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Monocytosis as a prognostic factor for survival in stage IB and IIA cervical cancer
Objective: To measure hematologic parameters derived from the white blood cell (WBC) count and differential count (DC) as prognostic factors for survival in patients with stage IB and IIA cervical cancer. Methods: We retrospectively examined demographic, clinicopathologic, and laboratory parameters...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5743712/ https://www.ncbi.nlm.nih.gov/pubmed/29290770 http://dx.doi.org/10.7150/jca.22234 |
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author | Eo, Wan Kyu Kwon, Byung Su Kim, Ki Hyung Kim, Heung Yeol Kim, Hong-bae Koh, Suk Bong Chun, Sungwook Ji, Yong Il Lee, Ji Young Namkung, Jeong Kwon, Sanghoon |
author_facet | Eo, Wan Kyu Kwon, Byung Su Kim, Ki Hyung Kim, Heung Yeol Kim, Hong-bae Koh, Suk Bong Chun, Sungwook Ji, Yong Il Lee, Ji Young Namkung, Jeong Kwon, Sanghoon |
author_sort | Eo, Wan Kyu |
collection | PubMed |
description | Objective: To measure hematologic parameters derived from the white blood cell (WBC) count and differential count (DC) as prognostic factors for survival in patients with stage IB and IIA cervical cancer. Methods: We retrospectively examined demographic, clinicopathologic, and laboratory parameters in a cohort of 233 patients with International Federation of Gynecology and Obstetrics stage IB and IIA cervical cancer who underwent surgical resection. We further assessed the effects of the WBC count and DC-derived hematologic parameters on progression-free survival (PFS) and overall survival (OS) after controlling for other parameters. Results: Patients were followed up for a median of 46.6 months (range, 9-142 months). The Kaplan-Meier estimates of PFS and OS at 5 years were 88.5% and 92.3%, respectively. In a multivariate analysis, we identified the absolute monocyte count (AMC) (hazard ratio [HR], 11.78; P <0.001) and tumor size (HR, 5.41; P = 0.003) as the strongest prognostic factors affecting PFS. We also identified AMC (HR, 23.29; P <0.001), tumor size, (HR, 5.27; P = 0.033), and lymph node involvement (HR, 3.90; P = 0.027) as the strongest prognostic factors affecting OS. AMC remained prognostic with respect to PFS or OS in a Cox model that controlled for the neutrophil-lymphocyte ratio or lymphocyte-monocyte ratio, although neither ratio was a significant prognostic factor for survival. Conclusions: Monocytosis and an increased tumor size were found to be independent prognostic factors affecting both PFS and OS in patients with stage IB and IIA cervical cancer. |
format | Online Article Text |
id | pubmed-5743712 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-57437122018-01-01 Monocytosis as a prognostic factor for survival in stage IB and IIA cervical cancer Eo, Wan Kyu Kwon, Byung Su Kim, Ki Hyung Kim, Heung Yeol Kim, Hong-bae Koh, Suk Bong Chun, Sungwook Ji, Yong Il Lee, Ji Young Namkung, Jeong Kwon, Sanghoon J Cancer Research Paper Objective: To measure hematologic parameters derived from the white blood cell (WBC) count and differential count (DC) as prognostic factors for survival in patients with stage IB and IIA cervical cancer. Methods: We retrospectively examined demographic, clinicopathologic, and laboratory parameters in a cohort of 233 patients with International Federation of Gynecology and Obstetrics stage IB and IIA cervical cancer who underwent surgical resection. We further assessed the effects of the WBC count and DC-derived hematologic parameters on progression-free survival (PFS) and overall survival (OS) after controlling for other parameters. Results: Patients were followed up for a median of 46.6 months (range, 9-142 months). The Kaplan-Meier estimates of PFS and OS at 5 years were 88.5% and 92.3%, respectively. In a multivariate analysis, we identified the absolute monocyte count (AMC) (hazard ratio [HR], 11.78; P <0.001) and tumor size (HR, 5.41; P = 0.003) as the strongest prognostic factors affecting PFS. We also identified AMC (HR, 23.29; P <0.001), tumor size, (HR, 5.27; P = 0.033), and lymph node involvement (HR, 3.90; P = 0.027) as the strongest prognostic factors affecting OS. AMC remained prognostic with respect to PFS or OS in a Cox model that controlled for the neutrophil-lymphocyte ratio or lymphocyte-monocyte ratio, although neither ratio was a significant prognostic factor for survival. Conclusions: Monocytosis and an increased tumor size were found to be independent prognostic factors affecting both PFS and OS in patients with stage IB and IIA cervical cancer. Ivyspring International Publisher 2018-01-01 /pmc/articles/PMC5743712/ /pubmed/29290770 http://dx.doi.org/10.7150/jca.22234 Text en © Ivyspring International Publisher This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) license (https://creativecommons.org/licenses/by-nc/4.0/). See http://ivyspring.com/terms for full terms and conditions. |
spellingShingle | Research Paper Eo, Wan Kyu Kwon, Byung Su Kim, Ki Hyung Kim, Heung Yeol Kim, Hong-bae Koh, Suk Bong Chun, Sungwook Ji, Yong Il Lee, Ji Young Namkung, Jeong Kwon, Sanghoon Monocytosis as a prognostic factor for survival in stage IB and IIA cervical cancer |
title | Monocytosis as a prognostic factor for survival in stage IB and IIA cervical cancer |
title_full | Monocytosis as a prognostic factor for survival in stage IB and IIA cervical cancer |
title_fullStr | Monocytosis as a prognostic factor for survival in stage IB and IIA cervical cancer |
title_full_unstemmed | Monocytosis as a prognostic factor for survival in stage IB and IIA cervical cancer |
title_short | Monocytosis as a prognostic factor for survival in stage IB and IIA cervical cancer |
title_sort | monocytosis as a prognostic factor for survival in stage ib and iia cervical cancer |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5743712/ https://www.ncbi.nlm.nih.gov/pubmed/29290770 http://dx.doi.org/10.7150/jca.22234 |
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