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Prognostic significance of red blood cell distribution width in gastrointestinal cancers: A meta-analysis
BACKGROUND: Many publications showed red blood cell distribution width (RDW) might associate with the prognosis of gastrointestinal (GI) cancers, however, the agreement has not been reached because of controversial results. This meta-analysis aimed to explore the prognostic value of RDW in GI cancer...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7220356/ https://www.ncbi.nlm.nih.gov/pubmed/32311927 http://dx.doi.org/10.1097/MD.0000000000019588 |
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author | Zhou, Yongping Li, Xiding Lu, Zhihua Zhang, Lei Dai, Tu |
author_facet | Zhou, Yongping Li, Xiding Lu, Zhihua Zhang, Lei Dai, Tu |
author_sort | Zhou, Yongping |
collection | PubMed |
description | BACKGROUND: Many publications showed red blood cell distribution width (RDW) might associate with the prognosis of gastrointestinal (GI) cancers, however, the agreement has not been reached because of controversial results. This meta-analysis aimed to explore the prognostic value of RDW in GI cancers. METHODS: Four common databases were comprehensively searched to look for relevant studies. The meta-analyses for overall survival (OS) and disease-free survival were performed using hazard ratio (HR) and 95% confidence interval (CI), and the meta-analyses for clinical parameters were conducted using odd ratio and 95% CI. RESULTS: A total of 13 studies involving with 3,509 patients with GI cancers were included into this study. The results showed, compared to patients with low RDW, patients with high RDW tended to have shorter OS (HR = 1.75, 95%CI = 1.57–1.94, P < .01) and disease-free survival (HR = 1.67, 95%CI = 1.39–2.00, P < .01). High RDW was associated with larger tumor size (P < .01), worse differentiation (P = .02), deeper invasion (P < .01), earlier lymph node metastasis (P < .01), more advanced clinical stage (P < .01) and higher carcinoembryonic antigen level (P < .01) when compared to low RDW. CONCLUSION: High RDW was significantly associated with worse prognosis of GI cancers, which could be regarded as a prognostic biomarker for GI cancers. More prospective studies with large sample size and long follow-up period should be carried out to determine the prognostic significance of RDW in GI cancers in future. |
format | Online Article Text |
id | pubmed-7220356 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-72203562020-06-15 Prognostic significance of red blood cell distribution width in gastrointestinal cancers: A meta-analysis Zhou, Yongping Li, Xiding Lu, Zhihua Zhang, Lei Dai, Tu Medicine (Baltimore) 5700 BACKGROUND: Many publications showed red blood cell distribution width (RDW) might associate with the prognosis of gastrointestinal (GI) cancers, however, the agreement has not been reached because of controversial results. This meta-analysis aimed to explore the prognostic value of RDW in GI cancers. METHODS: Four common databases were comprehensively searched to look for relevant studies. The meta-analyses for overall survival (OS) and disease-free survival were performed using hazard ratio (HR) and 95% confidence interval (CI), and the meta-analyses for clinical parameters were conducted using odd ratio and 95% CI. RESULTS: A total of 13 studies involving with 3,509 patients with GI cancers were included into this study. The results showed, compared to patients with low RDW, patients with high RDW tended to have shorter OS (HR = 1.75, 95%CI = 1.57–1.94, P < .01) and disease-free survival (HR = 1.67, 95%CI = 1.39–2.00, P < .01). High RDW was associated with larger tumor size (P < .01), worse differentiation (P = .02), deeper invasion (P < .01), earlier lymph node metastasis (P < .01), more advanced clinical stage (P < .01) and higher carcinoembryonic antigen level (P < .01) when compared to low RDW. CONCLUSION: High RDW was significantly associated with worse prognosis of GI cancers, which could be regarded as a prognostic biomarker for GI cancers. More prospective studies with large sample size and long follow-up period should be carried out to determine the prognostic significance of RDW in GI cancers in future. Wolters Kluwer Health 2020-04-17 /pmc/articles/PMC7220356/ /pubmed/32311927 http://dx.doi.org/10.1097/MD.0000000000019588 Text en Copyright © 2020 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0 |
spellingShingle | 5700 Zhou, Yongping Li, Xiding Lu, Zhihua Zhang, Lei Dai, Tu Prognostic significance of red blood cell distribution width in gastrointestinal cancers: A meta-analysis |
title | Prognostic significance of red blood cell distribution width in gastrointestinal cancers: A meta-analysis |
title_full | Prognostic significance of red blood cell distribution width in gastrointestinal cancers: A meta-analysis |
title_fullStr | Prognostic significance of red blood cell distribution width in gastrointestinal cancers: A meta-analysis |
title_full_unstemmed | Prognostic significance of red blood cell distribution width in gastrointestinal cancers: A meta-analysis |
title_short | Prognostic significance of red blood cell distribution width in gastrointestinal cancers: A meta-analysis |
title_sort | prognostic significance of red blood cell distribution width in gastrointestinal cancers: a meta-analysis |
topic | 5700 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7220356/ https://www.ncbi.nlm.nih.gov/pubmed/32311927 http://dx.doi.org/10.1097/MD.0000000000019588 |
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