Plazomicin: A Novel Aminoglycoside for the Treatment of Resistant Gram-Negative Bacterial Infections.
Animals
Anti-Bacterial Agents
/ pharmacology
Carbapenems
/ pharmacology
Clinical Trials as Topic
Colistin
/ pharmacology
Dose-Response Relationship, Drug
Drug Approval
Drug Resistance, Multiple, Bacterial
Drug Therapy, Combination
Gram-Negative Bacteria
/ drug effects
Gram-Negative Bacterial Infections
/ drug therapy
Humans
Meropenem
/ pharmacology
Randomized Controlled Trials as Topic
Sisomicin
/ analogs & derivatives
United States
United States Food and Drug Administration
Urinary Tract Infections
/ drug therapy
Journal
Drugs
ISSN: 1179-1950
Titre abrégé: Drugs
Pays: New Zealand
ID NLM: 7600076
Informations de publication
Date de publication:
Feb 2019
Feb 2019
Historique:
pubmed:
7
2
2019
medline:
8
10
2019
entrez:
7
2
2019
Statut:
ppublish
Résumé
Plazomicin is a novel semisynthetic parenteral aminoglycoside that inhibits bacterial protein synthesis. It was approved by the United States Food and Drug Administration for use in adults with complicated urinary tract infections (cUTI), including pyelonephritis. Plazomicin displays potent in vitro activity against Enterobacteriaceae, including both extended-spectrum β-lactamase-producing and carbapenem-resistant isolates. Plazomicin's enhanced Enterobacteriaceae activity is due to its stability to commonly encountered aminoglycoside-modifying enzymes that compromise the activity of traditional aminoglycosides. Plazomicin resistance in Enterobacteriaceae is via modification of the ribosomal binding site due to expression of 16S rRNA methyltransferases. Plazomicin does not display improved activity over traditional aminoglycosides against other problematic resistant Gram-negative bacteria, namely Pseudomonas aeruginosa and Acinetobacter baumannii. Plazomicin has been assessed in two phase III randomized controlled trials. The EPIC trial compared plazomicin and meropenem for the management of cUTI. In this trial, plazomicin demonstrated superiority in composite cure (81.7% vs 70.1%; difference 11.6%; 95% confidence interval [CI] 2.7-25.7) at the test-of-cure visit, which was driven by enhanced sustained microbiological eradication. The CARE trial compared plazomicin-based and colistin-based combinations in patients with serious infections due to carbapenem-resistant Enterobacteriaceae (CRE). In this analysis, plazomicin-based combinations were associated with numerically decreased mortality or serious disease-related complications when compared with colistin-based combinations (23.5% vs 50%, respectively; 90% CI -0.7 to 51.2). Furthermore, plazomicin was also associated with a lower incidence of nephrotoxicity than colistin. However, small sample sizes limit the interpretation of the findings in the CARE trial. Plazomicin is a novel aminoglycoside that offers clinicians an additional option for the management of CRE infections, with superior activity compared with traditional aminoglycosides and potentially improved efficacy and decreased toxicity compared with colistin.
Identifiants
pubmed: 30723876
doi: 10.1007/s40265-019-1054-3
pii: 10.1007/s40265-019-1054-3
doi:
Substances chimiques
Anti-Bacterial Agents
0
Carbapenems
0
Meropenem
FV9J3JU8B1
plazomicin
LYO9XZ250J
Sisomicin
X55XSL74YQ
Colistin
Z67X93HJG1
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
243-269Références
Antimicrob Agents Chemother. 1999 Apr;43(4):727-37
pubmed: 10103173
Antimicrob Agents Chemother. 2009 Oct;53(10):4504-7
pubmed: 19770287
Chembiochem. 2010 May 3;11(7):880-902
pubmed: 20397253
J Antimicrob Chemother. 2010 Oct;65(10):2123-7
pubmed: 20667885
Expert Opin Ther Pat. 2010 Oct;20(10):1321-41
pubmed: 20670208
J Med Primatol. 2011 Feb;40(1):6-17
pubmed: 20722770
Antimicrob Agents Chemother. 2010 Nov;54(11):4636-42
pubmed: 20805391
Curr Opin Microbiol. 2010 Oct;13(5):565-73
pubmed: 20932796
J Antimicrob Chemother. 2011 Jan;66(1):48-53
pubmed: 21078604
Chemotherapy. 2010;56(6):492-500
pubmed: 21099222
J Antimicrob Chemother. 2011 Feb;66(2):332-4
pubmed: 21131322
Antimicrob Agents Chemother. 2011 Apr;55(4):1728-33
pubmed: 21282439
Int J Antimicrob Agents. 2011 Oct;38(4):352-4
pubmed: 21820877
Antimicrob Agents Chemother. 2011 Dec;55(12):5874-80
pubmed: 21911572
Ann N Y Acad Sci. 2011 Dec;1241:122-52
pubmed: 22191530
J Chemother. 2012 Aug;24(4):191-4
pubmed: 23040681
Antimicrob Agents Chemother. 2014 May;58(5):2554-63
pubmed: 24550325
J Infect Dis. 2014 Oct 15;210(8):1319-24
pubmed: 24760199
Antimicrob Agents Chemother. 2014 Aug;58(8):4443-51
pubmed: 24867988
Int J Antimicrob Agents. 2015 Jan;45(1):76-8
pubmed: 25459738
Int J Antimicrob Agents. 2015 Dec;46(6):616-21
pubmed: 26391381
Int J Antimicrob Agents. 2016 Apr;47(4):250-8
pubmed: 27005457
Przegl Epidemiol. 2015;69(4):723-9, 865-70
pubmed: 27139351
Infect Dis Clin North Am. 2016 Jun;30(2):523-537
pubmed: 27208771
Clin Infect Dis. 2016 Dec 15;63(12):1615-1618
pubmed: 27624958
Antimicrob Agents Chemother. 2017 Jan 24;61(2):
pubmed: 27919895
Clin Infect Dis. 2017 Mar 15;64(suppl_1):S30-S35
pubmed: 28350901
Antimicrob Agents Chemother. 2017 Jul 25;61(8):
pubmed: 28559250
Int J Antimicrob Agents. 2017 Aug;50(2):191-196
pubmed: 28577932
Clin Infect Dis. 2018 Jan 6;66(2):163-171
pubmed: 29020404
J Antimicrob Chemother. 2017 Oct 1;72(10):2787-2791
pubmed: 29091226
Diagn Microbiol Infect Dis. 2018 Mar;90(3):228-232
pubmed: 29223516
Molecules. 2017 Dec 19;22(12):
pubmed: 29257114
Antimicrob Agents Chemother. 2018 Feb 23;62(3):
pubmed: 29263067
Antimicrob Agents Chemother. 2018 Mar 27;62(4):
pubmed: 29378708
Antimicrob Agents Chemother. 2018 Jul 27;62(8):
pubmed: 29866866
Antimicrob Agents Chemother. 2018 Jul 27;62(8):null
pubmed: 29866876
J Clin Invest. 1986 May;77(5):1492-500
pubmed: 3700652
Jpn J Antibiot. 1982 Aug;35(8):2034-46
pubmed: 7154249
J Infect Dis. 1976 Aug;134 Suppl:S97-103
pubmed: 787452