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Incidence and risk factors of second primary cancer after the initial primary human papillomavirus related neoplasms

Comprehensive studies in second primary cancer (SPC) after the initial primary human papillomavirus (HPV)‐related cancer still remain warranted. We aimed to analyze the incidence and risk factors of SPC after HPV‐related cancer. We identified 86 790 patients diagnosed with initial primary HPV‐relate...

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Autores principales: Shen, Jiayi, Zhou, Huaqiang, Liu, Jiaqing, Zhang, Zhonghan, Fang, Wenfeng, Yang, Yunpeng, Hong, Shaodong, Xian, Wei, Ma, Yuxiang, Zhou, Ting, Zhang, Yaxiong, Zhao, Hongyun, Huang, Yan, Zhang, Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8491207/
https://www.ncbi.nlm.nih.gov/pubmed/34766131
http://dx.doi.org/10.1002/mco2.43
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author Shen, Jiayi
Zhou, Huaqiang
Liu, Jiaqing
Zhang, Zhonghan
Fang, Wenfeng
Yang, Yunpeng
Hong, Shaodong
Xian, Wei
Ma, Yuxiang
Zhou, Ting
Zhang, Yaxiong
Zhao, Hongyun
Huang, Yan
Zhang, Li
author_facet Shen, Jiayi
Zhou, Huaqiang
Liu, Jiaqing
Zhang, Zhonghan
Fang, Wenfeng
Yang, Yunpeng
Hong, Shaodong
Xian, Wei
Ma, Yuxiang
Zhou, Ting
Zhang, Yaxiong
Zhao, Hongyun
Huang, Yan
Zhang, Li
author_sort Shen, Jiayi
collection PubMed
description Comprehensive studies in second primary cancer (SPC) after the initial primary human papillomavirus (HPV)‐related cancer still remain warranted. We aimed to analyze the incidence and risk factors of SPC after HPV‐related cancer. We identified 86 790 patients diagnosed with initial primary HPV‐related cancer between 1973 and 2010 in the SEER database. Standardized incidence ratio (SIR) and cumulative incidence were calculated to assess the risk of SPC after HPV‐related cancer. The SIR of SPC after HPV‐related cancer was 1.60 (95% confidence interval [CI], 1.55‐1.65) for male and 1.25 (95% CI, 1.22‐1.28) for female. SIR of second primary HPV‐related cancer (7.39 [95% CI, 6.26‐8.68] male and 4.35 [95% CI, 4.04‐4.67] female) was significantly higher than that of HPV‐unrelated cancer (1.54 [95% CI, 1.49‐1.60] male and 1.16 [95% CI, 1.13‐1.19] female). The 5‐year cumulative incidence of SPC was 7.22% (95% CI, 6.89‐7.55%) for male and 3.72% (95% CI, 3.58‐3.88%) for female. Risk factors for SPC included being married and having initial primary cancer (IPC) diagnosed at earlier stage for both genders, and IPC diagnosed at older age as well as surgery performed for female. Patients diagnosed with HPV‐related cancer are more likely to develop another primary cancer, compared with the age‐specific reference population.
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spelling pubmed-84912072021-11-10 Incidence and risk factors of second primary cancer after the initial primary human papillomavirus related neoplasms Shen, Jiayi Zhou, Huaqiang Liu, Jiaqing Zhang, Zhonghan Fang, Wenfeng Yang, Yunpeng Hong, Shaodong Xian, Wei Ma, Yuxiang Zhou, Ting Zhang, Yaxiong Zhao, Hongyun Huang, Yan Zhang, Li MedComm (2020) Original Articles Comprehensive studies in second primary cancer (SPC) after the initial primary human papillomavirus (HPV)‐related cancer still remain warranted. We aimed to analyze the incidence and risk factors of SPC after HPV‐related cancer. We identified 86 790 patients diagnosed with initial primary HPV‐related cancer between 1973 and 2010 in the SEER database. Standardized incidence ratio (SIR) and cumulative incidence were calculated to assess the risk of SPC after HPV‐related cancer. The SIR of SPC after HPV‐related cancer was 1.60 (95% confidence interval [CI], 1.55‐1.65) for male and 1.25 (95% CI, 1.22‐1.28) for female. SIR of second primary HPV‐related cancer (7.39 [95% CI, 6.26‐8.68] male and 4.35 [95% CI, 4.04‐4.67] female) was significantly higher than that of HPV‐unrelated cancer (1.54 [95% CI, 1.49‐1.60] male and 1.16 [95% CI, 1.13‐1.19] female). The 5‐year cumulative incidence of SPC was 7.22% (95% CI, 6.89‐7.55%) for male and 3.72% (95% CI, 3.58‐3.88%) for female. Risk factors for SPC included being married and having initial primary cancer (IPC) diagnosed at earlier stage for both genders, and IPC diagnosed at older age as well as surgery performed for female. Patients diagnosed with HPV‐related cancer are more likely to develop another primary cancer, compared with the age‐specific reference population. John Wiley and Sons Inc. 2020-12-03 /pmc/articles/PMC8491207/ /pubmed/34766131 http://dx.doi.org/10.1002/mco2.43 Text en © 2020 The Authors. MedComm published by Sichuan International Medical Exchange & Promotion Association (SCIMEA) and John Wiley & Sons Australia, 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 Original Articles
Shen, Jiayi
Zhou, Huaqiang
Liu, Jiaqing
Zhang, Zhonghan
Fang, Wenfeng
Yang, Yunpeng
Hong, Shaodong
Xian, Wei
Ma, Yuxiang
Zhou, Ting
Zhang, Yaxiong
Zhao, Hongyun
Huang, Yan
Zhang, Li
Incidence and risk factors of second primary cancer after the initial primary human papillomavirus related neoplasms
title Incidence and risk factors of second primary cancer after the initial primary human papillomavirus related neoplasms
title_full Incidence and risk factors of second primary cancer after the initial primary human papillomavirus related neoplasms
title_fullStr Incidence and risk factors of second primary cancer after the initial primary human papillomavirus related neoplasms
title_full_unstemmed Incidence and risk factors of second primary cancer after the initial primary human papillomavirus related neoplasms
title_short Incidence and risk factors of second primary cancer after the initial primary human papillomavirus related neoplasms
title_sort incidence and risk factors of second primary cancer after the initial primary human papillomavirus related neoplasms
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8491207/
https://www.ncbi.nlm.nih.gov/pubmed/34766131
http://dx.doi.org/10.1002/mco2.43
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