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Hepatocellular Carcinoma in Pacific Islanders: Comparison of Pacific Island-born . US-born

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Journal Hepatoma Res
Date 2023 Apr 10
PMID 37035453
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Abstract

Aim: To describe demographic, clinical, and outcome differences in Pacific Island-born (PI-born) compared to US-born hepatocellular carcinoma (HCC) patients of Pacific Island ancestry within a clinical cohort in Hawaii.

Methods: A prospectively collected database of 1608 patients diagnosed with HCC over a 30-year period (1993-2022) identified 252 patients of Pacific Islander ethnicity. Data collected: demographics, medical history, laboratory data, tumor characteristics, treatment, and survival. Patients were divided into two groups: PI-born and US-born. Categorical variables were analyzed using ANOVA and chi-square analysis. Odds ratios with 95% confidence intervals were calculated using univariate and multivariate logistic regression. Overall survival was evaluated using Kaplan-Meier analysis.

Results: PI-born patients were younger (57.3 . 61.8 years, = 0.002) and more likely to have hepatitis B (OR 14.10, 7.50-26.50) and underlying cirrhosis (OR 2.28, 1.17-4.45). In comparison, US-born patients had a significantly higher likelihood of Hepatitis C, nonalcoholic steatohepatitis/nonalcoholic fatty liver disease, history of non-HCC cancer, and positive smoking history compared to PI-born patients. PI-born patients were more likely to forego treatment (OR 3.22, 1.77-5.87) and be lost to follow-up (OR 9.21, 1.97-43.03). Both groups were equally likely to have the opportunity for curative surgical treatment (liver resection or transplant). US-born status was associated with higher mortality risk, while transplantation was associated with lower mortality risk. The PI-born cohort demonstrated higher overall survival at 3 and 5 years compared to US-born.

Conclusion: HBV remains the primary risk factor for HCC in PI-born patients, whereas HCC in US-born patients is more associated with the adoption of a Westernized lifestyle.

References
1.
Sliz E, Sebert S, Wurtz P, Kangas A, Soininen P, Lehtimaki T . NAFLD risk alleles in PNPLA3, TM6SF2, GCKR and LYPLAL1 show divergent metabolic effects. Hum Mol Genet. 2018; 27(12):2214-2223. PMC: 5985737. DOI: 10.1093/hmg/ddy124. View

2.
Younossi Z . Non-alcoholic fatty liver disease - A global public health perspective. J Hepatol. 2018; 70(3):531-544. DOI: 10.1016/j.jhep.2018.10.033. View

3.
Kessaram T, McKenzie J, Girin N, Roth A, Vivili P, Williams G . Alcohol use in the Pacific region: Results from the STEPwise approach to surveillance, Global School-Based Student Health Survey and Youth Risk Behavior Surveillance System. Drug Alcohol Rev. 2015; 35(4):412-23. PMC: 5049666. DOI: 10.1111/dar.12328. View

4.
Abara W, Collier M, Teshale E . Impact of universal infant hepatitis B vaccination in the US-affiliated Pacific Islands, 1985-2015. Vaccine. 2017; 35(7):997-1000. PMC: 10168596. DOI: 10.1016/j.vaccine.2017.01.020. View

5.
Harlan L, Parsons H, Wiggins C, Stevens J, Patt Y . Treatment of hepatocellular carcinoma in the community: disparities in standard therapy. Liver Cancer. 2015; 4(1):70-83. PMC: 4439839. DOI: 10.1159/000367729. View