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Optimal radiotherapy dose in cervical esophageal squamous cell carcinoma patients treated with definitive concurrent chemoradiotherapy: A population based study

BACKGROUND: The optimal radiotherapy dose for locally advanced cervical esophageal squamous cell carcinoma (C‐ESqCC) treated with definitive concurrent chemoradiotherapy (dCCRT) is unclear. Here, we aimed to compare the survival of those treated with high dose versus standard dose via a population b...

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Autores principales: Li, Chia‐Chin, Chen, Chih‐Yi, Chou, Ying‐Hsiang, Huang, Chih‐Jen, Ku, Hsiu‐Ying, Chien, Chun‐Ru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons Australia, Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8287021/
https://www.ncbi.nlm.nih.gov/pubmed/34028200
http://dx.doi.org/10.1111/1759-7714.14009
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author Li, Chia‐Chin
Chen, Chih‐Yi
Chou, Ying‐Hsiang
Huang, Chih‐Jen
Ku, Hsiu‐Ying
Chien, Chun‐Ru
author_facet Li, Chia‐Chin
Chen, Chih‐Yi
Chou, Ying‐Hsiang
Huang, Chih‐Jen
Ku, Hsiu‐Ying
Chien, Chun‐Ru
author_sort Li, Chia‐Chin
collection PubMed
description BACKGROUND: The optimal radiotherapy dose for locally advanced cervical esophageal squamous cell carcinoma (C‐ESqCC) treated with definitive concurrent chemoradiotherapy (dCCRT) is unclear. Here, we aimed to compare the survival of those treated with high dose versus standard dose via a population based approach. METHODS: Eligible C‐ESqCC patients diagnosed between 2011 and 2017 were identified via the Taiwan Cancer Registry. We used propensity score (PS) weighting to balance observable potential confounders between groups. The hazard ratio (HR) of death and incidence of esophageal cancer mortality (IECM) were compared between high (60–70 Gy) and standard dose (50–50.4 Gy). We also evaluated the outcome in supplementary analyses via alternative approaches. RESULTS: Our primary analysis consisted of 141 patients in whom covariates were well balanced after PS weighting. The HR of death when high dose was compared with standard dose was 0.65 (95% confidence interval [CI]: 0.4–1.03, p = 0.07). The HR of IECM was 0.74 (p = 0.45). The HR of OS remained similarly insignificant in supplementary analyses. CONCLUSIONS: We observed a trend in favor of high radiotherapy dose versus standard dose for C‐ESqCC treated with dCCRT in this population‐based nonrandomized study. Further studies are needed to confirm the findings of the study.
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spelling pubmed-82870212021-07-21 Optimal radiotherapy dose in cervical esophageal squamous cell carcinoma patients treated with definitive concurrent chemoradiotherapy: A population based study Li, Chia‐Chin Chen, Chih‐Yi Chou, Ying‐Hsiang Huang, Chih‐Jen Ku, Hsiu‐Ying Chien, Chun‐Ru Thorac Cancer Original Articles BACKGROUND: The optimal radiotherapy dose for locally advanced cervical esophageal squamous cell carcinoma (C‐ESqCC) treated with definitive concurrent chemoradiotherapy (dCCRT) is unclear. Here, we aimed to compare the survival of those treated with high dose versus standard dose via a population based approach. METHODS: Eligible C‐ESqCC patients diagnosed between 2011 and 2017 were identified via the Taiwan Cancer Registry. We used propensity score (PS) weighting to balance observable potential confounders between groups. The hazard ratio (HR) of death and incidence of esophageal cancer mortality (IECM) were compared between high (60–70 Gy) and standard dose (50–50.4 Gy). We also evaluated the outcome in supplementary analyses via alternative approaches. RESULTS: Our primary analysis consisted of 141 patients in whom covariates were well balanced after PS weighting. The HR of death when high dose was compared with standard dose was 0.65 (95% confidence interval [CI]: 0.4–1.03, p = 0.07). The HR of IECM was 0.74 (p = 0.45). The HR of OS remained similarly insignificant in supplementary analyses. CONCLUSIONS: We observed a trend in favor of high radiotherapy dose versus standard dose for C‐ESqCC treated with dCCRT in this population‐based nonrandomized study. Further studies are needed to confirm the findings of the study. John Wiley & Sons Australia, Ltd 2021-05-24 2021-07 /pmc/articles/PMC8287021/ /pubmed/34028200 http://dx.doi.org/10.1111/1759-7714.14009 Text en © 2021 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Li, Chia‐Chin
Chen, Chih‐Yi
Chou, Ying‐Hsiang
Huang, Chih‐Jen
Ku, Hsiu‐Ying
Chien, Chun‐Ru
Optimal radiotherapy dose in cervical esophageal squamous cell carcinoma patients treated with definitive concurrent chemoradiotherapy: A population based study
title Optimal radiotherapy dose in cervical esophageal squamous cell carcinoma patients treated with definitive concurrent chemoradiotherapy: A population based study
title_full Optimal radiotherapy dose in cervical esophageal squamous cell carcinoma patients treated with definitive concurrent chemoradiotherapy: A population based study
title_fullStr Optimal radiotherapy dose in cervical esophageal squamous cell carcinoma patients treated with definitive concurrent chemoradiotherapy: A population based study
title_full_unstemmed Optimal radiotherapy dose in cervical esophageal squamous cell carcinoma patients treated with definitive concurrent chemoradiotherapy: A population based study
title_short Optimal radiotherapy dose in cervical esophageal squamous cell carcinoma patients treated with definitive concurrent chemoradiotherapy: A population based study
title_sort optimal radiotherapy dose in cervical esophageal squamous cell carcinoma patients treated with definitive concurrent chemoradiotherapy: a population based study
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8287021/
https://www.ncbi.nlm.nih.gov/pubmed/34028200
http://dx.doi.org/10.1111/1759-7714.14009
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