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首页> 外文期刊>Radiological physics and technology >Utility of respiratory-gated small-animal PET/CT in the chronologic evaluation of an orthotopic lung cancer transplantation mouse model
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Utility of respiratory-gated small-animal PET/CT in the chronologic evaluation of an orthotopic lung cancer transplantation mouse model

机译:呼吸门控小动物PET / CT在原位肺癌移植小鼠模型的时间评估中的应用

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摘要

Our aim in this study was to clarify the effects of respiratory-gated PET in the evaluation of lung cancer according to the 18F-FDG uptake in an orthotopic transplantation mouse model. We created such a model, and we performed PET/CT. The mice were divided into two groups according to tumor volume: a small-tumor group (<20 mm3) and a large-tumor group (>20 mm3). We reconstructed the following conditions based on list-mode data: non-gated (3D) images and gated (4D) images, divided based on the respiratory cycle (expiration phase, stable phase, and inspiration phase). We calculated the maximum standardized uptake values (SUVmax) in each phase. We used the % difference [= (4D SUVmax ? 3D SUVmax)/3D PET SUVmax × 100 (%)] to evaluate the differences in the 4D SUVmax and 3D SUVmax. The 4D SUVmax values were significantly higher than the 3D SUVmax, regardless of the tumor size. The % difference for the small tumors was greater than that for the large tumors, and it was highest in the stable phase. We conclude that the SUVmax in the stable phase under respiratory-gated PET are the most reliable. The SUVmax observed under non-gated PET are considered to be more frequently underestimated in cases involving small tumors than in those involving large tumors. In the chronologic study evaluating the time course of tumor development, the size of the tumor is small in early stage, and respiratory-gated PET is effective in reducing the underestimation of such tumors caused by respiratory motion.
机译:我们在本研究中的目的是根据在原位移植小鼠模型中18F-FDG的摄取来阐明呼吸门控PET在评估肺癌中的作用。我们创建了这样的模型,并执行了PET / CT。根据肿瘤体积将小鼠分为两组:小肿瘤组(<20 mm3)和大肿瘤组(> 20 mm3)。我们基于列表模式数据重构了以下条件:非门控(3D)图像和门控(4D)图像,根据呼吸周期(呼气阶段,稳定阶段和吸气阶段)进行划分。我们计算了每个阶段的最大标准化摄取值(SUV max )。我们使用百分比差异[=(4D SUV max ?3D SUV max )/ 3D PET SUV max ×100(%)]进行评估4D SUV max 和3D SUV max 的差异。无论肿瘤大小如何,4D SUV max 值均显着高于3D SUV max 。小肿瘤的%差异大于大肿瘤的%差异,并且在稳定期最高。我们得出结论,在呼吸门控PET下处于稳定阶段的SUV max 是最可靠的。在非门控PET下观察到的SUV max 在涉及小肿瘤的情况下比对涉及大肿瘤的情况更被低估。在评估肿瘤发展过程的时间顺序研究中,肿瘤的大小在早期很小,而呼吸门控PET可以有效地减少由呼吸运动引起的这种肿瘤的低估。

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