Efficacy of ceftolozane/tazobactam against urinary tract and intra-abdominal infections caused by ESBL-producing Escherichia coli and Klebsiella pneumoniae: a pooled analysis of Phase 3 clinical trials

被引:106
作者
Popejoy, Myra W. [1 ]
Paterson, David L. [2 ]
Cloutier, Daniel [1 ]
Huntington, Jennifer A. [1 ]
Miller, Benjamin [1 ]
Bliss, Caleb A. [1 ]
Steenbergen, Judith N. [1 ]
Hershberger, Ellie [1 ]
Umeh, Obiamiwe [1 ]
Kaye, Keith S. [3 ,4 ]
机构
[1] Merck & Co Inc, Kenilworth, NJ USA
[2] Univ Queensland, Clin Res Ctr, Brisbane, Qld, Australia
[3] Wayne State Univ, Detroit Med Ctr, Detroit, MI USA
[4] Wayne State Univ, Dept Med, Detroit, MI 48202 USA
关键词
LACTAMASE-PRODUCING ENTEROBACTERIACEAE; SPECTRUM BETA-LACTAMASES; DOUBLE-BLIND; TAZOBACTAM; BACTEREMIA; RESISTANCE; THERAPY;
D O I
10.1093/jac/dkw374
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Objectives: The increase in infections caused by drug-resistant ESBL-producing Enterobacteriaceae (ESBL-ENT) is a global concern. The characteristics and outcomes of patients infected with ESBL-ENT were examined in a pooled analysis of Phase 3 clinical trials of ceftolozane/tazobactam in patients with complicated urinary tract infections (ASPECT-cUTI) and complicated intra-abdominal infections (ASPECT-cIAI). Methods: Trials were randomized and double blind. The ASPECT-cUTI regimen was 7 days of either intravenous ceftolozane/tazobactam (1.5 g) every 8 h or levofloxacin (750 mg) once daily. The ASPECT-cIAI regimen was 4-14 days of either intravenous ceftolozane/tazobactam (1.5 g) plus metronidazole (500 mg) or meropenem (1 g) every 8 h. Baseline cultures were obtained in both indications. Enterobacteriaceae were selected for ESBL characterization based on predefined criteria and were verified genotypically. Outcomes were assessed at the test-of-cure visit 5-9 days post-therapy in ASPECT-cUTI and 24-32 days post-randomization in ASPECT-cIAI among microbiologically evaluable (ME) patients. Results: Of 2076 patients randomized, 1346 were included in the pooled ME population and 150 of 1346 (11.1%) had ESBL-ENT at baseline. At US FDA/EUCAST breakpoints of <= 2/<= 1 mg/L, 81.8%/72.3% of ESBL-ENT (ESBL-Escherichia coli, 95%/88.1%; ESBL-Klebsiella pneumoniae, 56.7%/36.7%) were susceptible to ceftolozane/tazobactam versus 25.3%/24.1% susceptible to levofloxacin and 98.3%/98.3% susceptible to meropenem at CLSI/EUCAST breakpoints. Clinical cure rates for ME patients with ESBL-ENT were 97.4% (76/78) for ceftolozane/ tazobactam [ESBL-E. coli, 98.0% (49 of 50); ESBL-K. pneumoniae, 94.4% (17 of 18)], 82.6% (38 of 46) for levofloxacin and 88.5% (23 of 26) for meropenem. Conclusions: Randomized trial data demonstrated high clinical cure rates with ceftolozane/tazobactam treatment of cIAI and cUTI caused by ESBL-ENT.
引用
收藏
页码:268 / 272
页数:5
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