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

Author:

Peltonen Sirkku1234ORCID,Serup Jørgen5,Tang Mimmi12,Gillstedt Martin12,Kantere Despoina12,Neittaanmäki Noora67,Holmström Peter1,Blakeley Jaishri O.8,Rosner Karli8,Roberts Joshua8,Bove Torsten9,Karmisholt Katrine Elisabeth5

Affiliation:

1. Department of Dermatology and Venereology, Sahlgrenska Academy University of Gothenburg Gothenburg Sweden

2. Department of Dermatology and Venereology Region Västra Götaland, Sahlgrenska University Hospital Gothenburg Sweden

3. Department of Dermatology and Allergology University of Helsinki Helsinki Finland

4. Department of Dermatology and Allergology HUS Helsinki University Hospital Helsinki Uusimaa Finland

5. Department of Dermatology Bispebjerg University Hospital Copenhagen Denmark

6. Department of Laboratory Medicine, Institute of Biomedicine Gothenburg University of Gothenburg Sahlgrenska Academy Gothenburg Sweden

7. Department of Clinical Pathology and Cytology Region Västra Götaland, Sahlgrenska University Hospital Gothenburg Sweden

8. Neurofibromatosis Therapeutic Acceleration Program (NTAP), Department of Neurology Johns Hopkins University School of Medicine Baltimore Maryland USA

9. TOOsonix A/S Hoersholm Denmark

Abstract

AbstractBackgroundHigh‐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.ObjectivesThe objective of this study was to investigate the safety, local tolerability and efficacy of a novel method utilizing HIFU for the treatment of cNFs.MethodsA 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.ResultsTwenty 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%).ConclusionsHIFU 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.

Publisher

Wiley

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