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Evaluation of prognostic biomarkers in a population-validated Finnish HNSCC patient cohort

INTRODUCTION: Prognostic biomarkers and novel therapeutic approaches have been slow to emerge in the treatment of head and neck squamous cell carcinoma (HNSCC). In this study, an HNSCC patient cohort is created and performance of putative prognostic biomarkers investigated in a population-validated...

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Autores principales: Routila, J., Leivo, I., Minn, H., Westermarck, J., Ventelä, Sami
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8486716/
https://www.ncbi.nlm.nih.gov/pubmed/33582846
http://dx.doi.org/10.1007/s00405-021-06650-7
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author Routila, J.
Leivo, I.
Minn, H.
Westermarck, J.
Ventelä, Sami
author_facet Routila, J.
Leivo, I.
Minn, H.
Westermarck, J.
Ventelä, Sami
author_sort Routila, J.
collection PubMed
description INTRODUCTION: Prognostic biomarkers and novel therapeutic approaches have been slow to emerge in the treatment of head and neck squamous cell carcinoma (HNSCC). In this study, an HNSCC patient cohort is created and performance of putative prognostic biomarkers investigated in a population-validated setting. The overall goal is to develop a novel way to combine biomarker analyses with population-level clinical data on HNSCC patients and thus to improve the carryover of biomarkers into clinical practice. MATERIALS AND METHODS: To avoid selection biases in retrospective study design, all HNSCC patients were identified and corresponding clinical data were collected from the Southwest Finland geographical area. A particular emphasis was laid on avoiding potential biases in sample selection for immunohistochemical staining analyses. Staining results were evaluated for potential prognostic resolution. RESULTS: After comprehensive evaluation, the patient cohort was found to be representative of the background population in terms of clinical characteristics such as patient age and TNM stage distribution. A negligible drop-out of 1.3% (6/476) was observed during the first follow-up year. By immunohistochemical analysis, the role of previously implicated HNSCC biomarkers (p53, EGFR, p16, CIP2A, Oct4, MET, and NDFIP1) was investigated. DISCUSSION: Our exceptionally representative patient material supports the use of population validation to improve the applicability of results to real-life situations. The failure of the putative prognostic biomarkers emphasizes the need for controlling bias in retrospective studies, especially in the heterogenous tumor environment of HNSCC. The resolution of simple prognostic examination is unlikely to be sufficient to identify biomarkers for clinical practice of HNSCC. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00405-021-06650-7.
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spelling pubmed-84867162021-10-04 Evaluation of prognostic biomarkers in a population-validated Finnish HNSCC patient cohort Routila, J. Leivo, I. Minn, H. Westermarck, J. Ventelä, Sami Eur Arch Otorhinolaryngol Short Communication INTRODUCTION: Prognostic biomarkers and novel therapeutic approaches have been slow to emerge in the treatment of head and neck squamous cell carcinoma (HNSCC). In this study, an HNSCC patient cohort is created and performance of putative prognostic biomarkers investigated in a population-validated setting. The overall goal is to develop a novel way to combine biomarker analyses with population-level clinical data on HNSCC patients and thus to improve the carryover of biomarkers into clinical practice. MATERIALS AND METHODS: To avoid selection biases in retrospective study design, all HNSCC patients were identified and corresponding clinical data were collected from the Southwest Finland geographical area. A particular emphasis was laid on avoiding potential biases in sample selection for immunohistochemical staining analyses. Staining results were evaluated for potential prognostic resolution. RESULTS: After comprehensive evaluation, the patient cohort was found to be representative of the background population in terms of clinical characteristics such as patient age and TNM stage distribution. A negligible drop-out of 1.3% (6/476) was observed during the first follow-up year. By immunohistochemical analysis, the role of previously implicated HNSCC biomarkers (p53, EGFR, p16, CIP2A, Oct4, MET, and NDFIP1) was investigated. DISCUSSION: Our exceptionally representative patient material supports the use of population validation to improve the applicability of results to real-life situations. The failure of the putative prognostic biomarkers emphasizes the need for controlling bias in retrospective studies, especially in the heterogenous tumor environment of HNSCC. The resolution of simple prognostic examination is unlikely to be sufficient to identify biomarkers for clinical practice of HNSCC. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00405-021-06650-7. Springer Berlin Heidelberg 2021-02-13 2021 /pmc/articles/PMC8486716/ /pubmed/33582846 http://dx.doi.org/10.1007/s00405-021-06650-7 Text en © The Author(s) 2021 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 Short Communication
Routila, J.
Leivo, I.
Minn, H.
Westermarck, J.
Ventelä, Sami
Evaluation of prognostic biomarkers in a population-validated Finnish HNSCC patient cohort
title Evaluation of prognostic biomarkers in a population-validated Finnish HNSCC patient cohort
title_full Evaluation of prognostic biomarkers in a population-validated Finnish HNSCC patient cohort
title_fullStr Evaluation of prognostic biomarkers in a population-validated Finnish HNSCC patient cohort
title_full_unstemmed Evaluation of prognostic biomarkers in a population-validated Finnish HNSCC patient cohort
title_short Evaluation of prognostic biomarkers in a population-validated Finnish HNSCC patient cohort
title_sort evaluation of prognostic biomarkers in a population-validated finnish hnscc patient cohort
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8486716/
https://www.ncbi.nlm.nih.gov/pubmed/33582846
http://dx.doi.org/10.1007/s00405-021-06650-7
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