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Survival rate variation with different histological subtypes of poor prognostic male anal squamous cell carcinoma: a population-based study
BACKGROUND AND OBJECTIVE: The prognosis of male anal squamous cell carcinoma (MASCC) and female anal squamous cell carcinoma (FASCC) is variable. The influence of tumor subtype on the survival rate and gender is poorly known. Our study is the largest population-based study and aims to outline the di...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5663601/ https://www.ncbi.nlm.nih.gov/pubmed/29137429 http://dx.doi.org/10.18632/oncotarget.20969 |
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author | Wan, Zihao Huang, Zhihao Vikash, Vikash Rai, Kelash Vikash, Sindhu Chen, Liaobin Li, Jingfeng |
author_facet | Wan, Zihao Huang, Zhihao Vikash, Vikash Rai, Kelash Vikash, Sindhu Chen, Liaobin Li, Jingfeng |
author_sort | Wan, Zihao |
collection | PubMed |
description | BACKGROUND AND OBJECTIVE: The prognosis of male anal squamous cell carcinoma (MASCC) and female anal squamous cell carcinoma (FASCC) is variable. The influence of tumor subtype on the survival rate and gender is poorly known. Our study is the largest population-based study and aims to outline the difference in survival between MASCC and FASCC patients. METHODS: A retrospective population-based study was performed to compare the disease-specific mortalities (DSMs) between genders related to the tumor subtypes. The Surveillance, Epidemiology, and End Results (SEER) program database was employed to obtain the data from January 1988 to December 2014. RESULTS: A total of 4,516, (3,249 males and 1,267 females), patients with anal squamous cell carcinomas (ASCC) were investigated. The 5-year DSMs were 24.18% and 18.08% for men and women, respectively. The univariate analysis of the male basaloid squamous cell carcinoma (BSCC) and cloacogenic carcinoma (CC) patients demonstrated higher DSMs (P <0.001). Moreover, in the multivariate analysis, BSCC and CC were associated with soaring DSMs in male patients (P < 0.05). CONCLUSIONS: In the cohort of BSCC and CC patients, male patients demonstrated a considerable decrease in survival rate compared to females. A more precise classification of ASCC and individualized management for MASCC are warranted. |
format | Online Article Text |
id | pubmed-5663601 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-56636012017-11-13 Survival rate variation with different histological subtypes of poor prognostic male anal squamous cell carcinoma: a population-based study Wan, Zihao Huang, Zhihao Vikash, Vikash Rai, Kelash Vikash, Sindhu Chen, Liaobin Li, Jingfeng Oncotarget Research Paper BACKGROUND AND OBJECTIVE: The prognosis of male anal squamous cell carcinoma (MASCC) and female anal squamous cell carcinoma (FASCC) is variable. The influence of tumor subtype on the survival rate and gender is poorly known. Our study is the largest population-based study and aims to outline the difference in survival between MASCC and FASCC patients. METHODS: A retrospective population-based study was performed to compare the disease-specific mortalities (DSMs) between genders related to the tumor subtypes. The Surveillance, Epidemiology, and End Results (SEER) program database was employed to obtain the data from January 1988 to December 2014. RESULTS: A total of 4,516, (3,249 males and 1,267 females), patients with anal squamous cell carcinomas (ASCC) were investigated. The 5-year DSMs were 24.18% and 18.08% for men and women, respectively. The univariate analysis of the male basaloid squamous cell carcinoma (BSCC) and cloacogenic carcinoma (CC) patients demonstrated higher DSMs (P <0.001). Moreover, in the multivariate analysis, BSCC and CC were associated with soaring DSMs in male patients (P < 0.05). CONCLUSIONS: In the cohort of BSCC and CC patients, male patients demonstrated a considerable decrease in survival rate compared to females. A more precise classification of ASCC and individualized management for MASCC are warranted. Impact Journals LLC 2017-09-16 /pmc/articles/PMC5663601/ /pubmed/29137429 http://dx.doi.org/10.18632/oncotarget.20969 Text en Copyright: © 2017 Wan et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License 3.0 (http://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Wan, Zihao Huang, Zhihao Vikash, Vikash Rai, Kelash Vikash, Sindhu Chen, Liaobin Li, Jingfeng Survival rate variation with different histological subtypes of poor prognostic male anal squamous cell carcinoma: a population-based study |
title | Survival rate variation with different histological subtypes of poor prognostic male anal squamous cell carcinoma: a population-based study |
title_full | Survival rate variation with different histological subtypes of poor prognostic male anal squamous cell carcinoma: a population-based study |
title_fullStr | Survival rate variation with different histological subtypes of poor prognostic male anal squamous cell carcinoma: a population-based study |
title_full_unstemmed | Survival rate variation with different histological subtypes of poor prognostic male anal squamous cell carcinoma: a population-based study |
title_short | Survival rate variation with different histological subtypes of poor prognostic male anal squamous cell carcinoma: a population-based study |
title_sort | survival rate variation with different histological subtypes of poor prognostic male anal squamous cell carcinoma: a population-based study |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5663601/ https://www.ncbi.nlm.nih.gov/pubmed/29137429 http://dx.doi.org/10.18632/oncotarget.20969 |
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