Department of Nuclear Medicine and Clinical Molecular Imaging, University Hospital Tuebingen, Tuebingen, Germany.
Advanced Clinical Imaging Technology, Siemens Healthineers International AG, Lausanne, Switzerland.
Eur J Nucl Med Mol Imaging. 2024 Sep;51(11):3346-3359. doi: 10.1007/s00259-024-06745-3. Epub 2024 May 20.
The long axial field of view, combined with the high sensitivity of the Biograph Vision Quadra PET/CT scanner enables the precise deviation of an image derived input function (IDIF) required for parametric imaging. Traditionally, this requires an hour-long dynamic PET scan for [F]-FDG, which can be significantly reduced by using a population-based input function (PBIF). In this study, we expand these examinations and include the scanner's ultra-high sensitivity (UHS) mode in comparison to the high sensitivity (HS) mode and evaluate the potential for further shortening of the scan time.
Patlak K and DV estimates were determined by the indirect and direct Patlak methods using dynamic [F]-FDG data of 6 oncological patients with 26 lesions (0-65 min p.i.). Both sensitivity modes for different number/duration of PET data frames were compared, together with the potential of using abbreviated scan durations of 20, 15 and 10 min by using a PBIF. The differences in parametric images and tumour-to-background ratio (TBR) due to the shorter scans using the PBIF method and between the sensitivity modes were assessed.
A difference of 3.4 ± 7.0% (K) and 1.2 ± 2.6% (DV) was found between both sensitivity modes using indirect Patlak and the full IDIF (0-65 min). For the abbreviated protocols and indirect Patlak, the UHS mode resulted in a lower bias and higher precision, e.g., 45-65 min p.i. 3.8 ± 4.4% (UHS) and 6.4 ± 8.9% (HS), allowing shorter scan protocols, e.g. 50-65 min p.i. 4.4 ± 11.2% (UHS) instead of 7.3 ± 20.0% (HS). The variation of K and DV estimates for both Patlak methods was comparable, e.g., UHS mode 3.8 ± 4.4% and 2.7 ± 3.4% (K) and 14.4 ± 2.7% and 18.1 ± 7.5% (DV) for indirect and direct Patlak, respectively. Only a minor impact of the number of Patlak frames was observed for both sensitivity modes and Patlak methods. The TBR obtained with direct Patlak and PBIF was not affected by the sensitivity mode, was higher than that derived from the SUV image (6.2 ± 3.1) and degraded from 20.2 ± 12.0 (20 min) to 10.6 ± 5.4 (15 min). K and DV estimate images showed good agreement (UHS mode, RC: 6.9 ± 2.3% (K), 0.1 ± 3.1% (DV), peak signal-to-noise ratio (PSNR): 64.5 ± 3.3 dB (K), 61.2 ± 10.6 dB (DV)) even for abbreviated scan protocols of 50-65 min p.i.
Both sensitivity modes provide comparable results for the full 65 min dynamic scans and abbreviated scans using the direct Patlak reconstruction method, with good K and DV estimates for 15 min short scans. For the indirect Patlak approach the UHS mode improved the K estimates for the abbreviated scans.
长轴向视野,结合 Biograph Vision Quadra PET/CT 扫描仪的高灵敏度,可实现精确的图像衍生输入功能(IDIF)偏差,这是参数成像所必需的。传统上,这需要进行长达一小时的 [F]-FDG 动态 PET 扫描,而使用基于人群的输入函数(PBIF)则可以显著缩短扫描时间。在这项研究中,我们扩展了这些检查,并将扫描仪的超高灵敏度(UHS)模式与高灵敏度(HS)模式进行比较,并评估了进一步缩短扫描时间的潜力。
使用 6 名肿瘤患者的 26 个病灶的 [F]-FDG 动态数据,通过间接和直接 Patlak 方法确定 Patlak K 和 DV 估计值(0-65 分钟)。比较了不同 PET 数据帧数的两种灵敏度模式,以及使用 PBIF 缩短扫描时间至 20、15 和 10 分钟的潜力。评估了使用 PBIF 方法进行较短扫描和两种灵敏度模式之间的参数图像和肿瘤与背景比(TBR)的差异。
间接 Patlak 和完整 IDIF(0-65 分钟)使用两种灵敏度模式时,K 和 DV 分别存在 3.4±7.0%(K)和 1.2±2.6%(DV)的差异。对于缩写协议和间接 Patlak,UHS 模式在缩短扫描协议方面具有更低的偏差和更高的精度,例如 45-65 分钟时的 K 值为 3.8±4.4%(UHS)和 6.4±8.9%(HS),可以采用 50-65 分钟时的 K 值为 4.4±11.2%(UHS)而不是 7.3±20.0%(HS)的协议。两种 Patlak 方法的 K 和 DV 估计值的变化是可比的,例如 UHS 模式下间接 Patlak 的 K 值为 3.8±4.4%,直接 Patlak 的 K 值为 2.7±3.4%,DV 值分别为 14.4±2.7%和 18.1±7.5%。两种灵敏度模式和 Patlak 方法均观察到 Patlak 帧数的影响较小。直接 Patlak 和 PBIF 获得的 TBR 不受灵敏度模式的影响,高于 SUV 图像(6.2±3.1),并从 20.2±12.0(20 分钟)下降至 10.6±5.4(15 分钟)。即使对于 50-65 分钟的缩写扫描协议,K 和 DV 估计图像也显示出良好的一致性(UHS 模式下,RC:6.9±2.3%(K),0.1±3.1%(DV),峰值信噪比(PSNR):64.5±3.3dB(K),61.2±10.6dB(DV))。
两种灵敏度模式均可为完整的 65 分钟动态扫描和使用直接 Patlak 重建方法的缩写扫描提供可比的结果,对于 15 分钟的短扫描也可以得到良好的 K 和 DV 估计值。对于间接 Patlak 方法,UHS 模式可改善缩写扫描的 K 估计值。