Epidermal Growth Factor Receptor (EGFR) Gene Mutation Analysis, Non−Small-cell Lung Cancer (Single-base Extension)
Also known as: Erlotinib Responsiveness in NSCLC, EGFR Mutation Analysis, Gefitinib Responsiveness in NSCLC, EGFR Mutation Analysis, IRESSA® Responsiveness in NSCLC, EGFR Mutation Analysis, Non−Small-cell Lung Cancer, EGFR Mutation, Tarceva® Responsiveness in NSCLC, EGFR Mutation Analysis
Use
In non-small cell lung cancer, many mutations in EGFR are associated with responsiveness to EGFR tyrosine kinase inhibitor (TKI) therapy. In contrast, some mutations in EGFR are associated with resistance to EGFR TKI therapy, including T790M and EGFR exon 20 insertions. The T790M mutation is a known mechanism of resistance and is commonly associated with relapse following initial therapy with EGFR TKI.
Special Instructions
Not provided.
Limitations
The EGFR test is designed to detect mutations in exon 18, 19, 20, and 21 of the EGFR gene. These mutations account for >99% of all reported EGFR mutations in NSCLC patients. Samples with results reported as "no mutation detected" may harbor EGFR mutations that are not detected by the assay.
Methodology
SNaPshot Multiplex PCR (primer extension-based method)
Biomarkers
LOINC Codes
- 21665-5
- 50398-7
- 48004-6
- 48005-3
- 21666-3
- 72486-4
- 57723-9
- 8100-0
- 18781-5
- 39111-0
- 31208-2
- 55752-0
- 62365-2
- 77202-0
- 49549-9
- 75608-0
- 19139-5
- 51969-4
Result Turnaround Time
5-7 days
Related Documents
For more information, please review the documents below
Specimen
Unknown
Volume
Not provided
Minimum Volume
Not provided
Causes for Rejection
Tumor block containing insufficient tumor; tissue or tumor fixed in a heavy metal fixative; broken or stained slides
