Breast center, University Hospital Schleswig-Holstein, Kiel.
Ultraschall Med. 2013 Jun;34(3):254-9. doi: 10.1055/s-0033-1335523. Epub 2013 May 24.
To determine the benefit of ShearWave™ Elastography (SWE™) in the ultrasound characterization of BI-RADS® 3 breast lesions in a diagnostic population.
303 BI-RADS® 3 lesions (mean size: 13.2 mm, SD: 7.5 mm) from the multicenter BE1 prospective study population were analyzed: 201 (66%) had cytology or core biopsy, and the remaining 102 had a minimum follow-up of one year; 8 (2.6%) were malignant. 7 SWE features were evaluated with regard to their ability to downgrade benign BI-RADS® 3 masses. The performance of each SWE feature was assessed by evaluating the number of lesions correctly reclassified and the impact on cancer rates within the new BI-RADS® 3' lesion group.
No malignancies were found with an E-color "black to dark blue", which allowed the downgrading of 110/303 benign masses (p < 0.0001), with a non-significant increase in BI-RADS® 3' malignancy rate from 2.6% to 4.1%. E-max ≤ 20 kPa (2.6 m/s) was able to downgrade 48/303 (p < 0.0001) lesions with a lower increase in BI-RADS® 3' malignancy rate (3.1%). No other SWE features were useful for reclassifying benign BI-RADS® 3 lesions.
Applying simple reclassification rules, SWE assessment of the maximum stiffness of lesions allowed the downgrading of a sub-group of benign BI-RADS® 3 lesions. This was accompanied by a non-significant increase in the malignancy rate in the new BI-RADS® 3 class.
在诊断人群中,确定剪切波弹性成像(SWE)在 BI-RADS® 3 乳腺病变的超声特征中的获益。
对多中心 BE1 前瞻性研究人群中的 303 个 BI-RADS® 3 病变(平均大小:13.2mm,SD:7.5mm)进行分析:201 个(66%)有细胞学或核心活检,其余 102 个有至少一年的随访;8 个(2.6%)为恶性病变。评估了 7 个 SWE 特征在将良性 BI-RADS® 3 肿块降级方面的能力。通过评估正确重新分类的病变数量以及对新 BI-RADS® 3'病变组中癌症发生率的影响,评估每个 SWE 特征的性能。
E 色为“黑色到深蓝色”的病变中未发现恶性病变,这使得 110/303 个良性肿块得以降级(p < 0.0001),新 BI-RADS® 3'恶性率无显著增加,从 2.6%增加到 4.1%。E-max ≤ 20kPa(2.6m/s)可使 48/303 个(p < 0.0001)病变降级,新 BI-RADS® 3 恶性率略有增加(3.1%)。其他 SWE 特征均不能用于重新分类良性 BI-RADS® 3 病变。
应用简单的重新分类规则,SWE 评估病变的最大硬度可使部分良性 BI-RADS® 3 病变降级。这伴随着新 BI-RADS® 3 类中恶性率的非显著增加。