美国男性hpv相关口咽癌结局的种族/民族差异:一项国家队列研究

S. Villalona, A. Stroup, Satsuki Villalona, J. Ferrante
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引用次数: 1

摘要

背景:关于男性人乳头瘤病毒(HPV)相关口咽癌(OPC)发病率和结局的种族/民族差异知之甚少。我们评估了经年龄调整的hpv相关OPC男性发病率趋势、晚期诊断、生存率和癌症特异性死亡率(CSM)。方法:在这项基于人群的回顾性队列研究中,我们在北美中央癌症登记协会(NAACCR)中确定了2005年至2016年美国诊断为OPC的男性。分别使用多变量logistic和Cox比例风险分析比较种族/民族与晚期诊断、癌症特异性生存和死亡率的关系,调整年龄、健康保险、居住和贫困的县级属性、诊断阶段和美国的地理区域。结果:162183例hpv相关OPCs中,大多数为非西班牙裔(NH)白人男性(84.2%),2005年至2016年白人男性晚期癌症发病率增加50%。尽管与白人男性有相似的晚期诊断几率,西班牙裔和NH黑人男性的CSM更高[调整风险比(aHR) 1.17;95%置信区间(CI): 1.08, 1.26, aHR 1.79;95% CI分别为1.71,1.88]。经治疗调整后,西班牙裔和黑人男性的高死亡率有所减弱,但并未消除。结论:NH白人男性受晚期hpv相关OPC的影响不成比例,而西班牙裔和NH黑人男性有更高的CSM,这不能用分期或治疗方式来解释。需要采取干预措施,增加HPV疫苗的摄取,早期发现和治疗男性OPC,以减少发病率和死亡率的差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Racial/ethnic disparities in HPV-related oropharyngeal cancer outcomes among males in the United States: a national cohort study
Background: Little is known regarding differences in male human papillomavirus (HPV)-related oropharyngeal cancer (OPC) incidence and outcomes by race/ethnicity. We evaluated age-adjusted incidence trends, late-stage diagnosis, survival, and cancer-specific mortality (CSM) among males diagnosed with HPV-related OPC. Methods: In this population-based retrospective cohort study, we identified males diagnosed with OPC in the United States from 2005 to 2016 in the North American Association of Central Cancer Registries (NAACCR). Associations of race/ethnicity with late-stage diagnosis, cancer-specific survival, and mortality were compared using multivariable logistic and Cox proportional hazard analysis, respectively, adjusting for age, health insurance, county level attributes of residence and poverty, stage at diagnosis, and geographic region of the United States. Results: The majority of the 162,183 HPV-related OPCs were in non-Hispanic (NH) White males (84.2%), with 50% increase in late-stage cancer incidence among White males from 2005 to 2016. Despite having similar odds of late-stage diagnosis as White males, Hispanic and NH Black males had higher CSM [adjusted hazard ratios (aHR) 1.17; 95% confidence interval (CI): 1.08, 1.26, and aHR 1.79; 95% CI: 1.71, 1.88, respectively]. Adjusting for treatment attenuated, but did not eliminate, the higher mortality in Hispanic and Black males. Conclusions: NH White males are disproportionately affected by late-stage HPV-related OPC, while Hispanic and NH Black males have higher CSM that was not explained by stage or treatment modality. Interventions to increase HPV vaccine uptake, early detection, and treatment of OPC in males are needed to decrease disparities in incidence and mortality.
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