Olafson Emily, Tonietto Matteo, Klein Gregory, Teng Edmond, Stephens Andrew W, Russell David S, Pickthorn Karen, Sanabria Bohorquez Sandra
gRED, Genentech, Inc., South San Francisco, California;
pRED, F. Hoffmann-La Roche, Ltd., Basel, Switzerland.
J Nucl Med. 2025 Feb 3;66(2):277-285. doi: 10.2967/jnumed.124.268623.
Alzheimer disease (AD) is characterized by the accumulation of tau neurofibrillary tangles that can be labeled with PET tracers. Multiple tau PET tracers have been used in clinical studies, including [F]GTP1, [F]PI-2620, and [F]MK-6240. Standardized harmonization scales for comparing tau PET signals across tracers are currently under development and can be informed by comparisons of signals between tracers in both target and off-target regions of the brain. We conducted a head-to-head study comparing [F]GTP1 with [F]PI-2620 and [F]MK-6240 in terms of dynamic range, magnitude of uptake, and correlation between tracers in participants with normal cognition and prodromal to mild AD. [F]GTP1 exhibited retention patterns that correlated with [F]PI-2620 and [F]MK-6240 for all Braak regions (except Braak II). Differences in tracer binding in AD target regions were relatively small, and off-target binding profiles were unique to each tracer. Our findings indicate that [F]GTP1, [F]PI-2620, and [F]MK-6240 display similar uptake patterns in AD patients, suggesting that they detect the same tau pathology. However, the tracer-specific off-target signal distribution may impact their direct comparability, and for some use cases, tracer-specific considerations should be taken into account in the development of a standardized harmonization scale for tau PET.
阿尔茨海默病(AD)的特征是tau神经原纤维缠结的积累,这些缠结可用PET示踪剂标记。多种tau PET示踪剂已用于临床研究,包括[F]GTP1、[F]PI-2620和[F]MK-6240。目前正在开发用于比较不同示踪剂的tau PET信号的标准化协调量表,这可通过比较大脑目标区域和非目标区域中不同示踪剂之间的信号来实现。我们进行了一项对比研究,在认知正常和轻度AD前驱期参与者中,比较了[F]GTP1与[F]PI-2620和[F]MK-6240在动态范围、摄取量以及示踪剂之间的相关性。对于所有Braak区域(除Braak II外),[F]GTP1表现出与[F]PI-2620和[F]MK-6240相关的滞留模式。AD目标区域中示踪剂结合的差异相对较小,且每种示踪剂的非目标结合谱都是独特的。我们的研究结果表明,[F]GTP1、[F]PI-2620和[F]MK-6240在AD患者中显示出相似的摄取模式,这表明它们检测到相同的tau病理学特征。然而,示踪剂特异性的非目标信号分布可能会影响它们的直接可比性,并且对于某些应用案例,在制定tau PET标准化协调量表时应考虑示踪剂特异性因素。