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Patterns and prognostic predictive value of perineural invasion in esophageal squamous cell carcinoma

BACKGROUND: The pathological phenotype of perineural invasion (PNI) in squamous cell carcinoma (ESCC) is prevalent but highly heterogeneous. METHODS: Postoperative specimens from all patients with ESCC at Shaanxi Provincial People’s Hospital were evaluated for PNI using haematoxylin and eosin (H&...

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Autores principales: Ma, Yu, Chen, Jie, Yao, Xi, Li, Zhenzhen, Li, Wensheng, Wang, Hongtao, Zhu, Jianfei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9733208/
https://www.ncbi.nlm.nih.gov/pubmed/36482313
http://dx.doi.org/10.1186/s12885-022-10386-w
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author Ma, Yu
Chen, Jie
Yao, Xi
Li, Zhenzhen
Li, Wensheng
Wang, Hongtao
Zhu, Jianfei
author_facet Ma, Yu
Chen, Jie
Yao, Xi
Li, Zhenzhen
Li, Wensheng
Wang, Hongtao
Zhu, Jianfei
author_sort Ma, Yu
collection PubMed
description BACKGROUND: The pathological phenotype of perineural invasion (PNI) in squamous cell carcinoma (ESCC) is prevalent but highly heterogeneous. METHODS: Postoperative specimens from all patients with ESCC at Shaanxi Provincial People’s Hospital were evaluated for PNI using haematoxylin and eosin (H&E) staining and S100 immunohistochemistry (IHC). We determined the correlation between PNI status and clinical outcomes. RESULTS: Among 349 ESCC cases, PNI was identified in 127 patients (36.3%), and four subtypes of PNI were identified in our study. Correlation analysis confirmed that PNI was related to tumour invasion depth (pT stage) and lymph node status (pN stage) (P < 0.05). Multivariate analysis showed that PNI (P = 0.001) was an independent factor affecting disease-free survival (DFS) in ESCC, and a similar result was found for overall survival (OS) (P = 0.017). Further analysis revealed that PNI status was a prognostic factor of DFS (P < 0.001) and OS (P = 0.003) exclusively in pN-negative patients. We also found that patients with the PNI-a subtype had better DFS (P = 0.002) and OS (P = 0.002) than patients with the other three subtypes (PNI-b, c, d). CONCLUSION: The pathological phenotypes of PNI are diverse, and the identification of PNI subtypes has important clinical guiding value.
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spelling pubmed-97332082022-12-10 Patterns and prognostic predictive value of perineural invasion in esophageal squamous cell carcinoma Ma, Yu Chen, Jie Yao, Xi Li, Zhenzhen Li, Wensheng Wang, Hongtao Zhu, Jianfei BMC Cancer Research BACKGROUND: The pathological phenotype of perineural invasion (PNI) in squamous cell carcinoma (ESCC) is prevalent but highly heterogeneous. METHODS: Postoperative specimens from all patients with ESCC at Shaanxi Provincial People’s Hospital were evaluated for PNI using haematoxylin and eosin (H&E) staining and S100 immunohistochemistry (IHC). We determined the correlation between PNI status and clinical outcomes. RESULTS: Among 349 ESCC cases, PNI was identified in 127 patients (36.3%), and four subtypes of PNI were identified in our study. Correlation analysis confirmed that PNI was related to tumour invasion depth (pT stage) and lymph node status (pN stage) (P < 0.05). Multivariate analysis showed that PNI (P = 0.001) was an independent factor affecting disease-free survival (DFS) in ESCC, and a similar result was found for overall survival (OS) (P = 0.017). Further analysis revealed that PNI status was a prognostic factor of DFS (P < 0.001) and OS (P = 0.003) exclusively in pN-negative patients. We also found that patients with the PNI-a subtype had better DFS (P = 0.002) and OS (P = 0.002) than patients with the other three subtypes (PNI-b, c, d). CONCLUSION: The pathological phenotypes of PNI are diverse, and the identification of PNI subtypes has important clinical guiding value. BioMed Central 2022-12-08 /pmc/articles/PMC9733208/ /pubmed/36482313 http://dx.doi.org/10.1186/s12885-022-10386-w Text en © The Author(s) 2022 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
Ma, Yu
Chen, Jie
Yao, Xi
Li, Zhenzhen
Li, Wensheng
Wang, Hongtao
Zhu, Jianfei
Patterns and prognostic predictive value of perineural invasion in esophageal squamous cell carcinoma
title Patterns and prognostic predictive value of perineural invasion in esophageal squamous cell carcinoma
title_full Patterns and prognostic predictive value of perineural invasion in esophageal squamous cell carcinoma
title_fullStr Patterns and prognostic predictive value of perineural invasion in esophageal squamous cell carcinoma
title_full_unstemmed Patterns and prognostic predictive value of perineural invasion in esophageal squamous cell carcinoma
title_short Patterns and prognostic predictive value of perineural invasion in esophageal squamous cell carcinoma
title_sort patterns and prognostic predictive value of perineural invasion in esophageal squamous cell carcinoma
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9733208/
https://www.ncbi.nlm.nih.gov/pubmed/36482313
http://dx.doi.org/10.1186/s12885-022-10386-w
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