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. 2025 Mar;135(3):1113-1119.
doi: 10.1002/lary.31907. Epub 2024 Nov 16.

Nasopharynx Cancer in the United States: Racial and Ethnic Disparities in Stage at Presentation

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Nasopharynx Cancer in the United States: Racial and Ethnic Disparities in Stage at Presentation

Edward Christopher Dee et al. Laryngoscope. 2025 Mar.

Abstract

Introduction: Although nasopharynx cancer (NPC) is rare in the United States, global epidemiology varies greatly. Therefore, understanding NPC disparities in the diverse US setting is critical.

Methods and materials: Data from the National Cancer Database (NCDB, 2004-2021) identified patients with NPC; NCDB allows disaggregation by Asian American (AA) subgroups. Multivariable ordinal logistic regression adjusting for demographic and socioeconomic factors defined adjusted odds ratios (aORs).

Results: Of 15,862 patients, 11,173 (70.4%) were male (median age 59). Commonest groups included 10,034 (63.3%) White, 2,272 (14.3%) Black, 1,103 (7.0%) Chinese, 442 (2.8%) Filipino, and 338 (2.1%) Vietnamese patients. Prior to disaggregation, the proportion of stage IV disease at presentation was 43.2% among White (ref), 50.0% among Black (aOR 1.12, p = 0.012), 52.0% among Native American (aOR 1.18, p > 0.05), 41.9% among AA (aOR 0.97, p > 0.05), and 55.1% among Native Hawaiian and Other Pacific Islander patients (aOR 1.47, p = 0.021). Upon disaggregation, the proportion of stage IV disease was the greatest (>50%) among Black (50.0%, aOR 1.12, p = 0.012), Laotian (61.5%, aOR 2.21, p = 0.001), Hmong (73.2%, aOR 2.92, p < 0.001), and Other Pacific Islander patients (60.9%, aOR 1.83, p = 0.004); 44.2% of Filipino patients also presented with stage IV disease (aOR 1.21, p = 0.033). Odds of presenting with advanced stage disease were lower among Chinese patients (35.7% stage IV, aOR 0.72, p < 0.001).

Conclusions: Although most NPC patients were Chinese, White, or Black, stage IV disease at presentation was most common among Hmong, Laotian, non-Hawaiian Pacific Islander, and Black patients. Efforts are needed to improve awareness of NPC among less canonically affected groups.

Level of evidence: 4 Laryngoscope, 135:1113-1119, 2025.

Keywords: cancer disparities; head and neck cancer; health services; nasopharyngeal cancer; nasopharynx cancer; racial disparities.

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Conflict of interest statement

AUTHOR DISCLOSURES: The authors have no conflicts of interest to declare.

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References

    1. Chang ET, Ye W, Zeng YX, Adami HO. The Evolving Epidemiology of Nasopharyngeal Carcinoma. Cancer Epidemiol Biomarkers Prev. 2021;30(6):1035–1047. doi: 10.1158/1055-9965.EPI-20-1702 - DOI - PubMed
    1. Nasopharyngeal Cancer Survival Rates | American Cancer Society. Accessed June 29, 2024. https://www.cancer.org/cancer/types/nasopharyngeal-cancer/detection-diag...
    1. Li WZ, Lv SH, Liu GY, Liang H, Xia WX, Xiang YQ. Age-dependent changes of gender disparities in nasopharyngeal carcinoma survival. Biol Sex Differ. 2021;12:18. doi: 10.1186/s13293-021-00361-8 - DOI - PMC - PubMed
    1. Mahdavifar N, Ghoncheh M, Mohammadian-Hafshejani A, Khosravi B, Salehiniya H. Epidemiology and Inequality in the Incidence and Mortality of Nasopharynx Cancer in Asia. Osong Public Health Res Perspect. 2016;7(6):360–372. doi: 10.1016/j.phrp.2016.11.002 - DOI - PMC - PubMed
    1. Ji X, Zhang W, Xie C, Wang B, Zhang G, Zhou F. Nasopharyngeal carcinoma risk by histologic type in central China: impact of smoking, alcohol and family history. Int J Cancer. 2011;129(3):724–732. doi: 10.1002/ijc.25696 - DOI - PubMed

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