68Ga DOTATATE PET/CT列表模式重建的对比噪声比建模:预测较短采集PET重建中肝转移的可检出性。

IF 2 Q3 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING American journal of nuclear medicine and molecular imaging Pub Date : 2023-01-01
Michael Silosky, Fuyong Xing, John Wehrend, Daniel V Litwiller, Scott D Metzler, Bennett B Chin
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引用次数: 0

摘要

背景:深度学习(DL)算法在PET/CT的病变识别和量化方面显示出前景。然而,这些算法的准确性和泛化性依赖于大量不同的数据集,这些数据集需要花费大量的时间和人力来管理。现代PET/CT扫描仪可以在列表模式下获取数据,允许在不同参数和成像时间下对同一数据集进行多次重建。这些重建可以提供广泛的图像特征,以增加数据集的大小和多样性。具有更短成像时间和更高噪声特性的训练算法要求病灶保持可检测性。本研究的目的是基于持续时间较长、噪声较低的68Ga DOTATATE PET肝脏病变图像的CNR,对较短成像时间的对比噪声比(CNR)进行建模和预测,并确定一个阈值,超过该阈值,病变仍可检测到。方法:68例ga DOTATATE肝病变患者(n=20)分为2个亚组。“模型”组(n=4);n = 9病变;n=36个数据点)来确定CNR与成像时间的关系。“Test”组(n=16);n = 44病变;N =176个数据点)用于评估模型提供的预测。结果:CNR作为识别对象子集的成像时间的函数非常适合二次模型。对于其余受试者,在所有成像时间内,测量的CNR与这些病变的预测CNR呈非常高的线性相关(R2 > 0.97)。从模型来看,5分钟时的阈值CNR=6.9预测2分钟时的CNR > 5。对2分钟图像中病变的目视检查进行评估,5分钟图像中CNR高于阈值,并评级为4或5(可能阳性或绝对阳性),证实在较短的2分钟PET图像中病变可检测到100%。结论:较短DOTATATE PET成像时间的CNR可以使用较长时间采集的列表模式重建来准确预测。阈值CNR可应用于较长持续时间的图像,以确保较短持续时间重建的病变可检测性。这种方法可以帮助选择病变,包括在深度学习的新型数据增强技术中。
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Modeling contrast-to-noise ratio from list mode reconstructions of 68Ga DOTATATE PET/CT: predicting detectability of hepatic metastases in shorter acquisition PET reconstructions.

Background: Deep learning (DL) algorithms have shown promise in identifying and quantifying lesions in PET/CT. However, the accuracy and generalizability of these algorithms relies on large, diverse datasets which are time and labor intensive to curate. Modern PET/CT scanners may acquire data in list mode, allowing for multiple reconstructions of the same datasets with different parameters and imaging times. These reconstructions may provide a wide range of image characteristics to increase the size and diversity of datasets. Training algorithms with shorter imaging times and higher noise properties requires that lesions remain detectable. The purpose of this study is to model and predict the contrast-to-noise ratio (CNR) for shorter imaging times based on CNR from longer duration, lower noise images for 68Ga DOTATATE PET hepatic lesions and identify a threshold above which lesions remain detectable.

Methods: 68Ga DOTATATE subjects (n=20) with hepatic lesions were divided into two subgroups. The "Model" group (n=4 subjects; n=9 lesions; n=36 datapoints) was used to identify the relationship between CNR and imaging time. The "Test" group (n=16 subjects; n=44 lesions; n=176 datapoints) was used to evaluate the prediction provided by the model.

Results: CNR plotted as a function of imaging time for a subset of identified subjects was very well fit with a quadratic model. For the remaining subjects, the measured CNR showed a very high linear correlation with the predicted CNR for these lesions (R2 > 0.97) for all imaging durations. From the model, a threshold CNR=6.9 at 5-minutes predicted CNR > 5 at 2-minutes. Visual inspection of lesions in 2-minute images with CNR above the threshold in 5-minute images were assessed and rated as a 4 or 5 (probably positive or definitely positive) confirming 100% lesion detectability on the shorter 2-minute PET images.

Conclusions: CNR for shorter DOTATATE PET imaging times may be accurately predicted using list mode reconstructions of longer acquisitions. A threshold CNR may be applied to longer duration images to ensure lesion detectability of shorter duration reconstructions. This method can aid in the selection of lesions to include in novel data augmentation techniques for deep learning.

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来源期刊
American journal of nuclear medicine and molecular imaging
American journal of nuclear medicine and molecular imaging RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING-
自引率
4.00%
发文量
4
期刊介绍: The scope of AJNMMI encompasses all areas of molecular imaging, including but not limited to: positron emission tomography (PET), single-photon emission computed tomography (SPECT), molecular magnetic resonance imaging, magnetic resonance spectroscopy, optical bioluminescence, optical fluorescence, targeted ultrasound, photoacoustic imaging, etc. AJNMMI welcomes original and review articles on both clinical investigation and preclinical research. Occasionally, special topic issues, short communications, editorials, and invited perspectives will also be published. Manuscripts, including figures and tables, must be original and not under consideration by another journal.
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