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Prognostic value of granulocyte colony-stimulating factor in patients with non-metastatic clear cell renal cell carcinoma

Granulocyte colony-stimulating factor is a well-known cytokine to stimulate inflammatory cells. We sought to investigate the prognostic value of its expression in patients with non-metastatic clear cell renal cell carcinoma. Enrolled in this study were 228 eligible patients treated with curative nep...

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Autores principales: Liu, Zheng, Zhu, Yu, Wang, Yiwei, Fu, Qiang, Fu, Hangcheng, Wang, Zewei, Zhang, Junyu, Li, Gaoxiang, Xu, Jiejie, Dai, Bo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5642530/
https://www.ncbi.nlm.nih.gov/pubmed/29050255
http://dx.doi.org/10.18632/oncotarget.19540
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author Liu, Zheng
Zhu, Yu
Wang, Yiwei
Fu, Qiang
Fu, Hangcheng
Wang, Zewei
Zhang, Junyu
Li, Gaoxiang
Xu, Jiejie
Dai, Bo
author_facet Liu, Zheng
Zhu, Yu
Wang, Yiwei
Fu, Qiang
Fu, Hangcheng
Wang, Zewei
Zhang, Junyu
Li, Gaoxiang
Xu, Jiejie
Dai, Bo
author_sort Liu, Zheng
collection PubMed
description Granulocyte colony-stimulating factor is a well-known cytokine to stimulate inflammatory cells. We sought to investigate the prognostic value of its expression in patients with non-metastatic clear cell renal cell carcinoma. Enrolled in this study were 228 eligible patients treated with curative nephrectomy for clear cell renal cell carcinoma during 2008. Granulocyte colony-stimulating factor expression was detected by immunohistochemistry in patient specimens, and was divided into three groups according to the distribution of its immunohistochemistry score. Subgroup analyses were performed to evaluate its risk stratification ability. Cox regression models were applied to analyze the impact of prognostic factors. We found that high granulocyte colony-stimulating factor expression was associated with diminished recurrence-free survival (P<0.001). Its expression had stronger stratification ability in late disease patients, and was further identified as an independent prognosticator for recurrence-free survival. Moreover, nomogram based on granulocyte colony-stimulating factor expression presented a better prognostic ability compared with current prognostic systems (the concordance index = 0.874). To conclude, intratumoal granulocyte colony-stimulating factor expression could be a potential prognosticator for recurrence-free survival in non-metastatic clear cell renal cell carcinoma patients. Incorporating its expression into other pathologic factors provided a finer individual model for non-metastatic clear cell renal cell patients.
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spelling pubmed-56425302017-10-18 Prognostic value of granulocyte colony-stimulating factor in patients with non-metastatic clear cell renal cell carcinoma Liu, Zheng Zhu, Yu Wang, Yiwei Fu, Qiang Fu, Hangcheng Wang, Zewei Zhang, Junyu Li, Gaoxiang Xu, Jiejie Dai, Bo Oncotarget Research Paper Granulocyte colony-stimulating factor is a well-known cytokine to stimulate inflammatory cells. We sought to investigate the prognostic value of its expression in patients with non-metastatic clear cell renal cell carcinoma. Enrolled in this study were 228 eligible patients treated with curative nephrectomy for clear cell renal cell carcinoma during 2008. Granulocyte colony-stimulating factor expression was detected by immunohistochemistry in patient specimens, and was divided into three groups according to the distribution of its immunohistochemistry score. Subgroup analyses were performed to evaluate its risk stratification ability. Cox regression models were applied to analyze the impact of prognostic factors. We found that high granulocyte colony-stimulating factor expression was associated with diminished recurrence-free survival (P<0.001). Its expression had stronger stratification ability in late disease patients, and was further identified as an independent prognosticator for recurrence-free survival. Moreover, nomogram based on granulocyte colony-stimulating factor expression presented a better prognostic ability compared with current prognostic systems (the concordance index = 0.874). To conclude, intratumoal granulocyte colony-stimulating factor expression could be a potential prognosticator for recurrence-free survival in non-metastatic clear cell renal cell carcinoma patients. Incorporating its expression into other pathologic factors provided a finer individual model for non-metastatic clear cell renal cell patients. Impact Journals LLC 2017-07-25 /pmc/articles/PMC5642530/ /pubmed/29050255 http://dx.doi.org/10.18632/oncotarget.19540 Text en Copyright: © 2017 Liu et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Liu, Zheng
Zhu, Yu
Wang, Yiwei
Fu, Qiang
Fu, Hangcheng
Wang, Zewei
Zhang, Junyu
Li, Gaoxiang
Xu, Jiejie
Dai, Bo
Prognostic value of granulocyte colony-stimulating factor in patients with non-metastatic clear cell renal cell carcinoma
title Prognostic value of granulocyte colony-stimulating factor in patients with non-metastatic clear cell renal cell carcinoma
title_full Prognostic value of granulocyte colony-stimulating factor in patients with non-metastatic clear cell renal cell carcinoma
title_fullStr Prognostic value of granulocyte colony-stimulating factor in patients with non-metastatic clear cell renal cell carcinoma
title_full_unstemmed Prognostic value of granulocyte colony-stimulating factor in patients with non-metastatic clear cell renal cell carcinoma
title_short Prognostic value of granulocyte colony-stimulating factor in patients with non-metastatic clear cell renal cell carcinoma
title_sort prognostic value of granulocyte colony-stimulating factor in patients with non-metastatic clear cell renal cell carcinoma
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5642530/
https://www.ncbi.nlm.nih.gov/pubmed/29050255
http://dx.doi.org/10.18632/oncotarget.19540
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