PF00299804, an Irreversible Pan-ERBB Inhibitor, Is Effective in Lung Cancer Models with EGFR and ERBB2 Mutations that Are Resistant to Gefitinib
Harvard University · Hadassah Medical Center · +11 more institutions
Abstract
Epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors gefitinib and erlotinib are effective treatments for a subset of non-small cell lung cancers. In particular, cancers with specific EGFR-activating mutations seem to be the most sensitive to these agents. However, despite their initial response, such cancers almost invariably develop resistance. In 50% of such cancers, a secondary EGFR mutation, T790M, has been identified that renders gefitinib and erlotinib ineffective inhibitors of EGFR kinase activity. Thus, there is a clinical need to develop novel EGFR inhibitors that can effectively inactivate T790M-containing EGFR proteins. In this study, we evaluate the effectiveness of a novel compound,…
Citation impact
- FWCI
- 15.61
- Percentile
- 100%
- References
- 58
Authors
18- JAJeffrey A. EngelmanCorresponding
Harvard University, Hadassah Medical Center, Massachusetts General Hospital, Center for Systems Biology
- KZKreshnik Zejnullahu
Center for Neuro-Oncology, Dana-Farber Cancer Institute
- CGChristopher-Michael Gale
Hadassah Medical Center, Harvard University Press
- ELEugene Lifshits
Boston Children's Hospital
- AJAndrea J. Gonzales
Pfizer (United States)
Topics & keywords
- Gefitinib
- Erlotinib
- T790M
- Epidermal growth factor receptor
- Cancer research
- EGFR inhibitors
- Lung cancer
- ERBB3
- Good health and well-being