Literature DB >> 29254387

The evolution into personalized therapies in pancreatic ductal adenocarcinoma: challenges and opportunities.

Anteneh A Tesfaye1,2, Mandana Kamgar1,2, Asfar Azmi1,2, Philip A Philip1,2,3.   

Abstract

INTRODUCTION: Pancreatic ductal adenocarcinoma (PDAC) is projected to be the second leading cause of cancer related mortality in the United States in 2030, with a 5-year overall survival of less than 10% despite decades of extensive research. Pancreatic cancer is marked by the accumulation of complex molecular changes, complex tumor-stroma interaction, and an immunosuppressive tumor microenvironment. PDAC has proven to be resistant to many cytotoxic, targeted and immunologic treatment approaches. Areas covered: In this paper, we review the major areas of research in PDAC, with highlights on the challenges and areas of opportunity for personalized treatment approaches. Expert commentary: The focus of research in pancreatic cancer has moved away from developing conventional cytotoxic combinations. The marked advances in understanding the molecular biology of this disease especially in the areas of the microenvironment, metabolism, and DNA repair have opened new opportunities for developing novel treatment strategies. Improved understanding of molecular abnormalities allows the development of personalized treatment approaches.

Entities:  

Keywords:  DNA repair pathways; Targeted therapy; pancreas cancer; personalized therapy; tumor microenvironment

Mesh:

Year:  2017        PMID: 29254387      PMCID: PMC6121777          DOI: 10.1080/14737140.2018.1417844

Source DB:  PubMed          Journal:  Expert Rev Anticancer Ther        ISSN: 1473-7140            Impact factor:   4.512


  198 in total

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Review 1.  miRNA and Gene Expression in Pancreatic Ductal Adenocarcinoma.

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4.  The identification of candidate effective combination regimens for pancreatic cancer using the histoculture drug response assay.

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5.  The added value of intravoxel incoherent motion diffusion weighted imaging parameters in differentiating high-grade pancreatic neuroendocrine neoplasms from pancreatic ductal adenocarcinoma.

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6.  ERK Inhibition Improves Anti-PD-L1 Immune Checkpoint Blockade in Preclinical Pancreatic Ductal Adenocarcinoma.

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Review 7.  Natural killer cells in pancreatic cancer stroma.

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8.  Construction of a Competitive Endogenous RNA Network for Pancreatic Adenocarcinoma Based on Weighted Gene Co-expression Network Analysis and a Prognosis Model.

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