多罗替拉韦加达鲁那韦抗逆转录病毒疗法的案例:药物剂量加倍是否总是有用?简短交流。

IF 2.8 4区 医学 Q2 MEDICAL LABORATORY TECHNOLOGY
Dario Cattaneo, Anna Lisa Ridolfo, Andrea Giacomelli, Antonella Castagna, Alberto Dolci, Spinello Antinori, Cristina Gervasoni
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引用次数: 0

摘要

背景抗逆转录病毒药物组合会影响多鲁特韦的谷浓度。在此,作者重点研究了多罗拉韦加达鲁那韦增强剂的抗逆转录病毒疗法,以探讨增强剂和/或给药时间对多罗拉韦和达鲁那韦血浆谷浓度的影响:这项回顾性观察研究纳入了连续接受多鲁特韦加达鲁那韦加强型抗逆转录病毒疗法至少3个月的HIV感染者(PWH),他们至少接受过一次多鲁特韦和达鲁那韦血浆谷浓度评估:结果:共纳入了 116 名 PWH 的 200 项药物治疗药物监测结果。多鲁曲韦和达鲁那韦的谷浓度范围分别为70至3648微克/升和102至11876微克/升。多罗拉韦谷浓度最高的抗逆转录病毒药物组合是多罗拉韦加达鲁那韦/考比司他(均为每日一次)(1410 ± 788 mcg/L),而多罗拉韦每日一次加达鲁那韦/利托那韦每日两次的谷浓度最低(686 ± 481 mcg/L)。与每日一次的治疗方案相比,多鲁曲韦剂量加倍并不能显著提高药物谷浓度。相反,利托那韦的达鲁那韦谷浓度最高(2850 ± 1456 mcg/L,与基于cobicistat的方案相比,P < 0.05)。药物剂量加倍会导致达芦那韦谷浓度显著增加(4445 ± 2926 mcg/L,P < 0.05):结论:每天两次服用达芦那韦/利托那韦的PWH患者体内的多罗替拉韦谷浓度明显降低。在需要较高多鲁曲韦暴露量的临床条件下,如与已知会降低多鲁曲韦生物利用度的药物发生药物相互作用时,或在经验丰富的PWH中,应仔细考虑这一证据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Case of Dolutegravir Plus Darunavir Antiretroviral Regimens: Is It Always Useful to Double the Drug Doses? A Short Communication.

Background: Antiretroviral drug combinations affect dolutegravir trough concentrations. Here, the authors focused on dolutegravir plus booster darunavir antiretroviral regimens to investigate the effect of the booster and/or timing of drug administration on dolutegravir and darunavir plasma trough concentrations.

Methods: This retrospective observational study included consecutive people with HIV (PWH) receiving dolutegravir plus booster darunavir antiretroviral regimens for at least 3 months, with at least one assessment of dolutegravir and darunavir plasma trough concentrations.

Results: A total of 200 drug therapeutic drug monitoring results from 116 PWH were included. Dolutegravir and darunavir trough concentrations ranged, respectively, from 70 to 3648 mcg/L and from 102 to 11,876 mcg/L. The antiretroviral drug combination associated with the highest dolutegravir trough concentration was dolutegravir plus darunavir/cobicistat, both once daily (1410 ± 788 mcg/L), whereas dolutegravir once daily plus darunavir/ritonavir twice daily had the lowest trough concentrations (686 ± 481 mcg/L). Doubling the dose of dolutegravir did not significantly increase drug trough concentrations compared with that of once-daily regimens. Instead, the highest darunavir trough concentrations were with ritonavir (2850 ± 1456 mcg/L, P < 0.05 versus cobicistat-based regimens). Doubling the drug dose resulted in a significant increase in the darunavir trough concentration (4445 ± 2926 mcg/L, P < 0.05).

Conclusions: Dolutegravir trough concentrations were significantly reduced in PWH receiving darunavir/ritonavir twice daily. This evidence should be carefully considered in clinical conditions requiring higher dolutegravir exposure, such as in the presence of drug-drug interactions with drugs known to reduce dolutegravir bioavailability or in highly experienced PWH.

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来源期刊
Therapeutic Drug Monitoring
Therapeutic Drug Monitoring 医学-毒理学
CiteScore
5.00
自引率
8.00%
发文量
213
审稿时长
4-8 weeks
期刊介绍: Therapeutic Drug Monitoring is a peer-reviewed, multidisciplinary journal directed to an audience of pharmacologists, clinical chemists, laboratorians, pharmacists, drug researchers and toxicologists. It fosters the exchange of knowledge among the various disciplines–clinical pharmacology, pathology, toxicology, analytical chemistry–that share a common interest in Therapeutic Drug Monitoring. The journal presents studies detailing the various factors that affect the rate and extent drugs are absorbed, metabolized, and excreted. Regular features include review articles on specific classes of drugs, original articles, case reports, technical notes, and continuing education articles.
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