Marais Suzaan, Cresswell Fiona V, Hamers Raph L, Te Brake Lindsey H M, Ganiem Ahmad R, Imran Darma, Bangdiwala Ananta, Martyn Emily, Kasibante John, Kagimu Enock, Musubire Abdu, Maharani Kartika, Estiasari Riwanti, Kusumaningrum Ardiana, Kusumadjayanti Nadytia, Yunivita Vycke, Naidoo Kogieleum, Lessells Richard, Moosa Yunus, Svensson Elin M, Huppler Hullsiek Katherine, Aarnoutse Rob E, Boulware David R, van Crevel Reinout, Ruslami Rovina, Meya David B
Department of Neurology, Inkosi Albert Luthuli Central Hospital, Durban, 4091, South Africa.
Infectious Diseases Institute, Mulago College of Health Sciences, Kampala, PO Box 22418, Uganda.
Wellcome Open Res. 2020 Aug 25;4:190. doi: 10.12688/wellcomeopenres.15565.2. eCollection 2019.
Tuberculous meningitis (TBM), the most severe form of tuberculosis (TB), results in death or neurological disability in >50%, despite World Health Organisation recommended therapy. Current TBM regimen dosages are based on data from pulmonary TB alone. Evidence from recent phase II pharmacokinetic studies suggests that high dose rifampicin (R) administered intravenously or orally enhances central nervous system penetration and may reduce TBM associated mortality. We hypothesize that, among persons with TBM, high dose oral rifampicin (35 mg/kg) for 8 weeks will improve survival compared to standard of care (10 mg/kg), without excess adverse events. We will perform a parallel group, randomised, placebo-controlled, double blind, phase III multicentre clinical trial comparing high dose oral rifampicin to standard of care. The trial will be conducted across five clinical sites in Uganda, South Africa and Indonesia. Participants are HIV-positive or negative adults with clinically suspected TBM, who will be randomised (1:1) to one of two arms: 35 mg/kg oral rifampicin daily for 8 weeks (in combination with standard dose isoniazid [H], pyrazinamide [Z] and ethambutol [E]) or standard of care (oral HRZE, containing 10 mg/kg/day rifampicin). The primary end-point is 6-month survival. Secondary end points are: i) 12-month survival ii) functional and neurocognitive outcomes and iii) safety and tolerability. Tertiary outcomes are: i) pharmacokinetic outcomes and ii) cost-effectiveness of the intervention. We will enrol 500 participants over 2.5 years, with follow-up continuing until 12 months post-enrolment. Our best TBM treatment still results in unacceptably high mortality and morbidity. Strong evidence supports the increased cerebrospinal fluid penetration of high dose rifampicin, however conclusive evidence regarding survival benefit is lacking. This study will answer the important question of whether high dose oral rifampicin conveys a survival benefit in TBM in HIV-positive and -negative individuals from Africa and Asia. ISRCTN15668391 (17/06/2019).
结核性脑膜炎(TBM)是最严重的结核病形式,尽管有世界卫生组织推荐的治疗方法,但仍有超过50%的患者死亡或出现神经功能残疾。目前的TBM治疗方案剂量仅基于肺结核的数据。近期II期药代动力学研究的证据表明,静脉或口服高剂量利福平(R)可增强中枢神经系统的穿透性,并可能降低TBM相关的死亡率。我们假设,在TBM患者中,与标准治疗(10mg/kg)相比,口服高剂量利福平(35mg/kg)持续8周将提高生存率,且不会增加不良事件。我们将进行一项平行组、随机、安慰剂对照、双盲、III期多中心临床试验,比较高剂量口服利福平与标准治疗。该试验将在乌干达、南非和印度尼西亚的五个临床地点进行。参与者为临床疑似TBM的HIV阳性或阴性成年人,他们将被随机(1:1)分配到两个组之一:每天口服35mg/kg利福平,持续8周(联合标准剂量异烟肼[H]、吡嗪酰胺[Z]和乙胺丁醇[E])或标准治疗(口服HRZE,含10mg/kg/天利福平)。主要终点是6个月生存率。次要终点包括:i)12个月生存率;ii)功能和神经认知结果;iii)安全性和耐受性。三级终点包括:i)药代动力学结果;ii)干预措施的成本效益。我们将在2.5年内招募500名参与者,随访持续至入组后12个月。我们目前最佳的TBM治疗方法仍导致高得令人无法接受的死亡率和发病率。有力证据支持高剂量利福平增加脑脊液穿透性,但缺乏关于生存获益的确凿证据。本研究将回答重要问题,即高剂量口服利福平是否能使来自非洲和亚洲的HIV阳性和阴性个体在TBM中获得生存获益。ISRCTN15668391(2019年6月17日)