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Analysis of simultaneous modulated accelerated radiotherapy (SMART) for nasopharyngeal carcinomas

The purpose of this study was to analyze the clinical outcomes of simultaneous modulated accelerated radiotherapy (SMART) in patients with nasopharyngeal carcinoma (NPC). A total of 97 patients who underwent SMART for NPC between August 2005 and November 2011 were evaluated. The prescribed dose was...

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Autores principales: Tang, Jian Min, Ma, Xiu Mei, Hou, Yan Li, Dai, Li Yan, Cao, Hong Bin, Ye, Ming, Bai, Yong Rui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4100004/
https://www.ncbi.nlm.nih.gov/pubmed/24614820
http://dx.doi.org/10.1093/jrr/rru012
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author Tang, Jian Min
Ma, Xiu Mei
Hou, Yan Li
Dai, Li Yan
Cao, Hong Bin
Ye, Ming
Bai, Yong Rui
author_facet Tang, Jian Min
Ma, Xiu Mei
Hou, Yan Li
Dai, Li Yan
Cao, Hong Bin
Ye, Ming
Bai, Yong Rui
author_sort Tang, Jian Min
collection PubMed
description The purpose of this study was to analyze the clinical outcomes of simultaneous modulated accelerated radiotherapy (SMART) in patients with nasopharyngeal carcinoma (NPC). A total of 97 patients who underwent SMART for NPC between August 2005 and November 2011 were evaluated. The prescribed dose was 69.9 Gy/30 fractions at 2.33 Gy/fraction to the primary gross tumor volume (PGTV) including the nasopharynx gross target volume and the positive neck lymph nodes, and 60 Gy/30 fraction at 2.0 Gy/fraction to the PCTV1; 54 Gy/30 fractions at 1.8 Gy/fraction was given to the PCTV2. Among 59 patients with local advanced disease, 31 patients received concurrent chemoradiotherapy (chemo-RT) with a regimen consisting of 135 mg/m(2) paclitaxel on Day 1 and 25 mg/m(2) cisplatin on Days 1–3. The median follow-up period was 42 months. The local control rate (LCR), distant metastases-free survival (DMFS) and overall survival (OS) rates were 93.3%, 90.3% and 91.6% at 3 years, and 87.6%, 87.9% and 85.7% at 5 years, respectively. There was no significant difference in outcome with respect to these three indicators for Stage III and IV disease treated with/without concurrent chemoradiotherapy (P > 0.05). Acute toxicities included Grade 3 mucositis, skin desquamation, and leucopenia, which occurred in 78 (80.4%), 8 (8.2%), and 45 (46.4%) patients, respectively. No patient had a Grade 3–4 late toxicity. SMART was associated with a favorable outcome for NPC with acceptable toxicity. The local-regional control was excellent but distant metastasis remains the main risk. The combination of SMART and chemotherapy needs to be optimized through further studies to enhance outcomes for locally advanced diseases.
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spelling pubmed-41000042014-08-12 Analysis of simultaneous modulated accelerated radiotherapy (SMART) for nasopharyngeal carcinomas Tang, Jian Min Ma, Xiu Mei Hou, Yan Li Dai, Li Yan Cao, Hong Bin Ye, Ming Bai, Yong Rui J Radiat Res Oncology The purpose of this study was to analyze the clinical outcomes of simultaneous modulated accelerated radiotherapy (SMART) in patients with nasopharyngeal carcinoma (NPC). A total of 97 patients who underwent SMART for NPC between August 2005 and November 2011 were evaluated. The prescribed dose was 69.9 Gy/30 fractions at 2.33 Gy/fraction to the primary gross tumor volume (PGTV) including the nasopharynx gross target volume and the positive neck lymph nodes, and 60 Gy/30 fraction at 2.0 Gy/fraction to the PCTV1; 54 Gy/30 fractions at 1.8 Gy/fraction was given to the PCTV2. Among 59 patients with local advanced disease, 31 patients received concurrent chemoradiotherapy (chemo-RT) with a regimen consisting of 135 mg/m(2) paclitaxel on Day 1 and 25 mg/m(2) cisplatin on Days 1–3. The median follow-up period was 42 months. The local control rate (LCR), distant metastases-free survival (DMFS) and overall survival (OS) rates were 93.3%, 90.3% and 91.6% at 3 years, and 87.6%, 87.9% and 85.7% at 5 years, respectively. There was no significant difference in outcome with respect to these three indicators for Stage III and IV disease treated with/without concurrent chemoradiotherapy (P > 0.05). Acute toxicities included Grade 3 mucositis, skin desquamation, and leucopenia, which occurred in 78 (80.4%), 8 (8.2%), and 45 (46.4%) patients, respectively. No patient had a Grade 3–4 late toxicity. SMART was associated with a favorable outcome for NPC with acceptable toxicity. The local-regional control was excellent but distant metastasis remains the main risk. The combination of SMART and chemotherapy needs to be optimized through further studies to enhance outcomes for locally advanced diseases. Oxford University Press 2014-07 2014-03-09 /pmc/articles/PMC4100004/ /pubmed/24614820 http://dx.doi.org/10.1093/jrr/rru012 Text en © The Author 2014. Published by Oxford University Press on behalf of The Japan Radiation Research Society and Japanese Society for Radiation Oncology. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Oncology
Tang, Jian Min
Ma, Xiu Mei
Hou, Yan Li
Dai, Li Yan
Cao, Hong Bin
Ye, Ming
Bai, Yong Rui
Analysis of simultaneous modulated accelerated radiotherapy (SMART) for nasopharyngeal carcinomas
title Analysis of simultaneous modulated accelerated radiotherapy (SMART) for nasopharyngeal carcinomas
title_full Analysis of simultaneous modulated accelerated radiotherapy (SMART) for nasopharyngeal carcinomas
title_fullStr Analysis of simultaneous modulated accelerated radiotherapy (SMART) for nasopharyngeal carcinomas
title_full_unstemmed Analysis of simultaneous modulated accelerated radiotherapy (SMART) for nasopharyngeal carcinomas
title_short Analysis of simultaneous modulated accelerated radiotherapy (SMART) for nasopharyngeal carcinomas
title_sort analysis of simultaneous modulated accelerated radiotherapy (smart) for nasopharyngeal carcinomas
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4100004/
https://www.ncbi.nlm.nih.gov/pubmed/24614820
http://dx.doi.org/10.1093/jrr/rru012
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