Liu Albert Y, Yang Qiyun, Huang Yong, Bacchetti Peter, Anderson Peter L, Jin Chengshi, Goggin Kathy, Stojanovski Kristefer, Grant Robert, Buchbinder Susan P, Greenblatt Ruth M, Gandhi Monica
Bridge HIV, San Francisco Department of Public Health, San Francisco, California, United States of America ; Department of Medicine, University of California San Francisco (UCSF), San Francisco, California, United States of America.
Department of Bioengineering and Therapeutic Sciences, University of California San Francisco, San Francisco, California, United States of America.
PLoS One. 2014 Jan 8;9(1):e83736. doi: 10.1371/journal.pone.0083736. eCollection 2014.
Pre-exposure prophylaxis (PrEP) trials using tenofovir-based regimens have demonstrated that high levels of adherence are required to evaluate efficacy; the incorporation of objective biomarkers of adherence in trial design has been essential to interpretation, given the inaccuracy of self-report. Antiretroviral measurements in scalp hair have been useful as a marker of long-term exposure in the HIV treatment setting, and hair samples are relatively easy and inexpensive to collect, transport, and store for analysis. To evaluate the relationship between dose and tenofovir concentrations in hair, we examined the dose proportionality of tenofovir in hair in healthy, HIV-uninfected adults.
A phase I, crossover pharmacokinetic study was performed in 24 HIV-negative adults receiving directly-observed oral tenofovir tablets administered 2, 4, and 7 doses/week for 6 weeks, with a ≥3-week break between periods. Small samples of hair were collected after each six-week period and analyzed for tenofovir concentrations. Geometric-mean-ratios compared levels between each pair of dosing conditions. Intensive plasma pharmacokinetic studies were performed during the daily-dosing period to calculate areas-under-the-time-concentration curves (AUCs).
Over 90% of doses were observed per protocol. Median tenofovir concentrations in hair increased monotonically with dose. A log-linear relationship was seen between dose and hair levels, with an estimated 76% (95% CI 60-93%) increase in hair level per 2-fold dose increase. Tenofovir plasma AUCs modestly predicted drug concentrations in hair.
This study found a strong linear relationship between frequency of dosing and tenofovir levels in scalp hair. The analysis of quantitative drug levels in hair has the potential to improve adherence measurement in the PrEP field and may be helpful in determining exposure thresholds for protection and explaining failures in PrEP trials. Hair measures for adherence monitoring may also facilitate adherence measurement in real-world settings and merit further investigation in upcoming PrEP implementation studies and programs.
ClinicalTrials.gov NCT00903084.
使用基于替诺福韦的方案进行暴露前预防(PrEP)试验表明,需要高度依从性才能评估疗效;鉴于自我报告的不准确性,在试验设计中纳入依从性的客观生物标志物对于解读至关重要。在HIV治疗环境中,头皮头发中的抗逆转录病毒药物测量已被用作长期暴露的标志物,并且头发样本相对容易收集、运输和储存用于分析。为了评估头发中替诺福韦剂量与浓度之间的关系,我们研究了健康、未感染HIV的成年人头发中替诺福韦的剂量比例关系。
对24名HIV阴性成年人进行了一项I期交叉药代动力学研究,这些成年人接受直接观察下的口服替诺福韦片,每周服用2、4和7剂,共6周,各阶段之间间隔≥3周。在每个六周阶段结束后收集少量头发样本,并分析其中替诺福韦的浓度。几何平均比比较了每对给药条件下的水平。在每日给药期间进行了强化血浆药代动力学研究,以计算时间-浓度曲线下面积(AUC)。
超过90%的剂量符合方案要求。头发中替诺福韦的中位浓度随剂量单调增加。剂量与头发水平之间呈对数线性关系,每2倍剂量增加,头发水平估计增加76%(95%CI 60-93%)。替诺福韦血浆AUC适度预测了头发中的药物浓度。
本研究发现给药频率与头皮头发中替诺福韦水平之间存在很强的线性关系。头发中定量药物水平的分析有可能改善PrEP领域的依从性测量,并可能有助于确定保护的暴露阈值以及解释PrEP试验中的失败情况。用于依从性监测的头发测量也可能有助于在现实环境中进行依从性测量,值得在即将开展的PrEP实施研究和项目中进一步研究。
ClinicalTrials.gov NCT00903084。