Laya M B, Larson E B, Taplin S H, White E
Department of Medicine, University of Washington, Seattle 98105-6920, USA.
J Natl Cancer Inst. 1996 May 15;88(10):643-9. doi: 10.1093/jnci/88.10.643.
Previous studies have demonstrated that mammographic breast density increases following the initiation of estrogen replacement therapy (ERT). The effect, if any, that this increase in density has on the specificity (related to false-positive readings) and the sensitivity (related to false-negative readings) of screening mammography is unknown.
Using a retrospective cohort study design, we assessed the effects of ERT on the specificity and the sensitivity of screening mammography.
Participants (n = 8779) were postmenopausal women, aged 50 years or older, who were enrolled in a health maintenance organization located in western Washington state and who entered a breast cancer screening program between January 1988 and June 1993. Two-view mammography was performed as part of a comprehensive breast cancer screening visit. Menopausal status, as well as demographic and risk-factor information, was recorded via self-administered questionnaires. Hormonal replacement therapy type and use were determined from questionnaire data and from an automated review of pharmacy records. Individuals diagnosed with breast cancer within 12 months of their first screening-program mammograms were identified through use of a regional cancer registry. Risk ratios (RRs) plus 95% confidence intervals (CIs) of false-positive as well as false-negative examinations among current and former ERT users (with never users as the reference group) were calculated. Reported P values are two-sided.
The specificity of mammographic screening was lower for current users of ERT than for never users or former users. Defining a positive mammographic reading as any non-normal reading (either suspicious for cancer or indeterminate), the adjusted RR (95% CI) of a false-positive reading for current users versus never users was 1.33 (1.15-1.54) (P < .001); for former users versus never users, the RR (95% CI) was 1.00 (0.87-1.15). The adjusted mammographic specificities (95% CIs) for never users, former users, and current users of ERT were 86% (84%-88%), 86% (84%-87%), and 82% (80%-84%), respectively. Defining a positive reading more rigorously (i.e., as suspicious for cancer only), the adjusted RRs (95% CIs) of false-positive readings for current users and former users (versus never users) were 1.71 (1.37-2.14) (P < .001) and 1.16 (0.93-1.45), respectively. Sensitivity was also lower in women currently receiving ERT. The unadjusted RR (95% CI) of a false-negative reading for current users versus never users was 5.23 (1.09-25.02) (P = .04); for former users versus never users, the RR (95% CI) was 1.06 (0.10-10.87). The unadjusted mammographic sensitivities (95% CI) for never users, former users, and current users of ERT were 94% (80%-99%), 94% (69%-99%), and 69% (38%-91%), respectively.
Current use of ERT is associated with lower specificity and lower sensitivity of screening mammography. Lower specificity could increase the cost of breast cancer screening, and lower sensitivity may decrease its effectiveness.
既往研究表明,开始雌激素替代疗法(ERT)后乳腺钼靶密度会增加。这种密度增加对乳腺钼靶筛查的特异性(与假阳性读数相关)和敏感性(与假阴性读数相关)是否有影响尚不清楚。
采用回顾性队列研究设计,我们评估了ERT对乳腺钼靶筛查特异性和敏感性的影响。
参与者(n = 8779)为年龄50岁及以上的绝经后女性,她们参加了位于华盛顿州西部的一个健康维护组织,并于1988年1月至1993年6月期间进入乳腺癌筛查项目。作为全面乳腺癌筛查访视的一部分,进行了双视图乳腺钼靶检查。绝经状态以及人口统计学和危险因素信息通过自行填写的问卷记录。激素替代疗法的类型和使用情况根据问卷数据和药房记录的自动审查确定。通过使用区域癌症登记处,识别出在首次筛查项目乳腺钼靶检查后12个月内被诊断为乳腺癌的个体。计算当前和既往ERT使用者(以从未使用者作为参照组)中假阳性以及假阴性检查的风险比(RRs)及其95%置信区间(CIs)。报告的P值为双侧。
当前ERT使用者的乳腺钼靶筛查特异性低于从未使用者或既往使用者。将乳腺钼靶阳性读数定义为任何非正常读数(可疑癌症或不确定),当前使用者与从未使用者相比,假阳性读数的调整后RR(95%CI)为1.33(1.15 - 1.54)(P <.001);既往使用者与从未使用者相比,RR(95%CI)为1.00(0.87 - 1.15)。ERT从未使用者、既往使用者和当前使用者的调整后乳腺钼靶特异性(95%CI)分别为86%(84% - 88%)、86%(84% - 87%)和82%(80% - 84%)。更严格地将阳性读数定义为(即仅可疑癌症),当前使用者和既往使用者(与从未使用者相比)假阳性读数的调整后RR(95%CI)分别为1.71(1.37 - 2.14)(P <.001)和1.16(0.93 - 1.45)。目前接受ERT治疗的女性的敏感性也较低。当前使用者与从未使用者相比,假阴性读数的未调整RR(95%CI)为5.23(1.09 - 25.02)(P =.04);既往使用者与从未使用者相比,RR(95%CI)为1.06(0.10 - 10.87)。ERT从未使用者、既往使用者和当前使用者的未调整乳腺钼靶敏感性(95%CI)分别为94%(80% - 99%)、94%(69% - 99%)和69%(38% - 91%)。
当前使用ERT与乳腺钼靶筛查的特异性降低和敏感性降低相关。较低的特异性可能会增加乳腺癌筛查的成本,而较低的敏感性可能会降低其有效性。