Predictive biomarkers for the treatment of resectable esophageal and esophago-gastric junction adenocarcinoma: from hypothesis generation to clinical validation

Expert Rev Mol Diagn. 2018 Apr;18(4):357-370. doi: 10.1080/14737159.2018.1454312. Epub 2018 Mar 21.

Abstract

Esophageal and esophago-gastric junction (EGJ) adenocarcinomas remain a major health problem worldwide with a worryingly increasing incidence. Recent trials indicate survivals benefit for preoperative or perioperative chemoradiotherapy compared to surgery alone. Beside standard chemoradiotherapy regimens, new therapeutic approaches with targeted therapies have been proposed for the treatment of resectable disease. However, clinical outcomes remain extremely poor due to drug resistance phenomena. The failure of these approaches could be partially ascribed to their incorrect application in patients. Therefore, the identification of strong biomarkers for optimal patient management is urgently needed. Areas covered: This review aims to summarize and critically discuss the most relevant findings regarding predictive biomarker development for neoadjuvant treatment of resectable esophageal and esophago-gastric junction adenocarcinoma patients. Expert commentary: Optimizing the currently available therapeutic modalities through a more accurate selection of patients may avoid the use of ineffective and potentially toxic treatments. During the last decade, the advent of high-throughput '-omics' technologies has set the basis for a new biomarker discovery approach from 'molecule by molecule' screening towards a large-scale systematic screening process with exponential increases in putative biomarkers, which often failed to provide adequate clinical validation.

Keywords: Esophageal adenocarcinoma; esophago-gastric junction adenocarcinoma; gastric adenocarcinoma; neoadjuvant therapy; predictive biomarker.

Publication types

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

MeSH terms

  • Adenocarcinoma / genetics
  • Adenocarcinoma / metabolism
  • Adenocarcinoma / surgery
  • Adenocarcinoma / therapy*
  • Adipokines / genetics
  • Adipokines / metabolism
  • Biomarkers, Tumor / genetics
  • Biomarkers, Tumor / metabolism*
  • Combined Modality Therapy
  • Drug Resistance, Neoplasm
  • Esophageal Neoplasms / genetics
  • Esophageal Neoplasms / metabolism
  • Esophageal Neoplasms / surgery
  • Esophageal Neoplasms / therapy*
  • Esophagogastric Junction
  • Humans
  • Inactivation, Metabolic / genetics
  • Lymphocytes, Tumor-Infiltrating / immunology
  • Neoadjuvant Therapy
  • Neoplastic Stem Cells / drug effects
  • Neoplastic Stem Cells / radiation effects
  • Receptor Protein-Tyrosine Kinases / genetics
  • Transcriptome

Substances

  • Adipokines
  • Biomarkers, Tumor
  • Receptor Protein-Tyrosine Kinases