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Re-irradiation for local primary-recurrence esophageal squamous cell carcinoma treated with IMRT/VMAT

PURPOSE: Local primary-recurrence of esophageal squamous cell carcinoma (ESCC) after definitive treatment has the potential for increasing overall survival with re-irradiation (Re-RT), especially with advanced technique. This study aimed to evaluate the efficacy and toxicities of Re-RT using intensi...

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Autores principales: Xiang, Geng, Xu, Chunsheng, Chai, Guangjin, Lyu, Bo, Li, Zhaohui, Wang, Bin, Shi, Mei, Zhao, Lina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10334638/
https://www.ncbi.nlm.nih.gov/pubmed/37430276
http://dx.doi.org/10.1186/s13014-023-02265-w
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author Xiang, Geng
Xu, Chunsheng
Chai, Guangjin
Lyu, Bo
Li, Zhaohui
Wang, Bin
Shi, Mei
Zhao, Lina
author_facet Xiang, Geng
Xu, Chunsheng
Chai, Guangjin
Lyu, Bo
Li, Zhaohui
Wang, Bin
Shi, Mei
Zhao, Lina
author_sort Xiang, Geng
collection PubMed
description PURPOSE: Local primary-recurrence of esophageal squamous cell carcinoma (ESCC) after definitive treatment has the potential for increasing overall survival with re-irradiation (Re-RT), especially with advanced technique. This study aimed to evaluate the efficacy and toxicities of Re-RT using intensity-modulated radiotherapy (IMRT)/volumetric modulated arc therapy (VMAT) for local primary-recurrence of ESCC. MATERIALS AND METHODS: A total of 130 ESCC patients with local primary-recurrence from Xijing hospital between 2008 and 2021 were enrolled and 30 patients underwent IMRT/VMAT based salvage Re-RT. Cox regression analysis was used to analyze the prognostic factors for overall survival (OS) and after recurrence survival (ARS). The toxicities of 30 patients receiving Re-RT were also assessed. RESULTS: The median OS and ARS of the 130 recurrent patients were 21 months (1−164 months) and 6 months (1−142 months). The 1-, 2-, and 3-year OS rates were 81.5%, 39.2%, and 23.8%, respectively. Besides, the 1-, 2-, and 3-year ARS rates were 30.0%, 10%, and 6.2%. Multivariate analysis showed that Re-RT ± chemotherapy (p = 0.043) and chemotherapy alone (p < 0.001) and esophageal stents (p = 0.004) were independent prognostic factors for OS. The median OS of 30 patients treated with Re-RT were significantly better than that of 29 patients treated with chemotherapy (34.5 months vs. 22 months, p = 0.030). Among 30 ESCC patients treated with Re-RT, the median OS and ARS were 34.5 months (range 12–163 months) and 6 months (range 1−132 months), respectively. The recurrence-free interval (RFI) (> 12 months) and initial radiation dose (> 60 Gy) were significantly associated with improved OS. Radiation esophagitis (Grade 1–2) occurred in 16 patients and myelosuppression (Grade1−2) occurred in 10 patients. Grade 3 toxicities (radiation esophagitis and myelosuppression) were only 13.3%. There were no grade 4 toxicities. CONCLUSION: Our results demonstrated that IMRT/VMAT-based Re-RT was an effective therapeutic option for ESCC patients with local primary-recurrence compared with chemotherapy alone or without any treatment. Re-RT had improved OS but unfavorable ARS. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13014-023-02265-w.
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spelling pubmed-103346382023-07-12 Re-irradiation for local primary-recurrence esophageal squamous cell carcinoma treated with IMRT/VMAT Xiang, Geng Xu, Chunsheng Chai, Guangjin Lyu, Bo Li, Zhaohui Wang, Bin Shi, Mei Zhao, Lina Radiat Oncol Research PURPOSE: Local primary-recurrence of esophageal squamous cell carcinoma (ESCC) after definitive treatment has the potential for increasing overall survival with re-irradiation (Re-RT), especially with advanced technique. This study aimed to evaluate the efficacy and toxicities of Re-RT using intensity-modulated radiotherapy (IMRT)/volumetric modulated arc therapy (VMAT) for local primary-recurrence of ESCC. MATERIALS AND METHODS: A total of 130 ESCC patients with local primary-recurrence from Xijing hospital between 2008 and 2021 were enrolled and 30 patients underwent IMRT/VMAT based salvage Re-RT. Cox regression analysis was used to analyze the prognostic factors for overall survival (OS) and after recurrence survival (ARS). The toxicities of 30 patients receiving Re-RT were also assessed. RESULTS: The median OS and ARS of the 130 recurrent patients were 21 months (1−164 months) and 6 months (1−142 months). The 1-, 2-, and 3-year OS rates were 81.5%, 39.2%, and 23.8%, respectively. Besides, the 1-, 2-, and 3-year ARS rates were 30.0%, 10%, and 6.2%. Multivariate analysis showed that Re-RT ± chemotherapy (p = 0.043) and chemotherapy alone (p < 0.001) and esophageal stents (p = 0.004) were independent prognostic factors for OS. The median OS of 30 patients treated with Re-RT were significantly better than that of 29 patients treated with chemotherapy (34.5 months vs. 22 months, p = 0.030). Among 30 ESCC patients treated with Re-RT, the median OS and ARS were 34.5 months (range 12–163 months) and 6 months (range 1−132 months), respectively. The recurrence-free interval (RFI) (> 12 months) and initial radiation dose (> 60 Gy) were significantly associated with improved OS. Radiation esophagitis (Grade 1–2) occurred in 16 patients and myelosuppression (Grade1−2) occurred in 10 patients. Grade 3 toxicities (radiation esophagitis and myelosuppression) were only 13.3%. There were no grade 4 toxicities. CONCLUSION: Our results demonstrated that IMRT/VMAT-based Re-RT was an effective therapeutic option for ESCC patients with local primary-recurrence compared with chemotherapy alone or without any treatment. Re-RT had improved OS but unfavorable ARS. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13014-023-02265-w. BioMed Central 2023-07-10 /pmc/articles/PMC10334638/ /pubmed/37430276 http://dx.doi.org/10.1186/s13014-023-02265-w Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Xiang, Geng
Xu, Chunsheng
Chai, Guangjin
Lyu, Bo
Li, Zhaohui
Wang, Bin
Shi, Mei
Zhao, Lina
Re-irradiation for local primary-recurrence esophageal squamous cell carcinoma treated with IMRT/VMAT
title Re-irradiation for local primary-recurrence esophageal squamous cell carcinoma treated with IMRT/VMAT
title_full Re-irradiation for local primary-recurrence esophageal squamous cell carcinoma treated with IMRT/VMAT
title_fullStr Re-irradiation for local primary-recurrence esophageal squamous cell carcinoma treated with IMRT/VMAT
title_full_unstemmed Re-irradiation for local primary-recurrence esophageal squamous cell carcinoma treated with IMRT/VMAT
title_short Re-irradiation for local primary-recurrence esophageal squamous cell carcinoma treated with IMRT/VMAT
title_sort re-irradiation for local primary-recurrence esophageal squamous cell carcinoma treated with imrt/vmat
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10334638/
https://www.ncbi.nlm.nih.gov/pubmed/37430276
http://dx.doi.org/10.1186/s13014-023-02265-w
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