We evaluated the amino acid and glucose metabolism of brain tumors by using PET with 3,4-dihydroxy-6-18F-fluoro- class='sc'>l-phenylalanine (18F-FDOPA) and 18F-FDG. >Methods: Eighty-one pati'/> 18F-FDOPA PET Imaging of Brain Tumors: Comparison Study with 18F-FDG PET and Evaluation of Diagnostic Accuracy
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18F-FDOPA PET Imaging of Brain Tumors: Comparison Study with 18F-FDG PET and Evaluation of Diagnostic Accuracy

机译:脑肿瘤的18F-FDOPA PET成像:与18F-FDG PET的比较研究和诊断准确性的评估

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id="p-1">We evaluated the amino acid and glucose metabolism of brain tumors by using PET with 3,4-dihydroxy-6-18F-fluoro- class="sc">l-phenylalanine (18F-FDOPA) and 18F-FDG. >Methods: Eighty-one patients undergoing evaluation for brain tumors were studied. Initially, 30 patients underwent PET with 18F-FDOPA and 18F-FDG within the same week. Tracer kinetics in normal brain and tumor tissues were estimated. PET uptake was quantified by use of standardized uptake values and the ratio of tumor uptake to normal hemispheric tissue uptake (T/N). In addition, PET uptake with 18F-FDOPA was quantified by use of ratios of tumor uptake to striatum uptake (T/S) and of tumor uptake to white matter uptake. The accuracies of 18F-FDOPA and 18F-FDG PET were determined by comparing imaging data with histologic findings and findings of clinical follow-up of up to 31 mo (mean, 20 mo). To further validate the accuracy of 18F-FDOPA PET, 18F-FDOPA PET was performed with an additional 51 patients undergoing brain tumor evaluation. >Results: Tracer uptake in tumors on 18F-FDOPA scans was rapid, peaking at approximately 15 min after intravenous injection. Tumor uptake could be distinguished from that of the striatum by the difference in peak times. Both high-grade and low-grade tumors were well visualized with 18F-FDOPA. The sensitivity for identifying tumors was substantially higher with 18F-FDOPA PET than with 18F-FDG PET at comparable specificities, as determined by simple visual inspection, especially for the assessment of low-grade tumors. Using receiver-operating-characteristic curve analysis, we found the optimal threshold for 18F-FDOPA to be a T/S of greater than 1.0 (sensitivity, 96%; specificity, 100%) or a T/N of greater than 1.3 (sensitivity, 96%; specificity, 86%). The high diagnostic accuracy of 18F-FDOPA PET at these thresholds was confirmed with the additional 51 patients (a total of 81 patients: sensitivity, 98%; specificity, 86%; positive predictive value, 95%; negative predictive value, 95%). No significant difference in tumor uptake on 18F-FDOPA scans was seen between low-grade and high-grade tumors (P = 0.40) or between contrast-enhancing and nonenhancing tumors (P = 0.97). Radiation necrosis was generally distinguishable from tumors on 18F-FDOPA scans (P 0.00001). >Conclusion: 18F-FDOPA PET was more accurate than 18F-FDG PET for imaging of low-grade tumors and evaluating recurrent tumors. 18F-FDOPA PET may prove especially useful for imaging of recurrent low-grade tumors and for distinguishing tumor recurrence from radiation necrosis.
机译:id =“ p-1”>我们通过将PET与3,4-二羟基-6- 18 F-氟- class =“一起使用,评估了脑肿瘤的氨基酸和葡萄糖代谢sc“> l -苯丙氨酸( 18 F-FDOPA)和 18 F-FDG。 >方法:研究了81例接受脑瘤评估的患者。最初,有30例患者在同一周内接受了 18 F-FDOPA和 18 F-FDG的PET治疗。示踪剂动力学在正常的大脑和肿瘤组织中。通过使用标准化摄取值和肿瘤摄取与正常半球组织摄取的比率(T / N)来量化PET摄取。另外,通过使用肿瘤摄取与纹状体摄取(T / S)和肿瘤摄取与白质摄取的比率来定量 18 F-FDOPA的PET摄取。通过比较影像学数据与组织学检查结果以及31 mo以下的临床随访结果,确定 18 F-FDOPA和 18 F-FDG PET的准确性,20个月)。为了进一步验证 18 F-FDOPA PET的准确性,对另外51名接受脑肿瘤评估的患者进行了 18 F-FDOPA PET。 >结果: 18 F-FDOPA扫描显示肿瘤中的示踪剂摄取迅速,在静脉注射后约15分钟达到峰值。肿瘤吸收与纹状体的吸收可以通过高峰时间的差异来区分。使用 18 F-FDOPA可以很好地看到高度和低度肿瘤。通过简单的目视检查确定, 18 F-FDOPA PET在可比较的特异性下,识别肿瘤的敏感性明显高于 18 F-FDG PET。低度肿瘤。使用接收器工作特征曲线分析,我们发现 18 F-FDOPA的最佳阈值是T / S大于1.0(敏感性,96%;特异性,100%)或T / N大于1.3(灵敏度为96%;特异性为86%)。在这些阈值下, 18 F-FDOPA PET的诊断准确性较高,另外51例患者(总共81例患者:敏感性98%;特异性86%;阳性预测值95% ;阴性预测值为95%)。低级和高级肿瘤( P = 0.40)或对比增强和非增强肿瘤在 18 F-FDOPA扫描中均未观察到显着差异( P = 0.97)。在 18 F-FDOPA扫描中( P <0.00001),通常可以将放射坏死与肿瘤区分开。 >结论: 18 F-FDOPA PET在诊断低度肿瘤和评估复发肿瘤方面比 18 F-FDG PET更准确。 18 F-FDOPA PET可能特别适用于复发性低度肿瘤的成像以及区分肿瘤复发与放射坏死。

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