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p16, HPV, and Cetuximab: What Is the Evidence?

Squamous cell carcinoma of the head and neck (SCCHN) is the sixth most common cancer worldwide. It has recently been appreciated that human papillomavirus (HPV) status (or p16 status, which is a frequently used surrogate for HPV status) is prognostic for oropharyngeal SCCHN. Here, we review and cont...

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Autores principales: Bonner, James A., Mesia, Ricard, Giralt, Jordi, Psyrri, Amanda, Keilholz, Ulrich, Rosenthal, David I., Beier, Frank, Schulten, Jeltje, Vermorken, Jan B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AlphaMed Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5507644/
https://www.ncbi.nlm.nih.gov/pubmed/28526718
http://dx.doi.org/10.1634/theoncologist.2016-0433
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author Bonner, James A.
Mesia, Ricard
Giralt, Jordi
Psyrri, Amanda
Keilholz, Ulrich
Rosenthal, David I.
Beier, Frank
Schulten, Jeltje
Vermorken, Jan B.
author_facet Bonner, James A.
Mesia, Ricard
Giralt, Jordi
Psyrri, Amanda
Keilholz, Ulrich
Rosenthal, David I.
Beier, Frank
Schulten, Jeltje
Vermorken, Jan B.
author_sort Bonner, James A.
collection PubMed
description Squamous cell carcinoma of the head and neck (SCCHN) is the sixth most common cancer worldwide. It has recently been appreciated that human papillomavirus (HPV) status (or p16 status, which is a frequently used surrogate for HPV status) is prognostic for oropharyngeal SCCHN. Here, we review and contextualize existing p16 and HPV data, focusing on the cetuximab registration trials in previously untreated, locoregionally advanced, nonmetastatic SCCHN (LA SCCHN) and in recurrent and/or metastatic SCCHN (R/M SCCHN): the IMCL‐9815 and EXTREME clinical trials, respectively. Taken together, the available data suggest that, while p16 and HPV are prognostic biomarkers in patients with LA SCCHN and R/M SCCHN, it could not be shown that they are predictive for the outcomes of the described cetuximab‐containing trial regimens. Consequently, although HPV status provides prognostic information, it is not shown to predict therapy response, and so is not helpful for assigning first‐line therapy in patients with SCCHN. In addition, we discuss assays currently used to assess p16 and HPV status, as well as the differentiation between these two biomarkers. Ultimately, we believe HPV E6/E7 polymerase chain reaction–based mRNA testing may represent the most informative technique for assessing HPV status in patients with SCCHN. While p16 is a valid surrogate for HPV status in oropharyngeal carcinoma (OPC), there is a higher risk of discordance between p16 and HPV status in non‐OPC SCCHN. Collectively, these discussions hold key implications for the clinical management of SCCHN. IMPLICATIONS FOR PRACTICE. Human papillomavirus (HPV) status (or its commonly utilized surrogate p16) is a known prognostic biomarker in oropharyngeal squamous‐cell carcinoma of the head and neck (SCCHN). We evaluated implications of the available evidence, including cetuximab registration trials in previously untreated locoregionally advanced (LA) SCCHN and recurrent and/or metastatic (R/M) SCCHN. We conclude that, although p16 and HPV are prognostic biomarkers for both LA and R/M SCCHN, they have not been shown to be predictive of response to the described cetuximab‐containing regimens for either indication. Thus, current evidence suggests that benefits of cetuximab are observed in both p16‐/HPV‐positive and ‐negative SCCHN.
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spelling pubmed-55076442018-07-01 p16, HPV, and Cetuximab: What Is the Evidence? Bonner, James A. Mesia, Ricard Giralt, Jordi Psyrri, Amanda Keilholz, Ulrich Rosenthal, David I. Beier, Frank Schulten, Jeltje Vermorken, Jan B. Oncologist Head and Neck Cancers Squamous cell carcinoma of the head and neck (SCCHN) is the sixth most common cancer worldwide. It has recently been appreciated that human papillomavirus (HPV) status (or p16 status, which is a frequently used surrogate for HPV status) is prognostic for oropharyngeal SCCHN. Here, we review and contextualize existing p16 and HPV data, focusing on the cetuximab registration trials in previously untreated, locoregionally advanced, nonmetastatic SCCHN (LA SCCHN) and in recurrent and/or metastatic SCCHN (R/M SCCHN): the IMCL‐9815 and EXTREME clinical trials, respectively. Taken together, the available data suggest that, while p16 and HPV are prognostic biomarkers in patients with LA SCCHN and R/M SCCHN, it could not be shown that they are predictive for the outcomes of the described cetuximab‐containing trial regimens. Consequently, although HPV status provides prognostic information, it is not shown to predict therapy response, and so is not helpful for assigning first‐line therapy in patients with SCCHN. In addition, we discuss assays currently used to assess p16 and HPV status, as well as the differentiation between these two biomarkers. Ultimately, we believe HPV E6/E7 polymerase chain reaction–based mRNA testing may represent the most informative technique for assessing HPV status in patients with SCCHN. While p16 is a valid surrogate for HPV status in oropharyngeal carcinoma (OPC), there is a higher risk of discordance between p16 and HPV status in non‐OPC SCCHN. Collectively, these discussions hold key implications for the clinical management of SCCHN. IMPLICATIONS FOR PRACTICE. Human papillomavirus (HPV) status (or its commonly utilized surrogate p16) is a known prognostic biomarker in oropharyngeal squamous‐cell carcinoma of the head and neck (SCCHN). We evaluated implications of the available evidence, including cetuximab registration trials in previously untreated locoregionally advanced (LA) SCCHN and recurrent and/or metastatic (R/M) SCCHN. We conclude that, although p16 and HPV are prognostic biomarkers for both LA and R/M SCCHN, they have not been shown to be predictive of response to the described cetuximab‐containing regimens for either indication. Thus, current evidence suggests that benefits of cetuximab are observed in both p16‐/HPV‐positive and ‐negative SCCHN. AlphaMed Press 2017-05-18 2017-07 /pmc/articles/PMC5507644/ /pubmed/28526718 http://dx.doi.org/10.1634/theoncologist.2016-0433 Text en © 2017 The Authors The Oncologist published by Wiley Periodicals, Inc. on behalf of AlphaMed Press http://creativecommons.org/licenses/by-nc/4.0/ This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Head and Neck Cancers
Bonner, James A.
Mesia, Ricard
Giralt, Jordi
Psyrri, Amanda
Keilholz, Ulrich
Rosenthal, David I.
Beier, Frank
Schulten, Jeltje
Vermorken, Jan B.
p16, HPV, and Cetuximab: What Is the Evidence?
title p16, HPV, and Cetuximab: What Is the Evidence?
title_full p16, HPV, and Cetuximab: What Is the Evidence?
title_fullStr p16, HPV, and Cetuximab: What Is the Evidence?
title_full_unstemmed p16, HPV, and Cetuximab: What Is the Evidence?
title_short p16, HPV, and Cetuximab: What Is the Evidence?
title_sort p16, hpv, and cetuximab: what is the evidence?
topic Head and Neck Cancers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5507644/
https://www.ncbi.nlm.nih.gov/pubmed/28526718
http://dx.doi.org/10.1634/theoncologist.2016-0433
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