Patient outcomes by baseline pathogen resistance phenotype and genotype in CERTAIN-1, a Phase 3 study of cefepime-taniborbactam versus meropenem in adults with complicated urinary tract infection
- PMID: 38780262
- PMCID: PMC11232400
- DOI: 10.1128/aac.00236-24
Patient outcomes by baseline pathogen resistance phenotype and genotype in CERTAIN-1, a Phase 3 study of cefepime-taniborbactam versus meropenem in adults with complicated urinary tract infection
Abstract
CERTAIN-1 was a Phase 3, double-blind, randomized, parallel group study of the efficacy and safety of cefepime-taniborbactam versus meropenem in the treatment of adults with complicated urinary tract infection (cUTI), including acute pyelonephritis. We determined susceptibility of Enterobacterales and Pseudomonas aeruginosa baseline pathogens to cefepime-taniborbactam and comparators and characterized β-lactam resistance mechanisms. Microbiologic response and clinical response were assessed in patient subsets defined by baseline pathogens that were of cefepime-, multidrug-, or carbapenem-resistant phenotype or that carried β-lactamase genes. Among Enterobacterales baseline pathogens, 26.8%, 4.1%, and 3.0% carried genes for extended-spectrum β-lactamases (ESBLs), AmpC, and carbapenemases, respectively. Within each treatment group, while composite success rates at Test of Cure in resistant subsets by pathogen species were similar to those by pathogen overall, composite success rates in meropenem patients were numerically lower for cefepime-resistant Escherichia coli (9/19; 47.4%) and ESBL E. coli (13/25; 52.0%) compared with E. coli overall (62/100; 62.0%). Cefepime-taniborbactam achieved composite success in 7/8 (87.5%) patients with carbapenem-resistant Enterobacterales and 8/9 (88.9%) patients with Enterobacterales with a carbapenemase gene (5 OXA-48-group; 2 KPC-3; 2 NDM-1). Cefepime-taniborbactam also achieved composite success in 8/16 (50.0%) patients and clinical success in 13/16 (81.3%) patients with P. aeruginosa; corresponding rates were 4/7 (57.1%) and 6/7 (85.7%) for meropenem. Cefepime-taniborbactam demonstrated efficacy in adult cUTI patients with cefepime-, multidrug-, and carbapenem-resistant pathogens including pathogens with ESBL, AmpC, and carbapenemase genes.
Clinical trials: This study is registered with ClinicalTrials.gov as NCT03840148.
Keywords: carbapenemase; cefepime-taniborbactam; complicated urinary tract infection; meropenem; outcome; β-lactamase inhibitor.
References
-
- World Health Organization . 2017. Prioritization of pathogens to guide discovery, research and development of new antibiotics for drug-resistant bacterial infections,including tuberculosis. World Health Organization (WHO), Geneva.
-
- CDC . 2019. Antibiotic resistance threats in the United States, 2019. Vol. 139. Atlanta, GA: Centers for Disease Control and Prevention (CDC). doi:10.15620/cdc:82532 - DOI
-
- Castanheira M, Doyle T, Kantro V, Mendes RE, Sader HS. 2022. 664. Increase in the occurrence of carbapenem-resistant Enterobacterales (CRE) in United States (US) hospitals from 2019 to 2021 and activity of novel β-lactam/β-lactamase Inhibitor (BL/BLI) combinations against these isolates. Open Forum Infect Dis 9. doi:10.1093/ofid/ofac492.716 - DOI
-
- Estabrook M, Muyldermans A, Sahm D, Pierard D, Stone G, Utt E. 2023. Epidemiology of resistance determinants identified in meropenem-nonsusceptible Enterobacterales collected as part of a global surveillance study, 2018 to 2019. Antimicrob Agents Chemother 67:e0140622. doi:10.1128/aac.01406-22 - DOI - PMC - PubMed
Publication types
MeSH terms
Substances
Associated data
Grants and funding
LinkOut - more resources
Full Text Sources
Medical