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Meta analysis: HPV and p16 pattern determines survival in patients with HNSCC and identifies potential new biologic subtype

Consistent discrepancies in the p16/HPV-positivity have been observed in head and neck squamous cell carcinoma (HNSCC). It is therefore questionable, if all HPV(+) and/or p16(+) tested cancers are HPV-driven. Patients down-staged according to the HPV-dependant TNM are at risk for undertreatment and...

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Autores principales: Albers, Andreas E., Qian, Xu, Kaufmann, Andreas M., Coordes, Annekatrin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5711807/
https://www.ncbi.nlm.nih.gov/pubmed/29196639
http://dx.doi.org/10.1038/s41598-017-16918-w
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author Albers, Andreas E.
Qian, Xu
Kaufmann, Andreas M.
Coordes, Annekatrin
author_facet Albers, Andreas E.
Qian, Xu
Kaufmann, Andreas M.
Coordes, Annekatrin
author_sort Albers, Andreas E.
collection PubMed
description Consistent discrepancies in the p16/HPV-positivity have been observed in head and neck squamous cell carcinoma (HNSCC). It is therefore questionable, if all HPV(+) and/or p16(+) tested cancers are HPV-driven. Patients down-staged according to the HPV-dependant TNM are at risk for undertreatment and data in clinical trials may be skewed due to false patient inclusion. We performed a meta-analysis to classify clinical outcomes of the distinct subgroups with combined p16 and HPV detection. 25 out of 1677 publications fulfilled the inclusion criteria. The proportion of the subgroups was 35.6% for HPV(+)/p16(+), 50.4% for HPV(−)/p16(−), 6.7% for HPV(−)/p16(+) and 7.3% for HPV(+)/P16(−). The HPV(+)/p16(+) subgroup had a significantly improved 5-year overall-survival (OS) and disease-free-survival in comparison to others both for HNSCC and oropharyngeal cancers. The 5-year OS of the HPV(−)/p16(+) HNSCC was intermediate while HPV(+)/p16(−) and HPV(−)/p16(−) had the shortest survival outcomes. The clearly distinct survival of HPV(−)/p16(+) cancers may characterize a new relevant HPV-independent subtype yet to be biologically characterized. The possibility also exists that in some HPV(+)/p16(+) cancers HPV is an innocent bystander and p16 is independently positive. Therefore, in perspective, HPV-testing should distinguish between bystander HPV and truly HPV-driven cancers to avoid potential undertreatment in HPV(+) but non-HPV-driven HNSCC.
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spelling pubmed-57118072017-12-06 Meta analysis: HPV and p16 pattern determines survival in patients with HNSCC and identifies potential new biologic subtype Albers, Andreas E. Qian, Xu Kaufmann, Andreas M. Coordes, Annekatrin Sci Rep Article Consistent discrepancies in the p16/HPV-positivity have been observed in head and neck squamous cell carcinoma (HNSCC). It is therefore questionable, if all HPV(+) and/or p16(+) tested cancers are HPV-driven. Patients down-staged according to the HPV-dependant TNM are at risk for undertreatment and data in clinical trials may be skewed due to false patient inclusion. We performed a meta-analysis to classify clinical outcomes of the distinct subgroups with combined p16 and HPV detection. 25 out of 1677 publications fulfilled the inclusion criteria. The proportion of the subgroups was 35.6% for HPV(+)/p16(+), 50.4% for HPV(−)/p16(−), 6.7% for HPV(−)/p16(+) and 7.3% for HPV(+)/P16(−). The HPV(+)/p16(+) subgroup had a significantly improved 5-year overall-survival (OS) and disease-free-survival in comparison to others both for HNSCC and oropharyngeal cancers. The 5-year OS of the HPV(−)/p16(+) HNSCC was intermediate while HPV(+)/p16(−) and HPV(−)/p16(−) had the shortest survival outcomes. The clearly distinct survival of HPV(−)/p16(+) cancers may characterize a new relevant HPV-independent subtype yet to be biologically characterized. The possibility also exists that in some HPV(+)/p16(+) cancers HPV is an innocent bystander and p16 is independently positive. Therefore, in perspective, HPV-testing should distinguish between bystander HPV and truly HPV-driven cancers to avoid potential undertreatment in HPV(+) but non-HPV-driven HNSCC. Nature Publishing Group UK 2017-12-01 /pmc/articles/PMC5711807/ /pubmed/29196639 http://dx.doi.org/10.1038/s41598-017-16918-w Text en © The Author(s) 2017 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Albers, Andreas E.
Qian, Xu
Kaufmann, Andreas M.
Coordes, Annekatrin
Meta analysis: HPV and p16 pattern determines survival in patients with HNSCC and identifies potential new biologic subtype
title Meta analysis: HPV and p16 pattern determines survival in patients with HNSCC and identifies potential new biologic subtype
title_full Meta analysis: HPV and p16 pattern determines survival in patients with HNSCC and identifies potential new biologic subtype
title_fullStr Meta analysis: HPV and p16 pattern determines survival in patients with HNSCC and identifies potential new biologic subtype
title_full_unstemmed Meta analysis: HPV and p16 pattern determines survival in patients with HNSCC and identifies potential new biologic subtype
title_short Meta analysis: HPV and p16 pattern determines survival in patients with HNSCC and identifies potential new biologic subtype
title_sort meta analysis: hpv and p16 pattern determines survival in patients with hnscc and identifies potential new biologic subtype
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5711807/
https://www.ncbi.nlm.nih.gov/pubmed/29196639
http://dx.doi.org/10.1038/s41598-017-16918-w
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