Current and Emerging Role of Monoclonal Antibody-Based First-Line Treatment in Advanced Gastro-Esophageal and Gastric Cancer

Curr Oncol. 2023 Oct 20;30(10):9304-9316. doi: 10.3390/curroncol30100672.

Abstract

Gastric cancer is the fifth most common malignancy worldwide and one of the main causes of cancer-related death. While surgical treatment is the only curative option for early disease, many have inoperable or advanced disease at diagnosis. Treatment in this case would be a combination of chemotherapy and immunotherapy. Gastro-esophageal (GEJ) and gastric cancer (GC) genetic profiling with current molecular diagnostic techniques has significantly changed the therapeutic landscape in advanced cancers. The identification of key players in GEJ and GC survival and proliferation, such as human epidermal growth factor 2 (HER2), vascular endothelial growth factor (VEGF), and programmed cell death protein 1 (PD-1)/programmed cell death ligand-1 (PD-L1), has allowed for the individualization of advanced cancer treatment and significant improvement in overall survival and progression-free survival of patients. This review comprehensively examines the current and emerging role of monoclonal antibody-based first-line treatments in advanced GEJ and GC. We explore the impact of monoclonal antibodies targeting HER2, VEGF, PD-1/PD-L1, and Claudin 18.2 (CLDN18.2) on the first-line treatment landscape by talking about key clinical trials. This review emphasizes the importance of biomarker testing for optimal treatment selection and provides practical recommendations based on ASCO guidelines.

Keywords: Claudin 18.2; advanced gastric cancer; immune-checkpoint inhibitors; monoclonal antibodies; targeted therapy; zolbetuximab.

Publication types

  • Review

MeSH terms

  • Antibodies, Monoclonal / therapeutic use
  • B7-H1 Antigen
  • Claudins / therapeutic use
  • Esophageal Neoplasms* / drug therapy
  • Humans
  • Programmed Cell Death 1 Receptor
  • Stomach Neoplasms* / drug therapy
  • Vascular Endothelial Growth Factor A / therapeutic use

Substances

  • Antibodies, Monoclonal
  • Programmed Cell Death 1 Receptor
  • Vascular Endothelial Growth Factor A
  • B7-H1 Antigen
  • CLDN18 protein, human
  • Claudins

Grants and funding

This research received no external funding.