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简化乳腺MRI对乳腺极度致密女性进行筛查的多阅片者诊断准确性

Multireader Diagnostic Accuracy of Abbreviated Breast MRI for Screening Women with Extremely Dense Breasts.

作者信息

van Grinsven Sophie E L, Mann Ritse M, Monninkhof Evelyn M, Duvivier Katya, de Jong Mathijn D F, de Koekkoek-Doll Petra K, Loo Claudette E, Pijnappel Ruud M, van der Sluijs Rogier, Veltman Jeroen, van Gils Carla H, Veldhuis Wouter B

机构信息

Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.

Department of Radiology, Radboud University Nijmegen Medical Center, Nijmegen, the Netherlands.

出版信息

Radiology. 2025 May;315(2):e241233. doi: 10.1148/radiol.241233.

Abstract

Background Abbreviated MRI may reduce costs and time of supplemental breast cancer screening. The Dense Tissue and Early Breast Neoplasm Screening (DENSE) trial provides an opportunity to study this protocol in a true screening population. Purpose To compare multireader diagnostic accuracy of various abbreviated screening breast MRI protocols with that of the full multiparametric protocol in the DENSE trial, focusing on identifying the minimal protocol necessary to maintain high diagnostic accuracy. Materials and Methods In this secondary analysis of a subset from the DENSE trial, seven radiologists performed incremental readings of first-round screening MRI scans in women with extremely dense breasts and findings negative for cancer at mammography. Different sequences were added in four incremental steps. The first step included both high-temporal low-spatial and low-temporal high-spatial dynamic T1-weighted series, up to 120 seconds after contrast agent injection. The final step added all full-protocol sequences. Each radiologist assessed the same MRI scans and provided Breast Imaging Reporting and Data System scores for all four incremental steps. Pooled sensitivity and specificity were calculated across all readers per step using a generalized estimating equation model, and pooled reading time per step was calculated using a linear mixed model. Results The first-round screening included 518 MRI scans from 518 women (median age, 53 years; IQR, 51-59 years), including 83 breast cancers: 68 invasive cancers (82%) and 15 ductal carcinomas in situ (18%). There was no evidence of a difference in sensitivity between abbreviated protocol (84.3%; 95% CI: 77.7, 89.2) and the full multiparametric MRI protocol (85.9%; 95% CI: 80.0, 90.3; = .68). There was also no evidence of a difference in specificity between abbreviated protocol (73.9%; 95% CI: 70.7, 76.9) and full protocol (75.8%; 95% CI: 72.8, 78.5; = .39). The abbreviated protocol had a pooled reading time (49.7 seconds; 95% CI: 48.5, 50.9) that was almost 50% shorter than the full protocol (96.4 seconds; 95% CI: 94.3, 98.5; < .001) with 70%-80% shorter scanning time, depending on hospital and scanner vendor. Conclusion In women in the DENSE trial with extremely dense breasts and findings that were negative for cancer at mammography, abbreviated breast MRI for first-round screening had high diagnostic accuracy that was comparable to full multiparametric protocol, at much shorter reading and scanning times. ClinicalTrials.gov Identifier: NCT01315015 © RSNA, 2025 See also the editorial by Kataoka and Honda in this issue.

摘要

背景 简化的MRI检查可能会降低补充性乳腺癌筛查的成本和时间。致密组织与早期乳腺肿瘤筛查(DENSE)试验提供了一个在真正的筛查人群中研究该方案的机会。目的 在DENSE试验中,比较各种简化的乳腺筛查MRI方案与全多参数方案的多阅片者诊断准确性,重点是确定维持高诊断准确性所需的最小方案。材料与方法 在对DENSE试验的一个子集进行的二次分析中,7名放射科医生对乳腺极度致密且乳腺X线摄影检查结果为癌症阴性的女性进行第一轮筛查MRI扫描的递增阅片。分四个递增步骤添加不同序列。第一步包括高时间分辨率低空间分辨率和低时间分辨率高空间分辨率的动态T1加权序列,在注射造影剂后长达120秒。最后一步添加所有全方案序列。每位放射科医生评估相同的MRI扫描,并为所有四个递增步骤提供乳腺影像报告和数据系统评分。使用广义估计方程模型计算每个步骤所有阅片者的合并敏感性和特异性,并使用线性混合模型计算每个步骤的合并阅片时间。结果 第一轮筛查包括来自518名女性的518次MRI扫描(中位年龄53岁;四分位间距51 - 59岁),其中包括83例乳腺癌:68例浸润性癌(82%)和15例导管原位癌(18%)。简化方案(84.3%;95%可信区间:77.7,89.2)与全多参数MRI方案(85.9%;95%可信区间:80.0,90.3;P = 0.68)之间在敏感性上没有差异证据。简化方案(73.9%;95%可信区间:70.7,76.9)与全方案(75.8%;95%可信区间:72.8,78.5;P = 0.39)之间在特异性上也没有差异证据。简化方案的合并阅片时间(49.7秒;95%可信区间:48.5,50.9)比全方案(96.4秒;95%可信区间:94.3,98.5;P < 0.001)短近50%,扫描时间根据医院和扫描仪供应商缩短70% - 80%。结论 在DENSE试验中乳腺极度致密且乳腺X线摄影检查结果为癌症阴性的女性中,用于第一轮筛查的简化乳腺MRI具有与全多参数方案相当的高诊断准确性,且阅片和扫描时间短得多。ClinicalTrials.gov标识符:NCT01315015 © RSNA,2025 另见本期中Kataoka和Honda的社论。

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