Clinical pharmacology considerations and drug-drug interactions with long-acting cabotegravir and rilpivirine relevant to sub-Saharan Africa

被引:2
|
作者
Steulet, Adrian [1 ]
Obura, Bonniface [2 ,3 ]
Waitt, Catriona [4 ,5 ]
Laker, Eva [5 ]
Nicol, Melanie R. [6 ]
Cresswell, Fiona V. [7 ,8 ]
机构
[1] Nyon Hosp GHOL, Dept Internal Med, Nyon, Switzerland
[2] Univ Liverpool, Dept Pharmacol & Therapeut, Antimicrobial Pharmacodynam & Therapeut Grp, Liverpool, England
[3] Lira Univ, Dept Pharmacol & Therapeut, Lira, Uganda
[4] Univ Liverpool, Dept Pharmacol & Therapeut, Liverpool, England
[5] Makerere Univ, Infect Dis Inst, Coll Hlth Sci, Kampala, Uganda
[6] Univ Minnesota Twin Cities, Dept Expt & Clin Pharmacol, Minneapolis, MN 55455 USA
[7] MRC UVRI LSHTM Uganda Res Unit, Entebbe, Uganda
[8] Brighton & Sussex Med Sch, Ctr Global Hlth Res, Brighton, England
关键词
antiretroviral; cabotegravir; HIV; interaction; long-acting; rilpivirine; CYTOCHROME-P450; 3A4; QT PROLONGATION; IN-VITRO; PHARMACOKINETICS; METRONIDAZOLE; ERYTHROMYCIN; METABOLISM; ANTIRETROVIRALS; DISPOSITION; ARTEMETHER;
D O I
10.1111/bcp.16154
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Long-acting injectable (LAI) cabotegravir and rilpivirine for HIV treatment and LAI cabotegravir for pre-exposure HIV prophylaxis are being rolled out in a multitude of countries worldwide. Due to the prolonged exposure, it can be challenging to undertake 'traditional' pharmacokinetic studies and current guidance is derived from their oral equivalents or physiologically based pharmacokinetic studies. This review aims to consider pharmacokinetic characteristics of cabotegravir and rilpivirine and describe anticipated drug-drug interactions (DDIs) with frequent concomitant medications in African settings. Relevant co-medications were identified from the WHO 2021 List of Essential Medicines. All original human and physiologically based pharmacokinetic studies published in English on PubMed, discussing DDIs with LAI cabotegravir and rilpivirine prior to April 2023, were reviewed. The Liverpool HIV interaction database was also reviewed (). LAI cabotegravir and rilpivirine have half-lives of 6-12 and 13-28 weeks, respectively. Cabotegravir is primarily metabolized by UDP-glucuronyltransferase (UGT)-1A1 and rilpivirine by cytochrome P450 (CYP)-3A4. LAI cabotegravir and rilpivirine themselves exhibit low risk of perpetrating interactions with co-medications as they do not induce or inhibit the major drug metabolizing enzymes. However, they are victims of DDIs relating to the induction of their metabolizing enzymes by concomitantly administered medication. Noteworthy contraindicated co-medications include rifamycins, carbamazepine, phenytoin, flucloxacillin and griseofulvin, which induce CYP3A4 and/or UGT1A1, causing clinically significant reduced concentrations of rilpivirine and/or cabotegravir. In addition to virologic failure, subtherapeutic concentrations resulting from DDIs can lead to emergent drug resistance. Clinicians should be aware of potential DDIs and counsel people receiving LAI cabotegravir/rilpivirine appropriately to minimize risk.
引用
收藏
页码:2079 / 2091
页数:13
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