MRI引导的前列腺部分腺体冷冻消融的程序规划和3D模拟:一项初步研究。

IF 3.2 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
Nicole Wake, Andrew B Rosenkrantz, Daniel K Sodickson, Hersh Chandarana, James S Wysock
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引用次数: 2

摘要

目的:本研究报告了一种新的3D手术计划技术的发展,为部分腺体前列腺冷冻消融(cPGA)提供消融前治疗计划。方法:对20例行部分腺体冷冻消融(cPGA)的患者进行术前图像分割,并根据多参数MRI数据对前列腺包膜、指数病变、尿道、直肠和神经血管束进行三维建模。设计治疗前三维规划模型,包括虚拟三维冷冻治疗探针,预测和规划实现融合治疗体积所需的冷冻治疗探针配置。通过术后6个月的MRI、3个月和6个月的血清前列腺特异性抗原(PSA)以及6个月的治疗区活检结果来衡量治疗效果。将3D计划的结果与20例采用传统2D计划技术进行cPGA的患者的结果进行比较。结果:40例患者行cPGA。接受3D治疗计划的队列中位年龄为64.8岁,中位预处理PSA为6.97 ng/mL。该队列中治疗的指数病变的Gleason分级组(GGG)包括1 (5%)GGG1, 11 (55%) GGG2, 7 (35%) GGG3和1 (5%)GGG4。其中2例(10%)为放射后补救性治疗。2D治疗队列包括20名男性,中位年龄为68.5岁。中位预处理PSA为6.76 ng/mL。该队列中治疗指数病变的Gleason分级组(GGG)为GGG1组3例(15%),GGG2组8例(40%),GGG3组8例(40%),GGG4组1例(5%)。其中2例(10%)为放射后补救性治疗。3D计划预测各组冷冻探针数量相同,但预期3D组在手术过程中使用的冷冻探针数量多于2D计划组(分别为4.10±1.37和3.25±0.44,p = 0.01)。cPGA后6个月,3D组和2D组的中位PSA分别为1.68 ng/mL和2.38 ng/mL, 3D组下降幅度更大(3D组下降75.9%,2D组下降64.8%,p 0.48)。在3D队列中,监测活检的现场疾病检出率为1/14(7.1%),在2D队列中为3/14 (21.4%),p = 0.056。在3D队列中,4例患者(20%)由于未检测到PSA、MRI阴性和MRI Axumin PET阴性而未进行6个月的活检。传统二维方案组治疗区活检阳性的患者占3/14 (21.4%),p = 0.056。结论:基于mpMRI数据的三维前列腺癌模型为规划cPGA融合治疗量提供了新的指导,并且比传统的二维规划方法预测更多的治疗探针。随着部分腺体消融治疗方案的发展,本研究促使进一步研究使用3D治疗计划技术。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

MRI guided procedure planning and 3D simulation for partial gland cryoablation of the prostate: a pilot study.

MRI guided procedure planning and 3D simulation for partial gland cryoablation of the prostate: a pilot study.

MRI guided procedure planning and 3D simulation for partial gland cryoablation of the prostate: a pilot study.

MRI guided procedure planning and 3D simulation for partial gland cryoablation of the prostate: a pilot study.

Purpose: This study reports on the development of a novel 3D procedure planning technique to provide pre-ablation treatment planning for partial gland prostate cryoablation (cPGA).

Methods: Twenty men scheduled for partial gland cryoablation (cPGA) underwent pre-operative image segmentation and 3D modeling of the prostatic capsule, index lesion, urethra, rectum, and neurovascular bundles based upon multi-parametric MRI data. Pre-treatment 3D planning models were designed including virtual 3D cryotherapy probes to predict and plan cryotherapy probe configuration needed to achieve confluent treatment volume. Treatment efficacy was measured with 6 month post-operative MRI, serum prostate specific antigen (PSA) at 3 and 6 months, and treatment zone biopsy results at 6 months. Outcomes from 3D planning were compared to outcomes from a series of 20 patients undergoing cPGA using traditional 2D planning techniques.

Results: Forty men underwent cPGA. The median age of the cohort undergoing 3D treatment planning was 64.8 years with a median pretreatment PSA of 6.97 ng/mL. The Gleason grade group (GGG) of treated index lesions in this cohort included 1 (5%) GGG1, 11 (55%) GGG2, 7 (35%) GGG3, and 1 (5%) GGG4. Two (10%) of these treatments were post-radiation salvage therapies. The 2D treatment cohort included 20 men with a median age of 68.5 yrs., median pretreatment PSA of 6.76 ng/mL. The Gleason grade group (GGG) of treated index lesions in this cohort included 3 (15%) GGG1, 8 (40%) GGG2, 8 (40%) GGG3, 1 (5%) GGG4. Two (10%) of these treatments were post-radiation salvage therapies. 3D planning predicted the same number of cryoprobes for each group, however a greater number of cryoprobes was used in the procedure for the prospective 3D group as compared to that with 2D planning (4.10 ± 1.37 and 3.25 ± 0.44 respectively, p = 0.01). At 6 months post cPGA, the median PSA was 1.68 ng/mL and 2.38 ng/mL in the 3D and 2D cohorts respectively, with a larger decrease noted in the 3D cohort (75.9% reduction noted in 3D cohort and 64.8% reduction 2D cohort, p 0.48). In-field disease detection was 1/14 (7.1%) on surveillance biopsy in the 3D cohort and 3/14 (21.4%) in the 2D cohort, p = 0.056) In the 3D cohort, 6 month biopsy was not performed in 4 patients (20%) due to undetectable PSA, negative MRI, and negative MRI Axumin PET. For the group with traditional 2D planning, treatment zone biopsy was positive in 3/14 (21.4%) of the patients, p = 0.056.

Conclusions: 3D prostate cancer models derived from mpMRI data provide novel guidance for planning confluent treatment volumes for cPGA and predicted a greater number of treatment probes than traditional 2D planning methods. This study prompts further investigation into the use of 3D treatment planning techniques as the increase of partial gland ablation treatment protocols develop.

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