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We report the development of a novel structurally distinct third-generation EGFR TKI, AZD9291, that irreversibly and selectively targets both sensitizing and resistant T790M(+) mutant EGFR while harboring less activity toward wild-type EGFR. AZD9291 is showing promising responses in a phase I trial even at the first-dose level, with first published clinical proof-of-principle validation being presented.
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Cross et al. (Wed,) studied this question.
www.synapsesocial.com/papers/69d849c85c3030ff03d19ae2 — DOI: https://doi.org/10.1158/2159-8290.cd-14-0337
Darren A.E. Cross
Susan Ashton
Serban Ghiorghiu
Cancer Discovery
University of Manchester
Vanderbilt University
Seoul National University Hospital
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