Molecular classification as prognostic factor and guide for treatment decision of pancreatic cancer

Biochim Biophys Acta Rev Cancer. 2018 Apr;1869(2):248-255. doi: 10.1016/j.bbcan.2018.02.001. Epub 2018 Feb 28.

Abstract

Clinico-pathological factors fail to consistently predict the outcome after pancreatic resection for pancreatic ductal adenocarcinoma (PDAC). PDACs show a high level of inter- and intra- tumor genetic heterogeneity. A molecular classification should help sort patients into less heterogeneous and more appropriate groups regarding the metastatic risk and the therapeutic response, with the consequences of better predicting evolution and better orienting the treatment. PDAC can be classified based on mutational subtypes and 18gene alterations. Whole-genome sequencing identified mutational signatures, mutational burden and hyper-mutated tumors with specific DNA repair defects. Their overlap/similarities allow the definition of molecular subtypes. DNA and RNA classifications can be used in prognosis assessment. They are useful in therapeutic choice for they allow the design of approaches that can predict the respective drug sensitivity of each molecular subtype. This review provides a comprehensive analysis of available molecular classifications in PDAC and how this can help guide clinical decisions.

Keywords: Expression profiling; Genomic alteration; Pancreatic cancer; Personalized medicine; Prognosis; Survival.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Antineoplastic Agents / therapeutic use*
  • Biomarkers, Tumor / metabolism*
  • Carcinoma, Pancreatic Ductal / classification
  • Carcinoma, Pancreatic Ductal / drug therapy*
  • Carcinoma, Pancreatic Ductal / genetics*
  • Carcinoma, Pancreatic Ductal / pathology
  • Clinical Decision-Making
  • DNA Mutational Analysis
  • Gene Expression Profiling
  • Gene Expression Regulation
  • Genetic Heterogeneity
  • Genetic Predisposition to Disease
  • Humans
  • Molecular Diagnostic Techniques*
  • Molecular Targeted Therapy
  • Mutation
  • Pancreatic Neoplasms / classification
  • Pancreatic Neoplasms / drug therapy*
  • Pancreatic Neoplasms / genetics*
  • Pancreatic Neoplasms / pathology
  • Phenotype
  • Precision Medicine*
  • Predictive Value of Tests
  • Transcriptome

Substances

  • Antineoplastic Agents
  • Biomarkers, Tumor