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Meta-Analysis of VTE Risk: Ovarian Cancer Patients by Stage, Histology, Cytoreduction, and Ascites at Diagnosis

Venous thromboembolisms (VTEs) have been a leading secondary cause of death among ovarian cancer patients, prompting multiple studies of risk factors. The objective of this meta-analysis is to quantify the associations between VTE and the most commonly reported risk factors among ovarian cancer pati...

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Autores principales: Weeks, Kristin S., Herbach, Emma, McDonald, Megan, Charlton, Mary, Schweizer, Marin L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7486642/
https://www.ncbi.nlm.nih.gov/pubmed/32963543
http://dx.doi.org/10.1155/2020/2374716
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author Weeks, Kristin S.
Herbach, Emma
McDonald, Megan
Charlton, Mary
Schweizer, Marin L.
author_facet Weeks, Kristin S.
Herbach, Emma
McDonald, Megan
Charlton, Mary
Schweizer, Marin L.
author_sort Weeks, Kristin S.
collection PubMed
description Venous thromboembolisms (VTEs) have been a leading secondary cause of death among ovarian cancer patients, prompting multiple studies of risk factors. The objective of this meta-analysis is to quantify the associations between VTE and the most commonly reported risk factors among ovarian cancer patients. PubMed, Embase, and Cumulative Index to Nursing and Allied Health Literature (CINAHL) were used to identify observational studies. Two reviewers independently abstracted data and assessed quality via the Newcastle–Ottawa tool. A random effects model was used to calculate the pooled odds ratios for VTE with each of the following exposures: advanced cancer stage, clear cell histology, serous histology, ascites at diagnosis, and complete cytoreduction. The I(2) and Q tests were used to evaluate heterogeneity. Twenty cohort studies with 6,324 total ovarian cancer patients, 769 of whom experienced a VTE, were included. The odds of VTE in ovarian cancer patients were higher among patients with cancer stage III/IV (versus cancer stage I/II, pooled odds ratio (OR) 2.73; 95% CI 1.84–4.06; I(2)= 64%), clear cell (versus nonclear cell) histology (OR 2.11; 95% CI 1.55–2.89; I(2) = 6%), and ascites (versus no ascites) at diagnosis (OR 2.12; 95% CI 1.51–2.96; I(2) = 32%). Serous (versus nonserous) histology (OR 1.26; 95% CI 0.91–1.75; I(2) = 42%) and complete (versus incomplete) cytoreduction (OR 1.05; 95% CI 0.27–4.11; I(2) = 88%) were not associated with VTE. This meta-analysis quantifies the significantly elevated odds of VTE in ovarian cancer patients with advanced stage at diagnosis, clear cell histology, and ascites at diagnosis. Further studies are needed to account for confounders and inform clinical decision-making tools.
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spelling pubmed-74866422020-09-21 Meta-Analysis of VTE Risk: Ovarian Cancer Patients by Stage, Histology, Cytoreduction, and Ascites at Diagnosis Weeks, Kristin S. Herbach, Emma McDonald, Megan Charlton, Mary Schweizer, Marin L. Obstet Gynecol Int Research Article Venous thromboembolisms (VTEs) have been a leading secondary cause of death among ovarian cancer patients, prompting multiple studies of risk factors. The objective of this meta-analysis is to quantify the associations between VTE and the most commonly reported risk factors among ovarian cancer patients. PubMed, Embase, and Cumulative Index to Nursing and Allied Health Literature (CINAHL) were used to identify observational studies. Two reviewers independently abstracted data and assessed quality via the Newcastle–Ottawa tool. A random effects model was used to calculate the pooled odds ratios for VTE with each of the following exposures: advanced cancer stage, clear cell histology, serous histology, ascites at diagnosis, and complete cytoreduction. The I(2) and Q tests were used to evaluate heterogeneity. Twenty cohort studies with 6,324 total ovarian cancer patients, 769 of whom experienced a VTE, were included. The odds of VTE in ovarian cancer patients were higher among patients with cancer stage III/IV (versus cancer stage I/II, pooled odds ratio (OR) 2.73; 95% CI 1.84–4.06; I(2)= 64%), clear cell (versus nonclear cell) histology (OR 2.11; 95% CI 1.55–2.89; I(2) = 6%), and ascites (versus no ascites) at diagnosis (OR 2.12; 95% CI 1.51–2.96; I(2) = 32%). Serous (versus nonserous) histology (OR 1.26; 95% CI 0.91–1.75; I(2) = 42%) and complete (versus incomplete) cytoreduction (OR 1.05; 95% CI 0.27–4.11; I(2) = 88%) were not associated with VTE. This meta-analysis quantifies the significantly elevated odds of VTE in ovarian cancer patients with advanced stage at diagnosis, clear cell histology, and ascites at diagnosis. Further studies are needed to account for confounders and inform clinical decision-making tools. Hindawi 2020-09-03 /pmc/articles/PMC7486642/ /pubmed/32963543 http://dx.doi.org/10.1155/2020/2374716 Text en Copyright © 2020 Kristin S. Weeks et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Weeks, Kristin S.
Herbach, Emma
McDonald, Megan
Charlton, Mary
Schweizer, Marin L.
Meta-Analysis of VTE Risk: Ovarian Cancer Patients by Stage, Histology, Cytoreduction, and Ascites at Diagnosis
title Meta-Analysis of VTE Risk: Ovarian Cancer Patients by Stage, Histology, Cytoreduction, and Ascites at Diagnosis
title_full Meta-Analysis of VTE Risk: Ovarian Cancer Patients by Stage, Histology, Cytoreduction, and Ascites at Diagnosis
title_fullStr Meta-Analysis of VTE Risk: Ovarian Cancer Patients by Stage, Histology, Cytoreduction, and Ascites at Diagnosis
title_full_unstemmed Meta-Analysis of VTE Risk: Ovarian Cancer Patients by Stage, Histology, Cytoreduction, and Ascites at Diagnosis
title_short Meta-Analysis of VTE Risk: Ovarian Cancer Patients by Stage, Histology, Cytoreduction, and Ascites at Diagnosis
title_sort meta-analysis of vte risk: ovarian cancer patients by stage, histology, cytoreduction, and ascites at diagnosis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7486642/
https://www.ncbi.nlm.nih.gov/pubmed/32963543
http://dx.doi.org/10.1155/2020/2374716
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