Low incidence of mutations in EGFR kinase domain in Caucasian patients with head and neck squamous cell carcinoma

• Published in: European journal of cancer (1990) 2006, Vol.42 (1), p.109-111
• Main Authors: Loeffler-Ragg, Judith, Witsch-Baumgartner, Martina, Tzankov, Alexandar, Hilbe, Wolgang, Schwentner, Ilona, Sprinzl, Georg M., Utermann, Gerd, Zwierzina, Heinz
• Format: Article
• Language: English
• Subjects: Adult; Aged; Aged, 80 and over; Biological and medical sciences; Carcinoma, Squamous Cell - genetics; DNA - analysis; EGFR; European Continental Ancestry Group - genetics; Female; Head and Neck Neoplasms - genetics; Head and neck squamous cell carcinoma; Humans; Male; Medical sciences; Middle Aged; Mutation; Mutation - genetics; Pharmacology. Drug treatments; Polymerase Chain Reaction - methods; Polymorphism, Single Nucleotide - genetics; Receptor, Epidermal Growth Factor - genetics; Tumors; Tyrosine kinase inhibitor
• ISSN: 0959-8049; 1879-0852
• DOI: 10.1016/j.ejca.2005.08.034

Somatic mutations in the tyrosine kinase domain of the epidermal growth factor receptor ( EGFR) gene are associated with increased sensitivity to tyrosine kinase inhibitors (TKIs) and are present in 10–30% of non-small cell lung carcinoma depending on ethnic origin. EGFR protein is also overexpressed in about 90% of squamous cell carcinoma of head and neck (HNSCC), and treatment with TKIs has shown clinical benefit in a subgroup of these patients. Recently, EGFR mutations were described in three Asian patients with larynx cancer. We screened for EGFR tyrosine kinase mutations in tumour DNA of 100 patients of Caucasian origin with HNSCC by direct sequencing of the hotspot regions. Only one patient with larynx cancer displayed a novel, somatic EGFR missense mutation, K745R, affecting a highly conserved residue within the ATP cleft. Similar to reports in lung cancer, EGFR kinase domain mutations in HNSCC patients seem to show a lower incidence in patients of Caucasian origin.