Department of Clinical Epidemiology, Institute of Clinical Medicine, Aarhus University Hospital, Aarhus, Denmark.
Clinical Institute, Aarhus University, Aarhus, Denmark.
JAMA Netw Open. 2018 Nov 2;1(7):e184909. doi: 10.1001/jamanetworkopen.2018.4909.
Data on the long-term risk of urologic and nonurologic cancer after hematuria diagnosis are sparse. Such data can improve understanding of hematuria and cancer and can provide insight into the clinical course of patients with hematuria.
To assess the risk of urologic or nonurologic cancer after a hospital-based diagnosis of hematuria.
DESIGN, SETTING, AND PARTICIPANTS: This cohort study used population-based, nationwide health care databases covering all hospitals in Denmark. The data set included records of all adults (n = 134 173) with an inpatient, outpatient, or emergency department diagnosis of hematuria. The study was conducted from January 1, 1995, to December 31, 2013. Follow-up ended on December 31, 2013. Data analysis was performed from January 16, 2017, to September 18, 2018.
Cumulative risk of cancer was computed, and observed cancer incidence was compared with incidence expected in the general population, using standardized incidence ratios.
Of the 134 173 patients included, 52 367 (39.0%) were women, 81 806 (61.0%) were men, and the median (interquartile range) age was 59 (44-72) years. Within 3 months after hematuria diagnosis, 2647 patients (1.9%) received an invasive bladder cancer diagnosis, 1077 (0.8%) a noninvasive bladder cancer diagnosis, 569 (0.4%) a kidney cancer diagnosis, and 908 (1.1%) a prostate cancer diagnosis. The 3-month cumulative incidence (or absolute risk) of any cancer diagnosis was 4.81% (95% CI, 4.70%-4.93%), the 1-year risk was 6.65% (95% CI, 6.51%-6.78%), and the 5-year risk was 12.34% (95% CI, 12.15%-12.53%). The cumulative incidence of bladder cancer only increased from 1.20% (95% CI, 1.11%-1.30%) after 1 year to 1.36% (95% CI, 1.26%-1.46%) after 5 years of follow-up in women and from 2.93% (95% CI, 2.82%-3.05%) to 3.31% (95% CI, 3.19%-3.44%) in men. For noninvasive bladder cancer, the standardized incidence ratio in the 1 year to less than 5 years of follow-up was 5.39 (95% CI, 4.58-6.30) in patients without initial cystoscopy and was 0.16 (95% CI, 0.04-0.42) in patients with cystoscopy within 3 months after hospital-based diagnosis of hematuria. For kidney cancer, the standardized incidence ratio in the 1 year to less than 5 years of follow-up was 2.63 (95% CI, 2.15-3.18) in patients without cystoscopy and 1.20 (95% CI, 0.87-1.61) in patients with cystoscopy within 3 months after hospital-based diagnosis of hematuria. After 1 year, the risk of gynecologic and colorectal cancers was as expected or even lower, whereas the risk of hematologic malignant neoplasms remained slightly elevated.
Increased risk of bladder and kidney cancers even more than 1 year after hospital-based hematuria diagnosis, as well as the slightly elevated risk of invasive bladder cancer after 5 years, may indicate that it is a marker of greater cancer risk; these findings could inform follow-up recommendations for hematuria.
血尿诊断后泌尿系统和非泌尿系统癌症的长期风险数据较为匮乏。此类数据可以增进人们对血尿和癌症的理解,并为血尿患者的临床病程提供深入认识。
评估基于医院的血尿诊断后发生泌尿系统或非泌尿系统癌症的风险。
设计、设置和参与者:本队列研究使用基于人群的、覆盖丹麦所有医院的全国性医疗保健数据库。该数据集包含所有成年人(n=134173)的住院、门诊或急诊诊断血尿记录。研究从 1995 年 1 月 1 日至 2013 年 12 月 31 日进行。随访于 2013 年 12 月 31 日结束。数据分析于 2017 年 1 月 16 日至 2018 年 9 月 18 日进行。
计算癌症累积风险,并使用标准化发病比比较观察到的癌症发病率与普通人群的预期发病率。
在纳入的 134173 例患者中,52367 例(39.0%)为女性,81806 例(61.0%)为男性,中位(四分位间距)年龄为 59(4472)岁。血尿诊断后 3 个月内,2647 例患者(1.9%)接受了浸润性膀胱癌诊断,1077 例(0.8%)接受了非浸润性膀胱癌诊断,569 例(0.4%)接受了肾癌诊断,908 例(1.1%)接受了前列腺癌诊断。任何癌症诊断的 3 个月累积发病率(或绝对风险)为 4.81%(95%CI,4.70%4.93%),1 年风险为 6.65%(95%CI,6.51%6.78%),5 年风险为 12.34%(95%CI,12.15%12.53%)。女性膀胱癌的累积发病率仅从 1 年后的 1.20%(95%CI,1.11%1.30%)增加到 5 年后的 1.36%(95%CI,1.26%1.46%),而男性则从 2.93%(95%CI,2.82%3.05%)增加到 3.31%(95%CI,3.19%3.44%)。对于非浸润性膀胱癌,在无初始膀胱镜检查的 1 年至不到 5 年的随访中,标准化发病比为 5.39(95%CI,4.586.30),而在血尿诊断后 3 个月内进行膀胱镜检查的患者中,标准化发病比为 0.16(95%CI,0.040.42)。在肾癌中,无膀胱镜检查的患者在 1 年至不到 5 年的随访中,标准化发病比为 2.63(95%CI,2.153.18),而在血尿诊断后 3 个月内进行膀胱镜检查的患者中,标准化发病比为 1.20(95%CI,0.871.61)。在 1 年后,妇科和结直肠癌的风险与预期相符,甚至更低,而血液恶性肿瘤的风险仍然略有升高。
基于医院的血尿诊断后 1 年以上,膀胱癌和肾癌的风险增加,甚至在 5 年后浸润性膀胱癌的风险仍然升高,这可能表明其是癌症风险较高的标志物;这些发现可以为血尿的随访建议提供信息。