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

Author:

Mirza Muhammad Bilal1ORCID,Choi Jungyoon2,Marincola Smith Paula1,Baechle Jordan J3,Padmanabhan Chandrasekhar1,Holowatyj Andreana N4,Shah Shailja C56,Guo Xingyi7ORCID,Idrees Kamran1ORCID

Affiliation:

1. Division of Surgical Oncology and Endocrine Surgery, Department of Surgery, Vanderbilt University Medical Center , Nashville, TN, USA

2. Division of Oncology/Hematology, Department of Internal Medicine, Korea University Ansan Hospital, Korea University College of Medicine , Ansan, Republic of Korea

3. Department of Bioengineering and Therapeutic Sciences, University of California San Francisco , San Francisco, CA, USA

4. Department of Medicine, Vanderbilt University Medical Center, Vanderbilt-Ingram Cancer Center , Nashville, TN, USA

5. GI Section, VA San Diego Health System , La Jolla, CA, USA

6. Division of Gastroenterology, Department of Medicine, University of California , San Diego, CA, USA

7. Department of Biomedical Informatics, Department of Medicine, Vanderbilt Epidemiology Center, and Vanderbilt-Ingram Cancer Center , Nashville, TN, USA

Abstract

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.

Funder

National Institutes of Health

NIH/National Cancer Institute

Publisher

Oxford University Press (OUP)

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