通过优化PET显像时间提高低吸收18 - fdg乳腺癌的病变检出率

K. Wangerin, M. Muzi, L. Peterson, Finbarr O 'sullivan, H. Linden, D. Mankoff, Paul Kinahan
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摘要

有传闻称,延迟FDG-PET肿瘤成像可以提高已知病变的信噪比。我们的目标是评估是否有可能通过调整FDG注射和图像采集之间的时间来优化病变的可检测性。方法:我们结合了三个组成部分:18FFDG放射性示踪剂摄取的动力学模型、PET数据采集的正演模型和估计病变可检测性的观察者模型。从早期乳腺癌患者的动态PET研究中估计模型参数和动脉输入函数。这些数据被用来生成时间-活动曲线(TACs)。对于每个TAC,模拟真实的PET图,并使用OSEM重建图像。每个案件有600个身份验证。使用非预白化匹配滤波器(NPWMF)和信道化酒店观察者(CHO)统计量生成接收者工作特征(ROC)曲线,并使用曲线下面积(AUC)对其进行总结。结果:AUC比目前标准的注射后成像窗口(1小时)增加数小时。这种改善是由于在放射性示踪剂衰变引起的噪声增加的影响开始占主导地位之前,FDG在肿瘤中的持续积累所驱动的。结论:这些结果表明,延迟PET成像可能会发现患者的低显著性病变,否则这些病变可能会被发现。然而,这种方法还需要进一步的验证。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Improving lesion detectability in low uptake 18 F-FDG breast cancer by optimizing PET imaging time
There have been anecdotal reports that delayed FDG-PET oncology imaging can improve the SNR for known lesions. Our goal was to evaluate if it is possible to optimize lesion detectability by adjusting the duration between FDG injection and image acquisition. Methods: We combined three components: a kinetic model of 18FFDG radiotracer uptake, a forward model of PET data acquisition, and observer models to estimate lesion detectability. Model parameters and arterial input functions were estimated from dynamic PET studies of patients with early-stage breast cancer. These were used to generate time-activity curves (TACs). For each TAC, realistic PET sinograms were simulated, and images were reconstructed using OSEM. There were 600 i.i.d. realizations for each case. Both nonprewhitening matched filter (NPWMF) and channelized Hoteling observer (CHO) statistics were used to generate receiver operating characteristic (ROC) curves, which were summarized using the area under the curve (AUC). Results: The AUC increased for several hours past the current standard post-injection imaging window of one hour. This improvement is driven by the continued accumulation of FDG in the tumor before the impact of increased noise due to radiotracer decay begins to dominate. Conclusion: These results imply that delayed PET imaging may reveal low-conspicuity lesions in patients that would have otherwise gone undetected. However, further validation of this approach is needed.
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