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Evaluation and Validation of the Prognostic Value of Serum Albumin to Globulin Ratio in Patients With Cancer Cachexia: Results From a Large Multicenter Collaboration
BACKGROUND: Recently, albumin–globulin ratio (AGR), a serological indicator that reflects nutritional status and systemic inflammatory, has been reported to be associated with the prognosis of various cancers. However, there is currently no research report on its relationship with cancer cachexia. O...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8461248/ https://www.ncbi.nlm.nih.gov/pubmed/34568033 http://dx.doi.org/10.3389/fonc.2021.707705 |
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author | Xie, Hai-Lun Zhang, Qi Ruan, Guo-Tian Ge, Yi-Zhong Hu, Chun-Lei Song, Meng-Meng Song, Chun-Hua Zhang, Xi Zhang, Xiao-Wei Li, Xiang-Rui Zhang, Kang-Ping Liu, Tong Yang, Ming Tang, Meng Xu, Hong-Xia Shi, Han-Ping |
author_facet | Xie, Hai-Lun Zhang, Qi Ruan, Guo-Tian Ge, Yi-Zhong Hu, Chun-Lei Song, Meng-Meng Song, Chun-Hua Zhang, Xi Zhang, Xiao-Wei Li, Xiang-Rui Zhang, Kang-Ping Liu, Tong Yang, Ming Tang, Meng Xu, Hong-Xia Shi, Han-Ping |
author_sort | Xie, Hai-Lun |
collection | PubMed |
description | BACKGROUND: Recently, albumin–globulin ratio (AGR), a serological indicator that reflects nutritional status and systemic inflammatory, has been reported to be associated with the prognosis of various cancers. However, there is currently no research report on its relationship with cancer cachexia. OBJECTIVES: This study aimed to explore the prognostic value of AGR in patients with cancer cachexia through a multicenter retrospective analysis. METHODS: We recruited 2,364 patients with cancer cachexia and randomly divided the patients into training and validation cohorts at a ratio of 7:3. The optimal stratification method was used to determine the optimal cutoff value of AGR. The survival curve was evaluated by the Kaplan–Meier method. Cox regression proportional-hazards model was used to determine independent prognostic factors in patients with cancer cachexia. The time-dependent receiver operating characteristic curve was used to compare the prognostic performance of different malnutrition evaluation tools. RESULTS: The optimal cutoff value of AGR is 1.24 in patients with cancer cachexia. Increasing AGR was associated with survival in a dose–response manner with a forward L-shape. Compared with the high AGR group, the low AGR group had a shorter overall survival; and there was consistency in training and validation cohorts. In the stratified analysis of TNM stage, AGR has good prognostic distinguishing ability for advanced patients. Multivariate survival analysis determined that low AGR was an independent risk factor affecting all-cause mortality in patients with cancer cachexia. In addition, compared with other malnutrition evaluation tools, AGR could effectively stratify the prognosis of patients with cancer cachexia. CONCLUSION: AGR was an independent prognostic factor affecting patients with cancer cachexia, especially in advanced patients. Compared with other malnutrition evaluation tools, AGR can effectively stratify the prognosis of patients with cancer cachexia. |
format | Online Article Text |
id | pubmed-8461248 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-84612482021-09-25 Evaluation and Validation of the Prognostic Value of Serum Albumin to Globulin Ratio in Patients With Cancer Cachexia: Results From a Large Multicenter Collaboration Xie, Hai-Lun Zhang, Qi Ruan, Guo-Tian Ge, Yi-Zhong Hu, Chun-Lei Song, Meng-Meng Song, Chun-Hua Zhang, Xi Zhang, Xiao-Wei Li, Xiang-Rui Zhang, Kang-Ping Liu, Tong Yang, Ming Tang, Meng Xu, Hong-Xia Shi, Han-Ping Front Oncol Oncology BACKGROUND: Recently, albumin–globulin ratio (AGR), a serological indicator that reflects nutritional status and systemic inflammatory, has been reported to be associated with the prognosis of various cancers. However, there is currently no research report on its relationship with cancer cachexia. OBJECTIVES: This study aimed to explore the prognostic value of AGR in patients with cancer cachexia through a multicenter retrospective analysis. METHODS: We recruited 2,364 patients with cancer cachexia and randomly divided the patients into training and validation cohorts at a ratio of 7:3. The optimal stratification method was used to determine the optimal cutoff value of AGR. The survival curve was evaluated by the Kaplan–Meier method. Cox regression proportional-hazards model was used to determine independent prognostic factors in patients with cancer cachexia. The time-dependent receiver operating characteristic curve was used to compare the prognostic performance of different malnutrition evaluation tools. RESULTS: The optimal cutoff value of AGR is 1.24 in patients with cancer cachexia. Increasing AGR was associated with survival in a dose–response manner with a forward L-shape. Compared with the high AGR group, the low AGR group had a shorter overall survival; and there was consistency in training and validation cohorts. In the stratified analysis of TNM stage, AGR has good prognostic distinguishing ability for advanced patients. Multivariate survival analysis determined that low AGR was an independent risk factor affecting all-cause mortality in patients with cancer cachexia. In addition, compared with other malnutrition evaluation tools, AGR could effectively stratify the prognosis of patients with cancer cachexia. CONCLUSION: AGR was an independent prognostic factor affecting patients with cancer cachexia, especially in advanced patients. Compared with other malnutrition evaluation tools, AGR can effectively stratify the prognosis of patients with cancer cachexia. Frontiers Media S.A. 2021-09-10 /pmc/articles/PMC8461248/ /pubmed/34568033 http://dx.doi.org/10.3389/fonc.2021.707705 Text en Copyright © 2021 Xie, Zhang, Ruan, Ge, Hu, Song, Song, Zhang, Zhang, Li, Zhang, Liu, Yang, Tang, Xu and Shi 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 Xie, Hai-Lun Zhang, Qi Ruan, Guo-Tian Ge, Yi-Zhong Hu, Chun-Lei Song, Meng-Meng Song, Chun-Hua Zhang, Xi Zhang, Xiao-Wei Li, Xiang-Rui Zhang, Kang-Ping Liu, Tong Yang, Ming Tang, Meng Xu, Hong-Xia Shi, Han-Ping Evaluation and Validation of the Prognostic Value of Serum Albumin to Globulin Ratio in Patients With Cancer Cachexia: Results From a Large Multicenter Collaboration |
title | Evaluation and Validation of the Prognostic Value of Serum Albumin to Globulin Ratio in Patients With Cancer Cachexia: Results From a Large Multicenter Collaboration |
title_full | Evaluation and Validation of the Prognostic Value of Serum Albumin to Globulin Ratio in Patients With Cancer Cachexia: Results From a Large Multicenter Collaboration |
title_fullStr | Evaluation and Validation of the Prognostic Value of Serum Albumin to Globulin Ratio in Patients With Cancer Cachexia: Results From a Large Multicenter Collaboration |
title_full_unstemmed | Evaluation and Validation of the Prognostic Value of Serum Albumin to Globulin Ratio in Patients With Cancer Cachexia: Results From a Large Multicenter Collaboration |
title_short | Evaluation and Validation of the Prognostic Value of Serum Albumin to Globulin Ratio in Patients With Cancer Cachexia: Results From a Large Multicenter Collaboration |
title_sort | evaluation and validation of the prognostic value of serum albumin to globulin ratio in patients with cancer cachexia: results from a large multicenter collaboration |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8461248/ https://www.ncbi.nlm.nih.gov/pubmed/34568033 http://dx.doi.org/10.3389/fonc.2021.707705 |
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