Screening the Implant-Augmented Breast with Digital Breast Tomosynthesis: Is Tomosynthesis Necessary for Non-implant-Displaced Views?

IF 2 Q3 ONCOLOGY
Derek L Nguyen, Lars J Grimm, Jeffrey S Nelson, Karen S Johnson, Sujata V Ghate
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Abstract

Objective: To determine cancer visualization utility and radiation dose for non-implant-displaced (ID) views using standard protocol with digital breast tomosynthesis (DBT) vs alternative protocol with 2D only when screening women with implant augmentation.

Methods: This retrospective cohort study identified women with implants who underwent screening DBT examinations that had abnormal findings from July 28, 2014, to December 31, 2021. Three fellowship-trained breast radiologists independently reviewed examinations retrospectively to determine if the initially identified abnormalities could be visualized on standard protocol (DBT with synthesized 2D (S2D) for ID and non-ID views) and alternate protocol (DBT with S2D for ID and only the S2D images for non-ID views). Estimated exam average glandular dose (AGD) and associations between cancer visualization with patient and implant characteristics for both protocols were evaluated.

Results: The study included 195 patients (mean age 55 years ± 10) with 223 abnormal findings. Subsequent biopsy was performed for 86 abnormalities: 59 (69%) benign, 8 (9%) high risk, and 19 (22%) malignant. There was no significant difference in malignancy visualization rate between standard (19/223, 8.5%) and alternate (18/223, 8.1%) protocols (P = .92), but inclusion of the DBT for non-ID views found one additional malignancy. Total examination AGD using standard protocol (21.9 mGy ± 5.0) was significantly higher than it would be for estimated alternate protocol (12.6 mGy ± 5.0, P <.001). This remained true when stratified by breast thickness: 6.0-7.9 cm, 8.0-9.9 cm, >10.0 cm (all P <.001).

Conclusion: The inclusion of DBT for non-ID views did not significantly increase the cancer visualization rate but did significantly increase overall examination AGD.

用数字乳腺断层合成技术筛查植入假体的乳房:非植入物移位视图是否需要断层合成?
目的:确定在对植入假体隆胸的女性进行筛查时,使用数字乳腺断层合成(DBT)的标准方案与仅使用 2D 的替代方案进行非植入物移位(ID)视图的癌症可视化效用和辐射剂量:这项回顾性队列研究确定了从 2014 年 7 月 28 日至 2021 年 12 月 31 日期间接受筛查 DBT 检查并发现异常的植入假体的女性。三位接受过研究员培训的乳腺放射科医生独立回顾性地审查了检查结果,以确定最初发现的异常是否可以通过标准方案(ID 和非 ID 视图采用合成 2D (S2D) DBT)和备用方案(ID 视图采用 S2D DBT,非 ID 视图仅采用 S2D 图像)观察到。对两种方案的估计检查平均腺体剂量(AGD)以及癌症可视化与患者和植入物特征之间的关联进行了评估:研究包括 195 名患者(平均年龄 55 岁 ± 10),共发现 223 个异常结果。随后对 86 例异常进行了活检:59例(69%)良性,8例(9%)高危,19例(22%)恶性。标准方案(19/223,8.5%)和备用方案(18/223,8.1%)在恶性肿瘤显像率方面没有明显差异(P =.92),但在非 ID 视图中加入 DBT 发现了一个额外的恶性肿瘤。使用标准方案进行检查的总 AGD(21.9 mGy ± 5.0)明显高于估计的备用方案(12.6 mGy ± 5.0,P 10.0 cm)(均为 P 结论):将DBT纳入非ID视图并未明显提高癌症显像率,但确实明显增加了整体检查的AGD。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.40
自引率
20.00%
发文量
81
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