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High preoperative Glasgow prognostic score is a negative prognostic factor for patients with endometrial carcinoma
The aim of the present study was to determine the prognostic value of the Glasgow prognostic score (GPS) in endometrial carcinoma (EC). Patients with EC who underwent surgery at the Shimane University Hospital between January 1997 and December 2013 were enrolled (n=118). The associations between pre...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5795600/ https://www.ncbi.nlm.nih.gov/pubmed/29456849 http://dx.doi.org/10.3892/mco.2018.1551 |
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author | Nakamura, Kohei Nakayama, Kentaro Minamoto, Toshiko Ishibashi, Tomoka Sanuki, Kaori Yamashita, Hitomi Ono, Ruriko Sasamori, Hiroki Komatsu-Fujii, Takayoshi Ishikawa, Masako Kyo, Satoru |
author_facet | Nakamura, Kohei Nakayama, Kentaro Minamoto, Toshiko Ishibashi, Tomoka Sanuki, Kaori Yamashita, Hitomi Ono, Ruriko Sasamori, Hiroki Komatsu-Fujii, Takayoshi Ishikawa, Masako Kyo, Satoru |
author_sort | Nakamura, Kohei |
collection | PubMed |
description | The aim of the present study was to determine the prognostic value of the Glasgow prognostic score (GPS) in endometrial carcinoma (EC). Patients with EC who underwent surgery at the Shimane University Hospital between January 1997 and December 2013 were enrolled (n=118). The associations between pretreatment GPS and clinical parameters, including age, histological type, International Federation of Gynecology and Obstetrics stage, tumor grade, carbohydrate antigen 19-9 and carcinoembryonic antigen levels, progression-free survival (PFS), and overall survival (OS), were investigated. Survival analysis was performed with the Kaplan-Meier method, and prognostic factors were evaluated with Cox's proportional hazards regression model. A high pretreatment GPS was associated with advanced clinical stage, histological type and tumor grade (P<0.001, P=0.007 and P=0.006, respectively). Multivariate analysis identified a high GPS as an independent negative prognostic factor for PFS and OS (P=0.025 and P=0.044, respectively). Therefore, a high pretreatment GPS has prognostic value and the potential to be a predictive marker for surgical outcome in patients with EC. Evaluation of pretreatment GPS may aid in the identification of high-risk populations, which may improve treatment selection and patient outcomes. |
format | Online Article Text |
id | pubmed-5795600 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-57956002018-02-16 High preoperative Glasgow prognostic score is a negative prognostic factor for patients with endometrial carcinoma Nakamura, Kohei Nakayama, Kentaro Minamoto, Toshiko Ishibashi, Tomoka Sanuki, Kaori Yamashita, Hitomi Ono, Ruriko Sasamori, Hiroki Komatsu-Fujii, Takayoshi Ishikawa, Masako Kyo, Satoru Mol Clin Oncol Articles The aim of the present study was to determine the prognostic value of the Glasgow prognostic score (GPS) in endometrial carcinoma (EC). Patients with EC who underwent surgery at the Shimane University Hospital between January 1997 and December 2013 were enrolled (n=118). The associations between pretreatment GPS and clinical parameters, including age, histological type, International Federation of Gynecology and Obstetrics stage, tumor grade, carbohydrate antigen 19-9 and carcinoembryonic antigen levels, progression-free survival (PFS), and overall survival (OS), were investigated. Survival analysis was performed with the Kaplan-Meier method, and prognostic factors were evaluated with Cox's proportional hazards regression model. A high pretreatment GPS was associated with advanced clinical stage, histological type and tumor grade (P<0.001, P=0.007 and P=0.006, respectively). Multivariate analysis identified a high GPS as an independent negative prognostic factor for PFS and OS (P=0.025 and P=0.044, respectively). Therefore, a high pretreatment GPS has prognostic value and the potential to be a predictive marker for surgical outcome in patients with EC. Evaluation of pretreatment GPS may aid in the identification of high-risk populations, which may improve treatment selection and patient outcomes. D.A. Spandidos 2018-03 2018-01-10 /pmc/articles/PMC5795600/ /pubmed/29456849 http://dx.doi.org/10.3892/mco.2018.1551 Text en Copyright: © Nakamura et al. 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 Nakamura, Kohei Nakayama, Kentaro Minamoto, Toshiko Ishibashi, Tomoka Sanuki, Kaori Yamashita, Hitomi Ono, Ruriko Sasamori, Hiroki Komatsu-Fujii, Takayoshi Ishikawa, Masako Kyo, Satoru High preoperative Glasgow prognostic score is a negative prognostic factor for patients with endometrial carcinoma |
title | High preoperative Glasgow prognostic score is a negative prognostic factor for patients with endometrial carcinoma |
title_full | High preoperative Glasgow prognostic score is a negative prognostic factor for patients with endometrial carcinoma |
title_fullStr | High preoperative Glasgow prognostic score is a negative prognostic factor for patients with endometrial carcinoma |
title_full_unstemmed | High preoperative Glasgow prognostic score is a negative prognostic factor for patients with endometrial carcinoma |
title_short | High preoperative Glasgow prognostic score is a negative prognostic factor for patients with endometrial carcinoma |
title_sort | high preoperative glasgow prognostic score is a negative prognostic factor for patients with endometrial carcinoma |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5795600/ https://www.ncbi.nlm.nih.gov/pubmed/29456849 http://dx.doi.org/10.3892/mco.2018.1551 |
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