Journal of Medicinal Chemistry · 2022 · 160 citations · 40 references
MedicineOncologyPharmacologyCancer PharmacologyDrug DesignDrug DiscoveryLung Cancer PharmacotherapyTargeted Cancer TherapyTyrosine Kinase InhibitorsEpidermal Growth Factor Receptor InhibitionKinase Inhibitor ResistanceMutation-driven ResistanceNon-small Cell Lung Cancer TherapyNon-small Cell Lung Cancer TreatmentResistance To Tyrosine Kinase InhibitorsReversible Tyrosine Kinase InhibitorsTherapeutic Tyrosine Kinase Inhibitors
) is a potent, reversible, wild-type-sparing inhibitor of EGFR+/T790M and EGFR+/T790M/C797S resistance mutants that maintains activity against the sensitizing mutations, especially L858R. Pre-clinical efficacy and safety studies supported progression of BLU-945 into clinical studies, and it is currently in phase 1/2 clinical trials for treatment-resistant EGFR-driven NSCLC.
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<i>EGFR</i> Mutation and Resistance of Non–Small-Cell Lung Cancer to Gefitinib
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