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Preoperative carcinoembryonic antigen to body mass index ratio contributes to prognosis prediction in colorectal cancer
Both carcinoembryonic antigen (CEA) level and body mass index (BMI) are traditional prognostic markers in colorectal cancer (CRC); however, to the best of our knowledge, the value of the CEA to BMI ratio (CBR) has never been addressed. In the present study, 191 patients with CRC treated using radica...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9554958/ https://www.ncbi.nlm.nih.gov/pubmed/36245819 http://dx.doi.org/10.3892/ol.2022.13536 |
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author | Xiang, Jia Ding, Mengyao Lin, Jixing Xue, Tianhui Ye, Qianwen Yan, Bing |
author_facet | Xiang, Jia Ding, Mengyao Lin, Jixing Xue, Tianhui Ye, Qianwen Yan, Bing |
author_sort | Xiang, Jia |
collection | PubMed |
description | Both carcinoembryonic antigen (CEA) level and body mass index (BMI) are traditional prognostic markers in colorectal cancer (CRC); however, to the best of our knowledge, the value of the CEA to BMI ratio (CBR) has never been addressed. In the present study, 191 patients with CRC treated using radical resection were retrospectively included, and the significance of the CBR in predicting disease-free survival (DFS) or overall survival (OS) rates was calculated. The prognostic efficacy of the CBR in predicting OS was compared with individual CEA and BMI values. The survival differences of the subgroups were calculated by Kaplan-Meier analysis, and corresponding risk factors were then estimated by a Cox proportional hazards model. As a result, 29.84% (57/191) of the patients were assigned to the high CBR group (cut-off, ≥0.28); the CBR had a sensitivity of 56.50 and 68.90%, and a specificity of 80.60 and 80.10% for DFS and OS, respectively. Patients with a high CBR more commonly underwent laparotomy and exhibited advanced T stages, the presence of tumor deposits and advanced Tumor-Node-Metastasis stages (stage II or III). The CBR was more efficient than the CEA or BMI alone in predicting OS. In addition, patients with a high CBR presented with a significantly worse outcome than patients with a low CBR. Finally, the CBR was an independent risk factor for both DFS and OS. In conclusion, the CBR was a more robust prognostic factor in CRC, and patients with a relatively high CBR exhibited poorer survival. |
format | Online Article Text |
id | pubmed-9554958 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-95549582022-10-13 Preoperative carcinoembryonic antigen to body mass index ratio contributes to prognosis prediction in colorectal cancer Xiang, Jia Ding, Mengyao Lin, Jixing Xue, Tianhui Ye, Qianwen Yan, Bing Oncol Lett Articles Both carcinoembryonic antigen (CEA) level and body mass index (BMI) are traditional prognostic markers in colorectal cancer (CRC); however, to the best of our knowledge, the value of the CEA to BMI ratio (CBR) has never been addressed. In the present study, 191 patients with CRC treated using radical resection were retrospectively included, and the significance of the CBR in predicting disease-free survival (DFS) or overall survival (OS) rates was calculated. The prognostic efficacy of the CBR in predicting OS was compared with individual CEA and BMI values. The survival differences of the subgroups were calculated by Kaplan-Meier analysis, and corresponding risk factors were then estimated by a Cox proportional hazards model. As a result, 29.84% (57/191) of the patients were assigned to the high CBR group (cut-off, ≥0.28); the CBR had a sensitivity of 56.50 and 68.90%, and a specificity of 80.60 and 80.10% for DFS and OS, respectively. Patients with a high CBR more commonly underwent laparotomy and exhibited advanced T stages, the presence of tumor deposits and advanced Tumor-Node-Metastasis stages (stage II or III). The CBR was more efficient than the CEA or BMI alone in predicting OS. In addition, patients with a high CBR presented with a significantly worse outcome than patients with a low CBR. Finally, the CBR was an independent risk factor for both DFS and OS. In conclusion, the CBR was a more robust prognostic factor in CRC, and patients with a relatively high CBR exhibited poorer survival. D.A. Spandidos 2022-09-29 /pmc/articles/PMC9554958/ /pubmed/36245819 http://dx.doi.org/10.3892/ol.2022.13536 Text en Copyright: © Xiang et al. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Xiang, Jia Ding, Mengyao Lin, Jixing Xue, Tianhui Ye, Qianwen Yan, Bing Preoperative carcinoembryonic antigen to body mass index ratio contributes to prognosis prediction in colorectal cancer |
title | Preoperative carcinoembryonic antigen to body mass index ratio contributes to prognosis prediction in colorectal cancer |
title_full | Preoperative carcinoembryonic antigen to body mass index ratio contributes to prognosis prediction in colorectal cancer |
title_fullStr | Preoperative carcinoembryonic antigen to body mass index ratio contributes to prognosis prediction in colorectal cancer |
title_full_unstemmed | Preoperative carcinoembryonic antigen to body mass index ratio contributes to prognosis prediction in colorectal cancer |
title_short | Preoperative carcinoembryonic antigen to body mass index ratio contributes to prognosis prediction in colorectal cancer |
title_sort | preoperative carcinoembryonic antigen to body mass index ratio contributes to prognosis prediction in colorectal cancer |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9554958/ https://www.ncbi.nlm.nih.gov/pubmed/36245819 http://dx.doi.org/10.3892/ol.2022.13536 |
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