Targeting tumor tolerance: A new hope for pancreatic cancer therapy?

被引:27
作者
Delitto, Daniel [1 ]
Wallet, Shannon M. [2 ]
Hughes, Steven J. [1 ]
机构
[1] Univ Florida, Dept Surg, Gainesville, FL USA
[2] Univ Florida, Dept Oral Biol, Gainesville, FL 32610 USA
关键词
Pancreatic cancer; Immunotherapy; Immune modulation; Cancer immunology; Tumor-associated stroma; Innate immunity; T-CELL RESPONSES; COLONY-STIMULATING FACTOR; FIBROBLAST ACTIVATION PROTEIN; MYELOID SUPPRESSOR-CELLS; BRUTONS TYROSINE KINASE; FAS LIGAND EXPRESSION; NATURAL-KILLER-CELLS; LONG-TERM SAFETY; PHASE-I TRIAL; GM-CSF GENE;
D O I
10.1016/j.pharmthera.2016.06.008
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
With a 5-year survival rate of just 8%, pancreatic cancer (PC) is projected to be the second leading cause of cancer deaths by 2030. Most PC patients are not eligible for surgery with curative intent upon diagnosis, emphasizing a need for more effective therapies. However, PC is notoriously resistant to chemoradiation regimens. As an alternative, immune modulating strategies have recently achieved success in melanoma, prompting their application to other solid tumors. For such therapeutic approaches to succeed, a state of immunologic tolerance must be reversed in the tumor microenvironment and that has been especially challenging in PC. Nonetheless, knowledge of the PC immune microenvironment has advanced considerably over the past decade, yielding new insights and perspectives to guide multimodal therapies. In this review, we catalog the historical groundwork and discuss the evolution of the cancer immunology field to its present state with a specific focus on PC. Strategies currently employing immune modulation in PC are reviewed, specifically highlighting 66 clinical trials across the United States and Europe. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:9 / 29
页数:21
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