VoiceS: voice quality after transoral CO<sub>2</sub> laser surgery versus single vocal cord irradiation for unilateral stage 0 and I glottic larynx cancer-a randomized phase III trial.

Détails

Ressource 1Télécharger: 36303192_BIB_AA7128E6DDF6.pdf (1902.41 [Ko])
Etat: Public
Version: Final published version
Licence: CC BY 4.0
ID Serval
serval:BIB_AA7128E6DDF6
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
VoiceS: voice quality after transoral CO<sub>2</sub> laser surgery versus single vocal cord irradiation for unilateral stage 0 and I glottic larynx cancer-a randomized phase III trial.
Périodique
Trials
Auteur⸱e⸱s
Reinhardt P., Giger R., Seifert E., Shelan M., Riggenbach E., Terribilini D., Joosten A., Schanne D.H., Aebersold D.M., Manser P., Dettmer M.S., Simon C., Ozsahin E.M., Moeckli R., Limacher A., Caparrotti F., Nair D., Bourhis J., Broglie M.A., Al-Mamgani A., Elicin O.
ISSN
1745-6215 (Electronic)
ISSN-L
1745-6215
Statut éditorial
Publié
Date de publication
27/10/2022
Peer-reviewed
Oui
Volume
23
Numéro
1
Pages
906
Langue
anglais
Notes
Publication types: Randomized Controlled Trial ; Multicenter Study ; Clinical Trial, Phase III ; Journal Article
Publication Status: epublish
Résumé
Surgery and radiotherapy are well-established standards of care for unilateral stage 0 and I early-stage glottic cancer (ESGC). Based on comparative studies and meta-analyses, functional and oncological outcomes after both treatment modalities are similar. Historically, radiotherapy (RT) has been performed by irradiation of the whole larynx. However, only the involved vocal cord is being treated with recently introduced hypofractionated concepts that result in 8 to 10-fold smaller target volumes. Retrospective data argues for an improvement in voice quality with non-inferior local control. Based on these findings, single vocal cord irradiation (SVCI) has been implemented as a routine approach in some institutions for ESGC in recent years. However, prospective data directly comparing SVCI with surgery is lacking. The aim of VoiceS is to fill this gap.
In this prospective randomized multi-center open-label phase III study with a superiority design, 34 patients with histopathologically confirmed, untreated, unilateral stage 0-I ESGC (unilateral cTis or cT1a) will be randomized to SVCI or transoral CO <sub>2</sub> -laser microsurgical cordectomy (TLM). Average difference in voice quality, measured by using the voice handicap index (VHI) will be modeled over four time points (6, 12, 18, and 24 months). Primary endpoint of this study will be the patient-reported subjective voice quality between 6 to 24 months after randomization. Secondary endpoints will include perceptual impression of the voice via roughness - breathiness - hoarseness (RBH) assessment at the above-mentioned time points. Additionally, quantitative characteristics of voice, loco-regional tumor control at 2 and 5 years, and treatment toxicity at 2 and 5 years based on CTCAE v.5.0 will be reported.
To our knowledge, VoiceS is the first randomized phase III trial comparing SVCI with TLM. Results of this study may lead to improved decision-making in the treatment of ESGC.
ClinicalTrials.gov NCT04057209. Registered on 15 August 2019. Cantonal Ethics Committee KEK-BE 2019-01506.
Mots-clé
Humans, Laryngeal Neoplasms/radiotherapy, Laryngeal Neoplasms/surgery, Laryngeal Neoplasms/pathology, Voice Quality/radiation effects, Vocal Cords/surgery, Vocal Cords/pathology, Vocal Cords/radiation effects, Carbon Dioxide, Retrospective Studies, Prospective Studies, Laser Therapy/methods, Treatment Outcome, Glottic cancer, Larynx, Radiotherapy, Randomized controlled trial, Transoral CO2-laser surgery, Vocal cord irradiation
Pubmed
Web of science
Open Access
Oui
Création de la notice
08/11/2022 12:42
Dernière modification de la notice
23/01/2024 8:32
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