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Beyond EGFR Targeting in SCCHN: Angiogenesis, PI3K, and Other Molecular Targets
Although the molecular landscape of squamous cell carcinoma of the head and neck (SCCHN) has been largely deciphered, only one targeted therapy has been approved to date without any molecular selection, namely cetuximab. Cetuximab is a monoclonal antibody targeting EGFR. It has been shown to improve...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6381014/ https://www.ncbi.nlm.nih.gov/pubmed/30815390 http://dx.doi.org/10.3389/fonc.2019.00074 |
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author | Saada-Bouzid, Esma Le Tourneau, Christophe |
author_facet | Saada-Bouzid, Esma Le Tourneau, Christophe |
author_sort | Saada-Bouzid, Esma |
collection | PubMed |
description | Although the molecular landscape of squamous cell carcinoma of the head and neck (SCCHN) has been largely deciphered, only one targeted therapy has been approved to date without any molecular selection, namely cetuximab. Cetuximab is a monoclonal antibody targeting EGFR. It has been shown to improve overall survival in the locally advanced setting in combination with radiotherapy and the recurrent and/or metastatic setting in combination with a platinum compound and 5FU. Beside EGFR targeting agents, antiangiogenic agents have been shown to produce antitumor activity but were associated with substantial toxicity. Buparlisib that targets PI3K was also shown to improve survival in combination with paclitaxel in an unselected patient population. Several other targeted therapies have been developed in SCCHN, most of time in all comers, potentially explaining the limited efficacy reported with them. The recent emergence of clinical trials of targeted therapies in enriched patient populations and precision medicine trials such as umbrella trials might boost the clinical development of targeted therapy in SCCHN. |
format | Online Article Text |
id | pubmed-6381014 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-63810142019-02-27 Beyond EGFR Targeting in SCCHN: Angiogenesis, PI3K, and Other Molecular Targets Saada-Bouzid, Esma Le Tourneau, Christophe Front Oncol Oncology Although the molecular landscape of squamous cell carcinoma of the head and neck (SCCHN) has been largely deciphered, only one targeted therapy has been approved to date without any molecular selection, namely cetuximab. Cetuximab is a monoclonal antibody targeting EGFR. It has been shown to improve overall survival in the locally advanced setting in combination with radiotherapy and the recurrent and/or metastatic setting in combination with a platinum compound and 5FU. Beside EGFR targeting agents, antiangiogenic agents have been shown to produce antitumor activity but were associated with substantial toxicity. Buparlisib that targets PI3K was also shown to improve survival in combination with paclitaxel in an unselected patient population. Several other targeted therapies have been developed in SCCHN, most of time in all comers, potentially explaining the limited efficacy reported with them. The recent emergence of clinical trials of targeted therapies in enriched patient populations and precision medicine trials such as umbrella trials might boost the clinical development of targeted therapy in SCCHN. Frontiers Media S.A. 2019-02-13 /pmc/articles/PMC6381014/ /pubmed/30815390 http://dx.doi.org/10.3389/fonc.2019.00074 Text en Copyright © 2019 Saada-Bouzid and Le Tourneau. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Oncology Saada-Bouzid, Esma Le Tourneau, Christophe Beyond EGFR Targeting in SCCHN: Angiogenesis, PI3K, and Other Molecular Targets |
title | Beyond EGFR Targeting in SCCHN: Angiogenesis, PI3K, and Other Molecular Targets |
title_full | Beyond EGFR Targeting in SCCHN: Angiogenesis, PI3K, and Other Molecular Targets |
title_fullStr | Beyond EGFR Targeting in SCCHN: Angiogenesis, PI3K, and Other Molecular Targets |
title_full_unstemmed | Beyond EGFR Targeting in SCCHN: Angiogenesis, PI3K, and Other Molecular Targets |
title_short | Beyond EGFR Targeting in SCCHN: Angiogenesis, PI3K, and Other Molecular Targets |
title_sort | beyond egfr targeting in scchn: angiogenesis, pi3k, and other molecular targets |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6381014/ https://www.ncbi.nlm.nih.gov/pubmed/30815390 http://dx.doi.org/10.3389/fonc.2019.00074 |
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