James P Wilmot Cancer Center, University of Rochester School of Medicine, Rochester, NY 14642, USA.
J Clin Oncol. 2010 Jul 20;28(21):3531-40. doi: 10.1200/JCO.2009.27.4787. Epub 2010 Jun 14.
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.
胆道癌(BTC)包括肝内和肝外胆管癌以及胆囊癌,是一组具有遗传异质性的癌症。有证据表明存在不同的分子和病理进展模式,越来越多的遗传学数据表明关键癌基因和肿瘤抑制基因的潜在突变具有异质性。尽管肿瘤遗传学已被用于针对个体治疗方案,并指导其他癌症的临床决策,但这些原则尚未应用于 BTC。最近针对靶向治疗的临床试验似乎很有希望,尽管对治疗有阳性反应的患者亚组与肿瘤遗传学之间的关系仍有待探索。在这里,我们总结了 BTC 的分子发病机制和遗传学,以及动物模型,并将其与最近和正在进行的靶向药物临床试验相关联。