Role of modern immunotherapy in gastrointestinal malignancies: a review of current clinical progress

J Hematol Oncol. 2017 Apr 24;10(1):86. doi: 10.1186/s13045-017-0454-7.

Abstract

Gastrointestinal (GI) cancers are a group of highly aggressive malignancies with a huge disease burden worldwide. There is clearly a significant unmet need for new drugs and therapies to further improve the treatment outcomes of GI malignancies. Immunotherapy is a novel treatment strategy that is emerging as an effective and promising treatment option against several types of cancers. CTLA-4 and PD-1 are critical immune checkpoint molecules that negatively regulate T cell activation via distinct mechanisms. Immune checkpoint blockade with antibodies directed against these pathways has already shown clinical efficacy that has led to their FDA approval in the treatment of several solid tumors including melanoma, non-small cell lung cancer, renal cell carcinoma, urothelial carcinoma, and head and neck cancer. This review will summarize the current clinical progress of modern immunotherapy in the field of GI tumors, with a special focus on immune checkpoint blockade.

Keywords: CTLA-4; Colorectal cancer; Esophageal cancer; Gastric cancer; Gastrointestinal cancers; Hepatocellular carcinoma; Immune checkpoint blockade; Immunotherapy; PD-1; PD-L1; Pancreatic cancer.

Publication types

  • Review

MeSH terms

  • Antineoplastic Agents, Immunological / therapeutic use*
  • B7-H1 Antigen / analysis
  • B7-H1 Antigen / antagonists & inhibitors
  • CTLA-4 Antigen / analysis
  • CTLA-4 Antigen / antagonists & inhibitors
  • Cancer Vaccines / therapeutic use
  • Carcinoma, Pancreatic Ductal / therapy
  • Clinical Trials as Topic
  • Digestive System Neoplasms / immunology
  • Digestive System Neoplasms / therapy*
  • Esophageal Neoplasms / therapy
  • Gastrointestinal Neoplasms / therapy
  • Humans
  • Immunotherapy*
  • Molecular Targeted Therapy
  • Neoplasm Proteins / analysis
  • Neoplasm Proteins / antagonists & inhibitors
  • Pancreatic Neoplasms / therapy
  • Programmed Cell Death 1 Receptor / analysis
  • Programmed Cell Death 1 Receptor / antagonists & inhibitors

Substances

  • Antineoplastic Agents, Immunological
  • B7-H1 Antigen
  • CD274 protein, human
  • CTLA-4 Antigen
  • Cancer Vaccines
  • Neoplasm Proteins
  • PDCD1 protein, human
  • Programmed Cell Death 1 Receptor