前列腺补救性HIFU中基准标记物引起光束畸变的实验研究。

Journal of therapeutic ultrasound Pub Date : 2018-03-22 eCollection Date: 2018-01-01 DOI:10.1186/s40349-018-0109-3
Marina Bakaric, Eleanor Martin, Panayiotis S Georgiou, Benjamin T Cox, Heather Payne, Bradley E Treeby
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引用次数: 8

摘要

背景:前列腺癌常用外束放射治疗(EBRT)治疗。在治疗之前,前列腺通常植入少量永久性基准标记物,用于监测治疗期间前列腺的位置。在局部癌症复发的情况下,高强度聚焦超声(HIFU)提供了一种非侵入性的抢救治疗选择。然而,基准标记物对HIFU治疗的影响至今尚未得到彻底的研究。本研究的目的是通过实验研究单一EBRT基准标志物对使用组织模拟材料(TMM)进行HIFU治疗效果的影响。方法:采用含有牛血清白蛋白的聚丙烯酰胺水凝胶制备具有前列腺声学特性的TMM。每个假体植入一个圆柱形基准标记,然后使用3.3 MHz聚焦碗状HIFU换能器进行超声处理。进行了两组实验。首先,在相对于标记物的前后轴或左右轴的不同位置创建单个病变。在第二种情况下,通过光栅扫描产生更大的烧蚀体积。消融体积的大小和位置使用覆盖在假体上的毫米网格进行评估。结果:当换向器病灶位于标记物前方7mm、后方18mm和外侧3mm范围内时,标记物对HIFU病灶位置和大小的影响显著。除此之外,所产生的病变不受影响。当病灶位于标记物前方时,病变因反射而增大。当病灶位于后方时,病灶大小减小或因阴影而不存在。结论:EBRT基准标记物的存在可能导致由于到达焦点的能量减少而导致标记物以外的区域治疗不足,并且由于反射而导致标记物前面的区域治疗过度。根据靶向区域的位置和标记物的分布,这两种作用都可能是不希望的,从而降低治疗效果。需要进一步研究这些结果是否表明在EBRT失败后需要重新考虑患者选择和前列腺挽救性HIFU的治疗计划。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Experimental study of beam distortion due to fiducial markers during salvage HIFU in the prostate.

Experimental study of beam distortion due to fiducial markers during salvage HIFU in the prostate.

Experimental study of beam distortion due to fiducial markers during salvage HIFU in the prostate.

Experimental study of beam distortion due to fiducial markers during salvage HIFU in the prostate.

Background: Prostate cancer is frequently treated using external beam radiation therapy (EBRT). Prior to therapy, the prostate is commonly implanted with a small number of permanent fiducial markers used to monitor the position of the prostate during therapy. In the case of local cancer recurrence, high-intensity focused ultrasound (HIFU) provides a non-invasive salvage treatment option. However, the impact of the fiducial markers on HIFU treatment has not been thoroughly studied to date. The objective of this study was to experimentally investigate the effect of a single EBRT fiducial marker on the efficacy of HIFU treatment delivery using a tissue-mimicking material (TMM).

Methods: A TMM with the acoustic properties of the prostate was developed based on a polyacrylamide hydrogel containing bovine serum albumin. Each phantom was implanted with a cylindrical fiducial marker and then sonicated using a 3.3 MHz focused bowl HIFU transducer. Two sets of experiments were performed. In the first, a single lesion was created at different positions along either the anteroposterior or left-right axes relative to the marker. In the second, a larger ablation volume was created by raster scanning. The size and position of the ablated volume were assessed using a millimetre grid overlaid on the phantom.

Results: The impact of the marker on the position and size of the HIFU lesion was significant when the transducer focus was positioned within 7 mm anteriorly, 18 mm posteriorly or within 3 mm laterally of the marker. Beyond this, the generated lesion was not affected. When the focus was anterior to the marker, the lesion increased in size due to reflections. When the focus was posterior, the lesion decreased in size or was not present due to shadowing.

Conclusions: The presence of an EBRT fiducial marker may result in an undertreated region beyond the marker due to reduced energy arriving at the focus, and an overtreated region in front of the marker due to reflections. Depending on the position of the targeted regions and the distribution of the markers, both effects may be undesirable and reduce treatment efficacy. Further work is necessary to investigate whether these results indicate the necessity to reconsider patient selection and treatment planning for prostate salvage HIFU after failed EBRT.

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