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Utility of Red Cell Distribution Width as a Prognostic Factor in Young Breast Cancer Patients

The prognosis of breast cancer occurs in young women is usually poor. Red cell distribution width (RDW), 1 of many routinely examined parameters, has recently been proposed as a prognostic marker in solid tumors. The aim of our study was to assess the predictive value of RDW for survival in young wo...

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Autores principales: Huang, Du-Ping, Ma, Rui-Min, Xiang, You-Qun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4998693/
https://www.ncbi.nlm.nih.gov/pubmed/27124030
http://dx.doi.org/10.1097/MD.0000000000003430
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author Huang, Du-Ping
Ma, Rui-Min
Xiang, You-Qun
author_facet Huang, Du-Ping
Ma, Rui-Min
Xiang, You-Qun
author_sort Huang, Du-Ping
collection PubMed
description The prognosis of breast cancer occurs in young women is usually poor. Red cell distribution width (RDW), 1 of many routinely examined parameters, has recently been proposed as a prognostic marker in solid tumors. The aim of our study was to assess the predictive value of RDW for survival in young women with breast cancer. We reviewed 203 consecutive young female patients (under 40) with invasive breast cancer diagnosed at the First Affiliated Hospital of Wenzhou Medical University between January 2008 and December 2012. Preoperational RDW, clinicopathological information, and prognostic data were collected. RDW levels were divided into 2 groups: 161 patients with low RDW (≤13.75%) and 42 patients with high RDW (>13.75%). Clinicopathological differences between the 2 groups were calculated by chi-squared test and Wilcoxon rank-sum test. Kaplan–Meier survival analysis and Cox proportional hazard regression analyses were used to examine the effect of RDW on survival. We found that high RDW was significantly associated with larger tumor size (P = 0.002), positive lymph node metastases (P = 0.011), and advanced stages (P = 0.004). Patients with high RDW showed significantly lower disease-free survival (DFS; P < 0.001) and lower overall survival (OS) rate (P < 0.001) than patients with low RDW. Moreover, the Cox regression multivariate analysis revealed that high pretreatment DRW was independently correlated with poor DFS and OS, with hazard ratio 4.819 (95% confidence interval [CI] 2.291–10.138, P < 0.001) and 5.887 (95% CI 1.666–20.802, P = 0.006), respectively. In conclusion, our study demonstrated that pretreatment RDW may be associated with DFS and OS in young women with breast cancer. Further validation and feasibility studies are required before the result of our study can be considered for clinical practice.
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spelling pubmed-49986932016-09-06 Utility of Red Cell Distribution Width as a Prognostic Factor in Young Breast Cancer Patients Huang, Du-Ping Ma, Rui-Min Xiang, You-Qun Medicine (Baltimore) 5750 The prognosis of breast cancer occurs in young women is usually poor. Red cell distribution width (RDW), 1 of many routinely examined parameters, has recently been proposed as a prognostic marker in solid tumors. The aim of our study was to assess the predictive value of RDW for survival in young women with breast cancer. We reviewed 203 consecutive young female patients (under 40) with invasive breast cancer diagnosed at the First Affiliated Hospital of Wenzhou Medical University between January 2008 and December 2012. Preoperational RDW, clinicopathological information, and prognostic data were collected. RDW levels were divided into 2 groups: 161 patients with low RDW (≤13.75%) and 42 patients with high RDW (>13.75%). Clinicopathological differences between the 2 groups were calculated by chi-squared test and Wilcoxon rank-sum test. Kaplan–Meier survival analysis and Cox proportional hazard regression analyses were used to examine the effect of RDW on survival. We found that high RDW was significantly associated with larger tumor size (P = 0.002), positive lymph node metastases (P = 0.011), and advanced stages (P = 0.004). Patients with high RDW showed significantly lower disease-free survival (DFS; P < 0.001) and lower overall survival (OS) rate (P < 0.001) than patients with low RDW. Moreover, the Cox regression multivariate analysis revealed that high pretreatment DRW was independently correlated with poor DFS and OS, with hazard ratio 4.819 (95% confidence interval [CI] 2.291–10.138, P < 0.001) and 5.887 (95% CI 1.666–20.802, P = 0.006), respectively. In conclusion, our study demonstrated that pretreatment RDW may be associated with DFS and OS in young women with breast cancer. Further validation and feasibility studies are required before the result of our study can be considered for clinical practice. Wolters Kluwer Health 2016-04-29 /pmc/articles/PMC4998693/ /pubmed/27124030 http://dx.doi.org/10.1097/MD.0000000000003430 Text en Copyright © 2016 Wolters Kluwer Health, Inc. All rights reserved. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0
spellingShingle 5750
Huang, Du-Ping
Ma, Rui-Min
Xiang, You-Qun
Utility of Red Cell Distribution Width as a Prognostic Factor in Young Breast Cancer Patients
title Utility of Red Cell Distribution Width as a Prognostic Factor in Young Breast Cancer Patients
title_full Utility of Red Cell Distribution Width as a Prognostic Factor in Young Breast Cancer Patients
title_fullStr Utility of Red Cell Distribution Width as a Prognostic Factor in Young Breast Cancer Patients
title_full_unstemmed Utility of Red Cell Distribution Width as a Prognostic Factor in Young Breast Cancer Patients
title_short Utility of Red Cell Distribution Width as a Prognostic Factor in Young Breast Cancer Patients
title_sort utility of red cell distribution width as a prognostic factor in young breast cancer patients
topic 5750
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4998693/
https://www.ncbi.nlm.nih.gov/pubmed/27124030
http://dx.doi.org/10.1097/MD.0000000000003430
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