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Increased risk of high-grade prostate cancer among testicular cancer survivors
INTRODUCTION: Testicular cancer survivors (TCS) have an increased risk of additional cancers, including prostate cancer. Our understanding of the natural history of prostate cancer in testicular cancer survivors is very limited due to its rare incidence. METHODS: Using the Surveillance, Epidemiology...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8843166/ https://www.ncbi.nlm.nih.gov/pubmed/35157714 http://dx.doi.org/10.1371/journal.pone.0263573 |
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author | Zhang, Hong Yang, Hongmei Bandyopadhyay, Sanjukta Milano, Michael T. Fung, Chunkit Messing, Edward M. Chen, Yuhchyau |
author_facet | Zhang, Hong Yang, Hongmei Bandyopadhyay, Sanjukta Milano, Michael T. Fung, Chunkit Messing, Edward M. Chen, Yuhchyau |
author_sort | Zhang, Hong |
collection | PubMed |
description | INTRODUCTION: Testicular cancer survivors (TCS) have an increased risk of additional cancers, including prostate cancer. Our understanding of the natural history of prostate cancer in testicular cancer survivors is very limited due to its rare incidence. METHODS: Using the Surveillance, Epidemiology, and End Results (SEER) Registry from 1978 to 2011, we identified 282 TCS with subsequent prostate cancer and examined the tumor grade and clinical outcomes in contrast to men with primary prostate cancer in the general population. RESULTS: TCS with a subsequent prostate cancer diagnosis were more likely to be diagnosed at a younger age than men with primary prostate cancer (65.2% vs. 37.6% for age ≤65, 34.8% vs. 62.4% for age >65, p<0.001) and were more likely to have grade III/IV tumors (46.2% vs. 37.0%, p<0.002). Longer latency between testicular and prostate cancer diagnoses was associated with a higher risk of grade III/IV (p<0.001) cancer. Despite the increased risk for high-grade tumors, 10-year prostate cancer-specific survival and overall survival were not significantly different between TCS and men with primary prostate cancer. Based on the available information in SEER, we found that prior history of radiotherapy for testicular cancer had no impact on tumor grade or survival outcomes. CONCLUSIONS: Prostate cancer in TCS was more likely to be diagnosed at a younger age and with higher grades. Risks of grade III/IV disease increased with longer latency between testicular and prostate cancer diagnoses. Radiotherapy for testicular cancer did not appear to have a significant impact on the outcome of subsequent prostate cancer. |
format | Online Article Text |
id | pubmed-8843166 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-88431662022-02-15 Increased risk of high-grade prostate cancer among testicular cancer survivors Zhang, Hong Yang, Hongmei Bandyopadhyay, Sanjukta Milano, Michael T. Fung, Chunkit Messing, Edward M. Chen, Yuhchyau PLoS One Research Article INTRODUCTION: Testicular cancer survivors (TCS) have an increased risk of additional cancers, including prostate cancer. Our understanding of the natural history of prostate cancer in testicular cancer survivors is very limited due to its rare incidence. METHODS: Using the Surveillance, Epidemiology, and End Results (SEER) Registry from 1978 to 2011, we identified 282 TCS with subsequent prostate cancer and examined the tumor grade and clinical outcomes in contrast to men with primary prostate cancer in the general population. RESULTS: TCS with a subsequent prostate cancer diagnosis were more likely to be diagnosed at a younger age than men with primary prostate cancer (65.2% vs. 37.6% for age ≤65, 34.8% vs. 62.4% for age >65, p<0.001) and were more likely to have grade III/IV tumors (46.2% vs. 37.0%, p<0.002). Longer latency between testicular and prostate cancer diagnoses was associated with a higher risk of grade III/IV (p<0.001) cancer. Despite the increased risk for high-grade tumors, 10-year prostate cancer-specific survival and overall survival were not significantly different between TCS and men with primary prostate cancer. Based on the available information in SEER, we found that prior history of radiotherapy for testicular cancer had no impact on tumor grade or survival outcomes. CONCLUSIONS: Prostate cancer in TCS was more likely to be diagnosed at a younger age and with higher grades. Risks of grade III/IV disease increased with longer latency between testicular and prostate cancer diagnoses. Radiotherapy for testicular cancer did not appear to have a significant impact on the outcome of subsequent prostate cancer. Public Library of Science 2022-02-14 /pmc/articles/PMC8843166/ /pubmed/35157714 http://dx.doi.org/10.1371/journal.pone.0263573 Text en © 2022 Zhang et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Zhang, Hong Yang, Hongmei Bandyopadhyay, Sanjukta Milano, Michael T. Fung, Chunkit Messing, Edward M. Chen, Yuhchyau Increased risk of high-grade prostate cancer among testicular cancer survivors |
title | Increased risk of high-grade prostate cancer among testicular cancer survivors |
title_full | Increased risk of high-grade prostate cancer among testicular cancer survivors |
title_fullStr | Increased risk of high-grade prostate cancer among testicular cancer survivors |
title_full_unstemmed | Increased risk of high-grade prostate cancer among testicular cancer survivors |
title_short | Increased risk of high-grade prostate cancer among testicular cancer survivors |
title_sort | increased risk of high-grade prostate cancer among testicular cancer survivors |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8843166/ https://www.ncbi.nlm.nih.gov/pubmed/35157714 http://dx.doi.org/10.1371/journal.pone.0263573 |
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