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Prognostic impact of hepatitis B virus infection in patients with primary cervical cancer
BACKGROUND: Hepatitis B virus (HBV) infection has been associated with an increased risk of a few malignancies. However, the prognostic impact of HBV infection remains unclear in cervical cancer. OBJECTIVE: To explore the association between HBV infection and survival outcomes of patients with prima...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8633261/ https://www.ncbi.nlm.nih.gov/pubmed/34672431 http://dx.doi.org/10.1002/cam4.4358 |
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author | Feng, Xiaoyan Lu, Huaiwu Wei, Yuan Guan, Meimei Wang, Junyi Liu, Changhao Shen, Tianran Chen, Qingsong Rao, Qunxian |
author_facet | Feng, Xiaoyan Lu, Huaiwu Wei, Yuan Guan, Meimei Wang, Junyi Liu, Changhao Shen, Tianran Chen, Qingsong Rao, Qunxian |
author_sort | Feng, Xiaoyan |
collection | PubMed |
description | BACKGROUND: Hepatitis B virus (HBV) infection has been associated with an increased risk of a few malignancies. However, the prognostic impact of HBV infection remains unclear in cervical cancer. OBJECTIVE: To explore the association between HBV infection and survival outcomes of patients with primary cervical cancer, using overall survival (OS) and disease‐free survival (DFS) as primary endpoints. METHODS: This analysis was performed retrospectively with newly diagnosed cervical cancer patients admitted to the Department of Gynecologic Oncology at the Sun Yat‐sen Memorial Hospital of Sun Yat‐sen University from June 2013 to October 2019, who were enrolled and followed up. The Kaplan–Meier method and Cox proportional hazard analysis were used to examine the performance of HBV infection in predicting OS and DFS. RESULTS: Patients were followed up for a median of 37.17 months (95% CI, 34.69–39.65). Among the 695 patients, 87 (12.5%) were serologically positive for hepatitis B surface antigen (HBsAg), and 276 (39.7%) had a prior history of HBV infection. There was no significant difference between HBsAg‐positive group and HBsAg‐negative patients concerning OS or DFS. Multivariate analysis showed prior HBV infection was an independent favorable prognosticator for OS (HR, 0.335; 95% CI, 0.153–0.0.734; p = 0.006) and DFS (HR, 0.398; 95% CI, 0.208–0.691; p = 0.002). CONCLUSION: We provide the first clinical evidence that suggests prior HBV infection as an independent favorable prognostic factor for patients with primary cervical cancer. |
format | Online Article Text |
id | pubmed-8633261 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-86332612021-12-06 Prognostic impact of hepatitis B virus infection in patients with primary cervical cancer Feng, Xiaoyan Lu, Huaiwu Wei, Yuan Guan, Meimei Wang, Junyi Liu, Changhao Shen, Tianran Chen, Qingsong Rao, Qunxian Cancer Med Clinical Cancer Research BACKGROUND: Hepatitis B virus (HBV) infection has been associated with an increased risk of a few malignancies. However, the prognostic impact of HBV infection remains unclear in cervical cancer. OBJECTIVE: To explore the association between HBV infection and survival outcomes of patients with primary cervical cancer, using overall survival (OS) and disease‐free survival (DFS) as primary endpoints. METHODS: This analysis was performed retrospectively with newly diagnosed cervical cancer patients admitted to the Department of Gynecologic Oncology at the Sun Yat‐sen Memorial Hospital of Sun Yat‐sen University from June 2013 to October 2019, who were enrolled and followed up. The Kaplan–Meier method and Cox proportional hazard analysis were used to examine the performance of HBV infection in predicting OS and DFS. RESULTS: Patients were followed up for a median of 37.17 months (95% CI, 34.69–39.65). Among the 695 patients, 87 (12.5%) were serologically positive for hepatitis B surface antigen (HBsAg), and 276 (39.7%) had a prior history of HBV infection. There was no significant difference between HBsAg‐positive group and HBsAg‐negative patients concerning OS or DFS. Multivariate analysis showed prior HBV infection was an independent favorable prognosticator for OS (HR, 0.335; 95% CI, 0.153–0.0.734; p = 0.006) and DFS (HR, 0.398; 95% CI, 0.208–0.691; p = 0.002). CONCLUSION: We provide the first clinical evidence that suggests prior HBV infection as an independent favorable prognostic factor for patients with primary cervical cancer. John Wiley and Sons Inc. 2021-10-21 /pmc/articles/PMC8633261/ /pubmed/34672431 http://dx.doi.org/10.1002/cam4.4358 Text en © 2021 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Clinical Cancer Research Feng, Xiaoyan Lu, Huaiwu Wei, Yuan Guan, Meimei Wang, Junyi Liu, Changhao Shen, Tianran Chen, Qingsong Rao, Qunxian Prognostic impact of hepatitis B virus infection in patients with primary cervical cancer |
title | Prognostic impact of hepatitis B virus infection in patients with primary cervical cancer |
title_full | Prognostic impact of hepatitis B virus infection in patients with primary cervical cancer |
title_fullStr | Prognostic impact of hepatitis B virus infection in patients with primary cervical cancer |
title_full_unstemmed | Prognostic impact of hepatitis B virus infection in patients with primary cervical cancer |
title_short | Prognostic impact of hepatitis B virus infection in patients with primary cervical cancer |
title_sort | prognostic impact of hepatitis b virus infection in patients with primary cervical cancer |
topic | Clinical Cancer Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8633261/ https://www.ncbi.nlm.nih.gov/pubmed/34672431 http://dx.doi.org/10.1002/cam4.4358 |
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