was also assessed. The PFS duration and 2-year OS rate were significantly higher in the chemotherapy vs. the non-chemotherapy group (P < 0.001), but did not differ significantly between patients who received chemotherapy before vs. simultaneously as cART (P > 0.05). Age, aaIPI, chemotherapy, LDH level, and the Burkitt/Burkitt-like lymphoma subtype were significant prognostic factors for 2-year OS; the other factors were not associated with prognosis. Our results show that cART plus chemotherapy significantly improves the survival of patients with ARL and identifies several prognostic factors. Nature Publishing Group UK 2019-03-29 /pmc/articles/PMC6441082/ /pubmed/30926889 http://dx.doi.org/10.1038/s41598-019-41869-9 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Wu, Dedong Chen, Chen Zhang, Mingzhi Li, Zhaoming Wang, Suqian Shi, Jijing Zhang, Yu Yao, Dingzhu Hu, Shuang The clinical features and prognosis of 100 AIDS-related lymphoma cases |
title | The clinical features and prognosis of 100 AIDS-related lymphoma cases |
title_full | The clinical features and prognosis of 100 AIDS-related lymphoma cases |
title_fullStr | The clinical features and prognosis of 100 AIDS-related lymphoma cases |
title_full_unstemmed | The clinical features and prognosis of 100 AIDS-related lymphoma cases |
title_short | The clinical features and prognosis of 100 AIDS-related lymphoma cases |
title_sort | clinical features and prognosis of 100 aids-related lymphoma cases |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6441082/ https://www.ncbi.nlm.nih.gov/pubmed/30926889 http://dx.doi.org/10.1038/s41598-019-41869-9 |
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