Ontology highlight
ABSTRACT: Background
Characterization of the driver mutations in an individual metastatic breast cancer (MBC) patient is critical to selecting effective targeted therapies. Currently, it is believed that the limited efficacy of many targeted drugs may be due to the expansion of drug resistant clones with different genotypes that were already present in the primary tumor. Identifying the genomic alterations of these clones, and introducing combined or sequential targeted drug regimens, could lead to a significant increase in the efficacy of currently available targeted therapies.Objective
The primary objective of this study is to assess the concordance/discordance of mutations between the primary tumor and metastatic tissue in MBC patients. Secondary objectives include comparing the g
SUBMITTER: Gonzalez-Rivera M
PROVIDER: S-EPMC5005674 | biostudies-literature | 2016 Aug
REPOSITORIES: biostudies-literature