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Second primary malignancy risk after radiotherapy in rectal cancer survivors
AIM: To investigate second primary malignancy (SPM) risk after radiotherapy in rectal cancer survivors METHODS: We used Taiwan’s National Health Insurance Research Database to identify rectal cancer patients between 1996 and 2011. Surgery-alone, preoperative short course, preoperative long course, a...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Baishideng Publishing Group Inc
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6209568/ https://www.ncbi.nlm.nih.gov/pubmed/30386108 http://dx.doi.org/10.3748/wjg.v24.i40.4586 |
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author | Wang, Ti-Hao Liu, Chia-Jen Chao, Tze-Fan Chen, Tzeng-Ji Hu, Yu-Wen |
author_facet | Wang, Ti-Hao Liu, Chia-Jen Chao, Tze-Fan Chen, Tzeng-Ji Hu, Yu-Wen |
author_sort | Wang, Ti-Hao |
collection | PubMed |
description | AIM: To investigate second primary malignancy (SPM) risk after radiotherapy in rectal cancer survivors METHODS: We used Taiwan’s National Health Insurance Research Database to identify rectal cancer patients between 1996 and 2011. Surgery-alone, preoperative short course, preoperative long course, and post-operative radiotherapy groups were defined. The overall and site-specific SPM incidence rates were compared among the radiotherapy groups by multivariate Cox regression, taking chemotherapy and comorbidities into account. Sensitivity tests were performed for attained-year adjustment and long-term survivors analysis. RESULTS: A total of 28220 patients were analyzed. The 10-year cumulative SPM incidence was 7.8% [95% confidence interval (CI): 7.2%-8.2%] using a competing risk model. The most common sites of SPM were the lung, liver, and prostate. Radiotherapy was not associated with increased SPM risk in multi-variate Cox model (hazard ratio = 1.05, 95%CI: 0.91-1.21, P = 0.494). The SPM hazard remained unchanged in 10-year-survivors. In addition, no SPM risk difference was found between the preoperative radiotherapy and postoperative radiotherapy groups. CONCLUSION: In this large population-based cohort study, we demonstrated that radiotherapy had no increase in SPM. |
format | Online Article Text |
id | pubmed-6209568 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-62095682018-11-01 Second primary malignancy risk after radiotherapy in rectal cancer survivors Wang, Ti-Hao Liu, Chia-Jen Chao, Tze-Fan Chen, Tzeng-Ji Hu, Yu-Wen World J Gastroenterol Retrospective Study AIM: To investigate second primary malignancy (SPM) risk after radiotherapy in rectal cancer survivors METHODS: We used Taiwan’s National Health Insurance Research Database to identify rectal cancer patients between 1996 and 2011. Surgery-alone, preoperative short course, preoperative long course, and post-operative radiotherapy groups were defined. The overall and site-specific SPM incidence rates were compared among the radiotherapy groups by multivariate Cox regression, taking chemotherapy and comorbidities into account. Sensitivity tests were performed for attained-year adjustment and long-term survivors analysis. RESULTS: A total of 28220 patients were analyzed. The 10-year cumulative SPM incidence was 7.8% [95% confidence interval (CI): 7.2%-8.2%] using a competing risk model. The most common sites of SPM were the lung, liver, and prostate. Radiotherapy was not associated with increased SPM risk in multi-variate Cox model (hazard ratio = 1.05, 95%CI: 0.91-1.21, P = 0.494). The SPM hazard remained unchanged in 10-year-survivors. In addition, no SPM risk difference was found between the preoperative radiotherapy and postoperative radiotherapy groups. CONCLUSION: In this large population-based cohort study, we demonstrated that radiotherapy had no increase in SPM. Baishideng Publishing Group Inc 2018-10-28 2018-10-28 /pmc/articles/PMC6209568/ /pubmed/30386108 http://dx.doi.org/10.3748/wjg.v24.i40.4586 Text en ©The Author(s) 2018. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. |
spellingShingle | Retrospective Study Wang, Ti-Hao Liu, Chia-Jen Chao, Tze-Fan Chen, Tzeng-Ji Hu, Yu-Wen Second primary malignancy risk after radiotherapy in rectal cancer survivors |
title | Second primary malignancy risk after radiotherapy in rectal cancer survivors |
title_full | Second primary malignancy risk after radiotherapy in rectal cancer survivors |
title_fullStr | Second primary malignancy risk after radiotherapy in rectal cancer survivors |
title_full_unstemmed | Second primary malignancy risk after radiotherapy in rectal cancer survivors |
title_short | Second primary malignancy risk after radiotherapy in rectal cancer survivors |
title_sort | second primary malignancy risk after radiotherapy in rectal cancer survivors |
topic | Retrospective Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6209568/ https://www.ncbi.nlm.nih.gov/pubmed/30386108 http://dx.doi.org/10.3748/wjg.v24.i40.4586 |
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