Efficacy and tolerability of a cocktail of bacteriophages to treat burn wounds infected by Pseudomonas aeruginosa (PhagoBurn): a randomised, controlled, double-blind phase 1/2 trial.


Journal

The Lancet. Infectious diseases
ISSN: 1474-4457
Titre abrégé: Lancet Infect Dis
Pays: United States
ID NLM: 101130150

Informations de publication

Date de publication:
01 2019
Historique:
received: 17 04 2018
revised: 12 07 2018
accepted: 23 07 2018
pubmed: 8 10 2018
medline: 10 5 2020
entrez: 8 10 2018
Statut: ppublish

Résumé

Wound infections are the main cause of sepsis in patients with burns and increase burn-related morbidity and mortality. Bacteriophages, natural bacterial viruses, are being considered as an alternative therapy to treat infections caused by multidrug-resistant bacteria. We aimed to compare the efficacy and tolerability of a cocktail of lytic anti-Pseudomonas aeruginosa bacteriophages with standard of care for patients with burns. In this randomised phase 1/2 trial, patients with a confirmed burn wound infection were recruited from nine burn centres in hospitals in France and Belgium. Patients were eligible if they were aged 18 years or older and had a burn wound clinically infected with P aeruginosa. Eligible participants were randomly assigned (1:1) by use of an interactive web response system to a cocktail of 12 natural lytic anti-P aeruginosa bacteriophages (PP1131; 1 × 10 Between July 22, 2015, and Jan 2, 2017, across two recruitment periods spanning 13 months, 27 patients were recruited and randomly assigned to receive phage therapy (n=13) or standard of care (n=14). One patient in the standard of care group was not exposed to treatment, giving a safety population of 26 patients (PP1131 n=13, standard of care n=13), and one patient in the PP1131 group did not have an infection at day 0, giving an efficacy population of 25 patients (PP1131 n=12, standard of care n=13). The trial was stopped on Jan 2, 2017, because of the insufficient efficacy of PP1131. The primary endpoint was reached in a median of 144 h (95% CI 48-not reached) in the PP1131 group versus a median of 47 h (23-122) in the standard of care group (hazard ratio 0·29, 95% CI 0·10-0·79; p=0·018). In the PP1131 group, six (50%) of 12 analysable participants had a maximal bacterial burden versus two (15%) of 13 in the standard of care group. PP1131 titre decreased after manufacturing and participants were given a lower concentration of phages than expected (1 × 10 At very low concentrations, PP1131 decreased bacterial burden in burn wounds at a slower pace than standard of care. Further studies using increased phage concentrations and phagograms in a larger sample of participants are warranted. European Commission: Framework Programme 7.

Sections du résumé

BACKGROUND
Wound infections are the main cause of sepsis in patients with burns and increase burn-related morbidity and mortality. Bacteriophages, natural bacterial viruses, are being considered as an alternative therapy to treat infections caused by multidrug-resistant bacteria. We aimed to compare the efficacy and tolerability of a cocktail of lytic anti-Pseudomonas aeruginosa bacteriophages with standard of care for patients with burns.
METHODS
In this randomised phase 1/2 trial, patients with a confirmed burn wound infection were recruited from nine burn centres in hospitals in France and Belgium. Patients were eligible if they were aged 18 years or older and had a burn wound clinically infected with P aeruginosa. Eligible participants were randomly assigned (1:1) by use of an interactive web response system to a cocktail of 12 natural lytic anti-P aeruginosa bacteriophages (PP1131; 1 × 10
FINDINGS
Between July 22, 2015, and Jan 2, 2017, across two recruitment periods spanning 13 months, 27 patients were recruited and randomly assigned to receive phage therapy (n=13) or standard of care (n=14). One patient in the standard of care group was not exposed to treatment, giving a safety population of 26 patients (PP1131 n=13, standard of care n=13), and one patient in the PP1131 group did not have an infection at day 0, giving an efficacy population of 25 patients (PP1131 n=12, standard of care n=13). The trial was stopped on Jan 2, 2017, because of the insufficient efficacy of PP1131. The primary endpoint was reached in a median of 144 h (95% CI 48-not reached) in the PP1131 group versus a median of 47 h (23-122) in the standard of care group (hazard ratio 0·29, 95% CI 0·10-0·79; p=0·018). In the PP1131 group, six (50%) of 12 analysable participants had a maximal bacterial burden versus two (15%) of 13 in the standard of care group. PP1131 titre decreased after manufacturing and participants were given a lower concentration of phages than expected (1 × 10
INTERPRETATION
At very low concentrations, PP1131 decreased bacterial burden in burn wounds at a slower pace than standard of care. Further studies using increased phage concentrations and phagograms in a larger sample of participants are warranted.
FUNDING
European Commission: Framework Programme 7.

Identifiants

pubmed: 30292481
pii: S1473-3099(18)30482-1
doi: 10.1016/S1473-3099(18)30482-1
pii:
doi:

Substances chimiques

Anti-Bacterial Agents 0

Banques de données

ClinicalTrials.gov
['NCT02116010']

Types de publication

Clinical Trial, Phase I Clinical Trial, Phase II Journal Article Multicenter Study Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

35-45

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Informations de copyright

Copyright © 2019 Elsevier Ltd. All rights reserved.

Auteurs

Patrick Jault (P)

Clinique de La Muette, Paris, France. Electronic address: jaultpatrick@gmail.com.

Thomas Leclerc (T)

Centre de traitement des brûlés, Hôpital d'Instruction des Armées Percy, Clamart, France.

Serge Jennes (S)

Burn unit, Queen Astrid Military Hospital, Brussels, Belgium.

Jean Paul Pirnay (JP)

Burn unit, Queen Astrid Military Hospital, Brussels, Belgium.

Yok-Ai Que (YA)

Klinik für Intensivmedizin Inselspital, Universitätsspital Bern, Bern, Switzerland.

Gregory Resch (G)

Department of Fundamental Microbiology, University of Lausanne, Lausanne, Switzerland.

Anne Françoise Rousseau (AF)

Centre des Brûlés et Soins Intensifs Généraux, CHU Sart-Tilman, Campus Universitaire du Sart-Tilman, Liège, Belgium.

François Ravat (F)

Burn unit, Centre Hospitalier St Joseph et St Luc, Lyon, France.

Hervé Carsin (H)

CHR Hôpital de Mercy Metz Thionville, Thionville, France.

Ronan Le Floch (R)

Réanimation chirurgicale et des brûlés, Plateau technique médico-chirurgical, CHU Nantes, Nantes, France.

Jean Vivien Schaal (JV)

Centre de traitement des brûlés, Hôpital d'Instruction des Armées Percy, Clamart, France.

Charles Soler (C)

Centre de traitement des brûlés, Hôpital d'Instruction des Armées Percy, Clamart, France.

Cindy Fevre (C)

Pherecydes Pharma SA, Romainville, France.

Isabelle Arnaud (I)

Clean Cells, Boufféré, France.

Laurent Bretaudeau (L)

Clean Cells, Boufféré, France.

Jérôme Gabard (J)

Pherecydes Pharma SA, Romainville, France.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH