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Radiotherapy- and Chemotherapy-Induced Myelodysplasia Syndrome: A Nationwide Population-Based Nested Case–Control Study
This study explored which kinds of cancer are related to a higher incidence of subsequent myelodysplastic syndrome (MDS) after radiotherapy (RT) and chemotherapy (CT). We performed a nested case–control study by using data from the Taiwanese National Health Insurance (NHI) system. The case group inc...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4603069/ https://www.ncbi.nlm.nih.gov/pubmed/25929909 http://dx.doi.org/10.1097/MD.0000000000000737 |
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author | Sun, Li-Min Lin, Cheng-Li Lin, Ming-Chia Liang, Ji-An Kao, Chia-Hung |
author_facet | Sun, Li-Min Lin, Cheng-Li Lin, Ming-Chia Liang, Ji-An Kao, Chia-Hung |
author_sort | Sun, Li-Min |
collection | PubMed |
description | This study explored which kinds of cancer are related to a higher incidence of subsequent myelodysplastic syndrome (MDS) after radiotherapy (RT) and chemotherapy (CT). We performed a nested case–control study by using data from the Taiwanese National Health Insurance (NHI) system. The case group included cancer patients who developed MDS. For the control group, 4 cancer patients without MDS were frequency-matched with each MDS case by age, sex, year of cancer diagnosis, and MDS index year. A multivariable logistic regression analysis was conducted, and odds ratios (ORs) and 95% confidence intervals (CIs) were estimated. Overall, cancer patients who received RT or CT exhibited secondary MDS more frequently than did those who did not (RT: OR = 1.53; 95% CI = 1.33–1.77; CT: OR = 1.51; 95% CI = 1.25–1.82). Analysis by cancer site showed that RT increased the risk of MDS for patients with stomach, colorectal, liver, breast, endometrial, prostate, and kidney cancers. By contrast, CT was more likely to increase the risk of MDS for patients with lung, endometrial, and cervical cancers. Further analysis revealed that RT and CT seemed to have a positive interaction. The major limitation of this study was the lack of certain essential data in the NHI Research Database, such as data regarding cancer stage and treatment dose details. This population-based nested case–control study determined that RT and CT predisposed patients in Taiwan to the development of MDS. This effect was more prominent when both modalities were used. |
format | Online Article Text |
id | pubmed-4603069 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-46030692015-10-27 Radiotherapy- and Chemotherapy-Induced Myelodysplasia Syndrome: A Nationwide Population-Based Nested Case–Control Study Sun, Li-Min Lin, Cheng-Li Lin, Ming-Chia Liang, Ji-An Kao, Chia-Hung Medicine (Baltimore) 4800 This study explored which kinds of cancer are related to a higher incidence of subsequent myelodysplastic syndrome (MDS) after radiotherapy (RT) and chemotherapy (CT). We performed a nested case–control study by using data from the Taiwanese National Health Insurance (NHI) system. The case group included cancer patients who developed MDS. For the control group, 4 cancer patients without MDS were frequency-matched with each MDS case by age, sex, year of cancer diagnosis, and MDS index year. A multivariable logistic regression analysis was conducted, and odds ratios (ORs) and 95% confidence intervals (CIs) were estimated. Overall, cancer patients who received RT or CT exhibited secondary MDS more frequently than did those who did not (RT: OR = 1.53; 95% CI = 1.33–1.77; CT: OR = 1.51; 95% CI = 1.25–1.82). Analysis by cancer site showed that RT increased the risk of MDS for patients with stomach, colorectal, liver, breast, endometrial, prostate, and kidney cancers. By contrast, CT was more likely to increase the risk of MDS for patients with lung, endometrial, and cervical cancers. Further analysis revealed that RT and CT seemed to have a positive interaction. The major limitation of this study was the lack of certain essential data in the NHI Research Database, such as data regarding cancer stage and treatment dose details. This population-based nested case–control study determined that RT and CT predisposed patients in Taiwan to the development of MDS. This effect was more prominent when both modalities were used. Wolters Kluwer Health 2015-05-01 /pmc/articles/PMC4603069/ /pubmed/25929909 http://dx.doi.org/10.1097/MD.0000000000000737 Text en Copyright © 2015 Wolters Kluwer Health, Inc. All rights reserved. http://creativecommons.org/licenses/by-nd/4.0 This is an open access article distributed under the Creative Commons Attribution-NoDerivatives License 4.0, which allows for redistribution, commercial and non-commercial, as long as it is passed along unchanged and in whole, with credit to the author. http://creativecommons.org/licenses/by-nd/4.0 |
spellingShingle | 4800 Sun, Li-Min Lin, Cheng-Li Lin, Ming-Chia Liang, Ji-An Kao, Chia-Hung Radiotherapy- and Chemotherapy-Induced Myelodysplasia Syndrome: A Nationwide Population-Based Nested Case–Control Study |
title | Radiotherapy- and Chemotherapy-Induced Myelodysplasia Syndrome: A Nationwide Population-Based Nested Case–Control Study |
title_full | Radiotherapy- and Chemotherapy-Induced Myelodysplasia Syndrome: A Nationwide Population-Based Nested Case–Control Study |
title_fullStr | Radiotherapy- and Chemotherapy-Induced Myelodysplasia Syndrome: A Nationwide Population-Based Nested Case–Control Study |
title_full_unstemmed | Radiotherapy- and Chemotherapy-Induced Myelodysplasia Syndrome: A Nationwide Population-Based Nested Case–Control Study |
title_short | Radiotherapy- and Chemotherapy-Induced Myelodysplasia Syndrome: A Nationwide Population-Based Nested Case–Control Study |
title_sort | radiotherapy- and chemotherapy-induced myelodysplasia syndrome: a nationwide population-based nested case–control study |
topic | 4800 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4603069/ https://www.ncbi.nlm.nih.gov/pubmed/25929909 http://dx.doi.org/10.1097/MD.0000000000000737 |
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