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In vitroactivity of eravacycline and comparator agents against bacterial pathogens isolated from patients with cancer

Authors :
Kenneth Rolston
Bahgat Gerges
Lior Nesher
Samuel A Shelburne
Randall Prince
Issam Raad
Source :
JAC-Antimicrobial Resistance. 5
Publication Year :
2023
Publisher :
Oxford University Press (OUP), 2023.

Abstract

BackgroundBacterial infections are common in patients with cancer, and many bacteria have developed resistance to currently used antibiotics.ObjectivesWe evaluated the in vitro activity of eravacycline (a recently developed fluorocycline) and comparators against bacterial pathogens isolated from patients with cancer.MethodsAntimicrobial susceptibility testing was performed using CLSI-approved methodology and interpretive criteria for 255 Gram-positive and 310 Gram-negative bacteria. MIC and susceptibility percentage were calculated according to CLSI and FDA breakpoints when available.ResultsEravacycline had potent activity against most Gram-positive bacteria, including MRSA. Of 80 Gram-positive isolates with available breakpoints, 74 (92.5%) were susceptible to eravacycline. Eravacycline had potent activity against most Enterobacterales, including ESBL-producing organisms. Of 230 Gram-negative isolates with available breakpoints, 201 (87.4%) were susceptible to eravacycline. Eravacycline had the best activity among comparators against carbapenem-resistant Enterobacterales, with 83% susceptibility. Eravacycline was also active against many non-fermenting Gram-negative bacteria, with the lowest MIC90 value among comparators.ConclusionsEravacycline was active against many clinically significant bacteria isolated from patients with cancer, including MRSA, carbapenem-resistant Enterobacterales, and non-fermenting Gram-negative bacilli. Eravacycline might play an important role in the treatment of bacterial infections in patients with cancer, and additional clinical evaluation is warranted.

Details

ISSN :
26321823
Volume :
5
Database :
OpenAIRE
Journal :
JAC-Antimicrobial Resistance
Accession number :
edsair.doi...........2e692a6c8750336bbecc8e3ffbbd47b2