This test detects mutations in EGFR exons 18, 19, 20 and 21 (codons 719, 745-753, 768, 790, 858, and 861).These mutations account for >99% of all reported EGFR mutations in NSCLC patients. Detection of mutation is dependent on sample integrity and the amount of amplifiable DNA present in the specimen. The methods used in this assay are highly selective and, depending on the total amount of DNA present, can detect approximately 2% to 20% of mutant in a background of wild-type genomic DNA.
Gefitinib (Kinase Inhibitor) is also known by its brand name Iressa. Gefitinib is a treatment for NSCLC that has spread into the surrounding tissues (locally advanced) or to other parts of the body. By considering the mutation profile of EGFR gene, physician can predict the suitability of Gefitinib to support the treatment of lung cancer. This test is developed and its performance characteristics determined by geneOmbio Technologies Pvt Ltd.