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Definitive radiotherapy dose escalation with chemotherapy for treating non-metastatic oesophageal cancer

The locoregional failure rate remains high after concurrent chemoradiotherapy with standard-dose radiotherapy (RT, 50–50.4 Gy) for oesophageal cancer (EC). This retrospective study evaluated whether RT dose escalation was effective among 115 consecutive patients with non-metastatic EC (July 2003 to...

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Autores principales: Fan, Chao-Yueh, Su, Yu-Fu, Huang, Wen-Yen, Chao, Hsing-Lung, Lin, Kuen-Tze, Lin, Chun-Shu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6110762/
https://www.ncbi.nlm.nih.gov/pubmed/30150679
http://dx.doi.org/10.1038/s41598-018-31302-y
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author Fan, Chao-Yueh
Su, Yu-Fu
Huang, Wen-Yen
Chao, Hsing-Lung
Lin, Kuen-Tze
Lin, Chun-Shu
author_facet Fan, Chao-Yueh
Su, Yu-Fu
Huang, Wen-Yen
Chao, Hsing-Lung
Lin, Kuen-Tze
Lin, Chun-Shu
author_sort Fan, Chao-Yueh
collection PubMed
description The locoregional failure rate remains high after concurrent chemoradiotherapy with standard-dose radiotherapy (RT, 50–50.4 Gy) for oesophageal cancer (EC). This retrospective study evaluated whether RT dose escalation was effective among 115 consecutive patients with non-metastatic EC (July 2003 to November 2016). Forty-four patients received an RT dose of <66 Gy and 71 patients received ≥66 Gy, with most patients receiving concurrent cisplatin plus fluorouracil. The median follow-up was 12 months for all patients (52 months for 18 surviving patients). The ≥66 Gy group had significantly higher 3-year rates of overall survival (17.9% vs. 32.1%, p = 0.026) and local progression-free survival (46.1% vs. 72.1%, p = 0.005), but not disease progression-free survival (11.4% vs. 21.9%, p = 0.059) and distant metastasis-free survival (49% vs. 52.6%, p = 0.852). The ≥66 Gy group also had significantly better 5-year overall survival compared with 41.4–65.9 Gy. The only significant difference in treatment-related toxicities involved acute dermatitis (7% vs. 28%, p = 0.009). Inferior overall survival was associated with poor performance status, clinical N2–3 stage and not receiving maintenance chemotherapy. In conclusion, patients with inoperable EC experienced better survival outcomes and acceptable toxicities if they received higher dose RT (≥66 Gy) rather than lower dose RT (<66 Gy).
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spelling pubmed-61107622018-08-30 Definitive radiotherapy dose escalation with chemotherapy for treating non-metastatic oesophageal cancer Fan, Chao-Yueh Su, Yu-Fu Huang, Wen-Yen Chao, Hsing-Lung Lin, Kuen-Tze Lin, Chun-Shu Sci Rep Article The locoregional failure rate remains high after concurrent chemoradiotherapy with standard-dose radiotherapy (RT, 50–50.4 Gy) for oesophageal cancer (EC). This retrospective study evaluated whether RT dose escalation was effective among 115 consecutive patients with non-metastatic EC (July 2003 to November 2016). Forty-four patients received an RT dose of <66 Gy and 71 patients received ≥66 Gy, with most patients receiving concurrent cisplatin plus fluorouracil. The median follow-up was 12 months for all patients (52 months for 18 surviving patients). The ≥66 Gy group had significantly higher 3-year rates of overall survival (17.9% vs. 32.1%, p = 0.026) and local progression-free survival (46.1% vs. 72.1%, p = 0.005), but not disease progression-free survival (11.4% vs. 21.9%, p = 0.059) and distant metastasis-free survival (49% vs. 52.6%, p = 0.852). The ≥66 Gy group also had significantly better 5-year overall survival compared with 41.4–65.9 Gy. The only significant difference in treatment-related toxicities involved acute dermatitis (7% vs. 28%, p = 0.009). Inferior overall survival was associated with poor performance status, clinical N2–3 stage and not receiving maintenance chemotherapy. In conclusion, patients with inoperable EC experienced better survival outcomes and acceptable toxicities if they received higher dose RT (≥66 Gy) rather than lower dose RT (<66 Gy). Nature Publishing Group UK 2018-08-27 /pmc/articles/PMC6110762/ /pubmed/30150679 http://dx.doi.org/10.1038/s41598-018-31302-y Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Fan, Chao-Yueh
Su, Yu-Fu
Huang, Wen-Yen
Chao, Hsing-Lung
Lin, Kuen-Tze
Lin, Chun-Shu
Definitive radiotherapy dose escalation with chemotherapy for treating non-metastatic oesophageal cancer
title Definitive radiotherapy dose escalation with chemotherapy for treating non-metastatic oesophageal cancer
title_full Definitive radiotherapy dose escalation with chemotherapy for treating non-metastatic oesophageal cancer
title_fullStr Definitive radiotherapy dose escalation with chemotherapy for treating non-metastatic oesophageal cancer
title_full_unstemmed Definitive radiotherapy dose escalation with chemotherapy for treating non-metastatic oesophageal cancer
title_short Definitive radiotherapy dose escalation with chemotherapy for treating non-metastatic oesophageal cancer
title_sort definitive radiotherapy dose escalation with chemotherapy for treating non-metastatic oesophageal cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6110762/
https://www.ncbi.nlm.nih.gov/pubmed/30150679
http://dx.doi.org/10.1038/s41598-018-31302-y
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