Pharmacokinetic and clinical associations between doravirine-containing ART and injectable and implantable hormonal contraceptive methods among women living with HIV in South Africa

杜鲁特格拉维尔 医学 耐受性 不利影响 药代动力学 置信区间 醋酸甲孕酮 药理学 内科学 病毒载量 人类免疫缺陷病毒(HIV) 抗逆转录病毒疗法 病毒学 激素
作者
Rena C. Patel,Nkosiphile Ndlovu,Pooja Maheria,Reolebogile Kgoa,Lindsay Kew,La-Donna Kapa,Krishnaveni Reddy,Merusha Govindasami,Nomasonto Matswake,Nompumelelo Sigcu,Mohamed Seedat,Lerato R Shale,Nashon Yongo,Shukri A. Hassan,Tommy Williams,David W. Erikson,Kimberly K. Scarsi,Thesla Palanee‐Phillips
出处
期刊:The Journal of Infectious Diseases [Oxford University Press]
标识
DOI:10.1093/infdis/jiaf196
摘要

Abstract Background Drug resistance and intolerance of dolutegravir-containing antiretroviral therapy (ART) are rising in low- and middle-income countries, resulting in a potentially increased use of doravirine-containing ART use. There are knowledge gaps regarding doravirine and hormonal contraceptive drug-drug interactions among women living with HIV (WLWH). Methods We conducted a five parallel group, prospective pharmacokinetic study among WLWH aged 18-45 years in Johannesburg, South Africa between November 2021 and February 2024. We included a sixth, historical comparator group from a Kenyan study. After a ≥6-week lead-in period with doravirine-containing ART, participants initiated injectable medroxyprogesterone acetate (MPA), implantable etonogestrel (ENG), or non-hormonal intrauterine device contraception and were observed every 2-4 weeks for an additional 12 or 24 weeks. We analyzed serum MPA and ENG and plasma doravirine or dolutegravir concentrations per visit, using validated liquid chromatography–mass spectrometry (LC-MS/MS) assays. We assessed log-transformed concentrations of each drug with geometric mean ratios (GMR; 90% confidence intervals) and a multivariate model adjusted for age and body mass index. We described safety, tolerability, and effectiveness (HIV viral load <40 copies/mL) of doravirine-containing ART. Results A total of 128 participants are included in this analysis. There were no significant reductions in the MPA, ENG, or doravirine concentrations. A total of 8 (3%) adverse events grade 2 or higher were considered attributable to doravirine-containing ART and 22 (8%) to the contraceptive method. ART satisfaction was 100%, and viral suppression at study exit ranged from 86-96%. Conclusions We found no detrimental bidirectional drug-drug interactions and few adverse events between doravirine and hormonal contraceptives.
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