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经 MRI 控制的经尿道超声治疗凝固人前列腺体积:凝胶模型的结果。

Coagulation of human prostate volumes with MRI-controlled transurethral ultrasound therapy: results in gel phantoms.

机构信息

Imaging Research, Sunnybrook Research Institute, Toronto, Ontario M4N3M5, Canada.

出版信息

Med Phys. 2012 Jul;39(7):4524-36. doi: 10.1118/1.4730288.

Abstract

PURPOSE

The feasibility and safety of magnetic resonance imaging (MRI)-controlled transurethral ultrasound therapy were demonstrated recently in a preliminary human study in which a small subvolume of prostate tissue was treated prior to radical prostatectomy. Translation of this technology to full clinical use, however, requires the capability to generate thermal coagulation in a volume up to that of the prostate gland itself. The aim of this study was to investigate the parameters required to treat a full 3D human prostate accurately with a multi-element transurethral applicator and multiplanar MR temperature control.

METHODS

The approach was a combination of simulations (to select appropriate parameters) followed by experimental confirmation in tissue-mimicking phantoms. A ten-channel, MRI-compatible transurethral ultrasound therapy system was evaluated using six human prostate models (average volume: 36 cm(3)) obtained from the preliminary human feasibility study. Real-time multiplanar MR thermometry at 3 T was used to control the spatial heating pattern in up to nine planes simultaneously. Treatment strategies incorporated both single (4.6 or 8.1 MHz) and dual (4.6 and 14.4 MHz) frequencies, as well as maximum acoustic surface powers of 10 or 20 W cm(-2).

RESULTS

Treatments at 4.6 MHz were capable of coagulating a volume equivalent to 97% of the prostate. Increasing power from 10 to 20 W cm(-2) reduced treatment times by approximately 50% with full treatments taking 26 ± 3 min at a coagulation rate of 1.8 ± 0.4 cm(3) min(-1). A dual-frequency 4.6∕14.4 MHz treatment strategy was shown to be the most effective configuration for achieving full human prostate treatment while maintaining good treatment accuracy for small treatment radii. The dual-frequency approach reduced overtreatment close to the prostate base and apex, confirming the simulations.

CONCLUSIONS

This study reinforces the capability of MRI-controlled transurethral ultrasound therapy to treat full prostate volumes in a short treatment time with good spatial targeting accuracy and provides key parameters necessary for the next clinical trial.

摘要

目的

最近的一项初步人体研究证明了磁共振成像(MRI)控制经尿道超声治疗的可行性和安全性,该研究在根治性前列腺切除术前对前列腺的一小部分组织进行了治疗。然而,要将这项技术完全应用于临床,就需要有能力在与前列腺本身一样大的体积内产生热凝固。本研究的目的是研究使用多通道经尿道应用器和多平面磁共振温度控制来准确治疗整个 3D 前列腺所需的参数。

方法

该方法是模拟(选择合适的参数)和实验验证(在组织模拟体模中进行)的结合。评估了一种 10 通道、MRI 兼容的经尿道超声治疗系统,该系统使用从初步人体可行性研究中获得的 6 个人体前列腺模型(平均体积为 36cm3)进行了评估。在 3T 下实时进行多平面磁共振测温,以同时控制多达 9 个平面的空间加热模式。治疗策略包括单(4.6 或 8.1MHz)和双(4.6 和 14.4MHz)频率,以及最大声表面功率为 10 或 20W/cm2。

结果

4.6MHz 的治疗能够凝固相当于前列腺 97%的体积。将功率从 10W/cm2 增加到 20W/cm2,可将治疗时间缩短约 50%,全治疗时间为 26±3min,凝固速率为 1.8±0.4cm3/min。双频 4.6/14.4MHz 治疗策略被证明是实现全前列腺治疗的最有效配置,同时保持小治疗半径的良好治疗准确性。双频方法减少了靠近前列腺底部和顶点的过度治疗,这与模拟结果一致。

结论

本研究进一步证实了 MRI 控制经尿道超声治疗能够在短时间内用良好的空间靶向准确性治疗整个前列腺体积,并提供了下一次临床试验所需的关键参数。

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