Wright Jonathan L, Morgan Todd M, Lin Daniel W
Department of Urology, University of Washington School of Medicine, Seattle, Washington 98195, USA.
Urology. 2008 Nov;72(5):1139-43. doi: 10.1016/j.urology.2008.06.043. Epub 2008 Sep 16.
Scrotal malignancies are rare; the published data come from small, single-institution series, with the largest comprising only 28 patients. Using a population-based cancer registry, we describe the demographic and pathologic characteristics of scrotal cancer and report the incidence trends over time.
The Surveillance, Epidemiology, and End Results cancer registry was used to identify incident cases of scrotal cancer from 1973 to 2002. The demographic and pathologic characteristics were recorded. The incidence rates were determined and age adjusted to the 2000 United States standard population. Multivariate Cox regression analysis was performed to determine the predictors of mortality.
A total of 471 patients were identified with primary scrotal cancer. The most common histologic types were squamous cell carcinoma (32%), extramammary Paget's disease (21%), basal cell carcinoma (18%), and sarcoma (18%). A squamous cell histologic type was more common in black men than in white men (69% vs 31%, P < .001). On multivariate analysis, nonsquamous histologic types were associated with a lower mortality risk than were squamous cell carcinoma (hazard ratio range 0.43-0.63). Black race (hazard ratio = 2.02, 95% confidence interval 1.20-3.40) was associated with a greater risk of mortality. The age-adjusted incidence rate of scrotal cancer increased from 5 cases per 10 million persons in 1973 to 10 cases per 10 million persons in 2002, with an annual percentage change of 3.18 (P < .05).
Although rare, the incidence of scrotal cancer has doubled during the past 30 years and we observed significant differences in histology between races. Survival was worse in patients with squamous histologic features. Additional epidemiologic study is needed to determine the factors associated with these trends.
阴囊恶性肿瘤较为罕见;已发表的数据来自小型单机构系列研究,其中最大的系列仅包含28例患者。我们利用基于人群的癌症登记系统,描述阴囊癌的人口统计学和病理学特征,并报告其随时间的发病趋势。
利用监测、流行病学和最终结果癌症登记系统,确定1973年至2002年期间阴囊癌的发病病例。记录人口统计学和病理学特征。确定发病率并根据2000年美国标准人群进行年龄调整。进行多变量Cox回归分析以确定死亡率的预测因素。
共识别出471例原发性阴囊癌患者。最常见的组织学类型为鳞状细胞癌(32%)、乳房外佩吉特病(21%)、基底细胞癌(18%)和肉瘤(18%)。鳞状细胞组织学类型在黑人男性中比在白人男性中更常见(69%对31%,P<.001)。多变量分析显示,非鳞状组织学类型与鳞状细胞癌相比,死亡风险较低(风险比范围为0.43 - 0.63)。黑人种族(风险比 = 2.02,95%置信区间1.20 - 3.40)与更高的死亡风险相关。阴囊癌的年龄调整发病率从1973年的每1000万人5例增加到2002年的每1000万人10例,年变化率为3.18(P<.05)。
尽管罕见,但阴囊癌的发病率在过去30年中翻了一番,并且我们观察到不同种族之间在组织学上存在显著差异。具有鳞状组织学特征的患者生存率较差。需要进一步的流行病学研究来确定与这些趋势相关的因素。