Suppr超能文献

临床乳房检查对 BRCA 基因突变携带者与一般至中度风险女性乳腺癌诊断的贡献。

Clinical breast exam contribution to breast cancer diagnosis in BRCA mutation carriers vs. average to intermediate risk women.

机构信息

Department of Surgery, Sheba Medical Center, Ramat Gan, Israel.

Tel Aviv School of Medicine, Tel Aviv University, Tel Aviv-Yafo, Israel.

出版信息

Breast Cancer Res Treat. 2024 Aug;207(1):111-118. doi: 10.1007/s10549-024-07345-3. Epub 2024 May 26.

Abstract

PURPOSE

The contribution of clinical breast exam (CBE) to breast cancer diagnosis in average risk women undergoing regular screening mammography is minimal. To evaluate the role of CBE in high-risk women, we compared BC diagnosis by CBE in BRCA mutation carriers undergoing regular BC surveillance to average to intermediate risk women undergoing regular breast cancer screening.

METHODS

A retrospective chart review of all consecutive screening visits of BRCA mutation carriers (January 2012-October 2022) and average to intermediate risk women (November 2016-December 2022) was completed. Women with histologically confirmed BC diagnosis were included. Additional CBE yield for BC diagnosis, defined as the percentage of all BC cases detected by CBE alone, was assessed in both groups.

RESULTS

Overall, 12,997 CBEs were performed in 1,328 BRCA mutation carriers in whom 134 BCs were diagnosed. In 7,949 average to intermediate risk women who underwent 15,518 CBEs, 87 BCs were diagnosed. CBE contributed to BC diagnosis in 3 (2%) BRCA mutation carriers and 3 (4%) non-carriers. In both groups, over 4,000 CBEs were needed in order to diagnose one cancer. In all 3 BRCA mutation carriers BC was palpated during the surveillance round that did not include MRI. In the average to intermediate risk group, 2 of 3 cancers diagnosed following CBE findings were in a different location from the palpable finding.

CONCLUSIONS

The contribution of CBE to BC diagnosis is marginal for all women including BRCA mutation carriers. In BRCA mutation carriers, CBE appears redundant during the MRI surveillance round.

摘要

目的

临床乳房检查(CBE)对接受常规筛查性乳房 X 光检查的普通风险女性乳腺癌诊断的贡献微乎其微。为了评估 CBE 在高风险女性中的作用,我们比较了接受常规乳腺癌监测的 BRCA 基因突变携带者的 CBE 与接受常规乳腺癌筛查的普通至中度风险女性的乳腺癌诊断。

方法

对所有连续的 BRCA 基因突变携带者(2012 年 1 月至 2022 年 10 月)和普通至中度风险女性(2016 年 11 月至 2022 年 12 月)的常规筛查就诊的回顾性图表审查。纳入经组织学证实的乳腺癌诊断的女性。还评估了两组中 CBE 对乳腺癌诊断的额外检出率,定义为单独通过 CBE 检出的所有乳腺癌病例的百分比。

结果

总体而言,在 1328 名 BRCA 基因突变携带者中进行了 12997 次 CBE,其中诊断出 134 例乳腺癌。在接受了 15518 次 CBE 的 7949 名普通至中度风险女性中,诊断出 87 例乳腺癌。CBE 对 3 名(2%)BRCA 基因突变携带者和 3 名(4%)非携带者的乳腺癌诊断有贡献。在这两组中,需要进行超过 4000 次 CBE 才能诊断出 1 例癌症。在所有 3 名 BRCA 基因突变携带者中,在不包括 MRI 的监测轮次中触诊到了乳腺癌。在普通至中度风险组中,3 例经 CBE 发现的癌症中有 2 例的位置与触诊发现的位置不同。

结论

CBE 对所有女性(包括 BRCA 基因突变携带者)的乳腺癌诊断贡献都微不足道。在 BRCA 基因突变携带者中,在 MRI 监测轮次中 CBE 似乎是多余的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/46b1/11230960/d41c5c682467/10549_2024_7345_Fig1_HTML.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验