Tóth Adrienn, Edelman Robert R, Hagar Muhammad Taha, Kravchenko Dmitrij, Vecsey-Nagy Milán, Griggers James Ira, Eernisse Jonathan, Emrich Tilman, Spampinato M Vittoria, Varga-Szemes Akos
Department of Radiology and Radiological Science, Medical University of South Carolina, Charleston, SC, USA; Medical Imaging Centre, Semmelweis University, Budapest, Hungary.
Department of Radiology, NorthShore University Health System, Evanston, IL, USA; Department of Radiology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Eur J Radiol. 2025 Jul 5;191:112283. doi: 10.1016/j.ejrad.2025.112283.
This study aimed to evaluate the image quality and lesion characterization with Dixon unbalanced T1 relaxation-enahnced steady-state (uT1RESS) in comparison to magnetization-prepared rapid acquisition gradient echo (MPRAGE) pulse sequence for detecting brain tumors, focusing on its potential to improve diagnostic accuracy and enhance brain tumor assessment.
This single-center prospective study enrolled 20 patients (12 males, aged 35-83), with primary brain tumors and brain metastases. Both MPRAGE and Dixon uT1RESS were acquired at 3 T. Objective image quality was assessed by contrast-to-noise ratio (CNR), tumor-to-brain contrast, and tumor volume. Subjective image quality was assessed by two independent readers focusing on lesion visibility, lesion margins, motion, and static artifacts. A side-by-side comparison assessed diagnostic performance regarding lesion detection, evaluation of internal structure and vascular or dural invasion.
Dixon uT1RESS had a reduced acquisition time (2 min 51 s vs. 4 min 52 s for MPRAGE) and showed significantly higher CNR and tumor-to-brain contrast compared to MPRAGE (p < 0.001). Subjectively, both sequences showed similar overall image quality. Dixon uT1RESS achieved more conspicuous lesions with better-defined lesion margins (p < 0.001), while MPRAGE performed better in evaluating internal lesion structure (p < 0.05). Dixon uT1RESS was rated better for lesion detection, with three lesions additionally identified on this sequence. Wilcoxon signed-rank test was used to assess differences.
Dixon uT1RESS significantly improved tumor conspicuity and detection, particularly for small metastatic lesions. This new technique offers promising potential for enhancing clinical brain tumor imaging, though additional sequences may be necessary for comprehensive lesion characterization.
本研究旨在评估与磁化准备快速采集梯度回波(MPRAGE)脉冲序列相比,Dixon非平衡T1弛豫增强稳态(uT1RESS)在检测脑肿瘤时的图像质量和病变特征,重点关注其提高诊断准确性和增强脑肿瘤评估的潜力。
这项单中心前瞻性研究纳入了20例患者(12例男性,年龄35 - 83岁),患有原发性脑肿瘤和脑转移瘤。在3T条件下采集MPRAGE和Dixon uT1RESS图像。通过对比噪声比(CNR)、肿瘤与脑的对比度以及肿瘤体积评估客观图像质量。由两名独立阅片者通过关注病变可见性、病变边缘、运动和静态伪影来评估主观图像质量。通过并排比较评估病变检测、内部结构评估以及血管或硬脑膜侵犯方面的诊断性能。
Dixon uT1RESS的采集时间缩短(2分51秒,而MPRAGE为4分52秒),与MPRAGE相比,其CNR和肿瘤与脑的对比度显著更高(p < 0.001)。主观上,两种序列的整体图像质量相似。Dixon uT1RESS能使病变更明显,病变边缘更清晰(p < 0.001),而MPRAGE在评估病变内部结构方面表现更好(p < 0.05)。Dixon uT1RESS在病变检测方面的评分更高,该序列还额外发现了3个病变。采用Wilcoxon符号秩检验评估差异。
Dixon uT1RESS显著提高了肿瘤的可见性和检测能力,特别是对于小的转移瘤。这项新技术为增强临床脑肿瘤成像提供了有前景的潜力,不过可能需要额外的序列来进行全面的病变特征描述。