Department of Surgery, Durham VA Health Care System, Durham, North Carolina.
Department of Mathematics and Computer Science, College of the Holy Cross, Worcester, Massachusetts.
JAMA Netw Open. 2024 Nov 4;7(11):e2445505. doi: 10.1001/jamanetworkopen.2024.45505.
Prostate cancer (PC) care has evolved rapidly as a result of changes in prostate-specific antigen testing, novel imaging, and newer treatments. The impact of these changes on PC epidemiology and racial disparities across disease states remains underexplored.
To characterize racial and ethnic differences in the epidemiology of PC states, including nonmetastatic hormone-sensitive PC (nmHSPC), metastatic HSPC (mHSPC), nonmetastatic castration-resistant PC (nmCRPC), and metastatic CRPC (mCRPC).
DESIGN, SETTING, AND PARTICIPANTS: This is a retrospective, population-based cohort study of male US veterans aged 40 years and older with known race and ethnicity and no non-PC malignant neoplasm before study entry receiving care through the Veterans Health Administration. The study period was from 2012 to 2020, with follow-up through 2021. To identify active users, data capture included visits 18 months before and after the study period. Data analysis was performed from March to August 2023.
Self-identified race and ethnicity, classified as Black, White, or Hispanic.
The primary outcomes were annual age-adjusted incidence rates (IRs) and point prevalence for PC states by race and ethnicity. Trends were evaluated using joinpoint regression. Time to disease progression or death was estimated using nonparametric cumulative incidence. Competing risk models adjusted for age assessed the association of race and ethnicity on disease progression.
The study included 6 539 001 veterans (median [IQR] age, 65 [56-74] years), of whom 476 227 had PC (median [IQR] age, 69 [63-75] years). IRs varied by time frame and disease state. Across all states and years, the relative risk among Black vs White patients ranged from 2.09 (95% CI, 2.01-2.18; P < .001) for nmHSPC in 2012 to 4.12 (95% CI, 3.39-5.02; P < .001) for nmCRPC in 2017. In nmHSPC, hazard ratios for progression to mHSPC and nmCRPC were 1.36 (95% CI, 1.33-1.40) and 1.60 (95% CI, 1.51-1.70), respectively, for Black patients and 1.38 (95% CI, 1.31-1.45) and 1.55 (95% CI, 1.40-1.72), respectively, for Hispanic patients vs White patients. In contrast, in mCRPC, the hazard ratio for death was lower for Black (0.84; 95% CI, 0.81-0.88) and Hispanic (0.76; 95% CI, 0.69-0.83) patients compared with White patients.
This cohort study of veterans found that Black patients had more than 2-fold higher incidence of all disease states vs White patients. Progression risk was higher for Black and Hispanic patients in early-stage disease, but lower in later disease stages. Despite equal access, Black patients disproportionately experience PC, although progression risks relative to White patients differed according to disease state.
由于前列腺特异性抗原检测、新型影像学技术和新型治疗方法的改变,前列腺癌 (PC) 的治疗已经迅速发展。这些变化对前列腺癌流行病学和疾病状态下的种族差异的影响仍未得到充分探索。
描述 PC 各状态(包括非转移性激素敏感型 PC (nmHSPC)、转移性 HSPC (mHSPC)、非转移性去势抵抗型 PC (nmCRPC) 和转移性 CRPC (mCRPC))中种族和民族差异的流行病学特征。
设计、地点和参与者:这是一项回顾性、基于人群的队列研究,纳入了年龄在 40 岁及以上、已知种族和民族、在研究入组前没有非 PC 恶性肿瘤的美国男性退伍军人,这些退伍军人通过退伍军人事务部 (Veterans Health Administration) 接受治疗。研究期间为 2012 年至 2020 年,随访至 2021 年。为了确定活跃用户,数据采集包括研究期间前 18 个月和后 18 个月的就诊情况。数据分析于 2023 年 3 月至 8 月进行。
自我认定的种族和民族,分为黑人、白人或西班牙裔。
主要结局是按种族和民族划分的各 PC 状态的年年龄调整发病率 (IR) 和时点患病率。采用联合点回归评估趋势。使用非参数累积发病率估计疾病进展或死亡的时间。调整年龄的竞争风险模型评估种族和民族对疾病进展的关联。
该研究纳入了 6539001 名退伍军人(中位数 [IQR] 年龄为 65 [56-74] 岁),其中 476227 人患有 PC(中位数 [IQR] 年龄为 69 [63-75] 岁)。IRs 因时间框架和疾病状态而异。在所有状态和年份中,与白人患者相比,黑人患者的相对风险范围从 2012 年 nmHSPC 的 2.09(95%CI,2.01-2.18;P<0.001)到 2017 年 nmCRPC 的 4.12(95%CI,3.39-5.02;P<0.001)。在 nmHSPC 中,黑人和西班牙裔患者进展为 mHSPC 和 nmCRPC 的风险比分别为 1.36(95%CI,1.33-1.40)和 1.60(95%CI,1.51-1.70),而白人和西班牙裔患者的风险比分别为 1.38(95%CI,1.31-1.45)和 1.55(95%CI,1.40-1.72)。相比之下,在 mCRPC 中,黑人和西班牙裔患者的死亡风险比白人患者低(0.84;95%CI,0.81-0.88)和(0.76;95%CI,0.69-0.83)。
这项对退伍军人的队列研究发现,与白人患者相比,黑人患者各疾病状态的发病率高出两倍以上。黑人患者和西班牙裔患者在早期疾病中进展风险较高,但在晚期疾病中风险较低。尽管获得了平等的机会,但黑人患者不成比例地患有 PC,尽管相对于白人患者,疾病进展的风险因疾病状态而异。