TY - JOUR
T1 - Advances and perspectives in the molecular diagnosis of head and neck cancer
AU - Mydlarz, Wojciech K.
AU - Hennessey, Patrick T.
AU - Califano, Joseph A.
N1 - Funding Information:
JA Califano is supported by the National Institute of Dental and Craniofacial Research and the National Cancer Institute SPORE (5P50CA096784-05). WK Mydlarz and PT Hennessey are supported, in part, by the NIH training Grant No. T32DC000027.
PY - 2010/1
Y1 - 2010/1
N2 - Head and neck squamous cell carcinoma (HNSCC) is a debilitating and lethal disease. Despite significant advances in radiotherapy and surgical management, the 5-year survival rate for head and neck cancer has remained a dismal 50%. Advances in early detection have been made, but to improve patient outcomes better biomarkers and targeted therapeutic agents are needed. New biomarkers can improve early detection and provide data to optimize therapeutic strategy and patient survival, and could lead to potentially effective targeted therapies. To report the advances in the discovery of new biomarkers for HNSCC, and review the potential utility of biomarkers in the molecular diagnosis of HNSCC. A review of the English literature (PubMed) from 1980 to 2009. At present, the most widely accepted biomarker for HNSCC is high-risk HPV status. EGFR is another promising biomarker; however, further research is necessary to determine its prognostic benefit. A large number of promising biomarker candidates are now being evaluated, including epigenetic, expression and genomic-based markers. Studies to validate the sensitivity and specificity of these biomarkers in clinical samples from adequately powered prospective cohorts are needed for successful translation of these findings into potential molecular diagnostic, prognostic and therapeutic biomarkers for HNSCC.
AB - Head and neck squamous cell carcinoma (HNSCC) is a debilitating and lethal disease. Despite significant advances in radiotherapy and surgical management, the 5-year survival rate for head and neck cancer has remained a dismal 50%. Advances in early detection have been made, but to improve patient outcomes better biomarkers and targeted therapeutic agents are needed. New biomarkers can improve early detection and provide data to optimize therapeutic strategy and patient survival, and could lead to potentially effective targeted therapies. To report the advances in the discovery of new biomarkers for HNSCC, and review the potential utility of biomarkers in the molecular diagnosis of HNSCC. A review of the English literature (PubMed) from 1980 to 2009. At present, the most widely accepted biomarker for HNSCC is high-risk HPV status. EGFR is another promising biomarker; however, further research is necessary to determine its prognostic benefit. A large number of promising biomarker candidates are now being evaluated, including epigenetic, expression and genomic-based markers. Studies to validate the sensitivity and specificity of these biomarkers in clinical samples from adequately powered prospective cohorts are needed for successful translation of these findings into potential molecular diagnostic, prognostic and therapeutic biomarkers for HNSCC.
KW - Biomarkers
KW - DNA methylation
KW - Diagnosis
KW - Epidermal growth factor receptor
KW - Epigenetics
KW - Head and neck cancer
KW - Human papillomavirus
KW - Loss of heterozygosity
KW - MicroRNA
KW - Molecular biology
KW - Proteomics
KW - RNA
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U2 - 10.1517/17530050903338068
DO - 10.1517/17530050903338068
M3 - Review article
C2 - 20161611
AN - SCOPUS:77953452311
SN - 1753-0059
VL - 4
SP - 53
EP - 65
JO - Expert Opinion on Medical Diagnostics
JF - Expert Opinion on Medical Diagnostics
IS - 1
ER -