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Prognostic Value of an Immunohistochemical Signature in Patients With Head and Neck Mucosal Melanoma

PURPOSE: We aimed to develop a prognostic immunohistochemistry (IHC) signature for patients with head and neck mucosal melanoma (MMHN). METHODS: In total, 190 patients with nonmetastatic MMHN with complete clinical and pathological data before treatment were included in our retrospective study. RESU...

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Autores principales: Xu, Qing-Qing, Li, Qing-Jie, Huang, Cheng-Long, Cai, Mu-Yan, Zhang, Mei-Fang, Yin, Shao-Han, Lu, Li-Xia, Chen, Lei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8358394/
https://www.ncbi.nlm.nih.gov/pubmed/34394109
http://dx.doi.org/10.3389/fimmu.2021.708293
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author Xu, Qing-Qing
Li, Qing-Jie
Huang, Cheng-Long
Cai, Mu-Yan
Zhang, Mei-Fang
Yin, Shao-Han
Lu, Li-Xia
Chen, Lei
author_facet Xu, Qing-Qing
Li, Qing-Jie
Huang, Cheng-Long
Cai, Mu-Yan
Zhang, Mei-Fang
Yin, Shao-Han
Lu, Li-Xia
Chen, Lei
author_sort Xu, Qing-Qing
collection PubMed
description PURPOSE: We aimed to develop a prognostic immunohistochemistry (IHC) signature for patients with head and neck mucosal melanoma (MMHN). METHODS: In total, 190 patients with nonmetastatic MMHN with complete clinical and pathological data before treatment were included in our retrospective study. RESULTS: We extracted five IHC markers associated with overall survival (OS) and then constructed a signature in the training set (n=116) with the least absolute shrinkage and selection operator (LASSO) regression model. The validation set (n=74) was further built to confirm the prognostic significance of this classifier. We then divided patients into high- and low-risk groups according to the IHC score. In the training set, the 5-year OS rate was 22.0% (95% confidence interval [CI]: 11.2%- 43.2%) for the high-risk group and 54.1% (95% CI: 41.8%-69.9%) for the low-risk group (P<0.001), and in the validation set, the 5-year OS rate was 38.1% (95% CI: 17.9%-81.1%) for the high-risk group and 43.1% (95% CI: 30.0%-61.9%) for the low-risk group (P=0.26). Multivariable analysis revealed that IHC score, T stage, and primary tumor site were independent variables for predicting OS (all P<0.05). We developed a nomogram incorporating clinicopathological risk factors (primary site and T stage) and the IHC score to predict 3-, 5-, and 10-year OS. CONCLUSIONS: A nomogram was generated and confirmed to be of clinical value. Our IHC classifier integrating five IHC markers could help clinicians make decisions and determine optimal treatments for patients with MMHN.
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spelling pubmed-83583942021-08-13 Prognostic Value of an Immunohistochemical Signature in Patients With Head and Neck Mucosal Melanoma Xu, Qing-Qing Li, Qing-Jie Huang, Cheng-Long Cai, Mu-Yan Zhang, Mei-Fang Yin, Shao-Han Lu, Li-Xia Chen, Lei Front Immunol Immunology PURPOSE: We aimed to develop a prognostic immunohistochemistry (IHC) signature for patients with head and neck mucosal melanoma (MMHN). METHODS: In total, 190 patients with nonmetastatic MMHN with complete clinical and pathological data before treatment were included in our retrospective study. RESULTS: We extracted five IHC markers associated with overall survival (OS) and then constructed a signature in the training set (n=116) with the least absolute shrinkage and selection operator (LASSO) regression model. The validation set (n=74) was further built to confirm the prognostic significance of this classifier. We then divided patients into high- and low-risk groups according to the IHC score. In the training set, the 5-year OS rate was 22.0% (95% confidence interval [CI]: 11.2%- 43.2%) for the high-risk group and 54.1% (95% CI: 41.8%-69.9%) for the low-risk group (P<0.001), and in the validation set, the 5-year OS rate was 38.1% (95% CI: 17.9%-81.1%) for the high-risk group and 43.1% (95% CI: 30.0%-61.9%) for the low-risk group (P=0.26). Multivariable analysis revealed that IHC score, T stage, and primary tumor site were independent variables for predicting OS (all P<0.05). We developed a nomogram incorporating clinicopathological risk factors (primary site and T stage) and the IHC score to predict 3-, 5-, and 10-year OS. CONCLUSIONS: A nomogram was generated and confirmed to be of clinical value. Our IHC classifier integrating five IHC markers could help clinicians make decisions and determine optimal treatments for patients with MMHN. Frontiers Media S.A. 2021-07-29 /pmc/articles/PMC8358394/ /pubmed/34394109 http://dx.doi.org/10.3389/fimmu.2021.708293 Text en Copyright © 2021 Xu, Li, Huang, Cai, Zhang, Yin, Lu and Chen https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Xu, Qing-Qing
Li, Qing-Jie
Huang, Cheng-Long
Cai, Mu-Yan
Zhang, Mei-Fang
Yin, Shao-Han
Lu, Li-Xia
Chen, Lei
Prognostic Value of an Immunohistochemical Signature in Patients With Head and Neck Mucosal Melanoma
title Prognostic Value of an Immunohistochemical Signature in Patients With Head and Neck Mucosal Melanoma
title_full Prognostic Value of an Immunohistochemical Signature in Patients With Head and Neck Mucosal Melanoma
title_fullStr Prognostic Value of an Immunohistochemical Signature in Patients With Head and Neck Mucosal Melanoma
title_full_unstemmed Prognostic Value of an Immunohistochemical Signature in Patients With Head and Neck Mucosal Melanoma
title_short Prognostic Value of an Immunohistochemical Signature in Patients With Head and Neck Mucosal Melanoma
title_sort prognostic value of an immunohistochemical signature in patients with head and neck mucosal melanoma
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8358394/
https://www.ncbi.nlm.nih.gov/pubmed/34394109
http://dx.doi.org/10.3389/fimmu.2021.708293
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