National Healthcare Group, 6 Commonwealth Lane, Singapore 149547, Singapore.
Antimicrob Agents Chemother. 2010 Jul;54(7):2775-80. doi: 10.1128/AAC.01564-09. Epub 2010 Apr 12.
Ritonavir-boosted darunavir with efavirenz may be considered a nucleoside-sparing regimen for treatment-naïve HIV-infected patients. However, the pharmacokinetics of this combination administered once daily have not been studied. We conducted a three-period interaction study with healthy volunteers. The subjects were given darunavir at 900 mg with ritonavir at 100 mg once daily for 10 days. Efavirenz at 600 mg once daily was added for 14 days. Darunavir-ritonavir was then stopped and efavirenz alone was given for 14 days. At the end of each period, blood was taken predosing and for up to 24 h postdosing to measure the drug concentrations. We recruited seven males and five females ages 24 to 49 years and weighing 50 to 83 kg. The darunavir trough concentrations were reduced after efavirenz administration (geometric mean ratio [GMR], 0.43; 90% confidence interval [CI], 0.32 to 0.57]; P < 0.001). The mean darunavir trough concentrations were 1,180 ng/ml (standard deviation, 1,138 ng/ml) after efavirenz administration, but all darunavir trough concentrations were above the 50% effective concentration (EC(50)) of 55 ng/ml for the wild-type virus. For darunavir, the area under the concentration-time curve from 0 to 24 h (AUC(0-24)) (GMR, 0.86; 90% CI, 0.75 to 0.97; P = 0.05) and the half-life (GMR, 0.56; 90% CI, 0.49 to 0.65; P < 0.001) were also significantly reduced. The darunavir peak concentrations were not significantly changed (GMR, 0.92; 90% CI, 0.82 to 1.03; P = 0.23). The ritonavir trough concentrations (GMR, 0.46; 90% CI, 0.33 to 0.63; P = 0.001), AUC(0-24) (GMR, 0.74; 90% CI, 0.64 to 0.86; P = 0.004), and half-life (GMR, 0.80; 90% CI, 0.75 to 0.86; P < 0.001) were also significantly reduced. The efavirenz half-life was significantly longer when it was coadministered with darunavir-ritonavir than when it was given alone (GMR, 1.66; 90% CI, 1.24 to 2.23; P = 0.01), but there were no differences in the efavirenz trough or peak concentration or AUC(0-24) when it was coadministered with darunavir-ritonavir. Efavirenz reduced the trough concentrations of darunavir significantly, but the concentrations remained above the EC(50) for the wild-type virus. This regimen should be evaluated with treatment-naïve patients with no preexisting resistance.
利托那韦增强的达芦那韦与依非韦伦联合方案可能被视为一种治疗初治 HIV 感染患者的不含核苷类药物的方案。然而,尚未研究过每日一次给予这种联合方案的药代动力学。我们进行了一项有健康志愿者参与的三周期相互作用研究。研究对象接受达芦那韦 900 mg 联合利托那韦 100 mg 每日一次治疗 10 天,然后加用依非韦伦 600 mg 每日一次治疗 14 天。停止达芦那韦-利托那韦治疗,单独给予依非韦伦治疗 14 天。在每个周期的最后,在给药前和给药后最多 24 小时取血,以测量药物浓度。我们招募了 7 名男性和 5 名女性,年龄 24 至 49 岁,体重 50 至 83 公斤。依非韦伦给药后达芦那韦谷浓度降低(几何均数比 [GMR],0.43;90%置信区间 [CI],0.32 至 0.57;P < 0.001)。依非韦伦给药后达芦那韦谷浓度为 1180ng/ml(标准差 1138ng/ml),但所有达芦那韦谷浓度均高于野生型病毒的 50%有效浓度(EC50)55ng/ml。对于达芦那韦,0 至 24 小时的浓度-时间曲线下面积(AUC0-24)(GMR,0.86;90%CI,0.75 至 0.97;P = 0.05)和半衰期(GMR,0.56;90%CI,0.49 至 0.65;P < 0.001)也显著降低。达芦那韦峰浓度无显著变化(GMR,0.92;90%CI,0.82 至 1.03;P = 0.23)。利托那韦谷浓度(GMR,0.46;90%CI,0.33 至 0.63;P = 0.001)、AUC0-24(GMR,0.74;90%CI,0.64 至 0.86;P = 0.004)和半衰期(GMR,0.80;90%CI,0.75 至 0.86;P < 0.001)也显著降低。依非韦伦与达芦那韦-利托那韦同时给药时半衰期显著延长(GMR,1.66;90%CI,1.24 至 2.23;P = 0.01),但与达芦那韦-利托那韦同时给药时,依非韦伦的谷浓度、峰浓度或 AUC0-24 无差异。依非韦伦显著降低了达芦那韦的谷浓度,但浓度仍高于野生型病毒的 EC50。该方案应在无预先存在耐药性的初治患者中进行评估。