A retrospective analysis of tissue, liquid, and germline testing in Hispanic and non-Hispanic men with advanced hormone-sensitive prostate cancer
- 1Department of Medicine, University of Arizona, Tucson, AZ.
- 2Division of Allergy, Asthma, and Clinical Immunology, Department of Medicine, Mayo Clinic, Scottsdale, AZ.
- 3University of Arizona Cancer Center, Tucson, AZ.
- 4Department of Surgery, University of Arizona, Tucson, AZ; University of Arizona Cancer Center, Tucson, AZ.
- 5Cancer Prevention & Control, Roswell Park Comprehensive Cancer Center, Buffalo, NY.
- 6Department of Urology, University of Arizona, Tucson, AZ.
- 0Department of Medicine, University of Arizona, Tucson, AZ.
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View abstract on PubMed
Summary
This summary is machine-generated.Hispanic American men with prostate cancer (PCa) present with more advanced disease and distinct genomic mutations, including TMPRSS2-ERG fusion and TMB-High. These findings underscore the need for tailored screening and treatment strategies for this underrepresented group.
Area Of Science
- Oncology
- Genomics
- Health Disparities
Background
- Prostate cancer (PCa) significantly impacts American men, with notable racial and ethnic disparities.
- Hispanic Americans (HAs) are underrepresented in PCa genomic research despite their disease burden.
Purpose Of The Study
- To investigate genomic differences in prostate cancer between Hispanic Americans (HAs) and Non-Hispanics (NHs).
- To understand the drivers of health disparities in PCa within the underrepresented HA population.
Main Methods
- Retrospective analysis of 111 metastatic prostate adenocarcinoma patients (2015-2023).
- Genomic data from tissue, liquid, and germline samples compared between HA and NH patient cohorts.
- Statistical analysis included t-tests, Kruskal-Wallis, Chi-square, Fisher's exact tests, and Kaplan-Meier methods.
Main Results
- Hispanic Americans (HAs) represented 41% of the study cohort.
- HAs exhibited higher PSA levels, more advanced pathological stages (T4, M1c), and shorter time to first-line treatment.
- TMPRSS2-ERG fusion and TMB-High mutations were significantly more prevalent in HAs.
Conclusions
- Hispanic American PCa patients present with more advanced disease compared to Non-Hispanics.
- Genomic disparities, including TMPRSS2-ERG fusion and TMB-High mutations, necessitate early detection and personalized treatments for HAs.
- Expanding genomic research and addressing treatment disparities are critical for improving outcomes in this underrepresented population.
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