Department of Gastrointestinal Oncolgy, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL 33612, USA.
Curr Treat Options Oncol. 2011 Jun;12(2):111-25. doi: 10.1007/s11864-011-0150-8.
Pancreatic cancer (PC) is the fourth leading cause of cancer death in the United States. Despite significant improvement in understanding disease biology, the 5-year survival rates remain less than 5%. Targeted agents failed to add any meaningful survival benefit in this patient population despite very promising pre-clinical data. The new paradigm for the treatment of PC must emphasize validation of targeted agents in the appropriate pre-clinical models, identification of predictive markers for disease response, and extending range of targets into cancer stem cells and tumor microenvironment. It is also necessary to perform studies that are designed to address the various stages of disease with respect to study endpoints and application of a multimodality approach in management. Phase III trials should only be considered when a strong efficacy signal is demonstrated in phase II studies that is based on a survival endpoint. This review will focus on the development of novel treatments in pancreas cancer and the proposed design of future clinical trials.
胰腺癌(PC)是美国第四大致癌死亡原因。尽管对疾病生物学的认识有了显著提高,但 5 年生存率仍低于 5%。尽管有非常有前景的临床前数据,但靶向药物并不能为这一患者群体带来任何有意义的生存获益。治疗 PC 的新模式必须强调在适当的临床前模型中验证靶向药物,确定疾病反应的预测标志物,并将目标范围扩展到癌症干细胞和肿瘤微环境。还需要进行旨在针对疾病的各个阶段进行研究的研究,包括研究终点和多模式管理方法的应用。只有在基于生存终点的 II 期研究中显示出强大的疗效信号时,才应考虑进行 III 期试验。本综述将重点介绍胰腺癌的新型治疗方法的开发以及未来临床试验的建议设计。