来自3期临床试验的汇总数据,比较头孢唑烷/他唑巴坦与美罗培南治疗复杂性腹腔内感染的临床活性。

IF 2.3
Zhiqiang Li, Yue Kang, Hongqiang Gao, Yingpeng Zhao, Ding Luo, Dongdong Wang, Xiang Zhang, Jieqi Yu, Guang Chu, Jun Cao, Fan Wang, Xiongqi Zhao, Erin Jensen, Gina Lin, Gang Chen
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引用次数: 0

摘要

背景:头孢唑烷/他唑巴坦(C/T)联合甲硝唑是一种用于治疗复杂性腹腔感染(cIAIs)的有效抗菌药物。方法:采用4项3期临床研究(CXA-cIAI-10-08、CXA-cIAI-10-09、NCT02739997和NCT03830333)的汇总数据,比较C/T联合甲硝唑与美罗培南治疗cIAIs的临床疗效。结果:共纳入1361例患者(C/T联合甲硝唑,n = 721;美罗培南,n = 640)。意向治疗组(ITT)和临床可评估人群的治愈试验(TOC)就诊时的临床缓解率分别为84.3%(608/721)和86.9%(556/640),93.4%(534/572)和93.8% (483/515),C/T联合甲硝唑和美罗培南治疗结束时的临床缓解率分别为90.6%(653/721)和91.9%(588/640),96.5%(552/572)和96.6%(499/515)。改良ITT人群TOC就诊时的微生物应答率分别为85.3%(440/516)和89.3%(442/495),扩展微生物可评价人群C/T联合甲硝唑和美罗培南的微生物应答率分别为93.7%(399/426)和94.3%(394/418)。C/T联合甲硝唑和美罗培南的不良事件发生率分别为341/716例(47.6%)和280/631例(44.4%)。各治疗组最常见的不良反应是腹泻、恶心、发热和失眠。没有发现新的严重的安全问题。结论:C/T联合甲硝唑治疗cIAI的疗效与美罗培南相当,C/T联合甲硝唑可能是cIAI的一种替代治疗方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pooled data from phase 3 clinical trials comparing the clinical activity of ceftolozane/tazobactam versus meropenem for the treatment of complicated intra-abdominal infections.

Background: Ceftolozane/tazobactam (C/T) in combination with metronidazole is an active antimicrobial therapy used to treat complicated intra-abdominal infections (cIAIs).

Methods: A comparison of the clinical efficacy of C/T plus metronidazole vs. meropenem for the treatment of cIAIs using pooled data from four phase 3 clinical studies (CXA-cIAI-10-08, CXA-cIAI-10-09, NCT02739997 and NCT03830333).

Results: In total, 1,361 patients (C/T plus metronidazole, n = 721; meropenem, n = 640) were included in the pooled analysis. Clinical response rates at the test of cure (TOC) visit in the intention-to-treat (ITT) and clinically evaluable populations were 84.3% (608/721) and 86.9% (556/640) as well as 93.4% (534/572) and 93.8% (483/515), and at the end of treatment visits the rates were 90.6% (653/721) and 91.9% (588/640) as well as 96.5% (552/572) and 96.6% (499/515) for C/T plus metronidazole and meropenem, respectively. Microbiological response rates at the TOC visits in the modified ITT population were 85.3% (440/516) and 89.3% (442/495), and in the extended microbiological evaluable population 93.7% (399/426) and 94.3% (394/418) for C/T plus metronidazole and meropenem, respectively. Adverse events occurred in 341/716 (47.6%) and 280/631 (44.4%) patients treated with C/T plus metronidazole and meropenem, respectively. The most common adverse events across treatment groups were diarrhoea, nausea, pyrexia and insomnia. No new serious safety findings were identified.

Conclusions: The efficacy of C/T plus metronidazole was comparable with meropenem even for cIAIs and C/T plus metronidazole might be an alternative treatment option for cIAI.

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