Omadacycline for Acute Bacterial Skin and Skin Structure Infections.
Acute Disease
/ therapy
Administration, Intravenous
Administration, Oral
Adolescent
Adult
Aged
Aged, 80 and over
Anti-Bacterial Agents
/ administration & dosage
Drug Administration Routes
Female
Humans
Linezolid
/ therapeutic use
Male
Methicillin-Resistant Staphylococcus aureus
/ drug effects
Middle Aged
Skin
/ drug effects
Skin Diseases, Bacterial
/ drug therapy
Soft Tissue Infections
/ drug therapy
Tetracyclines
/ administration & dosage
Young Adult
MRSA
acute bacterial skin and skin structure infections
omadacycline
skin infection
tetracyclines
Journal
Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
ISSN: 1537-6591
Titre abrégé: Clin Infect Dis
Pays: United States
ID NLM: 9203213
Informations de publication
Date de publication:
01 08 2019
01 08 2019
Historique:
entrez:
2
8
2019
pubmed:
2
8
2019
medline:
4
8
2020
Statut:
ppublish
Résumé
Within the last decade, methicillin-resistant Staphylococcus aureus (MRSA) has emerged as a frequent cause of purulent skin and soft tissue infections. New therapeutic options are being investigated for these infections. We report an integrated analysis of 2 randomized, controlled studies involving omadacycline, a novel aminomethylcycline, and linezolid for the treatment of acute bacterial skin and skin structure infections (ABSSSI). Omadacycline in Acute Skin and Skin Structure Infections Study 1 (OASIS-1) initiated patients on intravenous omadacycline or linezolid, with the option to transition to an oral formulation after day 3. OASIS-2 was an oral-only study of omadacycline versus linezolid. In total, 691 patients received omadacycline and 689 patients received linezolid. Infection types included wound infection in 46.8% of patients, cellulitis/erysipelas in 30.5%, and major abscess in 22.7%. Pathogens were identified in 73.2% of patients. S. aureus was detected in 74.7% and MRSA in 32.4% of patients in whom a pathogen was identified. Omadacycline was noninferior to linezolid using the Food and Drug Administration primary endpoint of early clinical response (86.2% vs 83.9%; difference 2.3, 95% confidence interval -1.5 to 6.2) and using the European Medicines Agency primary endpoint of investigator-assessed clinical response at the posttreatment evaluation. Clinical responses were similar across different infection types and infections caused by different pathogens. Treatment-emergent adverse events, mostly described as mild or moderate, were reported by 51.1% of patients receiving omadacycline and 41.2% of those receiving linezolid. Omadacycline was effective and safe in ABSSSI. NCT02378480 and NCT02877927.
Sections du résumé
BACKGROUND
Within the last decade, methicillin-resistant Staphylococcus aureus (MRSA) has emerged as a frequent cause of purulent skin and soft tissue infections. New therapeutic options are being investigated for these infections.
METHODS
We report an integrated analysis of 2 randomized, controlled studies involving omadacycline, a novel aminomethylcycline, and linezolid for the treatment of acute bacterial skin and skin structure infections (ABSSSI). Omadacycline in Acute Skin and Skin Structure Infections Study 1 (OASIS-1) initiated patients on intravenous omadacycline or linezolid, with the option to transition to an oral formulation after day 3. OASIS-2 was an oral-only study of omadacycline versus linezolid.
RESULTS
In total, 691 patients received omadacycline and 689 patients received linezolid. Infection types included wound infection in 46.8% of patients, cellulitis/erysipelas in 30.5%, and major abscess in 22.7%. Pathogens were identified in 73.2% of patients. S. aureus was detected in 74.7% and MRSA in 32.4% of patients in whom a pathogen was identified. Omadacycline was noninferior to linezolid using the Food and Drug Administration primary endpoint of early clinical response (86.2% vs 83.9%; difference 2.3, 95% confidence interval -1.5 to 6.2) and using the European Medicines Agency primary endpoint of investigator-assessed clinical response at the posttreatment evaluation. Clinical responses were similar across different infection types and infections caused by different pathogens. Treatment-emergent adverse events, mostly described as mild or moderate, were reported by 51.1% of patients receiving omadacycline and 41.2% of those receiving linezolid.
CONCLUSIONS
Omadacycline was effective and safe in ABSSSI.
CLINICAL TRIALS REGISTRATION
NCT02378480 and NCT02877927.
Identifiants
pubmed: 31367742
pii: 5541769
doi: 10.1093/cid/ciz396
pmc: PMC6669297
doi:
Substances chimiques
Anti-Bacterial Agents
0
Tetracyclines
0
omadacycline
090IP5RV8F
Linezolid
ISQ9I6J12J
Banques de données
ClinicalTrials.gov
['NCT02378480', 'NCT02877927']
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
S23-S32Informations de copyright
© The Author(s) 2019. Published by Oxford University Press for the Infectious Diseases Society of America.
Références
Antimicrob Agents Chemother. 2009 Dec;53(12):4961-7
pubmed: 19721075
Emerg Infect Dis. 2009 Sep;15(9):1516-8
pubmed: 19788830
J Clin Microbiol. 2012 Feb;50(2):238-45
pubmed: 22116149
Can J Infect Dis. 1990 Winter;1(4):133-5
pubmed: 22553455
JAMA. 2012 Jul 4;308(1):50-9
pubmed: 22760291
PLoS One. 2013;8(1):e52722
pubmed: 23300988
BMC Infect Dis. 2013 May 30;13:252
pubmed: 23721377
Virulence. 2014 Jan 1;5(1):20-6
pubmed: 24280933
Antimicrob Agents Chemother. 2014;58(2):1127-35
pubmed: 24295985
BMC Infect Dis. 2014 Jun 02;14:296
pubmed: 24889406
Clin Infect Dis. 2014 Jul 15;59(2):147-59
pubmed: 24947530
J Emerg Med. 2015 Apr;48(4):508-19
pubmed: 25605319
Hosp Pract (1995). 2015;43(3):137-43
pubmed: 26224423
PLoS One. 2015 Nov 24;10(11):e0143276
pubmed: 26599005
Intern Emerg Med. 2016 Aug;11(5):637-48
pubmed: 27084183
Expert Rev Clin Pharmacol. 2016 Aug;9(8):1039-45
pubmed: 27248789
Bioorg Med Chem. 2016 Dec 15;24(24):6409-6419
pubmed: 27469981
Pediatr Infect Dis J. 2018 Mar;37(3):235-241
pubmed: 28859018
Ther Adv Infect Dis. 2017 Sep;4(5):143-161
pubmed: 28959445
Antimicrob Agents Chemother. 2018 Mar 27;62(4):
pubmed: 29378719
Antimicrob Agents Chemother. 2018 Mar 27;62(4):
pubmed: 29439961
Med Sci (Basel). 2018 Jan 18;6(1):null
pubmed: 30720776
N Engl J Med. 2019 Feb 7;380(6):528-538
pubmed: 30726689
N Engl J Med. 2019 Feb 7;380(6):517-527
pubmed: 30726692
Am Health Drug Benefits. 2018 Dec;11(9):449-459
pubmed: 30746017
Stat Med. 1985 Apr-Jun;4(2):213-26
pubmed: 4023479
Infect Dis Clin North Am. 1997 Dec;11(4):813-49
pubmed: 9421702