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Tumour-infiltrating lymphocytes predict response to definitive chemoradiotherapy in head and neck cancer

BACKGROUND: We aimed to investigate the prognostic value of tumour-infiltrating lymphocytes' (TILs) expression in pretreatment specimens from patients with head and neck squamous cell carcinoma (HNSCC) treated with definitive chemoradiotherapy (CRT). METHODS: The prevalence of CD3+, CD8+, CD4+...

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Autores principales: Balermpas, P, Michel, Y, Wagenblast, J, Seitz, O, Weiss, C, Rödel, F, Rödel, C, Fokas, E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3899751/
https://www.ncbi.nlm.nih.gov/pubmed/24129245
http://dx.doi.org/10.1038/bjc.2013.640
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author Balermpas, P
Michel, Y
Wagenblast, J
Seitz, O
Weiss, C
Rödel, F
Rödel, C
Fokas, E
author_facet Balermpas, P
Michel, Y
Wagenblast, J
Seitz, O
Weiss, C
Rödel, F
Rödel, C
Fokas, E
author_sort Balermpas, P
collection PubMed
description BACKGROUND: We aimed to investigate the prognostic value of tumour-infiltrating lymphocytes' (TILs) expression in pretreatment specimens from patients with head and neck squamous cell carcinoma (HNSCC) treated with definitive chemoradiotherapy (CRT). METHODS: The prevalence of CD3+, CD8+, CD4+ and FOXP3+ TILs was assessed using immunohistochemistry in tumour tissue obtained from 101 patients before CRT and was correlated with clinicopathological characteristics as well as local failure-free- (LFFS), distant metastases free- (DMFS), progression-free (PFS) and overall survival (OS). Survival curves were measured using the Kaplan–Meier method, and differences in survival between the groups were estimated using the log-rank test. Prognostic effects of TIL subset density were determined using the Cox regression analysis. RESULTS: With a mean follow-up of 25 months (range, 2.3–63 months), OS at 2 years was 57.4% for the entire cohort. Patients with high immunohistochemical CD3 and CD8 expression had significantly increased OS (P=0.024 and P=0.028), PFS (P=0.044 and P=0.047) and DMFS (P=0.021 and P=0.026) but not LFFS (P=0.90 and P=0.104) in multivariate analysis that included predictive clinicopathologic factors, such as age, sex, T-stage, N-stage, tumour grading and localisation. Neither CD4 nor FOXP3 expression showed significance for the clinical outcome. The lower N-stage was associated with improved OS in the multivariate analysis (P=0.049). CONCLUSION: The positive correlation between a high number of infiltrating CD3+ and CD8+ cells and clinical outcome indicates that TILs may have a beneficial role in HNSCC patients and may serve as a biomarker to identify patients likely to benefit from definitive CRT.
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spelling pubmed-38997512015-01-21 Tumour-infiltrating lymphocytes predict response to definitive chemoradiotherapy in head and neck cancer Balermpas, P Michel, Y Wagenblast, J Seitz, O Weiss, C Rödel, F Rödel, C Fokas, E Br J Cancer Molecular Diagnostics BACKGROUND: We aimed to investigate the prognostic value of tumour-infiltrating lymphocytes' (TILs) expression in pretreatment specimens from patients with head and neck squamous cell carcinoma (HNSCC) treated with definitive chemoradiotherapy (CRT). METHODS: The prevalence of CD3+, CD8+, CD4+ and FOXP3+ TILs was assessed using immunohistochemistry in tumour tissue obtained from 101 patients before CRT and was correlated with clinicopathological characteristics as well as local failure-free- (LFFS), distant metastases free- (DMFS), progression-free (PFS) and overall survival (OS). Survival curves were measured using the Kaplan–Meier method, and differences in survival between the groups were estimated using the log-rank test. Prognostic effects of TIL subset density were determined using the Cox regression analysis. RESULTS: With a mean follow-up of 25 months (range, 2.3–63 months), OS at 2 years was 57.4% for the entire cohort. Patients with high immunohistochemical CD3 and CD8 expression had significantly increased OS (P=0.024 and P=0.028), PFS (P=0.044 and P=0.047) and DMFS (P=0.021 and P=0.026) but not LFFS (P=0.90 and P=0.104) in multivariate analysis that included predictive clinicopathologic factors, such as age, sex, T-stage, N-stage, tumour grading and localisation. Neither CD4 nor FOXP3 expression showed significance for the clinical outcome. The lower N-stage was associated with improved OS in the multivariate analysis (P=0.049). CONCLUSION: The positive correlation between a high number of infiltrating CD3+ and CD8+ cells and clinical outcome indicates that TILs may have a beneficial role in HNSCC patients and may serve as a biomarker to identify patients likely to benefit from definitive CRT. Nature Publishing Group 2014-01-21 2013-10-15 /pmc/articles/PMC3899751/ /pubmed/24129245 http://dx.doi.org/10.1038/bjc.2013.640 Text en Copyright © 2014 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/3.0/ From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/
spellingShingle Molecular Diagnostics
Balermpas, P
Michel, Y
Wagenblast, J
Seitz, O
Weiss, C
Rödel, F
Rödel, C
Fokas, E
Tumour-infiltrating lymphocytes predict response to definitive chemoradiotherapy in head and neck cancer
title Tumour-infiltrating lymphocytes predict response to definitive chemoradiotherapy in head and neck cancer
title_full Tumour-infiltrating lymphocytes predict response to definitive chemoradiotherapy in head and neck cancer
title_fullStr Tumour-infiltrating lymphocytes predict response to definitive chemoradiotherapy in head and neck cancer
title_full_unstemmed Tumour-infiltrating lymphocytes predict response to definitive chemoradiotherapy in head and neck cancer
title_short Tumour-infiltrating lymphocytes predict response to definitive chemoradiotherapy in head and neck cancer
title_sort tumour-infiltrating lymphocytes predict response to definitive chemoradiotherapy in head and neck cancer
topic Molecular Diagnostics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3899751/
https://www.ncbi.nlm.nih.gov/pubmed/24129245
http://dx.doi.org/10.1038/bjc.2013.640
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