Burman William J, Goldberg Stefan, Johnson John L, Muzanye Grace, Engle Melissa, Mosher Ann W, Choudhri Shurjeel, Daley Charles L, Munsiff Sonal S, Zhao Zhen, Vernon Andrew, Chaisson Richard E
Denver Public Health and the Department of Medicine, University of Colorado Health Sciences; National Jewish Medical and Research Center, Denver, Colorado, USA.
Am J Respir Crit Care Med. 2006 Aug 1;174(3):331-8. doi: 10.1164/rccm.200603-360OC. Epub 2006 May 4.
Moxifloxacin has promising preclinical activity against Mycobacterium tuberculosis, but has not been evaluated in multidrug treatment of tuberculosis in humans.
To compare the impact of moxifloxacin versus ethambutol, both in combination with isoniazid, rifampin, and pyrazinamide, on sputum culture conversion at 2 mo as a measure of the potential sterilizing activity of alternate induction regimens.
Adults with smear-positive pulmonary tuberculosis were randomized in a factorial design to receive moxifloxacin (400 mg) versus ethambutol given 5 d/wk versus 3 d/wk (after 2 wk of daily therapy). All doses were directly observed.
The primary endpoint was sputum culture status at 2 mo of treatment.
Of 336 patients enrolled, 277 (82%) were eligible for the efficacy analysis, 186 (67%) were male, 175 (63%) were enrolled at African sites, 206 (74%) had cavitation on chest radiograph, and 60 (22%) had HIV infection. Two-month cultures were negative in 71% of patients (99 of 139) treated with moxifloxacin versus 71% (98 of 138) treated with ethambutol (p = 0.97). Patients receiving moxifloxacin, however, more often had negative cultures after 4 wk of treatment. Patients treated with moxifloxacin more often reported nausea (22 vs. 9%, p = 0.002), but similar proportions completed study treatment (88 vs. 89%). Dosing frequency had little effect on 2-mo culture status or tolerability of therapy.
The addition of moxifloxacin to isoniazid, rifampin, and pyrazinamide did not affect 2-mo sputum culture status but did show increased activity at earlier time points.
莫西沙星对结核分枝杆菌具有良好的临床前活性,但尚未在人类结核病的多药治疗中进行评估。
比较莫西沙星与乙胺丁醇(均与异烟肼、利福平及吡嗪酰胺联合使用)对2个月时痰培养转阴的影响,以此作为替代诱导方案潜在杀菌活性的衡量指标。
涂片阳性的成年肺结核患者采用析因设计进行随机分组,分别接受莫西沙星(400毫克)、每周5天给药的乙胺丁醇与每周3天给药的乙胺丁醇(每日治疗2周后)。所有剂量均直接观察给药。
主要终点为治疗2个月时的痰培养状况。
在纳入的336例患者中,277例(82%)符合疗效分析条件,其中男性186例(67%),175例(63%)在非洲地区入组,206例(74%)胸部X线片有空洞形成,60例(22%)感染HIV。接受莫西沙星治疗的患者中71%(139例中的99例)2个月时培养结果为阴性,接受乙胺丁醇治疗的患者中这一比例为71%(138例中的98例)(p = 0.97)。然而,接受莫西沙星治疗的患者在治疗4周后培养结果阴性的情况更为常见。接受莫西沙星治疗的患者恶心报告更为频繁(22%对9%,p = 0.002),但完成研究治疗的比例相似(88%对89%)。给药频率对2个月时的培养状况或治疗耐受性影响不大。
在异烟肼、利福平及吡嗪酰胺中添加莫西沙星不影响2个月时的痰培养状况,但在更早时间点显示出活性增加。