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Radical thoracic radiotherapy may provide favorable outcomes for stage IV non‐small cell lung cancer

BACKGROUND: This study investigates the outcome of synchronous stage IV non‐small cell lung cancer (NSCLC) patients who received radical thoracic radiotherapy (TRT). METHODS: We retrospectively reviewed the charts of stage IV NSCLC patients treated with TRT between January 2007 and December 2011. Ra...

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Autores principales: Wang, Jingbo, Ji, Zhe, Wang, Xiaozhen, Liang, Jun, Hui, Zhouguang, Lv, Jima, Zhou, Zongmei, Yin, Weibo, Wang, Luhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4773305/
https://www.ncbi.nlm.nih.gov/pubmed/27042220
http://dx.doi.org/10.1111/1759-7714.12305
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author Wang, Jingbo
Ji, Zhe
Wang, Xiaozhen
Liang, Jun
Hui, Zhouguang
Lv, Jima
Zhou, Zongmei
Yin, Weibo
Wang, Luhua
author_facet Wang, Jingbo
Ji, Zhe
Wang, Xiaozhen
Liang, Jun
Hui, Zhouguang
Lv, Jima
Zhou, Zongmei
Yin, Weibo
Wang, Luhua
author_sort Wang, Jingbo
collection PubMed
description BACKGROUND: This study investigates the outcome of synchronous stage IV non‐small cell lung cancer (NSCLC) patients who received radical thoracic radiotherapy (TRT). METHODS: We retrospectively reviewed the charts of stage IV NSCLC patients treated with TRT between January 2007 and December 2011. Radiotherapy was considered radical if it was the primary therapy with non‐symptom driven intent, or consolidation therapy after initial chemotherapy and the biologically equivalent dose ≥53 Gy halted disease progression. The patients' demographics, disease characteristics, and treatment parameters were uniformly collected. RESULTS: Eighty‐one patients were irradiated with radical intent, including 52% with more than five metastatic lesions. The minimum follow‐up was 31.5 months for survivors. The median overall survival (OS) was 20.8 months, with three and four‐year OS rates of 23% and 18%, respectively. The median progression‐free survival (PFS) was 8.2 months, with one and two‐year PFS rates of 23% and 9%, respectively. Partial response (PR) after TRT and administration of targeted therapy were predictive of longer OS. The factors associated with favorable PFS included earlier local tunor node stage, absence of concurrent chemotherapy, and post‐TRT PR. No correlation was found between the number of metastatic lesions and survival outcome. Incidences of grade ≥2 toxicities in the lung and esophagus were 9% and 26%, respectively. CONCLUSIONS: Radical TRT may result in advantageous outcomes for selected stage IV NSCLC patients, regardless of the number of metastatic foci. Patients who achieved post‐TRT PR attained the best outcomes.
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spelling pubmed-47733052016-04-01 Radical thoracic radiotherapy may provide favorable outcomes for stage IV non‐small cell lung cancer Wang, Jingbo Ji, Zhe Wang, Xiaozhen Liang, Jun Hui, Zhouguang Lv, Jima Zhou, Zongmei Yin, Weibo Wang, Luhua Thorac Cancer Original Articles BACKGROUND: This study investigates the outcome of synchronous stage IV non‐small cell lung cancer (NSCLC) patients who received radical thoracic radiotherapy (TRT). METHODS: We retrospectively reviewed the charts of stage IV NSCLC patients treated with TRT between January 2007 and December 2011. Radiotherapy was considered radical if it was the primary therapy with non‐symptom driven intent, or consolidation therapy after initial chemotherapy and the biologically equivalent dose ≥53 Gy halted disease progression. The patients' demographics, disease characteristics, and treatment parameters were uniformly collected. RESULTS: Eighty‐one patients were irradiated with radical intent, including 52% with more than five metastatic lesions. The minimum follow‐up was 31.5 months for survivors. The median overall survival (OS) was 20.8 months, with three and four‐year OS rates of 23% and 18%, respectively. The median progression‐free survival (PFS) was 8.2 months, with one and two‐year PFS rates of 23% and 9%, respectively. Partial response (PR) after TRT and administration of targeted therapy were predictive of longer OS. The factors associated with favorable PFS included earlier local tunor node stage, absence of concurrent chemotherapy, and post‐TRT PR. No correlation was found between the number of metastatic lesions and survival outcome. Incidences of grade ≥2 toxicities in the lung and esophagus were 9% and 26%, respectively. CONCLUSIONS: Radical TRT may result in advantageous outcomes for selected stage IV NSCLC patients, regardless of the number of metastatic foci. Patients who achieved post‐TRT PR attained the best outcomes. John Wiley and Sons Inc. 2015-09-13 2016-03 /pmc/articles/PMC4773305/ /pubmed/27042220 http://dx.doi.org/10.1111/1759-7714.12305 Text en © 2015 The Authors. Thoracic Cancer published by China Lung Oncology Group and Wiley Publishing Asia Pty Ltd. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Articles
Wang, Jingbo
Ji, Zhe
Wang, Xiaozhen
Liang, Jun
Hui, Zhouguang
Lv, Jima
Zhou, Zongmei
Yin, Weibo
Wang, Luhua
Radical thoracic radiotherapy may provide favorable outcomes for stage IV non‐small cell lung cancer
title Radical thoracic radiotherapy may provide favorable outcomes for stage IV non‐small cell lung cancer
title_full Radical thoracic radiotherapy may provide favorable outcomes for stage IV non‐small cell lung cancer
title_fullStr Radical thoracic radiotherapy may provide favorable outcomes for stage IV non‐small cell lung cancer
title_full_unstemmed Radical thoracic radiotherapy may provide favorable outcomes for stage IV non‐small cell lung cancer
title_short Radical thoracic radiotherapy may provide favorable outcomes for stage IV non‐small cell lung cancer
title_sort radical thoracic radiotherapy may provide favorable outcomes for stage iv non‐small cell lung cancer
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4773305/
https://www.ncbi.nlm.nih.gov/pubmed/27042220
http://dx.doi.org/10.1111/1759-7714.12305
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