Mechanisms of and therapeutic approaches for overcoming resistance to epidermal growth factor receptor (EGFR)-targeted therapy in squamous cell carcinoma of the head and neck (SCCHN)
- PMID: 25725588
- DOI: 10.1016/j.oraloncology.2015.01.018
Mechanisms of and therapeutic approaches for overcoming resistance to epidermal growth factor receptor (EGFR)-targeted therapy in squamous cell carcinoma of the head and neck (SCCHN)
Abstract
The majority of squamous cell carcinoma of the head and neck (SCCHN) overexpress epidermal growth factor receptor (EGFR), which has been associated with poor treatment response and survival. However, only modest success has been achieved with the use of single agents that target EGFR, possibly due to primary and acquired resistance. This review will discuss key mechanisms of and therapeutic approaches to overcoming resistance to EGFR-targeted therapy in SCCHN. Recent preclinical and clinical investigations have demonstrated that other ErbB family receptors (eg, HER2 and HER3) and other horizontal resistance mechanisms, as well as activation of downstream signaling pathways, epigenetic events, and nuclear EGFR, are possible mediators of resistance to anti-EGFR therapeutics. Key downstream pathways that may be implicated in EGFR resistance include phosphatidylinositol-3-kinase/protein kinase B, vascular endothelial growth factor (VEGF), and mammalian target of rapamycin (mTOR). Multiple agents that target EGFR and other ErbB family members (ie, lapatinib, afatinib, and dacomitinib), as well as combination therapies that target EGFR and selected other pathways (eg, VEGF, mTOR, and c-Met) are being investigated clinically. In addition, several phase II and III trials continue to investigate strategies to enhance the efficacy of EGFR-targeted therapy in SCCHN.
Keywords: Clinical trial; Drug resistance; Epidermal growth factor receptor; HER2; HER3; Molecular targeted therapy; Squamous cell carcinoma of the head and neck.
Copyright © 2015 Elsevier Ltd. All rights reserved.
Similar articles
-
Molecular-targeted therapy of head and neck squamous cell carcinoma: beyond cetuximab-based therapy.Curr Opin Oncol. 2011 May;23(3):241-8. doi: 10.1097/CCO.0b013e328344f581. Curr Opin Oncol. 2011. PMID: 21358328 Review.
-
Targeting pathways mediating resistance to anti-EGFR therapy in squamous cell carcinoma of the head and neck.Expert Rev Anticancer Ther. 2016 Aug;16(8):847-58. doi: 10.1080/14737140.2016.1202116. Epub 2016 Jul 11. Expert Rev Anticancer Ther. 2016. PMID: 27400139 Review.
-
Molecular-targeted therapies in the treatment of squamous cell carcinomas of the head and neck.Curr Opin Oncol. 2008 May;20(3):256-63. doi: 10.1097/CCO.0b013e3282f9b575. Curr Opin Oncol. 2008. PMID: 18391623 Review.
-
The challenge of blocking a wider family members of EGFR against head and neck squamous cell carcinomas.Oral Oncol. 2015 May;51(5):423-30. doi: 10.1016/j.oraloncology.2015.02.092. Epub 2015 Mar 6. Oral Oncol. 2015. PMID: 25753560 Review.
-
Epidermal growth factor receptor directed therapy in head and neck cancer.Crit Rev Oncol Hematol. 2006 Jan;57(1):25-43. doi: 10.1016/j.critrevonc.2005.06.002. Epub 2005 Oct 3. Crit Rev Oncol Hematol. 2006. PMID: 16207530 Review.
Cited by
-
The Tumour Suppressor CYLD Is Required for Clathrin-Mediated Endocytosis of EGFR and Cetuximab-Induced Apoptosis in Head and Neck Squamous Cell Carcinoma.Cancers (Basel). 2021 Dec 30;14(1):173. doi: 10.3390/cancers14010173. Cancers (Basel). 2021. PMID: 35008337 Free PMC article.
-
Prognostic value of the PIK3CA, AKT, and PTEN mutations in oral squamous cell carcinoma: literature review.Arch Med Sci. 2020 Nov 13;17(1):207-217. doi: 10.5114/aoms.2020.100780. eCollection 2021. Arch Med Sci. 2020. PMID: 33488873 Free PMC article.
-
Any Role of PIK3CA and PTEN Biomarkers in the Prognosis in Oral Squamous Cell Carcinoma?Life (Basel). 2020 Dec 3;10(12):325. doi: 10.3390/life10120325. Life (Basel). 2020. PMID: 33287350 Free PMC article.
-
Role of epidermal growth factor receptor inhibitor-induced interferon pathway signaling in the head and neck squamous cell carcinoma therapeutic response.J Transl Med. 2021 Jan 23;19(1):43. doi: 10.1186/s12967-021-02706-8. J Transl Med. 2021. PMID: 33485341 Free PMC article.
-
Transactivation of ErbB Family of Receptor Tyrosine Kinases Is Inhibited by Angiotensin-(1-7) via Its Mas Receptor.PLoS One. 2015 Nov 4;10(11):e0141657. doi: 10.1371/journal.pone.0141657. eCollection 2015. PLoS One. 2015. PMID: 26536590 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Research Materials
Miscellaneous