Richter Antonia, Knorr Karina, Schlapschy Martin, Robu Stephanie, Morath Volker, Mendler Claudia, Yen Hsi-Yu, Steiger Katja, Kiechle Marion, Weber Wolfgang, Skerra Arne, Schwaiger Markus
1Nuklearmedizinische Klinik und Poliklinik, Klinikum rechts der Isar, Technische Universität München, Ismaninger Straße 22, 81675 Munich, Germany.
2Lehrstuhl für Biologische Chemie, Technische Universität München, Emil-Erlenmeyer-Forum 5, 85354 Freising, Germany.
Nucl Med Mol Imaging. 2020 Apr;54(2):114-119. doi: 10.1007/s13139-020-00638-7. Epub 2020 Apr 20.
PASylation® offers the ability to systematically tune and optimize the pharmacokinetics of protein tracers for molecular imaging. Here we report the first clinical translation of a PASylated Fab fragment (Zr∙Df-HER2-Fab-PAS) for the molecular imaging of tumor-related HER2 expression.
A patient with HER2-positive metastatic breast cancer received 37 MBq of Zr∙Df-HER2-Fab-PAS at a total mass dose of 70 μg. PET/CT was carried out 6, 24, and 45 h after injection, followed by image analysis of biodistribution, normal organ uptake, and lesion targeting.
Images show a biodistribution typical for protein tracers, characterized by a prominent blood pool 6 h p.i., which decreased over time. Lesions were detectable as early as 24 h p.i. Zr∙Df-HER2-Fab-PAS was tolerated well.
This study demonstrates that a PASylated Fab tracer shows appropriate blood clearance to allow sensitive visualization of small tumor lesions in a clinical setting.
PASylation®能够系统地调节和优化用于分子成像的蛋白质示踪剂的药代动力学。在此,我们报告了一种用于肿瘤相关HER2表达分子成像的PAS化Fab片段(Zr∙Df-HER2-Fab-PAS)的首次临床转化。
一名HER2阳性转移性乳腺癌患者接受了37 MBq的Zr∙Df-HER2-Fab-PAS,总质量剂量为70 μg。在注射后6、24和45小时进行PET/CT检查,随后对生物分布、正常器官摄取和病变靶向进行图像分析。
图像显示出蛋白质示踪剂典型的生物分布,其特征是注射后6小时血池明显,随时间推移而减少。病变最早在注射后24小时即可检测到。Zr∙Df-HER2-Fab-PAS耐受性良好。
本研究表明,PAS化Fab示踪剂显示出适当的血液清除率,能够在临床环境中灵敏地显示小肿瘤病变。