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乳腺摄影密度与乳腺筛查间期癌:迈向更个体化的筛查。

Mammographic density and interval cancers in mammographic screening: Moving towards more personalized screening.

机构信息

Section for Breast Cancer Screening, Cancer Registry of Norway, Oslo, Norway.

Nykøbing Falster Hospital, University of Copenhagen, Nykøbing Falster, Denmark.

出版信息

Breast. 2023 Jun;69:306-311. doi: 10.1016/j.breast.2023.03.010. Epub 2023 Mar 21.

Abstract

PURPOSE

The European Society on Breast Imaging has recommended supplemental magnetic resonance imaging (MRI) every two to four years for women with mammographically dense breasts. This may not be feasible in many screening programs. Also, the European Commission Initiative on Breast Cancer suggests not implementing screening with MRI. By analyzing interval cancers and time from screening to diagnosis by density, we present alternative screening strategies for women with dense breasts.

METHODS

Our BreastScreen Norway cohort included 508 536 screening examinations, including 3125 screen-detected and 945 interval breast cancers. Time from screening to interval cancer was stratified by density measured by an automated software and classified into Volpara Density Grades (VDGs) 1-4. Examinations with volumetric density ≤3.4% were categorized as VDG1, 3.5%-7.4% as VDG2, 7.5%-15.4% as VDG3, and ≥15.5% as VDG4. Interval cancer rates were also determined by continuous density measures.

RESULTS

Median time from screening to interval cancer was 496 (IQR: 391-587) days for VDG1, 500 (IQR: 350-616) for VDG2, 482 (IQR: 309-595) for VDG3 and 427 (IQR: 266-577) for VDG4. A total of 35.9% of the interval cancers among VDG4 were detected within the first year of the biennial screening interval. For VDG2, 26.3% were detected within the first year. The highest annual interval cancer rate (2.7 per 1000 examinations) was observed for VDG4 in the second year of the biennial interval.

CONCLUSIONS

Annual screening of women with extremely dense breasts may reduce the interval cancer rate and increase program-wide sensitivity, especially in settings where supplemental MRI screening is not feasible.

摘要

目的

欧洲乳房成像学会建议对乳腺致密的女性每 2 至 4 年进行补充磁共振成像(MRI)检查。但在许多筛查项目中,这可能并不可行。此外,欧盟乳腺癌倡议建议不采用 MRI 筛查。通过分析间隔期癌症和按密度分层的从筛查到诊断的时间,我们为乳腺致密的女性提出了替代筛查策略。

方法

我们的挪威乳腺筛查队列纳入了 508536 次筛查检查,包括 3125 例筛查发现的乳腺癌和 945 例间隔期乳腺癌。根据自动软件测量的密度,将从筛查到间隔期癌症的时间分层,并分为 Volpara 密度分级(VDG)1-4 级。容积密度≤3.4%的检查归入 VDG1,3.5%-7.4%归入 VDG2,7.5%-15.4%归入 VDG3,≥15.5%归入 VDG4。间隔期癌症的发生率也通过连续密度测量来确定。

结果

VDG1 的中位从筛查到间隔期癌症的时间为 496(IQR:391-587)天,VDG2 为 500(IQR:350-616)天,VDG3 为 482(IQR:309-595)天,VDG4 为 427(IQR:266-577)天。VDG4 中有 35.9%的间隔期癌症发生在两年筛查间隔的第一年。VDG2 中有 26.3%发生在第一年。在两年筛查间隔的第二年,VDG4 的间隔期癌症年发生率最高(每 1000 次检查 2.7 例)。

结论

对乳腺极度致密的女性进行每年筛查可能会降低间隔期癌症的发生率,并提高整个项目的敏感性,特别是在无法进行补充性 MRI 筛查的情况下。

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