Toward the Goal of Personalized Therapy in Pancreatic Cancer by Targeting the Molecular Phenotype

被引:13
|
作者
Yee, Nelson S. [1 ,2 ]
机构
[1] Penn State Univ, Milton S Hershey Med Ctr, Div Hematol Oncol,Dept Med, Penn State Coll Med,Penn State Hershey Canc Inst, Hershey, PA 17033 USA
[2] Milton S Hershey Med Ctr, Penn State Hershey Canc Inst, Hershey, PA 17033 USA
关键词
Pancreatic cancer; Genetic targets; Biomarkers; Personalized therapy; EPIDERMAL-GROWTH-FACTOR; PHASE-III TRIAL; MATRIX-METALLOPROTEINASE INHIBITION; HISTONE DEACETYLASE INHIBITOR; DEPENDENT KINASE INHIBITOR; GEMCITABINE PLUS PLACEBO; FACTOR RECEPTOR; IN-VITRO; EXOCRINE PANCREAS; TUMOR-GROWTH;
D O I
10.1007/978-1-4614-6176-0_5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The purpose of this article is to provide a critical review of the molecular alterations in pancreatic cancer that are clinically investigated as therapeutic targets and their potential impact on clinical outcomes. Adenocarcinoma of exocrine pancreas is generally associated with poor prognosis and the conventional therapies are marginally effective. Advances in understanding the genetic regulation of normal and neoplastic development of pancreas have led to development and clinical evaluation of new therapeutic strategies that target the signaling pathways and molecular alterations in pancreatic cancer. Applications have begun to utilize the genetic targets as biomarkers for prediction of therapeutic responses and selection of treatment options. The goal of accomplishing personalized tumor-specific therapy with tolerable side effects for patients with pancreatic cancer is hopefully within reach in the foreseeable future.
引用
收藏
页码:91 / 143
页数:53
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