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High C-Reactive Protein to Albumin Ratio Predicts Inferior Clinical Outcomes in Extranodal Natural Killer T-Cell Lymphoma
OBJECTIVE: The prognostic value of C-reactive protein to albumin ratio (CAR) has been identified in several cancers but not in extranodal natural killer T-cell lymphoma (ENKTL) as yet. We aimed to evaluate the prognostic value of CAR in ENKTL. METHODS: A retrospective study with 246 patients with EN...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7139182/ https://www.ncbi.nlm.nih.gov/pubmed/32284703 http://dx.doi.org/10.1177/1559325820917824 |
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author | Di, Quan-shu Xu, Tao Song, Ying Zuo, Zhi-gang Cao, Feng-jun Yu, Xiong-jie Tang, Ji-ying Zhang, Wei Li, Chen Wan, Guo-xing Cai, Xiao-jun |
author_facet | Di, Quan-shu Xu, Tao Song, Ying Zuo, Zhi-gang Cao, Feng-jun Yu, Xiong-jie Tang, Ji-ying Zhang, Wei Li, Chen Wan, Guo-xing Cai, Xiao-jun |
author_sort | Di, Quan-shu |
collection | PubMed |
description | OBJECTIVE: The prognostic value of C-reactive protein to albumin ratio (CAR) has been identified in several cancers but not in extranodal natural killer T-cell lymphoma (ENKTL) as yet. We aimed to evaluate the prognostic value of CAR in ENKTL. METHODS: A retrospective study with 246 patients with ENKTL was performed to determine the prognostic value of pretreatment CAR and examine the prognostic performance of CAR incorporating with International Prognostic Index (IPI) or natural killer/T-cell lymphoma prognostic index (NKPI) by nomogram. RESULTS: The Cox regression analyses showed that high CAR (>0.3) independently predicted unfavorable progression-free survival (PFS, P = .011) and overall survival (OS, P = .012). In the stratification analysis, the CAR was able to separate patients into different prognoses regarding both OS and PFS in Ann Arbor stage I+II as well as III+IV, IPI score 0 to 1, and NKPI score 1 to 2 subgroups (all P < .05). Additionally, the predictive accuracy of the IPI-based nomogram incorporating CAR, albumin to globulin ratio (AGR), and IPI for OS and PFS appeared to be lower than the NKPI-based nomogram incorporating CAR, age, AGR, extranodal site, and NKPI. CONCLUSION: Pretreatment CAR is a simple and easily accessible parameter for independently predicting OS and PFS in patients with ENKTL. |
format | Online Article Text |
id | pubmed-7139182 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-71391822020-04-13 High C-Reactive Protein to Albumin Ratio Predicts Inferior Clinical Outcomes in Extranodal Natural Killer T-Cell Lymphoma Di, Quan-shu Xu, Tao Song, Ying Zuo, Zhi-gang Cao, Feng-jun Yu, Xiong-jie Tang, Ji-ying Zhang, Wei Li, Chen Wan, Guo-xing Cai, Xiao-jun Dose Response Original Article OBJECTIVE: The prognostic value of C-reactive protein to albumin ratio (CAR) has been identified in several cancers but not in extranodal natural killer T-cell lymphoma (ENKTL) as yet. We aimed to evaluate the prognostic value of CAR in ENKTL. METHODS: A retrospective study with 246 patients with ENKTL was performed to determine the prognostic value of pretreatment CAR and examine the prognostic performance of CAR incorporating with International Prognostic Index (IPI) or natural killer/T-cell lymphoma prognostic index (NKPI) by nomogram. RESULTS: The Cox regression analyses showed that high CAR (>0.3) independently predicted unfavorable progression-free survival (PFS, P = .011) and overall survival (OS, P = .012). In the stratification analysis, the CAR was able to separate patients into different prognoses regarding both OS and PFS in Ann Arbor stage I+II as well as III+IV, IPI score 0 to 1, and NKPI score 1 to 2 subgroups (all P < .05). Additionally, the predictive accuracy of the IPI-based nomogram incorporating CAR, albumin to globulin ratio (AGR), and IPI for OS and PFS appeared to be lower than the NKPI-based nomogram incorporating CAR, age, AGR, extranodal site, and NKPI. CONCLUSION: Pretreatment CAR is a simple and easily accessible parameter for independently predicting OS and PFS in patients with ENKTL. SAGE Publications 2020-04-07 /pmc/articles/PMC7139182/ /pubmed/32284703 http://dx.doi.org/10.1177/1559325820917824 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Article Di, Quan-shu Xu, Tao Song, Ying Zuo, Zhi-gang Cao, Feng-jun Yu, Xiong-jie Tang, Ji-ying Zhang, Wei Li, Chen Wan, Guo-xing Cai, Xiao-jun High C-Reactive Protein to Albumin Ratio Predicts Inferior Clinical Outcomes in Extranodal Natural Killer T-Cell Lymphoma |
title | High C-Reactive Protein to Albumin Ratio Predicts Inferior Clinical
Outcomes in Extranodal Natural Killer T-Cell Lymphoma |
title_full | High C-Reactive Protein to Albumin Ratio Predicts Inferior Clinical
Outcomes in Extranodal Natural Killer T-Cell Lymphoma |
title_fullStr | High C-Reactive Protein to Albumin Ratio Predicts Inferior Clinical
Outcomes in Extranodal Natural Killer T-Cell Lymphoma |
title_full_unstemmed | High C-Reactive Protein to Albumin Ratio Predicts Inferior Clinical
Outcomes in Extranodal Natural Killer T-Cell Lymphoma |
title_short | High C-Reactive Protein to Albumin Ratio Predicts Inferior Clinical
Outcomes in Extranodal Natural Killer T-Cell Lymphoma |
title_sort | high c-reactive protein to albumin ratio predicts inferior clinical
outcomes in extranodal natural killer t-cell lymphoma |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7139182/ https://www.ncbi.nlm.nih.gov/pubmed/32284703 http://dx.doi.org/10.1177/1559325820917824 |
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