Lan Nguyen Thi Ngoc, Thu Nguyen Thi Nguyet, Barrail-Tran Aurélie, Duc Nguyen Hong, Lan Nguyen Ngoc, Laureillard Didier, Lien Truong Thi Xuan, Borand Laurence, Quillet Catherine, Connolly Catherine, Lagarde Dominique, Pym Alexander, Lienhardt Christian, Dung Nguyen Huy, Taburet Anne-Marie, Harries Anthony D
Pham Ngoc Thach Hospital, Ho Chi Minh City, Vietnam.
Pasteur Institute, Ho Chi Minh City, Vietnam.
PLoS One. 2014 Jan 22;9(1):e84866. doi: 10.1371/journal.pone.0084866. eCollection 2014.
Rifampicin and protease inhibitors are difficult to use concomitantly in patients with HIV-associated tuberculosis because of drug-drug interactions. Rifabutin has been proposed as an alternative rifamycin, but there is concern that the current recommended dose is suboptimal. The principal aim of this study was to compare bioavailability of two doses of rifabutin (150 mg three times per week and 150 mg daily) in patients with HIV-associated tuberculosis who initiated lopinavir/ritonavir-based antiretroviral therapy in Vietnam. Concentrations of lopinavir/ritonavir were also measured.
This was a randomized, open-label, multi-dose, two-arm, cross-over trial, conducted in Vietnamese adults with HIV-associated tuberculosis in Ho Chi Minh City (Clinical trial registry number NCT00651066). Rifabutin pharmacokinetics were evaluated before and after the introduction of lopinavir/ritonavir -based antiretroviral therapy using patient randomization lists. Serial rifabutin and 25-O-desacetyl rifabutin concentrations were measured during a dose interval after 2 weeks of rifabutin 300 mg daily, after 3 weeks of rifabutin 150 mg daily with lopinavir/ritonavir and after 3 weeks of rifabutin 150 mg three times per week with lopinavir/ritonavir.
Sixteen and seventeen patients were respectively randomized to the two arms, and pharmacokinetic analysis carried out in 12 and 13 respectively. Rifabutin 150 mg daily with lopinavir/ritonavir was associated with a 32% mean increase in rifabutin average steady state concentration compared with rifabutin 300 mg alone. In contrast, the rifabutin average steady state concentration decreased by 44% when rifabutin was given at 150 mg three times per week with lopinavir/ritonavir. With both dosing regimens, 2 - 5 fold increases of the 25-O-desacetyl- rifabutin metabolite were observed when rifabutin was given with lopinavir/ritonavir compared with rifabutin alone. The different doses of rifabutin had no significant effect on lopinavir/ritonavir plasma concentrations.
Based on these findings, rifabutin 150 mg daily may be preferred when co-administered with lopinavir/ritonavir in patients with HIV-associated tuberculosis.
ClinicalTrials.gov NCT00651066.
由于药物相互作用,利福平与蛋白酶抑制剂难以在人类免疫缺陷病毒(HIV)相关结核病患者中联合使用。利福布汀已被提议作为替代利福霉素,但有人担心目前推荐的剂量并非最佳。本研究的主要目的是比较在越南开始基于洛匹那韦/利托那韦的抗逆转录病毒治疗的HIV相关结核病患者中,两种剂量利福布汀(每周三次,每次150毫克和每日150毫克)的生物利用度。同时也测量了洛匹那韦/利托那韦的浓度。
这是一项随机、开放标签、多剂量、双臂、交叉试验,在胡志明市的越南成年HIV相关结核病患者中进行(临床试验注册号NCT00651066)。使用患者随机列表,在引入基于洛匹那韦/利托那韦的抗逆转录病毒治疗之前和之后评估利福布汀的药代动力学。在每日300毫克利福布汀治疗2周后、每日150毫克利福布汀与洛匹那韦/利托那韦联合治疗3周后以及每周三次150毫克利福布汀与洛匹那韦/利托那韦联合治疗3周后的一个剂量间隔内,测量利福布汀和25 - O - 去乙酰利福布汀的系列浓度。
分别有16名和17名患者被随机分配到两组,分别对12名和13名患者进行了药代动力学分析。与单独使用300毫克利福布汀相比,每日150毫克利福布汀与洛匹那韦/利托那韦联合使用时,利福布汀平均稳态浓度平均增加32%。相比之下,当利福布汀与洛匹那韦/利托那韦联合使用,每周三次,每次150毫克时,利福布汀平均稳态浓度下降了44%。在两种给药方案中与单独使用利福布汀相比,当利福布汀与洛匹那韦/利托那韦联合使用时,25 - O - 去乙酰利福布汀代谢物增加了2 - 5倍。不同剂量的利福布汀对洛匹那韦/利托那韦血浆浓度没有显著影响。
基于这些发现,在HIV相关结核病患者中,当与洛匹那韦/利托那韦联合使用时,每日150毫克利福布汀可能是更优选择。
ClinicalTrials.gov NCT00651066