Virological History Predicts Non-sustained Viral Suppression with Long-Acting Cabotegravir and Rilpivirine Therapy, Independent of Pharmacokinetic Parameters.
CLINICAL INFECTIOUS DISEASES（2024）
Univ Miguel Hernandez | Hosp Gen Univ Elche
Abstract
Background This study aimed to investigate factors contributing to non-sustained viral suppression, including intermittent viremia and persistent low-level viremia, during cabotegravir (CAB) plus rilpivirine (RPV) long-acting (LA) injectable therapy, with a focus on pharmacokinetics (PK).Methods A prospective cohort study was conducted on people with human immunodeficiency virus (HIV, PWH) transitioning from stable oral antiretroviral therapy (ART) to bimonthly CAB + RPV LA. Standardized follow-up included close monitoring through blood sampling for plasma human immunodeficiency virus type 1 (HIV-1) viral load (VL) and multiple plasma drug concentrations measurements to analyze the connection between PK parameters and virologic outcomes.Results Among 173 patients with a median (interquartile range [IQR]) follow-up of 11.1(7.1-13.2) months and 789 pre-dose measurements, 38.7% experienced VL >= 20 copies/mL, and 16.2% had levels >= 50 copies/mL. Intermittent viremia occurred in 34.7% of patients, and persistent low-level viremia in 4%. Virological failure developed in 2 cases. Predictors of non-sustained viral suppression included VL at HIV diagnosis (adjusted hazard ratio [AHR]: 1.49 per log10 VL, 95% confidence interval [CI]: 1.04-2.12, P = .027), detectable viremia on oral ART (AHR: 2.45, 95% CI: 1.29-4.65, P = .006), and the level of viral suppression at transition (AHR: 0.38, 95% CI: .19-.75, P = .004). We found a significant association between low trough concentrations of CAB and RPV and episodes of detectable viremia exceeding 50 copies/mL. However, none of the assessed PK covariates predicted non-sustained viral suppression in multivariable models.Conclusions Non-sustained viral suppression in PWH transitioning from stable oral ART to CAB + RPV LA was linked to preexisting factors before transition. Higher VL pre-ART and incomplete suppression on oral therapy increased the risk, independent of PK parameters. In people with human immunodeficiency virus (HIV) transitioning to injectable cabotegravir plus rilpivirine, non-sustained viral suppression was associated with higher pre-antiretroviral therapy (ART) viral loads and incomplete suppression during oral therapy, with no significant pharmacokinetic factors identified.
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Key words
long-acting cabotegravir and rilpivirine,pharmacokinetics,non-sustained viral suppression,viral blips,low-level viremia
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