Indication

Non-small cell lung cancer with EGFR exon 19 deletion

Non-small cell lung cancer with EGFR exon 19 deletion is a biologically distinct subset of pulmonary epithelial malignancy defined by specific in-frame deletions within exon 19 of the epidermal growth factor receptor gene. Read more about Non-small cell lung cancer with EGFR exon 19 deletion

4 drugs 2 manufacturers

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Drugs that treat it

Common Non-small cell lung cancer with EGFR exon 19 deletion therapies.

Showing 1–4 of 4 drugs

TAGRISSO (osimertinib mesylate)

ANTINEOPLASTIC - PROTEIN-TYROSINE KINASE INHIBITORS·EGFR T790M MUTATION-POSITIVE NON-SMALL CELL LUNG CANCER·+2
AstraZeneca Pharmaceuticals

RYBREVANT (amivantamab-vmjw)

ANTINEOPLASTIC - BISPECIFIC EGFR AND MET REC INHIBITOR MC AB·NON-SMALL CELL LUNG CANCER WITH EGFR EXON 19 DELETION·+2
JANSSEN BIOTECH, Inc.

LAZCLUZE (lazertinib mesylate)

ANTINEOPLASTIC - PROTEIN-TYROSINE KINASE INHIBITORS·NON-SMALL CELL LUNG CANCER WITH EGFR EXON 19 DELETION·+1
JANSSEN BIOTECH, Inc.
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About Non-small cell lung cancer with EGFR exon 19 deletion.

Non-small cell lung cancer with EGFR exon 19 deletion is a biologically distinct subset of pulmonary epithelial malignancy defined by specific in-frame deletions within exon 19 of the epidermal growth factor receptor gene.

Affecting the respiratory system, this subtype is most frequently identified in lung adenocarcinomas and occurs with higher frequency among women, individuals with minimal or no smoking history, and populations of East Asian descent.

Pathophysiologically, these deletions alter the kinase domain near the ATP-binding pocket, leading to ligand-independent, constitutive activation of downstream oncogenic signaling pathways that promote dysregulated cellular proliferation and survival.

As one of the most prevalent classical activating mutations in non-small cell lung cancer, it characteristically predicts heightened tumor sensitivity to EGFR tyrosine kinase inhibitors.

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