Cefiderocol Treatment for Patients with Multidrug- and Carbapenem-Resistant Pseudomonas aeruginosa Infections in the
Michael J Satlin1, Patricia J Simner2, Christine M Slover3
1Transplant-Oncology Infectious Diseases Program, Division of Infectious Diseases, Department of Medicine, Weill Cornell Medicine, New York, New York, USA.
Abstract:
Cefiderocol is an option for infections caused by multidrug-resistant Pseudomonas aeruginosa, but its in vitro activity against these isolates and its clinical effectiveness for isolates with MICs of >1 μg/mL is unclear. We investigated the in vitro activity of cefiderocol against P. aeruginosa isolates collected from patients treated with cefiderocol through the compassionate use program and assessed physician-reported clinical response and 28-day all-cause mortality by cefiderocol MIC values. P. aeruginosa isolates underwent susceptibility testing to cefiderocol and comparator agents by using reference broth microdilution. U.S. Food and Drug Administration (FDA; susceptible, ≤1 μg/mL) and Clinical and Laboratory Standards Institute (CLSI; susceptible, ≤4 μg/mL) cefiderocol breakpoints were applied. Additionally, molecular characterization of β-lactamase genes was performed. Clinical response and vital status were reported by treating physicians. Forty-six patients with P. aeruginosa infections were evaluated. Twenty-nine (63%) and 42 (91%) isolates were susceptible to cefiderocol using FDA and CLSI breakpoints, respectively. Thirty-seven (80%) and 32 (70%) isolates were not susceptible to ceftolozane-tazobactam and ceftazidime-avibactam, respectively. The clinical response rate was 69% (20/29) with a cefiderocol MIC of ≤1 μg/mL, 69% (9/13) with a cefiderocol MIC of 2 to 4 μg/mL, and 100% (4/4) with an MIC of ≥8 μg/mL, while day 28 all-cause mortality rates were 23% (6/26; MIC ≤ 1 μg/mL), 33% (4/12; MIC, 2 to 4 μg/mL), and 0% (0/4; MIC ≥8 μg/mL), respectively. Cefiderocol was active in vitro against most P. aeruginosa isolated from patients with limited or no alternative therapies. Patients with cefiderocol MICs of 2 to 4 μg/mL did not have significantly worse outcomes than those with MICs of ≤1 μg/mL.
Insights
Cefiderocol shows in vitro activity against multidrug-resistant Pseudomonas aeruginosa. Patients with cefiderocol MICs of 2-4 μg/mL had similar outcomes to those with MICs ≤1 μg/mL.
Area of Science:
- Infectious Diseases
- Antimicrobial Resistance
- Pharmacology
Background:
- Cefiderocol offers a treatment option for multidrug-resistant Pseudomonas aeruginosa infections.
- Its in vitro activity and clinical effectiveness, particularly for isolates with elevated Minimum Inhibitory Concentrations (MICs), require further investigation.
Purpose of the Study:
- To evaluate the in vitro activity of cefiderocol against P. aeruginosa isolates from patients in a compassionate use program.
- To assess the clinical effectiveness and mortality rates associated with different cefiderocol MIC values.
Main Methods:
- Susceptibility testing of P. aeruginosa isolates to cefiderocol and comparator agents using broth microdilution.
- Application of FDA (≤1 μg/mL) and CLSI (≤4 μg/mL) cefiderocol breakpoints.
- Molecular characterization of beta-lactamase genes and physician-reported clinical outcomes and mortality.
Main Results:
- Cefiderocol demonstrated in vitro activity against 63% (FDA) and 91% (CLSI) of P. aeruginosa isolates.
- High rates of non-susceptibility were observed for ceftolozane-tazobactam (80%) and ceftazidime-avibactam (70%).
- Clinical response rates were 69% for MICs ≤1 μg/mL and 2-4 μg/mL, with 100% response for MICs ≥8 μg/mL. 28-day mortality rates were 23% (MIC ≤1) and 33% (MIC 2-4).
Conclusions:
- Cefiderocol exhibits in vitro activity against a majority of P. aeruginosa isolates from patients with limited therapeutic options.
- Clinical outcomes for patients with cefiderocol MICs of 2-4 μg/mL were comparable to those with MICs ≤1 μg/mL, suggesting potential clinical utility even with moderately elevated MICs.
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