Department of Radiology, Section of Interventional Radiology, Northwestern University, Chicago, IL.
Department of Radiology, Section of Interventional Radiology, Northwestern University, Chicago, IL.
J Vasc Interv Radiol. 2021 Aug;32(8):1103-1112.e12. doi: 10.1016/j.jvir.2021.01.282. Epub 2021 Apr 9.
To investigate the feasibility, safety, and absorbed-dose distribution of prostatic artery radioembolization (RE) in a canine model.
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 (Y) 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.
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.
Prostate Y 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.
研究前列腺动脉放射性栓塞(RE)在犬模型中的可行性、安全性和吸收剂量分布。
14 只雄性去势比格犬接受二氢睾丸酮/雌二醇治疗以诱导前列腺增生,持续整个研究过程。每只狗都接受了荧光透视前列腺动脉导管插入术。钇-90(Y)微球(TheraSphere;波士顿科学,马萨诸塞州马尔伯勒)被输送到 1 个前列腺半腺体(剂量递增至 60 至 200Gy),对侧作为对照。在整个随访过程中(不良事件通用术语标准 5.0 版)进行不良事件评估。正电子发射断层扫描/磁共振(MR)成像在输送吸收剂量分布后提供了确认。MR 成像在 RE 前、3、20 和 40 天后进行。RE 后 60 天,对前列腺、直肠、膀胱、尿道、阴茎和神经血管束进行了组织采集。
所有动物均成功接受 RE。正电子发射断层扫描/MR 成像显示仅靶向并很好地覆盖治疗的半腺体。未发生不良事件。MR 成像显示,治疗后 40 天,受治疗的半腺体大小呈剂量依赖性显著缩小(25%-60%,P<.001)。未观察到前列腺外的放射学变化。尸检未发现直肠、尿道、阴茎或膀胱的大体变化。组织学显示,最高剂量组的治疗前列腺组织发生了 RE 诱导的变化,表现为腺体萎缩和局灶性坏死。未观察到前列腺外与 RE 相关的组织学发现。
在犬模型中,前列腺 YRE 是安全可行的,可导致腺体局灶性、剂量依赖性变化,而不会引起不必要的前列腺外效应。这些结果表明,有必要对非手术治疗的前列腺癌进行研究。