Yang Jennifer, Farren Matthew R, Ahn Daniel, Bekaii-Saab Tanios, Lesinski Gregory B
a Molecular Cellular and Developmental Biology Graduate Program , The Ohio State University , Columbus , OH , USA.
b Department of Hematology and Medical Oncology , The Winship Cancer Institute of Emory University , Atlanta , GA , USA.
Expert Opin Ther Targets. 2017 May;21(5):485-498. doi: 10.1080/14728222.2017.1306055. Epub 2017 Mar 17.
The incidence of biliary tract cancer (BTC) is increasing, and the disease is frequently diagnosed during advanced stages, leading to poor overall survival. Limited treatment options are currently available and novel therapeutic approaches are needed. A number of completed clinical trials have evaluated the role of chemotherapy for BTC, demonstrating a marginal benefit. Thus, there is increased interest in applying targeted therapies for this disease. Areas covered: This review article summarizes the role of chemotherapeutic regimens for the treatment of BTC, and highlights key signal transduction pathways of interest for targeted inhibition. Of particular interest are the MEK or MAP2K (mitogen-activated protein kinase kinase), phosphatidylinositol-3 kinase (PI3K) and signal transducer and activator of transcription-3 (STAT3) pathways. We discuss the available data on several promising inhibitors of these pathways, both in the pre-clinical and clinical settings. Expert opinion: Future treatment strategies should address targeting of MEK, PI3K and STAT3 for BTC, with a focus on combined therapeutic approaches.
胆道癌(BTC)的发病率正在上升,且该疾病常在晚期被诊断出来,导致总体生存率较低。目前可用的治疗选择有限,需要新的治疗方法。一些已完成的临床试验评估了化疗在BTC治疗中的作用,显示出一定的益处。因此,人们对将靶向治疗应用于该疾病的兴趣日益增加。涵盖领域:本文综述总结了化疗方案在BTC治疗中的作用,并强调了靶向抑制感兴趣的关键信号转导通路。特别值得关注的是MEK或MAP2K(丝裂原活化蛋白激酶激酶)、磷脂酰肌醇-3激酶(PI3K)和信号转导及转录激活因子3(STAT3)通路。我们讨论了在临床前和临床环境中关于这些通路几种有前景的抑制剂的现有数据。专家意见:未来的治疗策略应针对BTC靶向MEK、PI3K和STAT3,重点是联合治疗方法。