| Literature DB >> 24403863 |
Abstract
The future of personalized oncological therapy will likely rely on evidence-based medicine to integrate all of the available evidence to delineate the most efficacious treatment option for the patient. To undertake evidence-based medicine through use of targeted therapy regimens, identification of the specific underlying causative mutation(s) driving growth and progression of a patient's tumor is imperative. Although molecular subtyping is important for planning and treatment, intraclonal genetic diversity has been recently highlighted as having significant implications for biopsy-based prognosis. Overall, delineation of the clonal architecture of a patient's cancer and how this will impact on the selection of the most efficacious therapy remain a topic of intense interest.Entities:
Mesh:
Year: 2013 PMID: 24403863 PMCID: PMC3884532 DOI: 10.1593/neo.131972
Source DB: PubMed Journal: Neoplasia ISSN: 1476-5586 Impact factor: 5.715