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Tumor-associated immune cell infiltrate density in penile squamous cell carcinomas

Penile squamous cell carcinomas are rare tumor entities throughout Europe. Early lymphonodal spread urges for aggressive therapeutic approaches in advanced tumor stages. Therefore, understanding tumor biology and its microenvironment and correlation with known survival data is of substantial interes...

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Autores principales: Hladek, Luca, Bankov, Katrin, von der Grün, Jens, Filmann, Natalie, Demes, Melanie, Vallo, Stefan, Wild, Peter J., Winkelmann, Ria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9184419/
https://www.ncbi.nlm.nih.gov/pubmed/35024940
http://dx.doi.org/10.1007/s00428-022-03271-1
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author Hladek, Luca
Bankov, Katrin
von der Grün, Jens
Filmann, Natalie
Demes, Melanie
Vallo, Stefan
Wild, Peter J.
Winkelmann, Ria
author_facet Hladek, Luca
Bankov, Katrin
von der Grün, Jens
Filmann, Natalie
Demes, Melanie
Vallo, Stefan
Wild, Peter J.
Winkelmann, Ria
author_sort Hladek, Luca
collection PubMed
description Penile squamous cell carcinomas are rare tumor entities throughout Europe. Early lymphonodal spread urges for aggressive therapeutic approaches in advanced tumor stages. Therefore, understanding tumor biology and its microenvironment and correlation with known survival data is of substantial interest in order to establish treatment strategies adapted to the individual patient. Fifty-five therapy naïve squamous cell carcinomas, age range between 41 and 85 years with known clinicopathological data, were investigated with the use of tissue microarrays (TMA) regarding the tumor-associated immune cell infiltrate density (ICID). Slides were stained with antibodies against CD3, CD8 and CD20. An image analysis software was applied for evaluation. Data were correlated with clinicopathological characteristics and overall survival. There was a significant increase of ICID in squamous cell carcinomas of the penis in relation to tumor adjacent physiological tissue. Higher CD3-positive ICID was significantly associated with lower tumor stage in our cohort. The ICID was not associated with overall survival. Our data sharpens the view on tumor-associated immune cell infiltrate in penile squamous cell carcinomas with an unbiased digital and automated cell count. Further investigations on the immune cell infiltrate and its prognostic and possible therapeutic impact are needed.
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spelling pubmed-91844192022-06-11 Tumor-associated immune cell infiltrate density in penile squamous cell carcinomas Hladek, Luca Bankov, Katrin von der Grün, Jens Filmann, Natalie Demes, Melanie Vallo, Stefan Wild, Peter J. Winkelmann, Ria Virchows Arch Original Article Penile squamous cell carcinomas are rare tumor entities throughout Europe. Early lymphonodal spread urges for aggressive therapeutic approaches in advanced tumor stages. Therefore, understanding tumor biology and its microenvironment and correlation with known survival data is of substantial interest in order to establish treatment strategies adapted to the individual patient. Fifty-five therapy naïve squamous cell carcinomas, age range between 41 and 85 years with known clinicopathological data, were investigated with the use of tissue microarrays (TMA) regarding the tumor-associated immune cell infiltrate density (ICID). Slides were stained with antibodies against CD3, CD8 and CD20. An image analysis software was applied for evaluation. Data were correlated with clinicopathological characteristics and overall survival. There was a significant increase of ICID in squamous cell carcinomas of the penis in relation to tumor adjacent physiological tissue. Higher CD3-positive ICID was significantly associated with lower tumor stage in our cohort. The ICID was not associated with overall survival. Our data sharpens the view on tumor-associated immune cell infiltrate in penile squamous cell carcinomas with an unbiased digital and automated cell count. Further investigations on the immune cell infiltrate and its prognostic and possible therapeutic impact are needed. Springer Berlin Heidelberg 2022-01-13 2022 /pmc/articles/PMC9184419/ /pubmed/35024940 http://dx.doi.org/10.1007/s00428-022-03271-1 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/) .
spellingShingle Original Article
Hladek, Luca
Bankov, Katrin
von der Grün, Jens
Filmann, Natalie
Demes, Melanie
Vallo, Stefan
Wild, Peter J.
Winkelmann, Ria
Tumor-associated immune cell infiltrate density in penile squamous cell carcinomas
title Tumor-associated immune cell infiltrate density in penile squamous cell carcinomas
title_full Tumor-associated immune cell infiltrate density in penile squamous cell carcinomas
title_fullStr Tumor-associated immune cell infiltrate density in penile squamous cell carcinomas
title_full_unstemmed Tumor-associated immune cell infiltrate density in penile squamous cell carcinomas
title_short Tumor-associated immune cell infiltrate density in penile squamous cell carcinomas
title_sort tumor-associated immune cell infiltrate density in penile squamous cell carcinomas
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9184419/
https://www.ncbi.nlm.nih.gov/pubmed/35024940
http://dx.doi.org/10.1007/s00428-022-03271-1
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