Department of Radiology, Maastricht University Medical Center, The Netherlands.
Ann Surg. 2011 Mar;253(3):539-45. doi: 10.1097/SLA.0b013e31820b01f1.
OBJECTIVE: To prospectively assess the accuracy of gadofosveset-enhanced magnetic resonance imaging (MRI) for nodal staging and restaging in rectal cancer. BACKGROUND: Accurate preoperative assessment of nodal disease in rectal cancer impacts treatment management. Staging with modern imaging techniques (computed tomography, MRI and endorectal ultrasound) is insufficiently accurate for clinical decision making. This study aims to assess the accuracy of MRI using a novel lymph node magnetic resonance contrast, gadofosveset, for nodal staging and restaging in rectal cancer using a per node comparison with histology as the reference standard. METHODS: Sixty-eight patients underwent gadofosveset-enhanced MRI at 1.5T. Twenty-six patients (primary staging group I) were treated with total mesorectal excision (with or without preoperative 5 × 5 Gy) and 42 (restaging group II) underwent a long course of chemoradiation followed by a restaging MRI and resection. Nodes were scored as benign or malignant by 2 radiologists (experienced and junior reader) first on standard MRI, then on gadofosveset-enhanced MRI. For group I the primary staging MRI was compared with histology. In group II the second, restaging MRI was compared with histology. RESULTS: For the experienced reader, sensitivity, specificity, and area under the ROC-curve (AUC) improved from 76%, 82% and 0.84 on standard MRI to 80%, 97% and 0.96 on gadofosveset-MRI (P < 0.001). For the junior reader results improved from 69%, 85%, and 0.85 on standard MRI to 70%, 95%, and 0.93 on gadofosveset-MRI (P = 0.03). Interobserver agreement was good on both standard MRI (κ 0.73) and gadofosveset-MRI (κ 0.71). CONCLUSIONS: This study shows high reproducibility and significantly improved accuracy compared to standard MRI for gadofosveset-enhanced MRI for nodal staging and restaging in rectal cancer.
目的:前瞻性评估钆塞酸增强磁共振成像(MRI)在直肠癌淋巴结分期和再分期中的准确性。
背景:准确术前评估直肠癌的淋巴结疾病会影响治疗管理。使用现代成像技术(计算机断层扫描、MRI 和直肠内超声)进行分期对于临床决策来说不够准确。本研究旨在评估使用新型淋巴结磁共振对比剂——钆塞酸,对直肠癌淋巴结分期和再分期的准确性,以每个淋巴结与组织学比较作为参考标准。
方法:68 例患者在 1.5T 下进行了钆塞酸增强 MRI。26 例患者(原发分期组 I)接受了全直肠系膜切除术(是否接受术前 5×5Gy),42 例(再分期组 II)接受了长程放化疗,然后进行再分期 MRI 和切除。2 名放射科医生(经验丰富的和初级读者)首先在标准 MRI 上,然后在钆塞酸增强 MRI 上对淋巴结进行良性或恶性评分。对于组 I,将原发分期 MRI 与组织学进行比较。对于组 II,将第二次再分期 MRI 与组织学进行比较。
结果:对于经验丰富的读者,敏感性、特异性和 ROC 曲线下面积(AUC)从标准 MRI 的 76%、82%和 0.84 提高到钆塞酸增强 MRI 的 80%、97%和 0.96(P<0.001)。对于初级读者,结果从标准 MRI 的 69%、85%和 0.85 提高到钆塞酸增强 MRI 的 70%、95%和 0.93(P=0.03)。在标准 MRI(κ0.73)和钆塞酸增强 MRI(κ0.71)上,观察者间的一致性都很好。
结论:与标准 MRI 相比,本研究显示了在直肠癌淋巴结分期和再分期方面,钆塞酸增强 MRI 具有高重复性和显著提高的准确性。
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