Black Noel F, McJames Scott, Kadrmas Dan J
Utah Center for Advanced Imaging Research, University of Utah, Salt Lake City, UT 84108-1218 USA.
IEEE Trans Nucl Sci. 2009 Oct 1;56(5):2750-2758. doi: 10.1109/TNS.2009.2026417.
Rapid multi-tracer PET, where two to three PET tracers are rapidly scanned with staggered injections, can recover certain imaging measures for each tracer based on differences in tracer kinetics and decay. We previously showed that single-tracer imaging measures can be recovered to a certain extent from rapid dual-tracer (62)Cu - PTSM (blood flow) + (62)Cu - ATSM (hypoxia) tumor imaging. In this work, the feasibility of rapidly imaging (18)F-FDG plus one or two of these shorter-lived secondary tracers was evaluated in the same tumor model. Dynamic PET imaging was performed in four dogs with pre-existing tumors, and the raw scan data was combined to emulate 60 minute long dual- and triple-tracer scans, using the single-tracer scans as gold standards. The multi-tracer data were processed for static (SUV) and kinetic (K(1), K(net)) endpoints for each tracer, followed by linear regression analysis of multi-tracer versus single-tracer results. Static and quantitative dynamic imaging measures of FDG were both accurately recovered from the multi-tracer scans, closely matching the single-tracer FDG standards (R > 0.99). Quantitative blood flow information, as measured by PTSM K(1) and SUV, was also accurately recovered from the multi-tracer scans (R = 0.97). Recovery of ATSM kinetic parameters proved more difficult, though the ATSM SUV was reasonably well recovered (R = 0.92). We conclude that certain additional information from one to two shorter-lived PET tracers may be measured in a rapid multi-tracer scan alongside FDG without compromising the assessment of glucose metabolism. Such additional and complementary information has the potential to improve tumor characterization in vivo, warranting further investigation of rapid multi-tracer techniques.
快速多示踪剂PET,即通过交错注射对两到三种PET示踪剂进行快速扫描,可根据示踪剂动力学和衰变的差异恢复每种示踪剂的某些成像指标。我们之前表明,单示踪剂成像指标可在一定程度上从快速双示踪剂(62)Cu - PTSM(血流)+(62)Cu - ATSM(缺氧)肿瘤成像中恢复。在这项工作中,在同一肿瘤模型中评估了快速成像(18)F - FDG加上一或两种这些短寿命次级示踪剂的可行性。对四只患有现有肿瘤的犬进行了动态PET成像,并将原始扫描数据合并以模拟60分钟长的双示踪剂和三示踪剂扫描,将单示踪剂扫描作为金标准。对多示踪剂数据进行处理以获得每种示踪剂的静态(SUV)和动力学(K(1),K(净))终点,随后对多示踪剂与单示踪剂结果进行线性回归分析。FDG的静态和定量动态成像指标均从多示踪剂扫描中准确恢复,与单示踪剂FDG标准密切匹配(R>0.99)。通过PTSM K(1)和SUV测量的定量血流信息也从多示踪剂扫描中准确恢复(R = 0.97)。虽然ATSM SUV恢复得相当好(R = 0.92),但ATSM动力学参数的恢复证明更困难。我们得出结论,在不影响葡萄糖代谢评估的情况下,可在快速多示踪剂扫描中与FDG一起测量来自一到两种短寿命PET示踪剂的某些额外信息。这种额外的补充信息有可能改善体内肿瘤特征,值得对快速多示踪剂技术进行进一步研究。