[44Sc]Sc-PSMA-617 Biodistribution and Dosimetry in Patients With Metastatic Castration-Resistant Prostate Carcinoma

医学 体内分布 核医学 脾脏 膀胱 前列腺 剂量学 腹部 泌尿系统 小肠 体内 病理 泌尿科 放射科 内科学 癌症 生物 生物技术
作者
Ambreen Khawar,Elisabeth Eppard,Jean Phlippe Sinnes,Frank Roesch,Hojjat Ahmadzadehfar,Stefan Kürpig,Michael Meisenheimer,Florian Gaertner,Markus Essler,Ralph A. Bundschuh
出处
期刊:Clinical Nuclear Medicine [Ovid Technologies (Wolters Kluwer)]
卷期号:43 (5): 323-330 被引量:24
标识
DOI:10.1097/rlu.0000000000002003
摘要

Aim [ 44 Sc]Sc-PSMA-617 with 3.9-hour half-life, in vitro and in vivo characteristics similar to [ 177 Lu]Lu-PSMA-617 and possibility of delayed imaging after 24 hours or later, implies it to be advantageous than [ 68 Ga]Ga-PSMA-617 for pretherapeutic dosimetric assessment for [ 177 Lu]Lu-PSMA-617 in metastatic castration-resistant prostate carcinoma (mCRPC) patients. In this study, we investigated biodistribution and radiation exposure to normal organs with [ 44 Sc]Sc-PSMA-617 in mCRPC patients. Methods Five mCRPC patients (mean age, 69 years) enrolled for [ 177 Lu]Lu-PSMA-617 therapy were injected with 40–62 MBq [ 44 Sc]Sc-PSMA-617 intravenously; Siemens Biograph 2 PET/CT system was used to acquire dynamic PET data (30 minutes) in list mode over the abdomen, followed by the collection of static PET/CT images (skull to mid-thigh) at 45 minutes, 2 and approximately 20 hours postinjection. Time-dependent changes in percentage activity in source organs (kidneys, bladder, salivary glands, small intestine, liver, spleen, and whole body) were determined. Bone marrow and urinary bladder contents residence time were also calculated. Source organs residence time, organ-absorbed doses, and effective doses were determined using OLINDA/EXM software. Results Physiological tracer uptake was seen in kidneys, liver, spleen, small intestine, urinary bladder, and salivary glands and in metastases. Kidneys with highest radiation absorbed dose of 3.19E-01 mSv/MBq were the critical organs, followed by urinary bladder wall (2.24E-01 mSv/MBq, spleen [1.85E-01], salivary glands [1.11E-01], and liver [1.07E-01] mSv/MBq). Red marrow dose was found to be 3.31E-02 mSv/MBq. The mean effective dose of 3.89E-02 mSv/MBq and effective dose of 1.95 mSv was estimated from 50 MBq (treatment planning dose) of [ 44 Sc]Sc-PSMA-617. Conclusions [ 44 Sc]Sc-PSMA-617 is found to be a very promising radiopharmaceutical that can be used for pre [ 177 Lu]Lu-PSMA-617 therapeutic dosimetric assessment.
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