Division of Infectious Diseases and Hospital Epidemiology, Departments of Medicine and Clinical Research, University Hospital of Basel and University of Basel, Basel, Switzerland.
Laboratory of Clinical Pharmacology, Service of Biomedicine, University Hospital of Lausanne and University of Lausanne, Lausanne, Switzerland.
J Antimicrob Chemother. 2017 Sep 1;72(9):2574-2577. doi: 10.1093/jac/dkx165.
Cobicistat and ritonavir have different inhibitory profiles for drug transporters that could impact the distribution of co-administered drugs. We compared darunavir concentrations in CSF when boosted by cobicistat versus ritonavir relative to plasma concentrations and with WT HIV-1 IC50 and IC90.
An open, single-arm, sequential clinical trial (NCT02503462) where paired CSF and blood samples were taken from seven HIV-infected patients presenting with HIV-associated neurocognitive disorders (HAND) and treated with a darunavir/ritonavir (800/100 mg) once-daily regimen. Ritonavir was subsequently replaced by cobicistat and paired CSF and blood samples were obtained from the same patients after treatment with the darunavir/cobicistat (800/150 mg) once-daily regimen. Darunavir concentrations at the end of the dosing interval were quantified by LC-MS/MS.
The median (IQR) darunavir concentrations in CSF with ritonavir and cobicistat boosting were 16.4 ng/mL (8.6-20.3) and 15.9 ng/mL (6.7-31.6), respectively (P = 0.58). The median (IQR) darunavir CSF:plasma ratios with ritonavir and cobicistat boosting were 0.007 (0.006-0.012) and 0.011 (0.007-0.015), respectively (P = 0.16). Darunavir concentrations in CSF exceeded the darunavir IC50 and IC90 by a median of 9.2- and 6.7-fold with ritonavir boosting, and by 8.9- and 6.5-fold with cobicistat boosting, respectively. All patients had darunavir CSF concentrations above the target inhibitory concentrations and remained virologically suppressed in the CSF and plasma.
This small study shows that cobicistat and ritonavir give comparable effective darunavir concentrations in CSF, thus suggesting that these boosters can be used interchangeably in once-daily darunavir regimens.
考比司他和利托那韦对药物转运体具有不同的抑制特性,这可能会影响合并用药的分布。我们比较了考比司他和利托那韦增强后的达芦那韦在脑脊液中的浓度与血浆浓度的比值,以及与野生型 HIV-1 的 IC50 和 IC90 的比值。
这是一项开放、单臂、连续临床试验(NCT02503462),共纳入 7 名患有 HIV 相关性认知障碍(HAND)的 HIV 感染患者,这些患者接受每日一次的达芦那韦/利托那韦(800/100mg)治疗方案,采集配对的脑脊液和血液样本。随后,将利托那韦替换为考比司他,并在这些患者接受每日一次的达芦那韦/考比司他(800/150mg)治疗方案后,再次采集配对的脑脊液和血液样本。通过 LC-MS/MS 定量分析达芦那韦在末端剂量间隔时的浓度。
利托那韦和考比司他增强后的脑脊液中达芦那韦的中位数(IQR)浓度分别为 16.4ng/mL(8.6-20.3)和 15.9ng/mL(6.7-31.6)(P=0.58)。利托那韦和考比司他增强后的脑脊液与血浆的达芦那韦比值中位数分别为 0.007(0.006-0.012)和 0.011(0.007-0.015)(P=0.16)。利托那韦增强后的脑脊液中达芦那韦浓度中位数超过达芦那韦 IC50 和 IC90 的 9.2 倍和 6.7 倍,考比司他增强后的脑脊液中达芦那韦浓度中位数超过达芦那韦 IC50 和 IC90 的 8.9 倍和 6.5 倍。所有患者的脑脊液中均有达芦那韦浓度超过目标抑制浓度,并且在脑脊液和血浆中病毒学仍得到抑制。
这项小型研究表明,考比司他和利托那韦在脑脊液中给予等效的有效达芦那韦浓度,因此提示这两种增强剂可以在每日一次的达芦那韦方案中互换使用。