The exon 20 T790M mutation is most common resistance associated with first- and second-generation EGFR tyrosine kinase inhibitor therapy. However, treatment decisions may be affected significantly by the sensitivity of the mutation detection method used and by the testing frequency. Other mutations in exons 18-21 include exon 18 G719X mutations, which are relatively uncommon in NSCLC, as well as exon 19 deletions and exon 21 L858R substitution mutations, which comprise approximately 85% of mutations in NSCLC.
Learn more about EGFR mutations in NSCLC.
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Cite this: Daniel S. Schwartz. Fast Five Quiz: Molecular and Biomarker Analysis in Non–Small Cell Lung Cancer (NSCLC) - Medscape - Jan 28, 2022.
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