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新型经支气管镜外部冷却射频消融导管消融周围肺部肿瘤的安全性和可行性:首例人体剂量递增研究。

Safety and Feasibility of a Novel Externally Cooled Bronchoscopic Radiofrequency Ablation Catheter for Ablation of Peripheral Lung Tumours: A First-In-Human Dose Escalation Study.

机构信息

Department of Respiratory Medicine, The Royal Melbourne Hospital, Melbourne, Victoria, Australia.

Department of Medicine, The University of Melbourne, Melbourne, Victoria, Australia.

出版信息

Respiration. 2023;102(3):211-219. doi: 10.1159/000529167. Epub 2023 Jan 31.

Abstract

BACKGROUND

Radiofrequency ablation (RFA) is an established modality for percutaneous ablation of non-small cell lung cancer (NSCLC) in medically inoperable patients but is underutilized clinically due to side effects. We have developed a novel, completely endobronchial RFA catheter with an externally cooled electrode.

OBJECTIVES

The objective of this study was to establish the safety and feasibility of bronchoscopic RFA using a novel, externally cooled catheter for ablation of peripheral NSCLC.

METHODS

Patients with stage I biopsy-confirmed NSCLC underwent bronchoscopic RFA of tumour 7 days prior to lobectomy. The RFA catheter was delivered bronchoscopically to peripheral NSCLC lesions, guided by radial endobronchial ultrasound, with positioning confirmed using intra-procedural cone beam CT. Pre-operative CT chest and histologic examination of resected specimens were used to establish distribution/uniformity of ablation and efficacy of tumour ablation.

RESULTS

RFA in the first patient was complicated by dispersal of heated saline due to cough, resulting in ICU admission. The patient recovered fully and underwent uncomplicated lobectomy. Subsequently, the protocol was altered to mandate neuromuscular blockade with a pre-determined dose escalation, with algorithm-restricted energy (kJ) and irrigated saline volume (mL) constraints. A further 10 patients consented and seven underwent successful bronchoscopic RFA of peripheral NSCLC. No significant adverse events were noted. Ablation zone included tumour in all cases (proportion of tumour ablated ranged 8-72%), with uniform necrosis of tissue within ablation zones observed at higher energy levels. Ablation zone diameter correlated with RFA energy delivered (R2 = 0.553), with maximum long axis diameter of ablation zone 3.1 cm (22.9 kJ).

CONCLUSION

Bronchoscopic RFA using an externally cooled catheter is feasible, appears safe, and achieves uniform ablation within the treatment zone. Uncontrolled escape of heated saline poses a major safety risk but can be prevented procedurally through neuromuscular blockade and by limiting irrigation.

摘要

背景

射频消融 (RFA) 是一种用于不能手术的非小细胞肺癌 (NSCLC) 经皮消融的成熟方法,但由于副作用,在临床上的应用并不广泛。我们开发了一种新型的、完全经支气管内的 RFA 导管,带有外部冷却电极。

目的

本研究的目的是建立使用新型外部冷却导管进行支气管内 RFA 的安全性和可行性,以消融周围型 NSCLC。

方法

接受支气管镜 RFA 的患者在肺叶切除术前 7 天接受肿瘤的支气管镜 RFA。RFA 导管经支气管镜送达外周性 NSCLC 病变部位,通过径向支气管内超声引导,使用术中锥形束 CT 确认定位。术前胸部 CT 和切除标本的组织学检查用于确定消融的分布/均匀性和肿瘤消融的效果。

结果

首例患者的 RFA 因咳嗽导致加热盐水扩散而复杂化,导致入住 ICU。患者完全康复并成功进行了肺叶切除术。随后,该方案改为要求使用预定剂量递增的神经肌肉阻滞剂,并限制算法能量 (kJ) 和灌洗盐水量 (mL)。另外有 10 名患者同意并进行了 7 例成功的支气管镜下周围性 NSCLC 的 RFA。没有观察到明显的不良事件。在所有病例中,消融区均包括肿瘤(消融的肿瘤比例范围为 8-72%),在较高能量水平下观察到消融区内组织的均匀坏死。消融区直径与 RFA 能量输送相关(R2=0.553),消融区最大长轴直径为 3.1cm(22.9kJ)。

结论

使用外部冷却导管的支气管镜 RFA 是可行的,似乎是安全的,并在治疗区内实现了均匀的消融。加热盐水的不受控制逸出构成了重大的安全风险,但可以通过神经肌肉阻滞剂和限制灌洗来预防。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0cb/9986835/dc499d0a9d68/res-0102-0211-g01.jpg

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