阿兹屈南
头孢他啶/阿维巴坦
医学
阿维巴坦
内科学
随机对照试验
肺炎克雷伯菌
抗生素
胃肠病学
微生物学
外科
生物
抗生素耐药性
基因
大肠杆菌
亚胺培南
生物化学
作者
George L. Daikos,José Miguel Cisneros,Yehuda Carmeli,Minggui Wang,Chee Loon Leong,Konstantinos Pontikis,Anastasia Anderzhanova,Simin Aysel Florescu,Roman S. Kozlov,Eduardo Rodríguez-Noriega,Mina Psichοgiou,Pinyo Rattanaumpawan,Anca Streinu‐Cercel,V Ramasubramanian,Francis F. Arhin,Halley Rogers,Michele Wible,Joanne L. Leaney,David Jacobson,Rienk Pypstra
标识
DOI:10.1093/jacamr/dlaf131
摘要
Abstract Background The Phase 3 ASSEMBLE study investigated aztreonam–avibactam versus best available therapy (BAT) for treatment of complicated intra-abdominal infection (cIAI), complicated urinary tract infection (cUTI), hospital-acquired/ventilator-associated pneumonia (HAP/VAP) or bloodstream infection (BSI) caused by confirmed MBL-producing multidrug-resistant pathogens. Methods This prospective, multicentre, randomized, open-label, central assessor-blinded study randomized hospitalized adults 2:1 to aztreonam–avibactam [+ metronidazole (cIAI)] or BAT for 5–14 (cIAI, cUTI and BSI) or 7–14 (HAP/VAP) days. Primary endpoint was clinical cure at test-of-cure (TOC) visit on Day 28 ± 3 [microbiological ITT (micro-ITT) analysis set]. Secondary endpoints included microbiological response at TOC, 28-day mortality and safety. No formal hypothesis testing was planned. Results Fifteen patients were randomized [aztreonam–avibactam, n = 12; BAT, n = 3 (ITT and micro-ITT analysis sets)]. Most frequent baseline pathogens were Enterobacterales; Klebsiella pneumoniae was most common [aztreonam–avibactam, 6/12 (50%); BAT, 2/3 (67%)]. MBL subtypes/variants identified in the aztreonam–avibactam group were NDM-1 (n = 7), NDM-5 (n = 3), VIM-2 (n = 2) and L1 (n = 3); and for BAT were NDM-1 (n = 2) and NDM-5 (n = 1). Clinical cure rates at TOC were 5/12 (42%) for aztreonam–avibactam and 0/3 (0%) for BAT. Per-patient microbiological responses were generally consistent with clinical responses. Twenty-eight-day all-cause mortality rates for aztreonam–avibactam and BAT were 1/12 (8%) and 1/3 (33%), respectively. Aztreonam–avibactam was generally well-tolerated, with no treatment-related serious adverse events. Conclusions These Phase 3 data provide support for aztreonam–avibactam as a potential therapeutic option for difficult-to-treat infections caused by MBL-producing Gram-negative bacteria.
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