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A retrospective study of shrinking field radiation therapy during chemoradiotherapy in stage III non-small cell lung cancer

BACKGROUND: and purpose: This retrospective study aimed to investigate the feasibility of shrinking field radiotherapy during chemoradiotherapy in non-small cell lung cancer (NSCLC). PATIENTS AND METHODS: Ninety-seven patients with stage III NSCLC who achieved a good response to chemoradiation were...

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Autores principales: Jiang, Chenxue, Han, Shuiyun, Chen, Wucheng, Ying, Xiaozhen, Wu, He, Zhu, Yaoyao, Shi, Guodong, Sun, Xiaojiang, Xu, Yaping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5844760/
https://www.ncbi.nlm.nih.gov/pubmed/29552324
http://dx.doi.org/10.18632/oncotarget.23849
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author Jiang, Chenxue
Han, Shuiyun
Chen, Wucheng
Ying, Xiaozhen
Wu, He
Zhu, Yaoyao
Shi, Guodong
Sun, Xiaojiang
Xu, Yaping
author_facet Jiang, Chenxue
Han, Shuiyun
Chen, Wucheng
Ying, Xiaozhen
Wu, He
Zhu, Yaoyao
Shi, Guodong
Sun, Xiaojiang
Xu, Yaping
author_sort Jiang, Chenxue
collection PubMed
description BACKGROUND: and purpose: This retrospective study aimed to investigate the feasibility of shrinking field radiotherapy during chemoradiotherapy in non-small cell lung cancer (NSCLC). PATIENTS AND METHODS: Ninety-seven patients with stage III NSCLC who achieved a good response to chemoradiation were analyzed. Computed tomography was performed after 40-50 Gy dose radiation to evaluate curative effect. Patients in the shrinking field group underwent resimulation CT scans and shrinking field radiotherapy. Acute symptomatic irradiation-induced pneumonia (ASIP), progression patterns and survival were assessed. RESULTS: Of the 97 patients who achieved response after a median total dose of 60 Gy, fifty patients received shrinking field radiotherapy. The incidence of acute symptomatic irradiation-induced pneumonia tended to be lower for the shrinking field group (18.0% vs. 23.4%, P = 0.51). The rate of disease progression was significantly higher in the non-shrinking than shrinking field group (95.7% vs. 66.0%, P < 0.001). Compared to the non-shrinking field group, the shrinking field group had similar overall survival (30.0 vs. 30.0 months, P = 0.58) but significantly better median progression-free survival (14.0 vs. 11.0 months, P = 0.006). CONCLUSIONS: Shrinking field radiotherapy during chemoradiotherapy in stage III non-small cell lung cancer seems safe with acceptable toxicities and relapse, and potentially spares normal tissues and enables dose escalation. Prospective trials are warranted.
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spelling pubmed-58447602018-03-16 A retrospective study of shrinking field radiation therapy during chemoradiotherapy in stage III non-small cell lung cancer Jiang, Chenxue Han, Shuiyun Chen, Wucheng Ying, Xiaozhen Wu, He Zhu, Yaoyao Shi, Guodong Sun, Xiaojiang Xu, Yaping Oncotarget Clinical Research Paper BACKGROUND: and purpose: This retrospective study aimed to investigate the feasibility of shrinking field radiotherapy during chemoradiotherapy in non-small cell lung cancer (NSCLC). PATIENTS AND METHODS: Ninety-seven patients with stage III NSCLC who achieved a good response to chemoradiation were analyzed. Computed tomography was performed after 40-50 Gy dose radiation to evaluate curative effect. Patients in the shrinking field group underwent resimulation CT scans and shrinking field radiotherapy. Acute symptomatic irradiation-induced pneumonia (ASIP), progression patterns and survival were assessed. RESULTS: Of the 97 patients who achieved response after a median total dose of 60 Gy, fifty patients received shrinking field radiotherapy. The incidence of acute symptomatic irradiation-induced pneumonia tended to be lower for the shrinking field group (18.0% vs. 23.4%, P = 0.51). The rate of disease progression was significantly higher in the non-shrinking than shrinking field group (95.7% vs. 66.0%, P < 0.001). Compared to the non-shrinking field group, the shrinking field group had similar overall survival (30.0 vs. 30.0 months, P = 0.58) but significantly better median progression-free survival (14.0 vs. 11.0 months, P = 0.006). CONCLUSIONS: Shrinking field radiotherapy during chemoradiotherapy in stage III non-small cell lung cancer seems safe with acceptable toxicities and relapse, and potentially spares normal tissues and enables dose escalation. Prospective trials are warranted. Impact Journals LLC 2018-01-03 /pmc/articles/PMC5844760/ /pubmed/29552324 http://dx.doi.org/10.18632/oncotarget.23849 Text en Copyright: © 2018 Jiang et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Clinical Research Paper
Jiang, Chenxue
Han, Shuiyun
Chen, Wucheng
Ying, Xiaozhen
Wu, He
Zhu, Yaoyao
Shi, Guodong
Sun, Xiaojiang
Xu, Yaping
A retrospective study of shrinking field radiation therapy during chemoradiotherapy in stage III non-small cell lung cancer
title A retrospective study of shrinking field radiation therapy during chemoradiotherapy in stage III non-small cell lung cancer
title_full A retrospective study of shrinking field radiation therapy during chemoradiotherapy in stage III non-small cell lung cancer
title_fullStr A retrospective study of shrinking field radiation therapy during chemoradiotherapy in stage III non-small cell lung cancer
title_full_unstemmed A retrospective study of shrinking field radiation therapy during chemoradiotherapy in stage III non-small cell lung cancer
title_short A retrospective study of shrinking field radiation therapy during chemoradiotherapy in stage III non-small cell lung cancer
title_sort retrospective study of shrinking field radiation therapy during chemoradiotherapy in stage iii non-small cell lung cancer
topic Clinical Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5844760/
https://www.ncbi.nlm.nih.gov/pubmed/29552324
http://dx.doi.org/10.18632/oncotarget.23849
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