Published online Jul 14, 2016. doi: 10.3748/wjg.v22.i26.5896
Peer-review started: March 18, 2016
First decision: May 12, 2016
Revised: May 25, 2016
Accepted: June 13, 2016
Article in press: June 13, 2016
Published online: July 14, 2016
Processing time: 113 Days and 16.4 Hours
Gastric cancer (GC) is a global health problem and a major cause of cancer-related death with high recurrence rates ranging from 25% to 40% for GC patients staging II-IV. Unfortunately, while the majority of GC patients usually present with advanced tumor stage; there is still limited evidence-based therapeutic options. Current approach to GC management consists mainly of; endoscopy followed by, gastrectomy and chemotherapy or chemo-radiotherapy. Recent studies in GC have confirmed that it is a heterogeneous disease. Many molecular characterization studies have been performed in GC. Recent discoveries of the molecular pathways underlying the disease have opened the door to more personalized treatment and better predictable outcome. The identification of molecular markers is a useful tool for clinical managementin GC patients, assisting in diagnosis, evaluation of response to treatment and development of novel therapeutic modalities. While chemotherapeutic agents have certain physiological effects on the tumor cells, the prediction of the response is different from one type of tumor to the other. The specificity of molecular biomarkers is a principal feature driving their application in anticancer therapies. Here we are trying to focus on the role of molecular pathways of GC and well-established molecular markers that can guide the therapeutic management.
Core tip: We tried to highlight the role of molecular biomarkers as a predictor to chemotherapeutic response to existing regimens, aiming for better personalized therapy. Also we provided a summary of molecular markers that may aid in the development of rational therapeutic options for gastric cancer (GC) patients, aiming for improving their outcomes. However, among the plethora of agents targeting VEGF, EGFR, HER-2, IGF and mTOR pathways, trastuzumab and ramucirumab have been the only approved therapeutic options for use in advanced GC. Despite having many promising studies in their early stages, a lot have failed to prove their effectiveness in GC on the long run.