Transoral laser microsurgery for supraglottic carcinomas: results of a prospective multicenter trial (SUPRATOL).

FEES MDADI VHI functional outcomes prospective multicenter trial supraglottic carcinoma transoral laser microsurgery

Journal

Frontiers in oncology
ISSN: 2234-943X
Titre abrégé: Front Oncol
Pays: Switzerland
ID NLM: 101568867

Informations de publication

Date de publication:
2024
Historique:
received: 28 05 2024
accepted: 19 08 2024
medline: 7 10 2024
pubmed: 7 10 2024
entrez: 7 10 2024
Statut: epublish

Résumé

A limited number of single institutions have published retrospective cohort studies on transoral laser microsurgery for supraglottic laryngectomy (TLM-SGL). These studies have shown that the oncologic outcomes of TLM-SGL are comparable to those of open SGL. However, there is limited information available regarding swallowing rehabilitation and quality of life (QoL). SUPRATOL is a prospective, multicenter trial assessing the functional outcomes of TLM-SGL +/- adjuvant radio-(chemo)-therapy. The primary endpoint was aspiration-free swallowing at 12 months, as established using fibreoptic endoscopic evaluation of swallowing (FEES) and defined as a grade < 6 on the penetration-aspiration scale. Secondary endpoints were swallowing- and voice-related QoL, the prevalence of temporary and permanent tracheostomy and percutaneous gastrostomy, local control, laryngectomy-free survival, overall survival, and disease-free survival, as well as the influence of treatment centers on outcomes. From April 2015 to February 2018, 102 patients were recruited from 26 German Otorhinolaryngology (ORL) hospitals. All patients had TLM-SGL and 96.1% underwent uni- or bilateral, mostly selective neck dissection. To 47.0% of patients, adjuvant radio-(chemo)-therapy (R(C)T) was administered. The median follow-up period was 24.1 months. At 12-month follow-up, completed by 84.3% of patients, 98.2%, 95.5%, and 98.8% were free of aspiration when tested with saliva, liquid, or pulp. Adjuvant R(C)T, pT category, and type of resection had no significant influence on swallowing rehabilitation. A total of 40.2% of patients had been tracheotomized, and in 46.1% of patients, a PEG tube was inserted. At the 24-month follow-up, 5.3% of patients still required a tracheostomy, and 8.0% continued to use a percutaneous endoscopic gastrostomy (PEG) tube. Deterioration of swallowing- and voice-related QoL was observed immediately after treatment, but patients recovered, and baseline values were reached again. The Kaplan-Meier 2-year rates for local control, laryngectomy-free survival, overall survival, and disease-free survival were 88%, 92%, 93%, and 82%, respectively. Our prospective multicenter trial shows that, at 12 months post-TLM-SGL +/- R(C)T, 95.5%-98.8% of patients achieved aspiration-free swallowing. Morbidity was higher than previously reported. The rates of permanent tracheostomy and gastrostomy tube placement correspond to previous cohort studies. The 2-year oncologic outcomes are within the reported range. https://drks.de/search/en/trial/DRKS00004641, identifier (DRKS00004641).

Sections du résumé

Background UNASSIGNED
A limited number of single institutions have published retrospective cohort studies on transoral laser microsurgery for supraglottic laryngectomy (TLM-SGL). These studies have shown that the oncologic outcomes of TLM-SGL are comparable to those of open SGL. However, there is limited information available regarding swallowing rehabilitation and quality of life (QoL).
Patients and methods UNASSIGNED
SUPRATOL is a prospective, multicenter trial assessing the functional outcomes of TLM-SGL +/- adjuvant radio-(chemo)-therapy. The primary endpoint was aspiration-free swallowing at 12 months, as established using fibreoptic endoscopic evaluation of swallowing (FEES) and defined as a grade < 6 on the penetration-aspiration scale. Secondary endpoints were swallowing- and voice-related QoL, the prevalence of temporary and permanent tracheostomy and percutaneous gastrostomy, local control, laryngectomy-free survival, overall survival, and disease-free survival, as well as the influence of treatment centers on outcomes.
Results UNASSIGNED
From April 2015 to February 2018, 102 patients were recruited from 26 German Otorhinolaryngology (ORL) hospitals. All patients had TLM-SGL and 96.1% underwent uni- or bilateral, mostly selective neck dissection. To 47.0% of patients, adjuvant radio-(chemo)-therapy (R(C)T) was administered. The median follow-up period was 24.1 months. At 12-month follow-up, completed by 84.3% of patients, 98.2%, 95.5%, and 98.8% were free of aspiration when tested with saliva, liquid, or pulp. Adjuvant R(C)T, pT category, and type of resection had no significant influence on swallowing rehabilitation. A total of 40.2% of patients had been tracheotomized, and in 46.1% of patients, a PEG tube was inserted. At the 24-month follow-up, 5.3% of patients still required a tracheostomy, and 8.0% continued to use a percutaneous endoscopic gastrostomy (PEG) tube. Deterioration of swallowing- and voice-related QoL was observed immediately after treatment, but patients recovered, and baseline values were reached again. The Kaplan-Meier 2-year rates for local control, laryngectomy-free survival, overall survival, and disease-free survival were 88%, 92%, 93%, and 82%, respectively.
Conclusions UNASSIGNED
Our prospective multicenter trial shows that, at 12 months post-TLM-SGL +/- R(C)T, 95.5%-98.8% of patients achieved aspiration-free swallowing. Morbidity was higher than previously reported. The rates of permanent tracheostomy and gastrostomy tube placement correspond to previous cohort studies. The 2-year oncologic outcomes are within the reported range.
Clinical trial registration UNASSIGNED
https://drks.de/search/en/trial/DRKS00004641, identifier (DRKS00004641).

Identifiants

pubmed: 39372873
doi: 10.3389/fonc.2024.1440024
pmc: PMC11449847
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1440024

Informations de copyright

Copyright © 2024 Ambrosch, Meuret, Dietz, Fazel, Fietkau, Tostmann, Schroeder, Lammert, Künzel, Jäckel, Boeger, Scherl, Deitmer, Breitenstein, Delank, Hilber, Vester, Knipping, Harreus, Scheich, Bartel, Plontke, Koscielny, Veit, Greve, Schilling, Linxweiler, Weiß, Psychogios, Arens, Wittekindt, Oeken, Grosheva and Borzikowsky.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. The author(s) declared that they were an editorial board member of Frontiers, at the time of submission. This had no impact on the peer review process and the final decision.

Auteurs

Petra Ambrosch (P)

Department of Otorhinolaryngology, Head and Neck Surgery, University Hospital Schleswig-Holstein (UKSH), University of Kiel, Kiel, Germany.

Sylvia Meuret (S)

Section of Phoniatrics and Audiology, Clinic of Otorhinolaryngology, University of Leipzig, Leipzig, Germany.

Andreas Dietz (A)

Clinic of Otorhinolaryngology, University of Leipzig, Leipzig, Germany.

Asita Fazel (A)

Department of Otorhinolaryngology, Head and Neck Surgery, University Hospital Schleswig-Holstein (UKSH), University of Kiel, Kiel, Germany.

Rainer Fietkau (R)

Department of Radiooncology, Friedrich-Alexander-University, Erlangen-Nuremberg, Erlangen, Germany.

Ralf Tostmann (R)

Clinical Trial Unit UMG, Universitätsmedizin Goettingen, Goettingen, Germany.

Ursula Schroeder (U)

Department of Otorhinolaryngology, Head and Neck Surgery, University Hospital Schleswig-Holstein (UKSH), University of Luebeck, Luebeck, Germany.

Anne Lammert (A)

Department of Otorhinolaryngology, Head and Neck Surgery, Medical Faculty Mannheim, University Hospital Mannheim, University of Heidelberg, Mannheim, Germany.

Julian Künzel (J)

Department of Otorhinolaryngology, Head and Neck Surgery, University Hospital of Regensburg, Regensburg, Germany.

Martin C Jäckel (MC)

Department of Otorhinolaryngology, Helios-Kliniken Schwerin, Schwerin, Germany.

Daniel Boeger (D)

Department of Otorhinolaryngology, SRH Zentralklinikum Suhl, Suhl, Germany.

Claudia Scherl (C)

Department of Otorhinolaryngology, Head and Neck Surgery, Medical Faculty Mannheim, University Hospital Mannheim, University of Heidelberg, Mannheim, Germany.

Thomas Deitmer (T)

German Society of Otorhinolaryngology, Head and Neck Surgery (DGHNO-KHC), Bonn, Germany.

Kerstin Breitenstein (K)

Department of Otorhinolaryngology, Helios-Klinikum Erfurt, Erfurt, Germany.

K-Wolfgang Delank (KW)

Department of Otorhinolaryngology, Head and Neck Surgery, Klinikum der Stadt Ludwigshafen gGmbH, Ludwigshafen, Germany.

Hermann Hilber (H)

Department of Otorhinolaryngology, Head and Neck Surgery, University Hospital of Regensburg and Private Medical Practice for Otorhinolaryngology, Regensburg, Germany.

Sarah Vester (S)

Department of Otorhinolaryngology, Head and Neck Surgery, University Hospital of Regensburg, Regensburg, Germany.

Stephan Knipping (S)

Department of Otorhinolaryngology, Head and Neck Surgery, Städtisches Klinikum Dessau, Dessau, Germany.

Ulrich Harreus (U)

Department of Otorhinolaryngology, Krankenhaus Bad Tölz, Bad Tölz, Germany.

Matthias Scheich (M)

Department of Otorhinolaryngology, Plastic, Aesthetic and Reconstructive Head and Neck Surgery, Julius-Maximilians-University Hospital Würzburg, Würzburg, Germany.

Sylva Bartel (S)

Department of Otorhinolaryngology, Head and Neck Surgery, Martin Luther University Halle-Wittenberg, Halle, Germany.

Stefan K Plontke (SK)

Department of Otorhinolaryngology, Head and Neck Surgery, Martin Luther University Halle-Wittenberg, Halle, Germany.

Sven Koscielny (S)

Department of Otorhinolaryngology, Head and Neck Surgery, University Hospital Jena, Jena, Germany.

Johannes A Veit (JA)

Department of Otorhinolaryngology, Head and Neck Surgery, Medical Faculty Mannheim, University Hospital Mannheim, University of Heidelberg, Mannheim, Germany.
Private Medical Practice for Nasal Surgery, Muenchen, Germany.

Jens Greve (J)

Department of Otorhinolaryngology, Head and Neck Surgery, Ulm University Hospital, Ulm, Germany.

Volker Schilling (V)

Department of Otorhinolaryngology, Head and Neck Surgery, Vivantes Klinikum Neukölln, Germany.

Maximilian Linxweiler (M)

Department of Otorhinolaryngology, Saarland University, Homburg, Germany.

Sonja Weiß (S)

Department of Otorhinolaryngology, Klinikum Kassel, Kassel, Germany.

Georgios Psychogios (G)

Clinic of Otorhinolaryngology, University of Ioannina, Ioannina, Greece.

Christoph Arens (C)

Department of Otorhinolaryngology, Head and Neck Surgery, University of Giessen, Giessen, Germany.

Claus Wittekindt (C)

Department of Otorhinolaryngology, Head and Neck Surgery, Klinikum Dortmund, Dortmund, Germany.

Jens Oeken (J)

Department of Otorhinolaryngology, Hospital Chemnitz, Chemnitz, Germany.

Maria Grosheva (M)

Department of Otorhinolaryngology, Head and Neck Surgery, University of Cologne, Cologne, Germany.

Christoph Borzikowsky (C)

Institute of Medical Informatics and Statistics, Christian-Albrechts-University Kiel, Kiel, Germany.

Classifications MeSH