HOPON (Hyperbaric Oxygen for the Prevention of Osteoradionecrosis): A Randomized Controlled Trial of Hyperbaric Oxygen to Prevent Osteoradionecrosis of the Irradiated Mandible After Dentoalveolar Surgery.


Journal

International journal of radiation oncology, biology, physics
ISSN: 1879-355X
Titre abrégé: Int J Radiat Oncol Biol Phys
Pays: United States
ID NLM: 7603616

Informations de publication

Date de publication:
01 07 2019
Historique:
received: 01 11 2018
revised: 28 01 2019
accepted: 21 02 2019
pubmed: 10 3 2019
medline: 30 11 2019
entrez: 10 3 2019
Statut: ppublish

Résumé

Hyperbaric oxygen (HBO) has been advocated in the prevention and treatment of osteoradionecrosis (ORN) of the jaw after head and neck radiation therapy, but supporting evidence is weak. The aim of this randomized trial was to establish the benefit of HBO in the prevention of ORN after high-risk surgical procedures to the irradiated mandible. HOPON was a randomized, controlled, phase 3 trial. Participants who required dental extractions or implant placement in the mandible with prior radiation therapy >50 Gy were recruited. Eligible patients were randomly assigned 1:1 to receive or not receive HBO. All patients received chlorhexidine mouthwash and antibiotics. For patients in the HBO arm, oxygen was administered in 30 daily dives at 100% oxygen to a pressure of 2.4 atmospheres absolute for 80 to 90 minutes. The primary outcome measure was the diagnosis of ORN 6 months after surgery, as determined by a blinded central review of clinical photographs and radiographs. The secondary endpoints included grade of ORN, ORN at other time points, acute symptoms, pain, and quality of life. A total of 144 patients were randomized, and data from 100 patients were analyzed for the primary endpoint. The incidence of ORN at 6 months was 6.4% and 5.7% for the HBO and control groups, respectively (odds ratio, 1.13; 95% confidence interval, 0.14-8.92; P = 1). Patients in the hyperbaric arm had fewer acute symptoms but no significant differences in late pain or quality of life. Dropout was higher in the HBO arm, but the baseline characteristics of the groups that completed the trial were comparable between the 2 arms. The low incidence of ORN makes recommending HBO for dental extractions or implant placement in the irradiated mandible unnecessary. These findings are in contrast with a recently published Cochrane review and previous trials reporting rates of ORN (non-HBO) of 14% to 30% and challenge a long-established standard of care.

Identifiants

pubmed: 30851351
pii: S0360-3016(19)30288-3
doi: 10.1016/j.ijrobp.2019.02.044
pii:
doi:

Substances chimiques

Anti-Bacterial Agents 0
Mouthwashes 0
Chlorhexidine R4KO0DY52L

Types de publication

Clinical Trial, Phase III Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

530-539

Subventions

Organisme : Cancer Research UK
ID : 12122
Pays : United Kingdom
Organisme : Cancer Research UK
ID : C23033/A9397
Pays : United Kingdom
Organisme : Cancer Research UK
ID : C23033/A12122
Pays : United Kingdom

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Informations de copyright

Copyright © 2019 Elsevier Inc. All rights reserved.

Auteurs

Richard J Shaw (RJ)

University of Liverpool, Liverpool, United Kingdom. Electronic address: rjshaw@liv.ac.uk.

Christopher J Butterworth (CJ)

Maxillofacial Prosthodontics, Department of Maxillofacial Surgery, University Hospital Aintree, Liverpool, United Kingdom.

Paul Silcocks (P)

Cancer Research UK Liverpool Clinical Trials Unit, University of Liverpool, Liverpool, United Kingdom.

Binyam T Tesfaye (BT)

Cancer Research UK Liverpool Cancer Trials Unit, Department of Molecular and Clinical Cancer Medicine, University of Liverpool, Liverpool, United Kingdom.

Matthew Bickerstaff (M)

Cancer Research UK Liverpool Clinical Trials Unit, University of Liverpool, Liverpool, United Kingdom.

Richard Jackson (R)

Cancer Research UK Liverpool Clinical Trials Unit, University of Liverpool, Liverpool, United Kingdom.

Anastios Kanatas (A)

OMFS Department, Leeds Dental Institute, Leeds, United Kingdom.

Peter Nixon (P)

Restorative Department, Leeds Dental Institute, Leeds, United Kingdom.

James McCaul (J)

Regional Maxillofacial Unit, Queen Elizabeth University Hospital, Glasgow, United Kingdom.

Prav Praveen (P)

Maxillofacial Office, Queen Elizabeth Hospital, Birmingham, United Kingdom.

Terry Lowe (T)

Aberdeen Royal Infirmary, Aberdeen, Scotland.

Manuel Blanco-Guzman (M)

Maxillofacial Unit, Musgrove Park Hospital, Taunton and Somerset NHS Foundation Trust, Taunton, United Kingdom.

Lone Forner (L)

Departments of Anesthesia and Oral and Maxillofacial Surgery, Centre of Head and Orthopedics, Copenhagen University Hospital, Copenhagen, Denmark.

Peter Brennan (P)

Maxillofacial Unit, Queen Alexandra Hospital, Portsmouth, United Kingdom.

Mike Fardy (M)

University Hospital of Wales, Cardiff, Wales, United Kingdom.

Richard Parkin (R)

OMFS Department, ABUHB, Newport, Wales, United Kingdom.

Gary Smerdon (G)

DDRC Healthcare, Hyperbaric Medical Centre, Plymouth, United Kingdom.

Ruth Stephenson (R)

NHS Grampian, Aberdeen Royal Infirmary, Aberdeen, Scotland.

Tristan Cope (T)

North West Recompression Unit, Murrayfield Hospital, Holmwood, United Kingdom.

Mark Glover (M)

Hyperbaric Medicine Unit, St. Richard's Hospital, Chichester, United Kingdom.

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Classifications MeSH