Photobiomodulation therapy for the prevention of acute radiation dermatitis in head and neck cancer patients (DERMISHEAD trial).

Acute radiodermatitis Head and neck cancer Photobiomodulation therapy Radiotherapy Skin toxicity Supportive care

Journal

Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology
ISSN: 1879-0887
Titre abrégé: Radiother Oncol
Pays: Ireland
ID NLM: 8407192

Informations de publication

Date de publication:
05 2021
Historique:
received: 14 12 2020
revised: 26 02 2021
accepted: 04 03 2021
pubmed: 13 3 2021
medline: 21 5 2021
entrez: 12 3 2021
Statut: ppublish

Résumé

The purpose of this study was to investigate the effectiveness of photobiomodulation therapy (PBMT) for the prevention of acute radiation dermatitis (ARD) in head and neck cancer (HNC) patients. A randomised, placebo-controlled trial (RCT) with 46 HNC patients who underwent radiotherapy (RT) with or without concomitant chemotherapy was set up (DERMISHEAD trial). Patients were randomised to receive PBM or placebo treatments from the first day of RT (2×/week) alongside the institutional skincare. The severity of skin reactions was assessed by the National Cancer Institute-Common Terminology Criteria for Adverse Events version 4.03 (NCI-CTCAE v4.03) and the Radiotherapy-Induced Skin Reaction Assessment Scale (RISRAS). Quality of life (QoL) was evaluated using the Skindex-16 questionnaire. PBMT significantly reduced NCI-CTCAE grade 2-3 ARD with 49% at the end of RT. The results of the first RCT in HNC patients showed that PBMT is an effective method to prevent the development of severe ARD. These results support the implementation of PBM in the clinical oncology - radiotherapy practice.

Sections du résumé

BACKGROUND AND PURPOSE
The purpose of this study was to investigate the effectiveness of photobiomodulation therapy (PBMT) for the prevention of acute radiation dermatitis (ARD) in head and neck cancer (HNC) patients.
MATERIALS AND METHODS
A randomised, placebo-controlled trial (RCT) with 46 HNC patients who underwent radiotherapy (RT) with or without concomitant chemotherapy was set up (DERMISHEAD trial). Patients were randomised to receive PBM or placebo treatments from the first day of RT (2×/week) alongside the institutional skincare. The severity of skin reactions was assessed by the National Cancer Institute-Common Terminology Criteria for Adverse Events version 4.03 (NCI-CTCAE v4.03) and the Radiotherapy-Induced Skin Reaction Assessment Scale (RISRAS). Quality of life (QoL) was evaluated using the Skindex-16 questionnaire.
RESULTS
PBMT significantly reduced NCI-CTCAE grade 2-3 ARD with 49% at the end of RT.
CONCLUSION
The results of the first RCT in HNC patients showed that PBMT is an effective method to prevent the development of severe ARD. These results support the implementation of PBM in the clinical oncology - radiotherapy practice.

Identifiants

pubmed: 33711412
pii: S0167-8140(21)06117-X
doi: 10.1016/j.radonc.2021.03.002
pii:
doi:

Types de publication

Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

268-275

Commentaires et corrections

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Informations de copyright

Copyright © 2021 The Author(s). Published by Elsevier B.V. All rights reserved.

Auteurs

Jolien Robijns (J)

Hasselt University, Faculty of Medicine & Life Sciences, LCRC, Hasselt, Belgium. Electronic address: jolien.robijns@uhasselt.be.

Joy Lodewijckx (J)

Hasselt University, Faculty of Medicine & Life Sciences, LCRC, Hasselt, Belgium.

Stefan Claes (S)

Limburg Oncology Center, Jessa Hospital - Campus Virga Jesse, Hasselt, Belgium.

Leen Van Bever (L)

Limburg Oncology Center, Jessa Hospital - Campus Virga Jesse, Hasselt, Belgium.

Luc Pannekoeke (L)

Limburg Oncology Center, Jessa Hospital - Campus Virga Jesse, Hasselt, Belgium.

Sandrine Censabella (S)

Limburg Oncology Center, Jessa Hospital - Campus Virga Jesse, Hasselt, Belgium.

Lore Bussé (L)

Hasselt University, Faculty of Medicine & Life Sciences, LCRC, Hasselt, Belgium.

Dora Colson (D)

Hasselt University, Faculty of Medicine & Life Sciences, LCRC, Hasselt, Belgium.

Iris Kaminski (I)

Hasselt University, Faculty of Medicine & Life Sciences, LCRC, Hasselt, Belgium.

Victoria Broux (V)

Hasselt University, Faculty of Medicine & Life Sciences, LCRC, Hasselt, Belgium.

Sofie Puts (S)

Hasselt University, Faculty of Medicine & Life Sciences, LCRC, Hasselt, Belgium.

Sofie Vanmechelen (S)

Hasselt University, Faculty of Medicine & Life Sciences, LCRC, Hasselt, Belgium.

An Timmermans (A)

Department of Dermatology, Jessa Hospital, Hasselt, Belgium.

Leen Noé (L)

Limburg Oncology Center, Jessa Hospital - Campus Virga Jesse, Hasselt, Belgium.

Paul Bulens (P)

Limburg Oncology Center, Jessa Hospital - Campus Virga Jesse, Hasselt, Belgium.

Mieke Govers (M)

Limburg Oncology Center, Ziekenhuis Oost-Limburg, Genk, Belgium.

Annelies Maes (A)

Limburg Oncology Center, Jessa Hospital - Campus Virga Jesse, Hasselt, Belgium; Limburg Oncology Center, Ziekenhuis Oost-Limburg, Genk, Belgium.

Jeroen Mebis (J)

Hasselt University, Faculty of Medicine & Life Sciences, LCRC, Hasselt, Belgium; Department of Medical Oncology, Jessa Hospital- Campus Virga Jesse, Hasselt, Belgium. Electronic address: Jeroen.mebis@jessazh.be.

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Classifications MeSH