Method to determine responsiveness of cancer to epidermal growth factor receptor targeting treatments
View Patent ↗The present invention is directed to a method for determining the responsiveness of cancer to an epidermal growth factor receptor (EGFR) treatment. In a preferred embodiment, the presence of at least one variance in the kinase domain of the erbB1 gene confers sensitivity to the tyrosine kinase inhibitor gefitinib. Thus, a diagnostic assay for these mutations will allow for the administration of gefitinib, erlotinib and other tyrosine kinase inhibitors to those patients most likely to respond to the drug.
1. A method to determine an increased likelihood of response to treatment with gefitinib or erlotinib in an individual affected with non-small cell lung cancer (NSCLC) comprising:
determining by polymerase chain reaction, the presence or absence of at least one nucleotide variance in exon 18, 19, or 21 of the epidermal growth factor receptor (EGFR) gene in DNA obtained from an NSCLC sample from said individual, wherein said at least one nucleotide variance is selected from:
1) an in-frame deletion in exon 19 of the EGFR gene comprising a deletion within codons 746 to 753 that results in amino acid changes consisting of a deletion of at least amino acids leucine, arginine, and glutamic acid at position 747, 748, and 749 of SEQ ID NO:512;
2) a substitution in exon 21 that results in an amino acid change comprising a substitution of arginine for leucine at position 858 (L858R) of SEQ ID NO:512, or a substitution in exon 21 that results in an amino acid change consisting of a substitution of glutamine for leucine at position 861 (L861Q) of SEQ ID NO:512; or
3) a substitution in exon 18 that results in an amino acid change comprising substitution of cysteine for glycine at position 719 (G719C) of SEQ ID NO:512;
wherein the presence of said at least one nucleotide variance indicates that said individual is likely to respond to treatment with gefitinib or erlotinib.
2. The method of claim 1 wherein said at least one nucleotide variance is an in-frame deletion in exon 19 within codons 746 to 753 that results in amino acid changes comprising a deletion of at least amino acids leucine, arginine, and glutamic acid at position 747, 748, and 749 of SEQ ID NO:512.
3. The method of claim 1 , wherein said at least one nucleotide variance is a substitution in exon 21 that results in a substitution of arginine for leucine at position 858 (L858R) of SEQ ID NO:512 or a substitution of glutamine for leucine at position 861 (L861Q) of SEQ ID NO:512.
4. The method of claim 1 , wherein said at least one nucleotide variance is a substitution in exon 18 that results in a substitution of cysteine for glycine at position 719 (G719C) of SEQ ID NO:512.