疑似前列腺癌转诊和诊断在伦敦东北部的社会人口景观

IF 1.6 Q3 UROLOGY & NEPHROLOGY
BJUI compass Pub Date : 2025-02-04 DOI:10.1002/bco2.495
Muhammad Haider, Jeffrey J. Leow, James S. A. Green, Chamkhor Dhillon, Angela S. Wong, Yin Zhou, Sara Paparini, Benjamin W. Lamb, Prabhakar Rajan, for the North East London Cancer Alliance Urology Expert Reference Group
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引用次数: 0

摘要

本研究的目的是确定在一个种族多样化和社会贫困的大城市地区,转诊和诊断疑似前列腺癌(PCa)的医疗保健不公平。方法回顾性队列研究2019年2月至2023年8月在伦敦东北部(NEL)两家急性NHS信托机构就诊的2周等待(2WW)疑似PCa患者(n = 1247)。从患者记录中收集社会人口统计学、诊断和预处理分期数据。我们检查了转诊和诊断统计数据、转诊时的年龄、诊断时的放射学t期、按种族划分的剥夺程度,以及COVID-19大流行封锁对按种族和诊断时t期划分的转诊和诊断比例的影响。采用单变量和多变量logistic回归来确定局部晚期(t期≥T3)疾病的预测因素。结果在所有转诊患者中,22%被诊断为前列腺癌。在COVID封锁期间与非封锁期间,按种族划分的PCa转诊、诊断或t分期无统计学差异(p > 0.05)。与其他种族的男性相比,黑人男性(来自英国黑人、非洲黑人和加勒比黑人族群)被诊断为较年轻(平均65岁),年龄调整后的PCa发病率最高,为每10万人年149例,来自最贫困的背景,被诊断为局部PCa的比例最高(74%)。患者亚组的多变量分析显示,71-80岁(OR 2.01, 95% CI 1.31-3.07)和80岁(OR 4.27, 95% CI 2.25-8.08)是局部晚期前列腺癌的独立阳性预测因子,黑人种族是局部疾病的独立预测因子(OR 0.66, 95% CI 0.43-1.00)。本研究的局限性包括排除了在2WW途径之外诊断的PCa病例,以及缺少前列腺特异性抗原(PSA)水平、远处放射学分期和组织病理学结果的数据。结论:在NEL的黑人男性中,我们发现了PCa发病率、分期、发病年龄以及社会经济剥夺方面的差异。需要有针对性的努力来缓解这些医疗不公平现象。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Sociodemographic landscape of suspected prostate cancer referrals and diagnoses across North East London

Sociodemographic landscape of suspected prostate cancer referrals and diagnoses across North East London

Objectives

The objective of this study is to identify healthcare inequities in referrals and diagnoses of suspected prostate cancer (PCa) in an ethnically diverse and socially deprived large urban region.

Methods

Retrospective cohort study of 2-Week Wait (2WW) suspected PCa patients (n = 12 947) referred to two acute NHS Trusts in North East London (NEL) from February 2019 to August 2023. Sociodemographics, diagnosis and pretreatment staging data were collected from patient records. We examined referral and diagnosis statistics, age at referral, radiological T-stage at diagnosis, levels of deprivation by ethnicity and the impact of COVID-19 pandemic lockdowns on proportion of referrals and diagnoses by ethnicity and T-stage at diagnosis. Uni- and multivariable logistic regression was performed to identify predictors of locally advanced (T-stage ≥T3) disease.

Results

Of all referrals, 22% were diagnosed with PCa. There were no statistically significant differences in referrals, diagnoses or T-stage of PCa by ethnicity during COVID lockdown versus non-lockdown periods (p > 0.05). Compared to men from any other ethnicity, Black men (from Black British, Black African and Black Caribbean ethnic groups) were diagnosed at a younger age (mean = 65 years), had the highest age-adjusted PCa incidence rate of 149 per 100 000 person-years, were from the most deprived backgrounds, and were diagnosed with the highest proportion of localised PCa (74%). Multivariable analysis of a patient subgroup revealed age bands 71–80 years (OR 2.01, 95% CI 1.31–3.07) and >80 (OR 4.27, 95% CI 2.25–8.08) as independent positive predictors of locally advanced PCa, and Black ethnicity as an independent predictor of localised disease (OR 0.66, 95% CI 0.43–1.00). Limitations of this study include the exclusion of PCa cases diagnosed outside the 2WW pathway, as well as missing data on Prostate-Specific Antigen (PSA) levels, distant radiological staging and histopathological findings.

Conclusion

We identify disparities in PCa incidence, stage and age at presentation, as well as socio-economic deprivation among Black men in NEL. Targeted efforts are needed to mitigate these healthcare inequities.

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