High-intensity focused ultrasound: Safety and efficacy of a novel treatment modality for neurofibromatosis type 1 cutaneous neurofibroma

Sirkku Peltonen, Jørgen Serup, Mimmi Tang, Martin Gillstedt, Despoina Kantere, Noora Neittaanmäki, Peter Holmström, Jaishri O. Blakeley, Karli Rosner, Joshua Roberts, Torsten Bove, Katrine Elisabeth Karmisholt
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Abstract

Background

High-intensity focused ultrasound (HIFU) is widely used in the treatment of deep tumours, but clinical trials on skin tumours are not yet available. Neurofibromatosis Type I (NF1) is among the most common single-gene inherited conditions worldwide and predisposes to benign and malignant neoplasms of the nervous system. Multiple cutaneous neurofibromas (cNFs) often cause social and functional limitations, itching and pain.

Objectives

The objective of this study was to investigate the safety, local tolerability and efficacy of a novel method utilizing HIFU for the treatment of cNFs.

Methods

A 20 MHz HIFU-device with an integrated dermoscopic guidance and a handpiece with a focus depth of 2.3 mm below the skin surface was used. Doses of acoustic energy with 0.7 J/dose and pulse duration of 250 ms/dose were manually positioned with 1–2 mm distance between each applied dose. Number of applied doses depended on the size of the cNF. No anaesthetic was applied.

Results

Twenty patients with NF1 were recruited in two centres, and 147 cNFs were treated. There were no serious adverse events. Immediate and transient wheal-and-flare reactions occurred at treatment sites and occasionally there was minor epidermal damage which healed in 1–2 weeks. Dyspigmentation occurred in some tumours after 3–9 months but no scarring was observed at 9-month follow-up. During treatment, the patient-reported pain-score median was 3.5 (range 1–7) on a 0–10-point scale. Clinical rating of cNFs after 9 months showed 48.9% full or major tumour reduction. The median reduction in tumour thickness measured by ultrasound at 9 months was 0.53 mm (range: –100% to +19%).

Conclusions

HIFU treatment is a new noninvasive, rapid and tolerable treatment modality that with high precision targets intradermal lesions. This study demonstrates acceptable safety, local tolerance and efficacy of HIFU for the treatment of cNFs that may further be developed also for other skin tumours.

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高强度聚焦超声:神经纤维瘤病 1 型皮肤神经纤维瘤新型治疗方式的安全性和有效性
高强度聚焦超声(HIFU)被广泛用于治疗深部肿瘤,但目前还没有针对皮肤肿瘤的临床试验。神经纤维瘤病 I 型(NF1)是世界上最常见的单基因遗传病之一,易导致神经系统良性和恶性肿瘤。本研究旨在探讨利用 HIFU 治疗多发性皮肤神经纤维瘤的新型方法的安全性、局部耐受性和疗效。本研究使用了 20 MHz HIFU 设备,该设备配有集成皮肤镜引导和聚焦深度为皮肤表面下 2.3 mm 的手机。声波能量剂量为 0.7 焦耳/剂量,脉冲持续时间为 250 毫秒/剂量,每个剂量之间的距离为 1-2 毫米。应用剂量的数量取决于 cNF 的大小。两个中心共招募了 20 名 NF1 患者,共治疗了 147 个 cNF。没有出现严重的不良反应。治疗部位出现了即刻性和短暂性麦粒肿和皮疹反应,偶尔会有轻微的表皮损伤,1-2周后痊愈。一些肿瘤在 3-9 个月后出现色素沉着,但在 9 个月的随访中未发现瘢痕。治疗期间,患者报告的疼痛评分中位数为 3.5(范围 1-7)(0-10 分)。9 个月后对 cNFs 的临床评分显示,48.9% 的肿瘤完全或主要缩小。9个月后,超声波测量的肿瘤厚度减少中位数为0.53毫米(范围:-100%至+19%)。这项研究证明了 HIFU 治疗 cNFs 的安全性、局部耐受性和疗效都是可以接受的。
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