Indication
Non-small cell lung cancer with EGFR exon 21 L858R substitution mutation
Non-small cell lung cancer with an EGFR exon 21 L858R substitution mutation is an oncogene-driven subtype of epithelial lung malignancy, most frequently diagnosed as adenocarcinoma. Read more about Non-small cell lung cancer with EGFR exon 21 L858R substitution mutation
4 drugs 2 manufacturers
Drugs that treat it
Common Non-small cell lung cancer with EGFR exon 21 L858R substitution mutation therapies.
RYBREVANT (amivantamab-vmjw)
LAZCLUZE (lazertinib mesylate)
RYBREVANT FASPRO (amivantamab-hyaluronidase, human recombinant-lpuj)
News & literature
Coming soonRelated codes
Coming soonRelated conditions & guidelines
Coming soonNon-small cell lung cancer with an EGFR exon 21 L858R substitution mutation is an oncogene-driven subtype of epithelial lung malignancy, most frequently diagnosed as adenocarcinoma.
It disproportionately impacts female patients, individuals who have never smoked or have a minimal smoking history, and populations of East Asian descent.
Pathophysiologically, this disease is characterized by a specific missense mutation where arginine replaces leucine at codon 858 within the tyrosine kinase domain of the epidermal growth factor receptor, resulting in ligand-independent constitutive kinase activation and downstream signaling that accelerates cell proliferation and survival.
Clinically, identification of this biomarker defines an actionable tumor profile conferring sensitivity to targeted EGFR tyrosine kinase inhibitors.
- medicalnewstoday.com
Non-small cell lung cancer with an EGFR exon 21 L858R substitution mutation is an oncogene-driven subtype of epithelial lung malignancy, most frequently diagnosed as adenocarcinoma
- nih.gov
It disproportionately impacts female patients, individuals who have never smoked or have a minimal smoking history, and populations of East Asian descent
- lcfamerica.org
It disproportionately impacts female patients, individuals who have never smoked or have a minimal smoking history, and populations of East Asian descent
- patsnap.com
Pathophysiologically, this disease is characterized by a specific missense mutation where arginine replaces leucine at codon 858 within the tyrosine kinase domain of the epidermal growth factor receptor, resulting in ligand-independent constitutive kinase activation and downstream signaling that accelerates cell proliferation and survival Clinically, identification of this biomarker defines an actionable tumor profile conferring sensitivity to targeted EGFR tyrosine kinase inhibitors
- everhope.care
Pathophysiologically, this disease is characterized by a specific missense mutation where arginine replaces leucine at codon 858 within the tyrosine kinase domain of the epidermal growth factor receptor, resulting in ligand-independent constitutive kinase activation and downstream signaling that accelerates cell proliferation and survival
- nih.gov
Clinically, identification of this biomarker defines an actionable tumor profile conferring sensitivity to targeted EGFR tyrosine kinase inhibitors
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