EXPLORER:用全身PET/CT改变分子成像范式(会议报告)

S. Cherry, R. Badawi, T. Jones
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引用次数: 0

摘要

正电子发射断层扫描(PET)是人体全身成像研究中灵敏度最高的技术。然而,目前的临床PET扫描仪不能充分利用可用的信号,因为它们一次只能成像15-25厘米的身体部分。鉴于有限的敏感区域,临床PET扫描仪的全身成像需要相对较长的扫描时间,并使患者接受高于必要的辐射剂量。探索者计划的目标是建立一个2米轴向长度的PET扫描仪,可以一次对整个对象进行成像,捕获几乎所有可用的PET信号。EXPLORER将以40倍的灵敏度获得数据,从而使重建的信噪比增加6倍,用于对整个身体进行成像。另外,在保持当前PET图像质量的同时,使用EXPLORER扫描仪可以在~30秒或~0.15 mSv的注射剂量下获得全身图像。优越的灵敏度将为生物医学研究开辟许多新的途径。特别是对于癌症应用,高灵敏度PET将能够检测较小的病变。此外,更高的灵敏度将允许成像到10个半衰期的正电子发射放射性示踪剂。这将使1)通过延长摄取和清除时间至3-5小时来实现FDG的代谢超分期,从而显着提高对比度;2)改善短寿命放射性同位素(如C-11)的动力学成像,这对药物开发研究至关重要。利用EXPLORER扫描仪的低剂量功能,可以对同一受试者进行频繁的成像研究,以研究疾病进展或跟踪对治疗的反应。低剂量的能力也将为儿科和青少年更好地研究发育障碍开辟新的成像可能性。本次演讲将回顾全身PET的发展基础,潜在的应用,并回顾迄今为止开发EXPLORER(第一款全身PET扫描仪)的进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
EXPLORER: Changing the molecular imaging paradigm with total-body PET/CT (Conference Presentation)
Positron emission tomography (PET) is the highest sensitivity technique for human whole-body imaging studies. However, current clinical PET scanners do not make full use of the available signal, as they only permit imaging of a 15-25 cm segment of the body at one time. Given the limited sensitive region, whole-body imaging with clinical PET scanners requires relatively long scan times and subjects the patient to higher than necessary radiation doses. The EXPLORER initiative aims to build a 2-meter axial length PET scanner to allow imaging the entire subject at once, capturing nearly the entire available PET signal. EXPLORER will acquire data with ~40-fold greater sensitivity leading to a six-fold increase in reconstructed signal-to-noise ratio for imaging the total body. Alternatively, total-body images with the EXPLORER scanner will be able to be acquired in ~30 seconds or with ~0.15 mSv injected dose, while maintaining current PET image quality. The superior sensitivity will open many new avenues for biomedical research. Specifically for cancer applications, high sensitivity PET will enable detection of smaller lesions. Additionally, greater sensitivity will allow imaging out to 10 half-lives of positron emitting radiotracers. This will enable 1) metabolic ultra-staging with FDG by extending the uptake and clearance time to 3-5 hours to significantly improve contrast and 2) improved kinetic imaging with short-lived radioisotopes such as C-11, crucial for drug development studies. Frequent imaging studies of the same subject to study disease progression or to track response to therapy will be possible with the low dose capabilities of the EXPLORER scanner. The low dose capabilities will also open up new imaging possibilities in pediatrics and adolescents to better study developmental disorders. This talk will review the basis for developing total-body PET, potential applications, and review progress to date in developing EXPLORER, the first total-body PET scanner.
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