Background: Taniborbactam is a β-lactamase inhibitor that, when combined with cefepime, may offer a potential treatment option for patients with serious and resistant Gram-negative bacterial (GNB) pathogens.
Objectives: This study evaluated activity of cefepime/taniborbactam and comparator agents against GNB pathogens isolated from patients with cancer at our institution.
Methods: A total of 270 GNB pathogens (2019-23) isolated from patients with cancer were tested against cefepime/taniborbactam and comparator agents commonly used for these patients. CLSI-approved broth microdilution methods were used. MIC, MIC, MIC range and percentage of susceptibility calculations were made using FDA breakpoints when available.
Results: Cefepime/taniborbactam showed highly potent activity against tested Enterobacterales, including isolates producing ESBLs and carbapenem-resistant Enterobacterales. At a provisional breakpoint of ≤16/4 mg/L, cefepime/taniborbactam inhibited most tested species of GNB pathogens, with overall 98.9% susceptibility, which was significantly (< 0.0001) higher than the susceptibility of the GNB isolates to all other tested comparator agents, ranging from 39.6% for cefepime to 86.3% for ceftazidime/avibactam.
Conclusions: Our results showed that taniborbactam in combination with cefepime improved activity against GNB pathogens isolated from patients with cancer, including MDR , carbapenem-resistant Enterobacterales, ESBL-producing Enterobacterales and isolates, with highest activity compared with all tested comparator agents, including other β-lactam/β-lactamase inhibitor combinations. Further studies are warranted to explore the efficacy of cefepime/taniborbactam for empirical initial treatment of GNB infections in cancer patients with high rates of febrile neutropenia requiring hospitalization.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11005172 | PMC |
http://dx.doi.org/10.1093/jacamr/dlae060 | DOI Listing |
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