Department of Radiology, University of Pennsylvania, Philadelphia, PA.
Department of Radiology, University of Washington, Seattle, WA.
Transl Oncol. 2014 Feb 1;7(1):48-54. doi: 10.1593/tlo.13850. eCollection 2014 Feb.
This study investigates measurement biases in longitudinal positron-emission tomography/computed tomography (PET/CT) studies that are due to instrumentation variability including human error. Improved estimation of variability between patient scans is of particular importance for assessing response to therapy and multicenter trials. We used National Institute of Standards and Technology-traceable calibration methodology for solid germanium-68/gallium-68 ((68)Ge/(68)Ga) sources used as surrogates for fluorine-18 ((18)F) in radionuclide activity calibrators. One cross-calibration kit was constructed for both dose calibrators and PET scanners using the same 9-month half-life batch of (68)Ge/(68)Ga in epoxy. Repeat measurements occurred in a local network of PET imaging sites to assess standardized uptake value (SUV) errors over time for six dose calibrators from two major manufacturers and for six PET/CT scanners from three major manufacturers. Bias in activity measures by dose calibrators ranged from -50% to 9% and was relatively stable over time except at one site that modified settings between measurements. Bias in activity concentration measures by PET scanners ranged from -27% to 13% with a median of 174 days between the six repeat scans (range, 29 to 226 days). Corresponding errors in SUV measurements ranged from -20% to 47%. SUV biases were not stable over time with longitudinal differences for individual scanners ranging from -11% to 59%. Bias in SUV measurements varied over time and between scanner sites. These results suggest that attention should be paid to PET scanner calibration for longitudinal studies and use of dose calibrator and scanner cross-calibration kits could be helpful for quality assurance and control.
本研究调查了由于仪器变化包括人为错误导致的纵向正电子发射断层扫描/计算机断层扫描(PET/CT)研究中的测量偏差。更好地估计患者扫描之间的变异性对于评估治疗反应和多中心试验非常重要。我们使用国家技术标准研究所可追踪的校准方法,对固体锗-68/镓-68((68)Ge/(68)Ga)源进行校准,这些源用作放射性核素活度校准器中的氟-18((18)F)的替代品。使用同一批在环氧树脂中的 9 个月半衰期的(68)Ge/(68)Ga,为剂量校准器和 PET 扫描仪构建了一个交叉校准套件。在本地 PET 成像站点网络中进行重复测量,以评估来自两个主要制造商的六个剂量校准器和来自三个主要制造商的六个 PET/CT 扫描仪的标准化摄取值(SUV)误差随时间的变化。剂量校准器的活性测量偏差范围为-50%至 9%,并且相对稳定,除非在一个站点在测量之间修改了设置。PET 扫描仪的活性浓度测量偏差范围为-27%至 13%,六个重复扫描之间的中位数为 174 天(范围为 29 至 226 天)。相应的 SUV 测量误差范围为-20%至 47%。SUV 偏差随时间不稳定,个别扫描仪的纵向差异范围为-11%至 59%。SUV 测量的偏差随时间和扫描仪站点而变化。这些结果表明,应注意纵向研究中的 PET 扫描仪校准,并且剂量校准器和扫描仪交叉校准套件的使用可能有助于质量保证和控制。