| Literature DB >> 20547994 |
Aram F Hezel1, Vikram Deshpande, Andrew X Zhu.
Abstract
Biliary tract cancers (BTC), which encompass intra- and extrahepatic cholangiocarcinomas and gallbladder carcinomas, are a genetically diverse collection of cancers. Evidence suggests distinct models of molecular and pathologic progression, and a growing body of genetics data points to a heterogeneous collection of underlying mutations in key oncogenes and tumor suppressor genes. Although tumor genetics have been used to tailor individual treatment regimens and guide clinical decision making in other cancers, these principles have not been applied in BTC. Recent clinical trials with targeted therapies seem promising, although the relationships between subsets of patients with positive responses to therapy and tumor genetics remain unexplored. Here, we summarize the molecular pathogenesis and genetics of BTCs and animal modeling and relate these to recent and ongoing clinical trials with targeted agents.Entities:
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Year: 2010 PMID: 20547994 PMCID: PMC2982782 DOI: 10.1200/JCO.2009.27.4787
Source DB: PubMed Journal: J Clin Oncol ISSN: 0732-183X Impact factor: 44.544