Erbas Bircan, Amos Alison, Fletcher Ashley, Kavanagh Anne M, Gertig Dorota M
Center for Genetic Epidemiology, School of Population Health, University of Melbourne, 723 Swanston Street, Carlton, Victoria 3053, Australia.
Cancer Epidemiol Biomarkers Prev. 2004 Oct;13(10):1569-73.
The evidence for the effectiveness of screening is strongest for women ages 50 to 69 years; however, there is variation in the target age group for screening programs between different countries. In particular, there is uncertainty over whether women should continue screening once they reach age 70. We therefore investigated incidence rates for invasive and in situ breast cancer by age as well as prognostic features of tumors within a screening program.
We studied 474,808 women who attended BreastScreen Victoria from January 1, 1993 to December 31, 2000. Of these women, 5,301 were diagnosed with invasive cancer and 1,127 were diagnosed with ductal carcinoma in situ. We used generalized additive models to model age-incidence rates for invasive cancers and ductal carcinoma in situ separately by users and nonusers of hormone replacement therapy at most recent screen. Nonparametric trends for ordered groups and regression methods were used to investigate trends in size, grade, and nodal involvement for invasive tumors by type of attendance and time since previous negative screen for age group.
The incidence of ductal carcinoma in situ among women with a previous negative screen clearly declined after age 70 irrespective of hormone replacement therapy use. At subsequent screen, the age-incidence curve for invasive breast cancer flattened at ages 60 to 75 years and then increased only for women taking hormone replacement therapy. Tumor size at diagnosis declined with age at both first round (P = 0.15) and subsequent round (P = 0.08). The proportion of poorly differentiated tumors also decreased with age, with the smallest proportion of grade III tumors diagnosed in women ages > or = 75 years (P = 0.09 for first screen and P = 0.05 for subsequent screen). The presence of positive nodes at diagnosis declined with age (P < 0.001) for both first and subsequent screening rounds.
Older age is associated with more favorable prognostic tumor features and a lower incidence of ductal carcinoma in situ among subsequent attenders of screening. When making decisions regarding continuing screening, older women and their physicians should also consider the presence of other comorbid conditions that may mitigate any impact of screening on mortality.
筛查有效性的证据在50至69岁女性中最为充分;然而,不同国家筛查项目的目标年龄组存在差异。特别是,女性70岁后是否应继续筛查尚不确定。因此,我们在一个筛查项目中按年龄调查了浸润性和原位乳腺癌的发病率以及肿瘤的预后特征。
我们研究了1993年1月1日至2000年12月31日期间参加维多利亚州乳腺癌筛查项目的474,808名女性。其中,5301名被诊断为浸润性癌,1127名被诊断为导管原位癌。我们使用广义相加模型分别对最近一次筛查时使用和未使用激素替代疗法的人群的浸润性癌和导管原位癌的年龄发病率进行建模。对于有序组的非参数趋势和回归方法,用于按就诊类型和自上次阴性筛查以来的时间,调查不同年龄组浸润性肿瘤的大小、分级和淋巴结受累情况的趋势。
既往筛查为阴性的女性中,导管原位癌的发病率在70岁后明显下降,无论是否使用激素替代疗法。在随后的筛查中,浸润性乳腺癌的年龄发病率曲线在60至75岁时趋于平缓,然后仅在使用激素替代疗法的女性中上升。诊断时的肿瘤大小在第一轮(P = 0.15)和随后一轮(P = 0.08)均随年龄下降。低分化肿瘤的比例也随年龄降低,年龄≥75岁的女性中诊断为III级肿瘤的比例最小(首次筛查时P = 0.09,随后筛查时P = 0.05)。诊断时阳性淋巴结的出现率在首次和随后的筛查轮次中均随年龄下降(P < 0.001)。
年龄较大与后续筛查参与者中更有利的肿瘤预后特征以及较低的导管原位癌发病率相关。在做出关于继续筛查的决策时,老年女性及其医生还应考虑是否存在其他合并症,这些合并症可能减轻筛查对死亡率的任何影响。