| Literature DB >> 28684409 |
Jordi Rodon1, Josep Tabernero2.
Abstract
<b/> Excitement and drug-development efforts aimed at targetable genetic aberrations in the PI3K/AKT/mTOR pathway have declined due to the limited clinical performance of these inhibitors as monotherapies. New, more isoform-selective treatments, such as taselisib, promise to both expand the therapeutic window and increase efficacy. Cancer Discov; 7(7); 666-9. ©2017 AACR.See related article by Juric et al., p. 704. ©2017 American Association for Cancer Research.Entities:
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Year: 2017 PMID: 28684409 DOI: 10.1158/2159-8290.CD-17-0500
Source DB: PubMed Journal: Cancer Discov ISSN: 2159-8274 Impact factor: 39.397