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Long-term survival and late complications of intensity-modulated radiotherapy for recurrent nasopharyngeal carcinoma

BACKGROUND: To evaluate the effectiveness and toxicities of intensity-modulated radiotherapy (IMRT) for locally recurrent nasopharyngeal carcinoma (NPC). METHODS: One hundred and eighty-four previously irradiated NPC patients with recurrent disease and re-irradiated by IMRT between February 2005 to...

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Autores principales: Kong, Fangfang, Zhou, Junjun, Du, Chengrun, He, Xiayun, Kong, Lin, Hu, Chaosu, Ying, Hongmei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245884/
https://www.ncbi.nlm.nih.gov/pubmed/30453915
http://dx.doi.org/10.1186/s12885-018-5055-5
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author Kong, Fangfang
Zhou, Junjun
Du, Chengrun
He, Xiayun
Kong, Lin
Hu, Chaosu
Ying, Hongmei
author_facet Kong, Fangfang
Zhou, Junjun
Du, Chengrun
He, Xiayun
Kong, Lin
Hu, Chaosu
Ying, Hongmei
author_sort Kong, Fangfang
collection PubMed
description BACKGROUND: To evaluate the effectiveness and toxicities of intensity-modulated radiotherapy (IMRT) for locally recurrent nasopharyngeal carcinoma (NPC). METHODS: One hundred and eighty-four previously irradiated NPC patients with recurrent disease and re-irradiated by IMRT between February 2005 to May 2013 had been reviewed. The disease was re-staged I in 33, II in 27, III in 70 and IV in 54 patients. Seventy-five percent of the patients received cisplatin-based chemotherapy. RESULTS: The median survival time was 33 months. The 3-year actuarial rates of local recurrence–free survival (LRFS), distant metastases–free survival (DMFS), and overall survival (OS) rates were 85.1, 91.1, and 46.0%, respectively. About 53% of the patients experienced Grade 3–4 late toxicities. Forty-four patients died of massive hemorrhage of the nasopharynx caused by radiation induced mucosal necrosis. Multivariate analysis indicated that chemotherapy and time interval between initial radiotherapy and re-irradiation were independent predictors for DMFS. CONCLUSION: IMRT is an effective method for patients with locally recurrent NPC. Massive hemorrhage of the nasopharynx is the major sever late complication and also the leading cause of death. Early recurrence is negative factor for DMFS. Combination of chemotherapy can improve DMFS, but not for OS. Optimal salvage treatment strategies focusing on improvement of survival and minimization of late toxicities are warranted.
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spelling pubmed-62458842018-11-26 Long-term survival and late complications of intensity-modulated radiotherapy for recurrent nasopharyngeal carcinoma Kong, Fangfang Zhou, Junjun Du, Chengrun He, Xiayun Kong, Lin Hu, Chaosu Ying, Hongmei BMC Cancer Research Article BACKGROUND: To evaluate the effectiveness and toxicities of intensity-modulated radiotherapy (IMRT) for locally recurrent nasopharyngeal carcinoma (NPC). METHODS: One hundred and eighty-four previously irradiated NPC patients with recurrent disease and re-irradiated by IMRT between February 2005 to May 2013 had been reviewed. The disease was re-staged I in 33, II in 27, III in 70 and IV in 54 patients. Seventy-five percent of the patients received cisplatin-based chemotherapy. RESULTS: The median survival time was 33 months. The 3-year actuarial rates of local recurrence–free survival (LRFS), distant metastases–free survival (DMFS), and overall survival (OS) rates were 85.1, 91.1, and 46.0%, respectively. About 53% of the patients experienced Grade 3–4 late toxicities. Forty-four patients died of massive hemorrhage of the nasopharynx caused by radiation induced mucosal necrosis. Multivariate analysis indicated that chemotherapy and time interval between initial radiotherapy and re-irradiation were independent predictors for DMFS. CONCLUSION: IMRT is an effective method for patients with locally recurrent NPC. Massive hemorrhage of the nasopharynx is the major sever late complication and also the leading cause of death. Early recurrence is negative factor for DMFS. Combination of chemotherapy can improve DMFS, but not for OS. Optimal salvage treatment strategies focusing on improvement of survival and minimization of late toxicities are warranted. BioMed Central 2018-11-20 /pmc/articles/PMC6245884/ /pubmed/30453915 http://dx.doi.org/10.1186/s12885-018-5055-5 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Kong, Fangfang
Zhou, Junjun
Du, Chengrun
He, Xiayun
Kong, Lin
Hu, Chaosu
Ying, Hongmei
Long-term survival and late complications of intensity-modulated radiotherapy for recurrent nasopharyngeal carcinoma
title Long-term survival and late complications of intensity-modulated radiotherapy for recurrent nasopharyngeal carcinoma
title_full Long-term survival and late complications of intensity-modulated radiotherapy for recurrent nasopharyngeal carcinoma
title_fullStr Long-term survival and late complications of intensity-modulated radiotherapy for recurrent nasopharyngeal carcinoma
title_full_unstemmed Long-term survival and late complications of intensity-modulated radiotherapy for recurrent nasopharyngeal carcinoma
title_short Long-term survival and late complications of intensity-modulated radiotherapy for recurrent nasopharyngeal carcinoma
title_sort long-term survival and late complications of intensity-modulated radiotherapy for recurrent nasopharyngeal carcinoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245884/
https://www.ncbi.nlm.nih.gov/pubmed/30453915
http://dx.doi.org/10.1186/s12885-018-5055-5
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