Thursday, July 11, 20244:00 PM - 5:00 PM MPP01 Presentation Time: 4:00 PM

IF 1.7 4区 医学 Q4 ONCOLOGY
Mahbubur Rahman PhD , Yash Soni MD , Mary Gronberg PhD , Ambrosia Simmons MD, PhD , Shaghayegh Rezaie M.S.N., APRN, FNP-C, OCN , Joseph Kwon MD , Brett Tortelli MD , Shameca Ragan BS, MBA , Jennifer Cleaton BS, MBA , Shahed Badiyan MD , Audra Schwalk MD , Muhanned Abu-Hijleh MD , Hsienchang Chiu MD , Kim Styrvoky MD , Brian Hrycushko PhD , Aurelie Garant MD
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引用次数: 0

Abstract

Purpose

There have been recent disruptions in supply chains related to centering baskets intended for use with high dose rate (HDR) endobronchial brachytherapy. The standard plastic catheter (1.6mm diameter) without a centering basket gives too high of a surface dose to the bronchial mucosa to safely prescribe at distances of 5-10mm. We present on the commissioning and first reported clinical use of intraluminal endobronchial HDR brachytherapy by placing a standard plastic catheter within a robotic bronchoscope working channel, functioning as a fixed spacer of the source from the bronchial mucosa.

Materials and Methods

In this first in-human hybrid technique, a 68-year-old patient with an endobronchial tumor obstructing the lower left lobe in the superior segment of the bronchus received a definitive treatment with the HDR source. The patient previously received external beam radiation to the right upper lobe (24Gy in 1 Fractions) and 2 nodules in the left lower lobe (60Gy in 5 Fractions) of the lungs. The system was commissioned by measuring attenuation from the robotic bronchoscope (Intuitive Surgical, Inc., Sunnyvale, CA, USA) to determine scaling required for water-based TG43 dose calculations. Well chamber readings were taken with the Ir-192 HDR source inside the plastic catheter with and without the bronchoscope using a custom 3D printed well chamber insert. In preparation for clinical use, standard treatment plans were created in Eclipse (Varian Medical Systems, Inc., Palo Alto, CA, USA) in cm increments prescribing at 5mm or 10mm from the bronchoscope wall. Following general anesthesia, a therapeutic bronchoscope was inserted to perform tumor ablation and mechanical dilation in the occluded airway. After airway patency was achieved, the shape sensing robotic assisted bronchoscope was passed distal the endobronchial tumor. Tumor length was determined with the robotic bronchoscope, by marking the junction of the robotic catheter at its intersection of the endotracheal tube, both distal and proximal to the tumor. The HDR brachytherapy catheter was then inserted through the robotic catheter and placement was verified with fluoroscopic imaging and a radiopaque wire with fiducials in cm increments. Once alignment was verified, the brachytherapy catheter was secured to the robotic catheter using adhesive. The treatment plan was created with 1 cm proximal and distal margins. Catheter length was confirmed and obstruction check through the catheter was completed prior to delivery.

Results

The attenuation measurements from the bronchoscope were <1% over a length of 1 to 8 cm indicating no need to scale treatment delivery time. The bronchoscope's diameter of 3.8 mm significantly reduced the bronchial mucosal dose (by ∼2 times, ∼70 Gy vs. ∼30 Gy at tissue surface for 7.5 Gy/Fraction) compared to the standard plastic catheter without a centering basket. The patients’ tumor was 2 cm in length, and the treatment plan ensured dose (22.5 Gy in 3 Fraction) ±1 cm of the tumor (4 cm treatment length) prescribed at a depth of 0.5 cm from tissue surface. The patient was discharged home the same day in stable condition without acute complications.

Conclusions

HDR brachytherapy with a catheter within a robotic bronchoscope's channel was feasible as an alternative to the standard plastic catheter for endobronchial treatment.
2024 年 7 月 11 日(星期四)下午 4:00 - 5:00 MPP01 演讲时间:下午 4:00
目的最近,与用于高剂量率(HDR)支气管内近距离放射治疗的定心篮有关的供应链出现了中断。不带定心篮的标准塑料导管(直径为 1.6 毫米)对支气管粘膜的表面剂量过高,无法在 5-10 毫米的距离内安全使用。我们通过在机器人支气管镜工作通道内放置标准塑料导管,作为放射源与支气管粘膜之间的固定间隔,介绍了腔内支气管内HDR近距离放射治疗的调试和首次临床应用情况。该患者之前曾接受过肺部右上叶(24Gy,1 分)和左下叶 2 个结节(60Gy,5 分)的外照射。该系统通过测量机器人支气管镜(直觉外科公司,美国加利福尼亚州森尼韦尔)的衰减进行调试,以确定基于水的 TG43 剂量计算所需的比例。在有支气管镜和没有支气管镜的情况下,使用定制的 3D 打印井室插入物在塑料导管内使用 Ir-192 HDR 源进行井室读数。在准备临床使用时,在 Eclipse(瓦里安医疗系统公司,美国加利福尼亚州帕洛阿尔托)中以厘米为单位创建了标准治疗计划,并在距支气管镜壁 5 毫米或 10 毫米处开具处方。全身麻醉后,插入治疗性支气管镜,在闭塞的气道中进行肿瘤消融和机械扩张。气道通畅后,将形状传感机器人辅助支气管镜通过支气管内肿瘤远端。通过机器人支气管镜在肿瘤远端和近端标记机器人导管与气管导管的交汇处,确定肿瘤的长度。然后通过机器人导管插入 HDR 近距离治疗导管,并通过透视成像和以厘米为单位增量的带有靶标的不透射线导线验证导管的位置。确认对准后,使用粘合剂将近距离治疗导管固定在机器人导管上。治疗计划的近端和远端边缘均为 1 厘米。结果支气管镜的衰减测量值在 1 至 8 厘米的长度范围内均为 1%,表明无需缩短治疗时间。支气管镜的直径为 3.8 毫米,与不带中心篮的标准塑料导管相比,支气管粘膜剂量明显减少(减少了 2 倍,70 Gy 与组织表面的 30 Gy 相比,7.5 Gy/Fraction)。患者的肿瘤长度为 2 厘米,治疗方案确保剂量(22.5 Gy,3 个分次)为肿瘤±1 厘米(治疗长度为 4 厘米),深度为组织表面 0.5 厘米。结论 在机器人支气管镜的通道内使用导管进行 HDR 近距离放射治疗是可行的,可以替代标准的塑料导管进行支气管内治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Brachytherapy
Brachytherapy 医学-核医学
CiteScore
3.40
自引率
21.10%
发文量
119
审稿时长
9.1 weeks
期刊介绍: Brachytherapy is an international and multidisciplinary journal that publishes original peer-reviewed articles and selected reviews on the techniques and clinical applications of interstitial and intracavitary radiation in the management of cancers. Laboratory and experimental research relevant to clinical practice is also included. Related disciplines include medical physics, medical oncology, and radiation oncology and radiology. Brachytherapy publishes technical advances, original articles, reviews, and point/counterpoint on controversial issues. Original articles that address any aspect of brachytherapy are invited. Letters to the Editor-in-Chief are encouraged.
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