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Analysis of late adverse events and their chronological changes after radiation therapy for cervical cancer
Several late adverse events occur after radiation therapy (RT) for cervical cancer. However, there has been little reported about their chronological changes. It is still unclear whether concurrent chemoradiotherapy (CCRT) increases late complications. We aimed to evaluate the late adverse events an...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nagoya University
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6295430/ https://www.ncbi.nlm.nih.gov/pubmed/30587863 http://dx.doi.org/10.18999/nagjms.80.4.487 |
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author | Yamada, Takehiro Ishihara, Shunichi Kawai, Michiyasu Itoh, Yoshiyuki Naganawa, Shinji Ikeda, Mitsuru |
author_facet | Yamada, Takehiro Ishihara, Shunichi Kawai, Michiyasu Itoh, Yoshiyuki Naganawa, Shinji Ikeda, Mitsuru |
author_sort | Yamada, Takehiro |
collection | PubMed |
description | Several late adverse events occur after radiation therapy (RT) for cervical cancer. However, there has been little reported about their chronological changes. It is still unclear whether concurrent chemoradiotherapy (CCRT) increases late complications. We aimed to evaluate the late adverse events and their chronological changes and whether CCRT increases their incidence and severity. For this purpose, we retrospectively analyzed 157 women with histologically proven cervical cancer. We reviewed all late adverse events and compared the frequency and severity between the patients who underwent CCRT and those who underwent RT alone. We calculated the cumulative occurrence rates of late adverse events stratified by the site and severity, and determined the chronological changes. With survivors’ median follow-up time of 74.3 months, late adverse events occurred in 49.0% and serious complications developed in 24.2% of all patients. There was no significant difference in the cumulative incidence rate of all late adverse events between the CCRT and RT-alone groups (p = 0.720). The incidence rate of rectal bleeding was 25.5%. Serious rectal bleeding developed in 5 patients, all within 20 months from the start of RT. Importantly, the symptoms of rectal bleeding disappeared or were relieved in most patients during follow-up. In conclusion, we evaluated the late adverse events and their chronological changes after RT for cervical cancer and showed that adding chemotherapy to RT did not affect the frequency and severity of late complications, and the symptoms of rectal bleeding were relieved over time. |
format | Online Article Text |
id | pubmed-6295430 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nagoya University |
record_format | MEDLINE/PubMed |
spelling | pubmed-62954302018-12-26 Analysis of late adverse events and their chronological changes after radiation therapy for cervical cancer Yamada, Takehiro Ishihara, Shunichi Kawai, Michiyasu Itoh, Yoshiyuki Naganawa, Shinji Ikeda, Mitsuru Nagoya J Med Sci Original Paper Several late adverse events occur after radiation therapy (RT) for cervical cancer. However, there has been little reported about their chronological changes. It is still unclear whether concurrent chemoradiotherapy (CCRT) increases late complications. We aimed to evaluate the late adverse events and their chronological changes and whether CCRT increases their incidence and severity. For this purpose, we retrospectively analyzed 157 women with histologically proven cervical cancer. We reviewed all late adverse events and compared the frequency and severity between the patients who underwent CCRT and those who underwent RT alone. We calculated the cumulative occurrence rates of late adverse events stratified by the site and severity, and determined the chronological changes. With survivors’ median follow-up time of 74.3 months, late adverse events occurred in 49.0% and serious complications developed in 24.2% of all patients. There was no significant difference in the cumulative incidence rate of all late adverse events between the CCRT and RT-alone groups (p = 0.720). The incidence rate of rectal bleeding was 25.5%. Serious rectal bleeding developed in 5 patients, all within 20 months from the start of RT. Importantly, the symptoms of rectal bleeding disappeared or were relieved in most patients during follow-up. In conclusion, we evaluated the late adverse events and their chronological changes after RT for cervical cancer and showed that adding chemotherapy to RT did not affect the frequency and severity of late complications, and the symptoms of rectal bleeding were relieved over time. Nagoya University 2018-11 /pmc/articles/PMC6295430/ /pubmed/30587863 http://dx.doi.org/10.18999/nagjms.80.4.487 Text en http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. To view the details of this license, please visit (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Paper Yamada, Takehiro Ishihara, Shunichi Kawai, Michiyasu Itoh, Yoshiyuki Naganawa, Shinji Ikeda, Mitsuru Analysis of late adverse events and their chronological changes after radiation therapy for cervical cancer |
title | Analysis of late adverse events and their chronological changes after radiation therapy for cervical cancer |
title_full | Analysis of late adverse events and their chronological changes after radiation therapy for cervical cancer |
title_fullStr | Analysis of late adverse events and their chronological changes after radiation therapy for cervical cancer |
title_full_unstemmed | Analysis of late adverse events and their chronological changes after radiation therapy for cervical cancer |
title_short | Analysis of late adverse events and their chronological changes after radiation therapy for cervical cancer |
title_sort | analysis of late adverse events and their chronological changes after radiation therapy for cervical cancer |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6295430/ https://www.ncbi.nlm.nih.gov/pubmed/30587863 http://dx.doi.org/10.18999/nagjms.80.4.487 |
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