ClearPoint Prism®激光消融系统:神经肿瘤学激光间质热治疗(LITT)的新平台。

Neurosurgery practice Pub Date : 2024-02-21 eCollection Date: 2024-03-01 DOI:10.1227/neuprac.0000000000000084
Hannah Wilson, Sanjay Dhawan, Truong Huy Do, Samuel H Jones, Clark C Chen
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引用次数: 0

摘要

背景与目的:激光间质热疗法(LITT)促进了脑癌的外科治疗。然而,第一代激光烧蚀系统的技术限制限制了该技术的全部潜力。ClearPoint Prism®激光消融系统的开发克服了许多这些限制,包括更大的消融窗口,更快的磁共振测温刷新率,以及与mri兼容的立体定向系统的集成。该系统于2022年被美国食品和药物管理局批准用于神经外科手术。方法:作为一项IDEAL一期研究,我们前瞻性地随访了前3名在美国使用ClearPoint Prism®激光消融系统接受LITT的患者,以确定该技术平台的可行性和安全性。结果:3例患者接受了mri引导下的穿刺活检,随后进行了LITT。相对于预定目标的立体定向径向误差范围为0.8 ~ 1.6 mm(中位数为1.0 mm)。所有病例均获得明确诊断。建立轨迹所需的平均时间为98.7±16.6分钟。活检和LITT的平均时间为110±19.3分钟。这些时间与我们发表的使用其他可用LITT系统的可比程序的统计结果没有统计学差异。实现半径为bbbb1 cm的消融所需的平均LITT时间为49秒(范围:29-133秒)。没有手术并发症。所有患者均于术后第3天出院。术后mri显示预期的消融结果与术中体温评估一致。中位随访219天(范围:185-259天),无30天再入院、90天急诊或伤口并发症。结论:在本研究中,我们介绍了ClearPoint Prism®激光烧蚀系统的设计原理,相对于其他现有系统的技术优点的理论考虑,并分享了我们的初步经验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The ClearPoint Prism® Laser Ablation System: A New Platform for Laser Interstitial Thermal Therapy (LITT) in Neuro-Oncology.

Background and objectives: Laser interstitial thermal therapy (LITT) has advanced the surgical treatment of brain cancer. However, technical constraints in the first-generation laser ablation systems limit the full potential of this technology. The ClearPoint Prism® Laser Ablation System was developed to overcome many of these limitations, including a larger ablation window, a faster refresh rate for magnetic resonance thermometry, and integration with an MRI-compatible stereotactic system. This system was US Food and Drug Administration-cleared for neurosurgical use in 2022.

Methods: As an IDEAL Stage 1 study, we prospectively followed the first 3 patients who underwent LITT using the ClearPoint Prism® Laser Ablation System in the United States to establish feasibility and safety of this technology platform.

Results: Three patients underwent procedures involving MRI-guided needle biopsy followed by LITT. The radial error of stereotaxis relative to the intended target ranged from 0.8 to 1.6 mm (with a median of 1.0 mm). Definitive diagnosis was achieved in all cases. The average time required to establish the trajectories was 98.7 ± 16.6 minutes. The average time required to perform the biopsy and LITT was 110 ± 19.3 minutes. These times are not statistically different from our published results for comparable procedures using other available LITT systems. The average LITT time required to achieve ablation of >1 cm radius was 49 seconds (range: 29-133 seconds). There were no procedural complications. All patients were discharged home by postoperative day 3. The postoperative MRIs demonstrated expected ablation findings consistent with intraoperative thermometric assessment. With a median follow-up of 219 days (range: 185-259 days), there were no 30-day readmission, 90-day emergency visits, or wound complications.

Conclusion: In this study, we introduced the design rationale for the ClearPoint Prism® Laser Ablation System, theoretical considerations for its technical merits relative to other existing systems, and to share our initial experience.

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