AZD9291, an Irreversible EGFR TKI, Overcomes T790M-Mediated Resistance to EGFR Inhibitors in Lung Cancer
Vanderbilt University · AstraZeneca (Singapore) · +3 more institutions
Abstract
UNLABELLED: First-generation EGFR tyrosine kinase inhibitors (EGFR TKI) provide significant clinical benefit in patients with advanced EGFR-mutant (EGFRm(+)) non-small cell lung cancer (NSCLC). Patients ultimately develop disease progression, often driven by acquisition of a second T790M EGFR TKI resistance mutation. AZD9291 is a novel oral, potent, and selective third-generation irreversible inhibitor of both EGFRm(+) sensitizing and T790M resistance mutants that spares wild-type EGFR. This mono-anilino-pyrimidine compound is structurally distinct from other third-generation EGFR TKIs and offers a pharmacologically differentiated profile from earlier generation EGFR TKIs. Preclinically, the drug potently…
Citation impact
- FWCI
- 115.85
- Percentile
- 100%
- References
- 64
Authors
26Topics & keywords
- T790M
- Mutant
- Cancer research
- Medicine
- Lung cancer
- EGFR inhibitors
- Mutation
- Cancer
- Good health and well-being