[11] C -蛋氨酸正电子发射断层扫描在原发性和复发性胶质瘤患者术后影像学及随访中的应用。

ISRN oncology Pub Date : 2014-02-04 eCollection Date: 2014-01-01 DOI:10.1155/2014/463152
Matteo Santoni, Cristina Nanni, Alessandro Bittoni, Gabriele Polonara, Alessandro Paccapelo, Roberto Trignani, Mariagrazia De Lisa, Franco Rychlicki, Luciano Burattini, Rossana Berardi, Stefano Fanti, Stefano Cascinu
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引用次数: 10

摘要

我们研究了[(11)C]-蛋氨酸正电子发射断层扫描([(11)C]-MET PET)在胶质瘤患者治疗中的敏感性和特异性。我们回顾性分析了53例原发性胶质瘤(16例低级别星形细胞瘤,15例间变性星形细胞瘤和22例胶质母细胞瘤)的数据,Karnofsky性能状态(KPS) > 70。患者接受了[(11)C]-MET PET扫描(N = 249)、平行增强MRI (N = 193)和/或CT (N = 113)对照。在低级别胶质瘤患者中,MRI或CT表现与[(11)C]-MET PET附加数据相关,96.22%的病例可以从术后改变中区分残留病变。[(11)C]-MET PET可早期发现低级别到间变性星形细胞瘤的恶性进展,具有较高的敏感性(91.56%)和特异性(95.18%)。在间变性星形细胞瘤中,我们在这些患者的术后影像学和随访中获得了高灵敏度(93.97%)和特异性(95.18%)。在GBM患者中,CT和/或MRI扫描加上额外的[(11)C]-MET PET数据,在术后评估和替莫唑胺治疗期间的肿瘤评估中,灵敏度为96.92%。[(11)C]-MET平均摄取指数与组织学分级之间存在显著相关性(P < 0.001)。这些发现支持了这样一种观点,即从[(11)C]-MET PET获得的补充信息可能有助于胶质瘤患者术后和后续的肿瘤评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

[ (11) C]-methionine positron emission tomography in the postoperative imaging and followup of patients with primary and recurrent gliomas.

[ (11) C]-methionine positron emission tomography in the postoperative imaging and followup of patients with primary and recurrent gliomas.

[ (11) C]-methionine positron emission tomography in the postoperative imaging and followup of patients with primary and recurrent gliomas.

[ (11) C]-methionine positron emission tomography in the postoperative imaging and followup of patients with primary and recurrent gliomas.

We investigated the sensitivity and specificity of [(11)C]-methionine positron emission tomography ([(11)C]-MET PET) in the management of glioma patients. We retrospectively analysed data from 53 patients with primary gliomas (16 low grade astrocytomas, 15 anaplastic astrocytomas and 22 glioblastomas) and Karnofsky Performance Status (KPS) > 70. Patients underwent [(11)C]-MET PET scans (N = 249) and parallel contrast-enhanced MRI (N = 193) and/or CT (N = 113) controls. In low grade glioma patients, MRI or CT findings associated with [(11)C]-MET PET additional data allowed discrimination residual disease from postsurgical changes in 96.22% of these cases. [(11)C]-MET PET early allowed detection of malignant progression from low grade to anaplastic astrocytoma with high sensitivity (91.56%) and specificity (95.18%). In anaplastic astrocytomas, we registered high sensitivity (93.97%) and specificity (95.18%) in the postoperative imaging and during the followup of these patients. In GBM patients, CT and/or MRI scans with additional [(11)C]-MET PET data registered a sensitivity of 96.92% in the postsurgical evaluation and in the tumour assessment during temozolomide therapy. A significant correlation was found between [(11)C]-MET mean uptake index and histologic grading (P < 0.001). These findings support the notion that complementary information derived from [(11)C]-MET PET may be helpful in postoperative and successive tumor assessment of glioma patients.

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