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T cell abundance in blood predicts acute organ toxicity in chemoradiotherapy for head and neck cancer
Treatment of head and neck squamous cell carcinoma (HNSCC) by chemoradiotherapy (CRT) often results in high-grade acute organ toxicity (HGAOT). As these adverse effects impair the patients' quality of life and the feasibility of the planned therapy, we sought to analyze immunological parameters...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5323201/ https://www.ncbi.nlm.nih.gov/pubmed/27589568 http://dx.doi.org/10.18632/oncotarget.11677 |
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author | Beschel, L. Milena Leu, Martin Reichardt, Sybille D. Rave-Fränk, Margret Schirmer, Markus A. Stadelmann, Christine Canis, Martin Wolff, Hendrik A. Reichardt, Holger M. |
author_facet | Beschel, L. Milena Leu, Martin Reichardt, Sybille D. Rave-Fränk, Margret Schirmer, Markus A. Stadelmann, Christine Canis, Martin Wolff, Hendrik A. Reichardt, Holger M. |
author_sort | Beschel, L. Milena |
collection | PubMed |
description | Treatment of head and neck squamous cell carcinoma (HNSCC) by chemoradiotherapy (CRT) often results in high-grade acute organ toxicity (HGAOT). As these adverse effects impair the patients' quality of life and the feasibility of the planned therapy, we sought to analyze immunological parameters in tumor material and blood samples obtained from 48 HNSCC patients in order to assess the potential to predict the individual acute organ toxicity. T cells in the tumor stroma were enriched in patients developing HGAOT whereas levels of soluble factors in the plasma and gene expression in whole blood did not coincide with the occurrence of acute organ toxicity. In contrast, the frequency and absolute numbers of selected leukocyte subpopulations measured in samples of peripheral blood mononuclear cells (PBMCs) directly before the beginning of CRT were significantly different in patients with HGAOT as compared to those without. When we validated several potential markers including the abundance of T cells in a small prospective study with 16 HNSCC patients, we were able to correctly predict acute organ toxicity in up to 81% of the patients. We conclude that analysis of PBMCs by fluorescence-activated cell sorting (FACS) might be a convenient strategy to identify patients at risk of developing HGAOT caused by CRT, which might allow to adapt the treatment regimen and possibly improve disease outcome. |
format | Online Article Text |
id | pubmed-5323201 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-53232012017-03-23 T cell abundance in blood predicts acute organ toxicity in chemoradiotherapy for head and neck cancer Beschel, L. Milena Leu, Martin Reichardt, Sybille D. Rave-Fränk, Margret Schirmer, Markus A. Stadelmann, Christine Canis, Martin Wolff, Hendrik A. Reichardt, Holger M. Oncotarget Research Paper Treatment of head and neck squamous cell carcinoma (HNSCC) by chemoradiotherapy (CRT) often results in high-grade acute organ toxicity (HGAOT). As these adverse effects impair the patients' quality of life and the feasibility of the planned therapy, we sought to analyze immunological parameters in tumor material and blood samples obtained from 48 HNSCC patients in order to assess the potential to predict the individual acute organ toxicity. T cells in the tumor stroma were enriched in patients developing HGAOT whereas levels of soluble factors in the plasma and gene expression in whole blood did not coincide with the occurrence of acute organ toxicity. In contrast, the frequency and absolute numbers of selected leukocyte subpopulations measured in samples of peripheral blood mononuclear cells (PBMCs) directly before the beginning of CRT were significantly different in patients with HGAOT as compared to those without. When we validated several potential markers including the abundance of T cells in a small prospective study with 16 HNSCC patients, we were able to correctly predict acute organ toxicity in up to 81% of the patients. We conclude that analysis of PBMCs by fluorescence-activated cell sorting (FACS) might be a convenient strategy to identify patients at risk of developing HGAOT caused by CRT, which might allow to adapt the treatment regimen and possibly improve disease outcome. Impact Journals LLC 2016-08-29 /pmc/articles/PMC5323201/ /pubmed/27589568 http://dx.doi.org/10.18632/oncotarget.11677 Text en Copyright: © 2016 Beschel et al. http://creativecommons.org/licenses/by/2.5/ 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 Beschel, L. Milena Leu, Martin Reichardt, Sybille D. Rave-Fränk, Margret Schirmer, Markus A. Stadelmann, Christine Canis, Martin Wolff, Hendrik A. Reichardt, Holger M. T cell abundance in blood predicts acute organ toxicity in chemoradiotherapy for head and neck cancer |
title | T cell abundance in blood predicts acute organ toxicity in chemoradiotherapy for head and neck cancer |
title_full | T cell abundance in blood predicts acute organ toxicity in chemoradiotherapy for head and neck cancer |
title_fullStr | T cell abundance in blood predicts acute organ toxicity in chemoradiotherapy for head and neck cancer |
title_full_unstemmed | T cell abundance in blood predicts acute organ toxicity in chemoradiotherapy for head and neck cancer |
title_short | T cell abundance in blood predicts acute organ toxicity in chemoradiotherapy for head and neck cancer |
title_sort | t cell abundance in blood predicts acute organ toxicity in chemoradiotherapy for head and neck cancer |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5323201/ https://www.ncbi.nlm.nih.gov/pubmed/27589568 http://dx.doi.org/10.18632/oncotarget.11677 |
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