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The impact of intratumoral metabolic heterogeneity on postoperative recurrence and survival in resectable esophageal squamous cell carcinoma

OBJECTIVE: To evaluate the impact of intratumoral metabolic heterogeneity measured by 18F-FDG PET imaging on postoperative recurrence and survival for patients with esophageal squamous cell carcinoma (ESCC). RESULTS: AUC-CSH, metabolic tumor volume and pN-stage were significant prognostic factors fo...

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Autores principales: Dong, Xinzhe, Sun, Xiaorong, Zhao, Xianguang, Zhu, Wanqi, Sun, Lu, Huang, Yong, Li, Wenwu, Wan, Honglin, Xing, Ligang, Yu, Jinming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5362458/
https://www.ncbi.nlm.nih.gov/pubmed/28122340
http://dx.doi.org/10.18632/oncotarget.14743
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author Dong, Xinzhe
Sun, Xiaorong
Zhao, Xianguang
Zhu, Wanqi
Sun, Lu
Huang, Yong
Li, Wenwu
Wan, Honglin
Xing, Ligang
Yu, Jinming
author_facet Dong, Xinzhe
Sun, Xiaorong
Zhao, Xianguang
Zhu, Wanqi
Sun, Lu
Huang, Yong
Li, Wenwu
Wan, Honglin
Xing, Ligang
Yu, Jinming
author_sort Dong, Xinzhe
collection PubMed
description OBJECTIVE: To evaluate the impact of intratumoral metabolic heterogeneity measured by 18F-FDG PET imaging on postoperative recurrence and survival for patients with esophageal squamous cell carcinoma (ESCC). RESULTS: AUC-CSH, metabolic tumor volume and pN-stage were significant prognostic factors for RFS. Additionally, tumor recurrence of the low AUC-CSH group (≤ 0.478) was 3 times higher than high group (P = 0.015). The median OS of patients with advanced AJCC stage or low AUC-CSH was also significantly shorter than that of patients with stage I & II or high AUC-CSH (P = 0.021, 0.009). Multivariate analysis identified the AUC-CSH to be the only significant risk factor for postoperative recurrence and overall survival in whole-group and stage III patients. MATERIALS AND METHODS: 116 ESCC patients who underwent staging 18F-FDG PET-CT scan and surgical resection were reviewed. The metabolic parameters were assessed as follows: maximum standardized uptake value (SUV(max)), metabolic tumor volume, and the area under the curve of the cumulative SUV-volume histogram (AUC-CSH), which is known to reflect the intratumoral metabolic heterogeneity. Regression analyses were used to identify clinicopathological and imaging variables associated with relapse-free survival (RFS) and overall survival (OS). CONCLUSIONS: Intratumoral metabolic heterogeneity characterized by AUC-CSH can predict postoperative recurrence and survival in patients with resectable ESCC.
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spelling pubmed-53624582017-04-24 The impact of intratumoral metabolic heterogeneity on postoperative recurrence and survival in resectable esophageal squamous cell carcinoma Dong, Xinzhe Sun, Xiaorong Zhao, Xianguang Zhu, Wanqi Sun, Lu Huang, Yong Li, Wenwu Wan, Honglin Xing, Ligang Yu, Jinming Oncotarget Research Paper OBJECTIVE: To evaluate the impact of intratumoral metabolic heterogeneity measured by 18F-FDG PET imaging on postoperative recurrence and survival for patients with esophageal squamous cell carcinoma (ESCC). RESULTS: AUC-CSH, metabolic tumor volume and pN-stage were significant prognostic factors for RFS. Additionally, tumor recurrence of the low AUC-CSH group (≤ 0.478) was 3 times higher than high group (P = 0.015). The median OS of patients with advanced AJCC stage or low AUC-CSH was also significantly shorter than that of patients with stage I & II or high AUC-CSH (P = 0.021, 0.009). Multivariate analysis identified the AUC-CSH to be the only significant risk factor for postoperative recurrence and overall survival in whole-group and stage III patients. MATERIALS AND METHODS: 116 ESCC patients who underwent staging 18F-FDG PET-CT scan and surgical resection were reviewed. The metabolic parameters were assessed as follows: maximum standardized uptake value (SUV(max)), metabolic tumor volume, and the area under the curve of the cumulative SUV-volume histogram (AUC-CSH), which is known to reflect the intratumoral metabolic heterogeneity. Regression analyses were used to identify clinicopathological and imaging variables associated with relapse-free survival (RFS) and overall survival (OS). CONCLUSIONS: Intratumoral metabolic heterogeneity characterized by AUC-CSH can predict postoperative recurrence and survival in patients with resectable ESCC. Impact Journals LLC 2017-01-19 /pmc/articles/PMC5362458/ /pubmed/28122340 http://dx.doi.org/10.18632/oncotarget.14743 Text en Copyright: © 2017 Dong et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Dong, Xinzhe
Sun, Xiaorong
Zhao, Xianguang
Zhu, Wanqi
Sun, Lu
Huang, Yong
Li, Wenwu
Wan, Honglin
Xing, Ligang
Yu, Jinming
The impact of intratumoral metabolic heterogeneity on postoperative recurrence and survival in resectable esophageal squamous cell carcinoma
title The impact of intratumoral metabolic heterogeneity on postoperative recurrence and survival in resectable esophageal squamous cell carcinoma
title_full The impact of intratumoral metabolic heterogeneity on postoperative recurrence and survival in resectable esophageal squamous cell carcinoma
title_fullStr The impact of intratumoral metabolic heterogeneity on postoperative recurrence and survival in resectable esophageal squamous cell carcinoma
title_full_unstemmed The impact of intratumoral metabolic heterogeneity on postoperative recurrence and survival in resectable esophageal squamous cell carcinoma
title_short The impact of intratumoral metabolic heterogeneity on postoperative recurrence and survival in resectable esophageal squamous cell carcinoma
title_sort impact of intratumoral metabolic heterogeneity on postoperative recurrence and survival in resectable esophageal squamous cell carcinoma
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5362458/
https://www.ncbi.nlm.nih.gov/pubmed/28122340
http://dx.doi.org/10.18632/oncotarget.14743
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