Center for Infectious Diseases Research and Experimental Therapeutics, Baylor Research Institute, Baylor University Medical Center, Dallas, TX, USA.
Praedicare Laboratories, Dallas, TX, USA.
J Antimicrob Chemother. 2020 Feb 1;75(2):392-399. doi: 10.1093/jac/dkz460.
Animal models have suggested that the combination of pretomanid with pyrazinamide and moxifloxacin (PaMZ) may shorten TB therapy duration to 3-4 months. Here, we tested that in the hollow-fibre system model of TB (HFS-TB).
A series of HFS-TB experiments were performed to compare the kill rates of the PaMZ regimen with the standard three-drug combination therapy. HFS-TB experiments were performed with bacilli in log-phase growth treated for 28 days, intracellular bacilli treated daily for 28 days and semi-dormant Mycobacterium tuberculosis treated with daily therapy for 56 days for sterilizing effect. Next, time-to-extinction equations were employed, followed by morphism transformation and Latin hypercube sampling, to determine the proportion of patients who achieved a time to extinction of 3, 4 or 6 months with each regimen.
Using linear regression, the HFS-TB sterilizing effect rates of the PaMZ regimen versus the standard-therapy regimen during the 56 days were 0.18 (95% credible interval=0.13-0.23) versus 0.15 (95% credible interval=0.08-0.21) log10 cfu/mL/day, compared with 0.16 (95% credible interval=0.13-0.18) versus 0.11 (95% credible interval=0.09-0.13) log10 cfu/mL/day in the Phase II clinical trial, respectively. Using time-to-extinction and Latin hypercube sampling modelling, the expected percentages of patients in which the PaMZ regimen would achieve sterilization were 40.37% (95% credible interval=39.1-41.34) and 72.30% (95% credible interval=71.41-73.17) at 3 and 4 months duration of therapy, respectively, versus 93.67% (95% credible interval=93.18-94.13) at 6 months for standard therapy.
The kill rates of the PaMZ regimen were predicted to be insufficient to achieve cure in less than 6 months in most patients.
动物模型表明,将贝达喹啉与吡嗪酰胺和莫西沙星(PaMZ)联合使用可能将结核病治疗时间缩短至 3-4 个月。在此,我们在中空纤维系统结核模型(HFS-TB)中对此进行了测试。
进行了一系列 HFS-TB 实验,以比较 PaMZ 方案与标准三联药物组合疗法的杀菌率。用对数期生长的杆菌进行 28 天的 HFS-TB 实验,用每日处理 28 天的细胞内杆菌和用每日治疗 56 天的半休眠结核分枝杆菌进行杀菌效果处理。然后,采用时间灭绝方程、形态转换和拉丁超立方抽样,确定每个方案达到 3、4 或 6 个月时间灭绝的患者比例。
使用线性回归,PaMZ 方案与标准治疗方案在 56 天的 HFS-TB 杀菌效果率分别为 0.18(95%可信区间=0.13-0.23)与 0.15(95%可信区间=0.08-0.21)log10cfu/mL/天,而 II 期临床试验分别为 0.16(95%可信区间=0.13-0.18)与 0.11(95%可信区间=0.09-0.13)log10cfu/mL/天。使用时间灭绝和拉丁超立方抽样建模,PaMZ 方案预计在 3 个月和 4 个月治疗期间实现杀菌的患者百分比分别为 40.37%(95%可信区间=39.1-41.34)和 72.30%(95%可信区间=71.41-73.17),而标准治疗方案则为 6 个月时的 93.67%(95%可信区间=93.18-94.13)。
预测 PaMZ 方案的杀菌率不足以在大多数患者中实现 6 个月内的治愈。