Department of Epidemiology, University of Pittsburgh Cancer Institute, Pittsburgh, PA 15232, USA.
Cancer Causes Control. 2010 Aug;21(8):1227-36. doi: 10.1007/s10552-010-9550-5. Epub 2010 Apr 7.
To identify trends in a residual category of cancers not typically associated with tobacco, screening, or human immunodeficiency virus (HIV) infection.
For persons aged 20-84, we used sex- and race-specific age-period-cohort (APC) models to describe temporal patterns of incidence (1975-2004) and mortality (1970-2004) in the U.S. for a residual cancer category that excluded non-Hodgkin lymphoma, Kaposi sarcoma, and cancer of the oral cavity and pharynx, esophagus, pancreas, larynx, lung and bronchus, urinary bladder, kidney and renal pelvis, colon and rectum, prostate, female breast, and cervix uteri.
Age-specific incidence rose (0.1-0.9% per year, on average) in every sex-race group, with factors related to both time period and birth cohort membership appearing to accelerate the increases in women. Age-specific mortality fell (0.6-0.9% per year, on average) for black and white men and women, with the declines decelerating in white women but accelerating in the other sex-race groups. Extrapolations of APC models predicted higher age-adjusted incidence rates in white women (11%), black women (5%), and white men (4%) in 2005-2009, relative to 2000-2004, and lower rates in black men (-3%), accompanied by lower age-adjusted mortality rates in every sex-race group (-8% in black men, -3% in black women, -1% in white men, and -1% in white women).
The possibility that increased incidence in women over time reflects changes in underlying risks, diagnostic practices, or better case ascertainment should be actively explored. Declining mortality may signify improvements in cancer care.
确定与烟草、筛查或人类免疫缺陷病毒(HIV)感染无关的癌症残留类别的趋势。
对于年龄在 20-84 岁的人群,我们使用性别和种族特异性的年龄-时期-队列(APC)模型来描述美国残留癌症类别的发病率(1975-2004 年)和死亡率(1970-2004 年)的时间模式,该模型排除了非霍奇金淋巴瘤、卡波西肉瘤和口腔和咽、食管、胰腺、喉、肺和支气管、膀胱癌、肾和肾盂、结肠和直肠、前列腺、女性乳房和子宫颈的癌症。
每个性别-种族组的特定年龄的发病率均有所上升(平均每年上升 0.1-0.9%),与时期和出生队列成员有关的因素似乎加速了女性发病率的上升。黑人和白人男性和女性的特定年龄死亡率均有所下降(平均每年下降 0.6-0.9%),白人女性的下降速度减缓,但其他性别-种族组的下降速度加快。APC 模型的外推预测,与 2000-2004 年相比,2005-2009 年白人女性(11%)、黑人女性(5%)和白人男性(4%)的年龄调整发病率将会更高,而黑人男性(-3%)的发病率将会更低,同时每个性别-种族组的年龄调整死亡率也会更低(黑人男性-8%,黑人女性-3%,白人男性-1%,白人女性-1%)。
随着时间的推移,女性发病率的增加可能反映了潜在风险、诊断实践或更好的病例发现的变化,应积极探索。死亡率的下降可能表明癌症治疗的改善。