Asian Americans and prostate cancer: A nationwide population-based analysis

Abstract Introduction It remains largely unknown if there are racial disparities in outcomes of prostate cancer (PCa) for Asian American and Pacific Islanders (PIs) (AAPIs). We examined differences in diagnosis, management, and survival of AAPI ethnic groups, relative to their non-Hispanic White (NH...

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Veröffentlicht in:Urologic oncology 2016-05, Vol.34 (5), p.233.e7-233.e15
Hauptverfasser: Chao, Grace F., B.A, Krishna, Nandita, B.A, Aizer, Ayal A., M.D., M.H.S, Dalela, Deepansh, M.D, Hanske, Julian, M.D, Li, Hanhan, M.D, Meyer, Christian P., M.D, Kim, Simon P., M.D, Mahal, Brandon A., M.D, Reznor, Gally, M.S, Schmid, Marianne, M.D, Choueiri, Toni K., M.D, Nguyen, Paul L., M.D, O׳Leary, Michael, M.D., M.P.H, Trinh, Quoc-Dien, M.D
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Sprache:eng
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Zusammenfassung:Abstract Introduction It remains largely unknown if there are racial disparities in outcomes of prostate cancer (PCa) for Asian American and Pacific Islanders (PIs) (AAPIs). We examined differences in diagnosis, management, and survival of AAPI ethnic groups, relative to their non-Hispanic White (NHW) counterparts. Methods Patients ( n = 891,100) with PCa diagnosed between 1988 and 2010 within the surveillance, epidemiology, and end results database were extracted and stratified by ethnic group: Chinese, Japanese, Filipino, Hawaiian, Korean, Vietnamese, Asian Indian/Pakistani, PI, and Other Asian. The effect of ethnic group on stage at presentation, rates of definitive treatment, and PCa-specific mortality was assessed. The severity at diagnosis was defined as: localized (TxN0M0), regional (TxN1M0), or metastatic (TxNxM1). Results Relative to NHWs, Asian Indian/Pakistani, Filipino, Hawaiian, and PI men had significantly worse outcomes. Filipino (odds ratio [OR] = 1.38, 95% CI: 1.27–1.51), Hawaiian, (OR = 1.70, 95% CI: 1.41–2.04), Asian Indian/Pakistani (OR = 1.37, 95% CI: 1.15–1.64), and PI men (OR = 1.90, 95% CI: 1.46–2.49) were more likely to present with metastatic PCa ( P
ISSN:1078-1439
1873-2496
DOI:10.1016/j.urolonc.2015.11.013