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Development and validation of platelet-to-albumin ratio as a clinical predictor for diffuse large B-cell lymphoma
INTRODUCTION: Diffuse large B-cell lymphoma (DLBCL) is the most common subtypes of lymphoma. Clinical biomarkers are still required for DLBCL patients to identify high-risk patients. Therefore, we developed and validated the platelet-to-albumin (PTA) ratio as a predictor for DLBCL patients. METHODS:...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10285288/ https://www.ncbi.nlm.nih.gov/pubmed/37361573 http://dx.doi.org/10.3389/fonc.2023.1138284 |
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author | Wang, Jinghan Li, Linjie Yu, Fang Zhang, Junyu Mao, Liping Chen, Bocheng Hu, Xuelian Zhou, Hongmei Xie, Wanzhuo Tong, Hongyan Jin, Jie |
author_facet | Wang, Jinghan Li, Linjie Yu, Fang Zhang, Junyu Mao, Liping Chen, Bocheng Hu, Xuelian Zhou, Hongmei Xie, Wanzhuo Tong, Hongyan Jin, Jie |
author_sort | Wang, Jinghan |
collection | PubMed |
description | INTRODUCTION: Diffuse large B-cell lymphoma (DLBCL) is the most common subtypes of lymphoma. Clinical biomarkers are still required for DLBCL patients to identify high-risk patients. Therefore, we developed and validated the platelet-to-albumin (PTA) ratio as a predictor for DLBCL patients. METHODS: A group of 749 patients was randomly divided into a training set (600 patients) and an internal validation set (149 cases). The independent cohort of 110 patients was enrolled from the other hospital as an external validation set. Penalized smoothing spline (PS) Cox regression models were used to explore the non-linear relationship between the PTA ratio and overall survival (OS) as well as progression-free survival (PFS), respectively. RESULTS: A U-shaped relation between the PTA ratio and PFS was identified in the training set. The PTA ratio less than 2.7 or greater than 8.6 was associated with the shorter PFS. Additionally, the PTA ratio had an additional prognostic value to the well-established predictors. What’s more, the U-shaped pattern of the PTA ratio and PFS was respectively validated in the two validation sets. DISCUSSION: A U-shaped association between the PTA ratio and PFS was found in patients with DLBCLs. The PTA ratio can be used as a biomarker, and may suggest abnormalities of both host nutritional aspect and systemic inflammation in DLBCL. |
format | Online Article Text |
id | pubmed-10285288 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-102852882023-06-23 Development and validation of platelet-to-albumin ratio as a clinical predictor for diffuse large B-cell lymphoma Wang, Jinghan Li, Linjie Yu, Fang Zhang, Junyu Mao, Liping Chen, Bocheng Hu, Xuelian Zhou, Hongmei Xie, Wanzhuo Tong, Hongyan Jin, Jie Front Oncol Oncology INTRODUCTION: Diffuse large B-cell lymphoma (DLBCL) is the most common subtypes of lymphoma. Clinical biomarkers are still required for DLBCL patients to identify high-risk patients. Therefore, we developed and validated the platelet-to-albumin (PTA) ratio as a predictor for DLBCL patients. METHODS: A group of 749 patients was randomly divided into a training set (600 patients) and an internal validation set (149 cases). The independent cohort of 110 patients was enrolled from the other hospital as an external validation set. Penalized smoothing spline (PS) Cox regression models were used to explore the non-linear relationship between the PTA ratio and overall survival (OS) as well as progression-free survival (PFS), respectively. RESULTS: A U-shaped relation between the PTA ratio and PFS was identified in the training set. The PTA ratio less than 2.7 or greater than 8.6 was associated with the shorter PFS. Additionally, the PTA ratio had an additional prognostic value to the well-established predictors. What’s more, the U-shaped pattern of the PTA ratio and PFS was respectively validated in the two validation sets. DISCUSSION: A U-shaped association between the PTA ratio and PFS was found in patients with DLBCLs. The PTA ratio can be used as a biomarker, and may suggest abnormalities of both host nutritional aspect and systemic inflammation in DLBCL. Frontiers Media S.A. 2023-06-08 /pmc/articles/PMC10285288/ /pubmed/37361573 http://dx.doi.org/10.3389/fonc.2023.1138284 Text en Copyright © 2023 Wang, Li, Yu, Zhang, Mao, Chen, Hu, Zhou, Xie, Tong and Jin https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Oncology Wang, Jinghan Li, Linjie Yu, Fang Zhang, Junyu Mao, Liping Chen, Bocheng Hu, Xuelian Zhou, Hongmei Xie, Wanzhuo Tong, Hongyan Jin, Jie Development and validation of platelet-to-albumin ratio as a clinical predictor for diffuse large B-cell lymphoma |
title | Development and validation of platelet-to-albumin ratio as a clinical predictor for diffuse large B-cell lymphoma |
title_full | Development and validation of platelet-to-albumin ratio as a clinical predictor for diffuse large B-cell lymphoma |
title_fullStr | Development and validation of platelet-to-albumin ratio as a clinical predictor for diffuse large B-cell lymphoma |
title_full_unstemmed | Development and validation of platelet-to-albumin ratio as a clinical predictor for diffuse large B-cell lymphoma |
title_short | Development and validation of platelet-to-albumin ratio as a clinical predictor for diffuse large B-cell lymphoma |
title_sort | development and validation of platelet-to-albumin ratio as a clinical predictor for diffuse large b-cell lymphoma |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10285288/ https://www.ncbi.nlm.nih.gov/pubmed/37361573 http://dx.doi.org/10.3389/fonc.2023.1138284 |
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