Defining New Paradigms for the Treatment of Pancreatic Cancer

被引:32
作者
Almhanna, Khaldoun [1 ]
Philip, Philip A. [2 ]
机构
[1] H Lee Moffitt Canc Ctr & Res Inst, Dept Gastrointestinal Oncol, Tampa, FL 33612 USA
[2] Wayne State Univ, Karmanos Canc Inst, Dept Hematol & Oncol, Detroit, MI 48201 USA
关键词
GROWTH-FACTOR RECEPTOR; PHASE-III TRIAL; PLUS GEMCITABINE; SIGNALING PATHWAYS; CARCINOMA CELLS; STEM-CELLS; INHIBITION; APOPTOSIS; THERAPY; COMBINATION;
D O I
10.1007/s11864-011-0150-8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页码:111 / 125
页数:15
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