Romagna Cancer Registry, IRST, 47014 Meldola, Forlì, Italy.
BMC Med. 2010 Feb 1;8:11. doi: 10.1186/1741-7015-8-11.
Although poorly described in the literature, the practice of early (short-interval) rescreen after a negative screening mammogram is controversial due to its financial and psychological burden and because it is of no proven benefit.
The present study targeted an Italian 2-yearly screening programme (Emilia-Romagna Region, 1997-2002). An electronic dataset of 647,876 eligible negative mammography records from 376,257 women aged 50-69 years was record-linked with the regional breast cancer registry. The statistical analysis addressed the following research questions: (1) the prevalence of recommendation for early (<24 months) rescreen (RES) among negative mammography reports; (2) factors associated with the likelihood of a women receiving RES; and (3) whether women receiving RES and women receiving standard negative reports differed in terms of proportional incidence of interval breast cancer, recall rate at the next rescreen, detection rate of breast cancer at the next rescreen and the odds of having late-stage breast cancer during the interscreening interval and at the next rescreen.
RES was used in eight out of 13 screening centres, where it was found in 4171 out of 313,320 negative reports (average rate 1.33%; range 0.05%-4.33%). Reports with RES were more likely for women aged 50-59 years versus older women (odds ratio (OR) 1.33; 95% CI 1.25-1.42), for the first versus subsequent screening rounds (OR 1.91; 95% CI 1.79-2.04) and with a centre-specific recall rate below the average of 6.2% (OR 1.41; 95% CI 1.32-1.50). RES predicted a 3.51-fold (95% CI 0.94-9.29) greater proportional incidence of first-year interval cancers, a 1.90-fold (95% CI 1.62-2.22) greater recall rate at the next screen, a 1.72-fold (95% CI 1.01-2.74) greater detection rate of cancer at the next screen and a non-significantly decreased risk of late disease stage (OR 0.59; 95% CI 0.23-1.53).
The prevalence of RES was in line with the maximum standard level established by the Italian national guidelines. RES identified a subset of women with greater incidence of interval cancers and greater prevalence of cancers detected at the next screen.
尽管文献中对此描述不佳,但由于其经济和心理负担,并且没有被证明有益,因此在阴性乳房 X 光筛检后进行早期(短间隔)复查的做法存在争议。
本研究针对意大利两年一次的筛查计划(艾米利亚-罗马涅地区,1997-2002 年)。对 376,257 名 50-69 岁女性的 647,876 份合格阴性乳房 X 光记录的电子数据集进行了记录链接,这些女性的乳房 X 光记录与区域乳腺癌登记处相关联。统计分析解决了以下研究问题:(1)阴性乳房 X 光报告中建议早期(<24 个月)复查(RES)的比例;(2)与女性接受 RES 可能性相关的因素;以及(3)接受 RES 的女性和接受标准阴性报告的女性在间隔期内和下一次复查期间间隔性乳腺癌的比例发生率、下一次复查的召回率、下一次复查时乳腺癌的检出率以及在筛查间隔和下一次复查时患有晚期乳腺癌的几率方面是否存在差异。
RES 用于 13 个筛查中心中的 8 个中心,在 313,320 份阴性报告中发现了 4171 份(平均率为 1.33%;范围 0.05%-4.33%)。与年龄较大的女性相比,年龄在 50-59 岁的女性(比值比(OR)1.33;95%置信区间(CI)1.25-1.42)、首次筛查与后续筛查相比(OR 1.91;95% CI 1.79-2.04)和中心特定召回率低于 6.2%(OR 1.41;95% CI 1.32-1.50)的女性更有可能接受 RES。RES 预测第一年间隔性癌症的比例发生率增加了 3.51 倍(95% CI 0.94-9.29),下一次筛查的召回率增加了 1.90 倍(95% CI 1.62-2.22),下一次筛查时癌症的检出率增加了 1.72 倍(95% CI 1.01-2.74),晚期疾病阶段的风险降低但无统计学意义(OR 0.59;95% CI 0.23-1.53)。
RES 的流行率符合意大利国家指南规定的最高标准水平。RES 确定了一组间隔性癌症发生率较高和下一次筛查时检出癌症率较高的女性。