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Effects of marital status on survival of hepatocellular carcinoma by race/ethnicity and gender
PURPOSE: It is well demonstrated that being married is associated with a better prognosis in multiple types of cancer. However, whether the protective effect of marital status varied across race/ethnicity and gender in patients with hepatocellular carcinoma remains unclear. Therefore, we aimed to ev...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5757210/ https://www.ncbi.nlm.nih.gov/pubmed/29379317 http://dx.doi.org/10.2147/CMAR.S142019 |
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author | Wu, Wenrui Fang, Daiqiong Shi, Ding Bian, Xiaoyuan Li, Lanjuan |
author_facet | Wu, Wenrui Fang, Daiqiong Shi, Ding Bian, Xiaoyuan Li, Lanjuan |
author_sort | Wu, Wenrui |
collection | PubMed |
description | PURPOSE: It is well demonstrated that being married is associated with a better prognosis in multiple types of cancer. However, whether the protective effect of marital status varied across race/ethnicity and gender in patients with hepatocellular carcinoma remains unclear. Therefore, we aimed to evaluate the roles of race/ethnicity and gender in this relationship. PATIENTS AND METHODS: We identified eligible patients from Surveillance, Epidemiology and End Results (SEER) database during 2004–2012. Overall and cancer-specific survival differences across marital status were compared by Kaplan–Meier curves. We also estimated crude hazard ratios (CHRs) and adjusted hazard ratios (AHRs) with 95% confidence intervals (CIs) for marital status associated with survival by race/ethnicity and gender in Cox proportional hazard models. RESULTS: A total of 12,168 eligible patients diagnosed with hepatocellular carcinoma were included. We observed that married status was an independent protective prognostic factor for overall and cancer-specific survival. In stratified analyses by race/ethnicity, the AHR of overall mortality (unmarried vs married) was highest for Hispanic (AHR =1.25, 95% CI, 1.13–1.39; P<0.001) and lowest for Asian or Pacific Islander (AHR =1.13; 95% CI, 1.00–1.28; P=0.042). Stratified by gender, the AHR was higher in males (AHR =1.27; 95% CI, 1.20–1.33; P<0.001). Conclusion: We demonstrated that married patients obtained better survival advantages. Race/ethnicity and gender could influence the magnitude of associations between marital status and risk of mortality. |
format | Online Article Text |
id | pubmed-5757210 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-57572102018-01-29 Effects of marital status on survival of hepatocellular carcinoma by race/ethnicity and gender Wu, Wenrui Fang, Daiqiong Shi, Ding Bian, Xiaoyuan Li, Lanjuan Cancer Manag Res Original Research PURPOSE: It is well demonstrated that being married is associated with a better prognosis in multiple types of cancer. However, whether the protective effect of marital status varied across race/ethnicity and gender in patients with hepatocellular carcinoma remains unclear. Therefore, we aimed to evaluate the roles of race/ethnicity and gender in this relationship. PATIENTS AND METHODS: We identified eligible patients from Surveillance, Epidemiology and End Results (SEER) database during 2004–2012. Overall and cancer-specific survival differences across marital status were compared by Kaplan–Meier curves. We also estimated crude hazard ratios (CHRs) and adjusted hazard ratios (AHRs) with 95% confidence intervals (CIs) for marital status associated with survival by race/ethnicity and gender in Cox proportional hazard models. RESULTS: A total of 12,168 eligible patients diagnosed with hepatocellular carcinoma were included. We observed that married status was an independent protective prognostic factor for overall and cancer-specific survival. In stratified analyses by race/ethnicity, the AHR of overall mortality (unmarried vs married) was highest for Hispanic (AHR =1.25, 95% CI, 1.13–1.39; P<0.001) and lowest for Asian or Pacific Islander (AHR =1.13; 95% CI, 1.00–1.28; P=0.042). Stratified by gender, the AHR was higher in males (AHR =1.27; 95% CI, 1.20–1.33; P<0.001). Conclusion: We demonstrated that married patients obtained better survival advantages. Race/ethnicity and gender could influence the magnitude of associations between marital status and risk of mortality. Dove Medical Press 2018-01-03 /pmc/articles/PMC5757210/ /pubmed/29379317 http://dx.doi.org/10.2147/CMAR.S142019 Text en © 2018 Wu et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Wu, Wenrui Fang, Daiqiong Shi, Ding Bian, Xiaoyuan Li, Lanjuan Effects of marital status on survival of hepatocellular carcinoma by race/ethnicity and gender |
title | Effects of marital status on survival of hepatocellular carcinoma by race/ethnicity and gender |
title_full | Effects of marital status on survival of hepatocellular carcinoma by race/ethnicity and gender |
title_fullStr | Effects of marital status on survival of hepatocellular carcinoma by race/ethnicity and gender |
title_full_unstemmed | Effects of marital status on survival of hepatocellular carcinoma by race/ethnicity and gender |
title_short | Effects of marital status on survival of hepatocellular carcinoma by race/ethnicity and gender |
title_sort | effects of marital status on survival of hepatocellular carcinoma by race/ethnicity and gender |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5757210/ https://www.ncbi.nlm.nih.gov/pubmed/29379317 http://dx.doi.org/10.2147/CMAR.S142019 |
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