ERBB2 amplification in gastric cancer: a genomic insight into ethnic disparities

J Natl Cancer Inst. 2024 Nov 1;116(11):1830-1833. doi: 10.1093/jnci/djae147.

Abstract

Overall, gastric adenocarcinoma (GC) incidence rates have declined in recent years, but racial and ethnic disparities persist. Individuals who identify as Hispanic/Spanish/Latino are diagnosed with GC at younger ages and have poorer outcomes than non-Hispanic individuals. However, our understanding of GC biology across racial/ethnic groups remains limited. We assessed tumor genomic patterns by race/ethnicity among 1019 patients with primary GC in the American Association for Cancer Research (AACR) Project GENIE Consortium. Hispanic individuals presented with significantly higher rates of ERBB2/HER2 amplification vs other racial/ethnic groups (Hispanic: 13.9% vs 9.8% non-Hispanic White, 8.1% non-Hispanic Asian, and 11.0% non-Hispanic Black; P < .001, FDR adjusted q < 0.001). Hispanic patients also had higher odds of an ERBB2 amplification vs non-Hispanic Whites in adjusted models (OR = 2.52, 95%CI = 1.20 to 5.33, P = .015). These findings underscore the important role of genomic factors in GC disparities. Ensuring equitable access to genomic profiling and targeted therapies, such as trastuzumab for HER2-overexpressing GC, is a promising avenue to mitigate GC disparities and improve outcomes.

MeSH terms

  • Adenocarcinoma / ethnology
  • Adenocarcinoma / genetics
  • Adult
  • Aged
  • Black or African American / genetics
  • Ethnicity / genetics
  • Female
  • Gene Amplification*
  • Genomics
  • Health Status Disparities*
  • Hispanic or Latino / genetics
  • Humans
  • Male
  • Middle Aged
  • Receptor, ErbB-2* / genetics
  • Receptor, ErbB-2* / metabolism
  • Stomach Neoplasms* / ethnology
  • Stomach Neoplasms* / genetics
  • United States / epidemiology
  • White / genetics

Substances

  • ERBB2 protein, human
  • Receptor, ErbB-2