Department of Biomedical Imaging and Image-guided Therapy, Division of Molecular and Gender Imaging, Medical University of Vienna, Vienna, Austria.
Department of Radiology, Breast Imaging Service, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
J Magn Reson Imaging. 2019 Apr;49(4):1157-1165. doi: 10.1002/jmri.26335. Epub 2018 Dec 15.
Contrast-enhanced magnetic resonance imaging (CE-MRI) of the breast is highly sensitive for breast cancer detection. Multichannel coils and 3T scanners can increase signal, spatial, and temporal resolution. In addition, the T -reduction effect of a gadolinium-based contrast agent (GBCA) is higher at 3T. Thus, it might be possible to reduce the dose of GBCA at 3T without losing diagnostic information.
To compare a three-quarter (0.075 mmol/kg) dose of the high-relaxivity GBCA gadobenate dimeglumine, with a 1.5-fold higher than on-label dose (0.15 mmol/kg) of gadoterate meglumine for breast lesion detection and characterization at 3T CE-MRI.
Prospective, randomized, intraindividual comparative study.
Eligible were patients with imaging abnormalities (BI-RADS 0, 4, 5) on conventional imaging. Each patient underwent two examinations, 24-72 hours apart, one with 0.075 mmol/kg gadobenate and the other with 0.15 mmol/kg gadoterate administered in a randomized order. In all, 109 patients were prospectively recruited.
FIELD STRENGTH/SEQUENCE: 3T MRI with a standard breast protocol (dynamic-CE, T w-TSE, STIR-T w, DWI).
Histopathology was the standard of reference. Three blinded, off-site breast radiologists evaluated the examinations using the BI-RADS lexicon.
Lesion detection, sensitivity, specificity, and diagnostic accuracy were calculated per-lesion and per-region, and compared by univariate and multivariate analysis (Generalized Estimating Equations, GEE).
Five patients were excluded, leaving 104 women with 142 histologically verified breast lesions (109 malignant, 33 benign) available for evaluation. Lesion detection with gadobenate (84.5-88.7%) was not inferior to gadoterate (84.5-90.8%) (P ≥ 0.165). At per-region analysis, gadobenate demonstrated higher specificity (96.4-98.7% vs. 92.6-97.3%, P ≤ 0.007) and accuracy (96.3-97.8% vs. 93.6-96.1%, P ≤ 0.001) compared with gadoterate. Multivariate analysis demonstrated superior, reader-independent diagnostic accuracy with gadobenate (odds ratio = 1.7, P < 0.001 using GEE).
A 0.075 mmol/kg dose of the high-relaxivity contrast agent gadobenate was not inferior to a 0.15 mmol/kg dose of gadoterate for breast lesion detection. Gadobenate allowed increased specificity and accuracy.
1 Technical Efficacy: Stage 2 J. Magn. Reson. Imaging 2019;49:1157-1165.
对比增强磁共振成像(CE-MRI)对乳腺癌具有高度的敏感性。多通道线圈和 3T 扫描仪可以提高信号、空间和时间分辨率。此外,基于钆的对比剂(GBCA)的 T 弛豫率降低效果在 3T 时更高。因此,在不丢失诊断信息的情况下,有可能在 3T 时降低 GBCA 的剂量。
比较高弛豫率 GBCA 钆贝葡胺的 0.075mmol/kg 剂量与标签推荐剂量的 1.5 倍(0.15mmol/kg)的钆特酸葡胺在 3T CE-MRI 中对乳腺病变检测和特征描述的效果。
前瞻性、随机、个体内比较研究。
适合有影像学异常(BI-RADS 0、4、5)的患者。每位患者接受两次检查,间隔 24-72 小时,一次给予 0.075mmol/kg 的钆贝葡胺,另一次给予随机顺序的 0.15mmol/kg 的钆特酸葡胺。共有 109 例患者前瞻性入组。
场强/序列:3T MRI 采用标准乳腺方案(动态 CE、T w-TSE、STIR-T w、DWI)。
组织病理学是参考标准。三位盲法、场外乳腺放射科医生使用 BI-RADS 词汇表进行检查评估。
对每例病变和每区病变进行病变检测、敏感性、特异性和诊断准确性的计算,并通过单变量和多变量分析(广义估计方程,GEE)进行比较。
5 例患者被排除,104 例女性的 142 个经组织学证实的乳腺病变(109 个恶性,33 个良性)可用于评估。钆贝葡胺的病变检出率(84.5-88.7%)并不逊于钆特酸葡胺(84.5-90.8%)(P≥0.165)。在区病变分析中,钆贝葡胺显示出更高的特异性(96.4-98.7%比 92.6-97.3%,P≤0.007)和准确性(96.3-97.8%比 93.6-96.1%,P≤0.001)与钆特酸葡胺相比。多变量分析显示,使用 GEE,钆贝葡胺具有优越的、读者独立的诊断准确性(比值比=1.7,P<0.001)。
高弛豫率对比剂钆贝葡胺的 0.075mmol/kg 剂量与 0.15mmol/kg 剂量的钆特酸葡胺相比,对乳腺病变的检出效果相当。钆贝葡胺可提高特异性和准确性。
1 技术功效:阶段 2 J. Magn. Reson. Imaging 2019;49:1157-1165.