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Oral mucositis: the hidden side of cancer therapy

Inflammation response of epithelial mucosa to chemo- radiotherapy cytotoxic effects leads to mucositis, a painful side effect of antineoplastic treatments. About 40% of the patients treated with chemotherapy develop mucositis; this percentage rises to about 90% for head and neck cancer patients (HNC...

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Autores principales: Pulito, Claudio, Cristaudo, Antonio, Porta, Caterina La, Zapperi, Stefano, Blandino, Giovanni, Morrone, Aldo, Strano, Sabrina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7542970/
https://www.ncbi.nlm.nih.gov/pubmed/33028357
http://dx.doi.org/10.1186/s13046-020-01715-7
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author Pulito, Claudio
Cristaudo, Antonio
Porta, Caterina La
Zapperi, Stefano
Blandino, Giovanni
Morrone, Aldo
Strano, Sabrina
author_facet Pulito, Claudio
Cristaudo, Antonio
Porta, Caterina La
Zapperi, Stefano
Blandino, Giovanni
Morrone, Aldo
Strano, Sabrina
author_sort Pulito, Claudio
collection PubMed
description Inflammation response of epithelial mucosa to chemo- radiotherapy cytotoxic effects leads to mucositis, a painful side effect of antineoplastic treatments. About 40% of the patients treated with chemotherapy develop mucositis; this percentage rises to about 90% for head and neck cancer patients (HNC) treated with both chemo- and radiotherapy. 19% of the latter will be hospitalized and will experience a delay in antineoplastic treatment for high-grade mucositis management, resulting in a reduction of the quality of life, a worse prognosis and an increase in patient management costs. Currently, several interventions and prevention guidelines are available, but their effectiveness is uncertain. This review comprehensively describes mucositis, debating the impact of standard chemo-radiotherapy and targeted therapy on mucositis development and pointing out the limits and the benefits of current mucositis treatment strategies and assessment guidelines. Moreover, the review critically examines the feasibility of the existing biomarkers to predict patient risk of developing oral mucositis and their role in early diagnosis. Despite the expression levels of some proteins involved in the inflammation response, such as TNF-α or IL-1β, partially correlate with mucositis process, their presence does not exclude others mucositis-independent inflammation events. This strongly suggests the need to discover biomarkers that specifically feature mucositis process development. Non-coding RNAs might hold this potential.
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spelling pubmed-75429702020-10-13 Oral mucositis: the hidden side of cancer therapy Pulito, Claudio Cristaudo, Antonio Porta, Caterina La Zapperi, Stefano Blandino, Giovanni Morrone, Aldo Strano, Sabrina J Exp Clin Cancer Res Review Inflammation response of epithelial mucosa to chemo- radiotherapy cytotoxic effects leads to mucositis, a painful side effect of antineoplastic treatments. About 40% of the patients treated with chemotherapy develop mucositis; this percentage rises to about 90% for head and neck cancer patients (HNC) treated with both chemo- and radiotherapy. 19% of the latter will be hospitalized and will experience a delay in antineoplastic treatment for high-grade mucositis management, resulting in a reduction of the quality of life, a worse prognosis and an increase in patient management costs. Currently, several interventions and prevention guidelines are available, but their effectiveness is uncertain. This review comprehensively describes mucositis, debating the impact of standard chemo-radiotherapy and targeted therapy on mucositis development and pointing out the limits and the benefits of current mucositis treatment strategies and assessment guidelines. Moreover, the review critically examines the feasibility of the existing biomarkers to predict patient risk of developing oral mucositis and their role in early diagnosis. Despite the expression levels of some proteins involved in the inflammation response, such as TNF-α or IL-1β, partially correlate with mucositis process, their presence does not exclude others mucositis-independent inflammation events. This strongly suggests the need to discover biomarkers that specifically feature mucositis process development. Non-coding RNAs might hold this potential. BioMed Central 2020-10-07 /pmc/articles/PMC7542970/ /pubmed/33028357 http://dx.doi.org/10.1186/s13046-020-01715-7 Text en © The Author(s) 2020 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/. The Creative Commons Public Domain Dedication waiver (http://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 Review
Pulito, Claudio
Cristaudo, Antonio
Porta, Caterina La
Zapperi, Stefano
Blandino, Giovanni
Morrone, Aldo
Strano, Sabrina
Oral mucositis: the hidden side of cancer therapy
title Oral mucositis: the hidden side of cancer therapy
title_full Oral mucositis: the hidden side of cancer therapy
title_fullStr Oral mucositis: the hidden side of cancer therapy
title_full_unstemmed Oral mucositis: the hidden side of cancer therapy
title_short Oral mucositis: the hidden side of cancer therapy
title_sort oral mucositis: the hidden side of cancer therapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7542970/
https://www.ncbi.nlm.nih.gov/pubmed/33028357
http://dx.doi.org/10.1186/s13046-020-01715-7
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