Cargando…
Delineation of clinical target volume for postoperative radiotherapy in stage IIIA-pN2 non-small-cell lung cancer
With the high locoregional relapse rate and the improvement of radiation technology, postoperative radiotherapy (PORT) has been widely used in the treatment of completely resected stage IIIA-pN2 non-small-cell lung cancer (NSCLC). However, there is still no definitive consensus on clinical target vo...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4767117/ https://www.ncbi.nlm.nih.gov/pubmed/26929651 http://dx.doi.org/10.2147/OTT.S98765 |
_version_ | 1782417783957487616 |
---|---|
author | Jing, Xuquan Meng, Xue Sun, Xindong Yu, Jinming |
author_facet | Jing, Xuquan Meng, Xue Sun, Xindong Yu, Jinming |
author_sort | Jing, Xuquan |
collection | PubMed |
description | With the high locoregional relapse rate and the improvement of radiation technology, postoperative radiotherapy (PORT) has been widely used in the treatment of completely resected stage IIIA-pN2 non-small-cell lung cancer (NSCLC). However, there is still no definitive consensus on clinical target volume for the pN2 subgroup. This review will discuss how to delineate the clinical target volume (CTV) for pN2 subgroups of IIIA-N2 NSCLC based on the published literature and to investigate the optimal PORT CTV in this cohort of patients. Besides overall survival (OS), locoregional recurrence (LR), and radiotherapy-related toxicity of this subset of the population in the modern PORT era, selection of proper patients will also be considered in this review. In summary, it is appropriate to include involved lymph node stations and uninvolved stations at high risk in PORT CTV for patients with pN2 disease when PORT is administered. PORT can reduce LR and has the potential to improve OS. In the current era of modern radiation technology, PORT can be administered safely with well-tolerated toxicity. Clinicopathological characteristics may be helpful in selecting proper candidates for PORT. |
format | Online Article Text |
id | pubmed-4767117 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-47671172016-02-29 Delineation of clinical target volume for postoperative radiotherapy in stage IIIA-pN2 non-small-cell lung cancer Jing, Xuquan Meng, Xue Sun, Xindong Yu, Jinming Onco Targets Ther Original Research With the high locoregional relapse rate and the improvement of radiation technology, postoperative radiotherapy (PORT) has been widely used in the treatment of completely resected stage IIIA-pN2 non-small-cell lung cancer (NSCLC). However, there is still no definitive consensus on clinical target volume for the pN2 subgroup. This review will discuss how to delineate the clinical target volume (CTV) for pN2 subgroups of IIIA-N2 NSCLC based on the published literature and to investigate the optimal PORT CTV in this cohort of patients. Besides overall survival (OS), locoregional recurrence (LR), and radiotherapy-related toxicity of this subset of the population in the modern PORT era, selection of proper patients will also be considered in this review. In summary, it is appropriate to include involved lymph node stations and uninvolved stations at high risk in PORT CTV for patients with pN2 disease when PORT is administered. PORT can reduce LR and has the potential to improve OS. In the current era of modern radiation technology, PORT can be administered safely with well-tolerated toxicity. Clinicopathological characteristics may be helpful in selecting proper candidates for PORT. Dove Medical Press 2016-02-19 /pmc/articles/PMC4767117/ /pubmed/26929651 http://dx.doi.org/10.2147/OTT.S98765 Text en © 2016 Jing et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Jing, Xuquan Meng, Xue Sun, Xindong Yu, Jinming Delineation of clinical target volume for postoperative radiotherapy in stage IIIA-pN2 non-small-cell lung cancer |
title | Delineation of clinical target volume for postoperative radiotherapy in stage IIIA-pN2 non-small-cell lung cancer |
title_full | Delineation of clinical target volume for postoperative radiotherapy in stage IIIA-pN2 non-small-cell lung cancer |
title_fullStr | Delineation of clinical target volume for postoperative radiotherapy in stage IIIA-pN2 non-small-cell lung cancer |
title_full_unstemmed | Delineation of clinical target volume for postoperative radiotherapy in stage IIIA-pN2 non-small-cell lung cancer |
title_short | Delineation of clinical target volume for postoperative radiotherapy in stage IIIA-pN2 non-small-cell lung cancer |
title_sort | delineation of clinical target volume for postoperative radiotherapy in stage iiia-pn2 non-small-cell lung cancer |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4767117/ https://www.ncbi.nlm.nih.gov/pubmed/26929651 http://dx.doi.org/10.2147/OTT.S98765 |
work_keys_str_mv | AT jingxuquan delineationofclinicaltargetvolumeforpostoperativeradiotherapyinstageiiiapn2nonsmallcelllungcancer AT mengxue delineationofclinicaltargetvolumeforpostoperativeradiotherapyinstageiiiapn2nonsmallcelllungcancer AT sunxindong delineationofclinicaltargetvolumeforpostoperativeradiotherapyinstageiiiapn2nonsmallcelllungcancer AT yujinming delineationofclinicaltargetvolumeforpostoperativeradiotherapyinstageiiiapn2nonsmallcelllungcancer |