Safety and Efficacy of Ceftolozane/Tazobactam Plus Metronidazole Versus Meropenem From a Phase 2, Randomized Clinical Trial in Pediatric Participants With Complicated Intra-abdominal Infection

被引:4
|
作者
Jackson, Carl-Christian A. [1 ]
Newland, Jason [2 ]
Dementieva, Nataliia [3 ]
Lonchar, Julia [4 ]
Su, Feng-Hsiu [4 ]
Huntington, Jennifer A. [4 ]
Bensaci, Mekki [4 ]
Popejoy, Myra W. [4 ]
Johnson, Matthew G. [4 ]
De Anda, Carisa [4 ]
Rhee, Elizabeth G. [4 ]
Bruno, Christopher J. [4 ]
机构
[1] Tufts Childrens Hosp, Div Pediat Surg, Boston, MA USA
[2] Washington Univ, St Louis Childrens Hosp, Dept Pediat, Sch Med, St Louis, MO USA
[3] Dnipropetrovsk Reg Childrens Clin Hosp, Dept Pediat Surg, Dnipro, Ukraine
[4] Merck & Co Inc, Rahway, NJ 07065 USA
关键词
adolescent; cIAI; children; Gram-negative; Enterobacterales; ANTIMICROBIAL SUSCEPTIBILITY; RESISTANCE;
D O I
10.1097/INF.0000000000003911
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background:Ceftolozane/tazobactam, a cephalosporin-beta-lactamase inhibitor combination, is approved for the treatment of complicated urinary tract infections and complicated intra-abdominal infections (cIAI). The safety and efficacy of ceftolozane/tazobactam in pediatric participants with cIAI were assessed. Methods:This phase 2 study (NCT03217136) randomized participants to either ceftolozane/tazobactam+metronidazole or meropenem for treatment of cIAI in pediatric participants (<18 years). The primary objective was to assess the safety and tolerability of intravenous ceftolozane/tazobactam+metronidazole. Clinical cure at end of treatment (EOT) and test of cure (TOC) visits were secondary end points. Results:The modified intent-to-treat (MITT) population included 91 participants (ceftolozane/tazobactam+metronidazole, n = 70; meropenem, n = 21). Complicated appendicitis was the most common diagnosis (93.4%); Escherichia coli was the most common pathogen (65.9%). Adverse events (AEs) occurred in 80.0% and 61.9% of participants receiving ceftolozane/tazobactam+metronidazole and meropenem, drug-related AEs occurred in 18.6% and 14.3% and serious AEs occurred in 11.4% and 0% of participants receiving ceftolozane/tazobactam+metronidazole and meropenem, respectively. No drug-related serious AEs or discontinuations due to drug-related AEs occurred. Rates of the clinical cure for ceftolozane/tazobactam+metronidazole and meropenem at EOT were 80.0% and 95.2% (difference: -14.3; 95% confidence interval: -26.67 to 4.93) and at TOC were 80.0% and 100.0% (difference: -19.1; 95% confidence interval: -30.18 to -2.89), respectively; 6 of the 14 clinical failures for ceftolozane/tazobactam+metronidazole at TOC were indeterminate responses imputed as failures per protocol. Conclusion:Ceftolozane/tazobactam+metronidazole was well tolerated in pediatric participants with cIAI and had a safety profile similar to the established safety profile in adults. In this descriptive efficacy analysis, ceftolozane/tazobactam+metronidazole appeared efficacious.
引用
收藏
页码:557 / 563
页数:7
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