Yttrium-90 Radioembolization to the Prostate Gland: Proof of Concept in a Canine Model and Clinical Translation

医学 磁共振成像 前列腺 神经血管束 泌尿科 不利影响 尿道 放射科 核医学 病理 内科学 癌症
作者
S. Mouli,Simone Raiter,Kathleen R. Harris,Amrutha Mylarapu,Malcolm Burks,Weiguo Li,Andrew C. Gordon,Ali Khan,Monica M. Matsumoto,Keith Bailey,Alexander S. Pasciak,Sasicha Manupipatpong,Clifford R. Weiss,David D. Casalino,Frank H. Miller,Vanessa L. Gates,Elias Hohlastos,Robert J. Lewandowski,Dong‐Hyun Kim,Matthew R. Dreher
出处
期刊:Journal of Vascular and Interventional Radiology [Elsevier BV]
卷期号:32 (8): 1103-1112.e12 被引量:16
标识
DOI:10.1016/j.jvir.2021.01.282
摘要

PURPOSE To investigate the feasibility, safety, and absorbed-dose distribution of prostatic artery radioembolization (RE) in a canine model. MATERIALS AND METHODS Fourteen male castrated beagles received dihydroandrosterone/estradiol to induce prostatic hyperplasia for the duration of the study. Each dog underwent fluoroscopic prostatic artery catheterization. Yttrium-90 (90Y) microspheres (TheraSphere; Boston Scientific, Marlborough, Massachusetts) were delivered to 1 prostatic hemigland (dose escalation from 60 to 200 Gy), with the contralateral side serving as a control. Assessments for adverse events were performed throughout the follow-up (Common Terminology Criteria for Adverse Events v5.0). Positron emission tomography/magnetic resonance (MR) imaging provided a confirmation after the delivery of absorbed-dose distribution. MR imaging was performed before and 3, 20, and 40 days after RE. Tissue harvest of the prostate, rectum, bladder, urethra, penis, and neurovascular bundles was performed 60 days after RE. RESULTS All the animals successfully underwent RE. Positron emission tomography/MR imaging demonstrated localization to and good coverage of only the treated hemigland. No adverse events occurred. The MR imaging showed a significant dose-dependent decrease in the treated hemigland size at 40 days (25%-60%, P < .001). No extraprostatic radiographic changes were observed. Necropsy demonstrated no gross rectal, urethral, penile, or bladder changes. Histology revealed RE-induced changes in the treated prostatic tissues of the highest dose group, with gland atrophy and focal necrosis. No extraprostatic RE-related histologic findings were observed. CONCLUSIONS Prostate 90Y RE is safe and feasible in a canine model and leads to focal dose-dependent changes in the gland without inducing unwanted extraprostatic effects. These results suggest that an investigation of nonoperative prostate cancer is warranted.
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