Real-world trough concentrations and effectiveness of long-acting cabotegravir and rilpivirine: a multicenter prospective observational study in Switzerland.

Détails

Ressource 1Télécharger: Thoueille P_ Lancet RHE.pdf (919.15 [Ko])
Etat: Public
Version: Final published version
Licence: CC BY-NC 4.0
ID Serval
serval:BIB_EE4919775F0F
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Real-world trough concentrations and effectiveness of long-acting cabotegravir and rilpivirine: a multicenter prospective observational study in Switzerland.
Périodique
The Lancet regional health. Europe
Auteur⸱e⸱s
Thoueille P., Saldanha S.A., Schaller F., Choong E., Munting A., Cavassini M., Braun D., Günthard H.F., Kusejko K., Surial B., Furrer H., Rauch A., Rougemont M., Ustero P., Calmy A., Stöckle M., Marzolini C., Di Benedetto C., Bernasconi E., Schmid P., Piso R.J., Andre P., Girardin F.R., Guidi M., Buclin T., Decosterd L.A.
Collaborateur⸱rice⸱s
Swiss HIV Cohort Study
ISSN
2666-7762 (Electronic)
ISSN-L
2666-7762
Statut éditorial
Publié
Date de publication
01/2024
Peer-reviewed
Oui
Volume
36
Pages
100793
Langue
anglais
Notes
Publication types: Journal Article
Publication Status: epublish
Résumé
The efficacy and tolerability of long-acting cabotegravir and rilpivirine were demonstrated in Phase III trials. However, low concentrations combined with other risk factors have been associated with an increased risk of virologic failure. This study aims to verify whether drug concentrations measured in a real-world setting are consistent with those previously reported.
SHCS-879 is a nationwide observational study within the Swiss HIV Cohort Study for the monitoring of people with HIV (PWH) on long-acting cabotegravir plus rilpivirine. Samples were collected from March 2022 to March 2023.
Overall, 725 samples were obtained from 186 PWH. Our data show a large inter-individual variability in cabotegravir and rilpivirine concentrations, with some individuals exhibiting repeatedly low concentrations. Rilpivirine trough concentrations were consistent with those from Phase III trials, while cabotegravir concentrations were lower. The first concentrations quartile was only slightly above the target of 664 ng/mL. Exploratory statistical analyses found 35% (p < 0·01) lower cabotegravir trough in males compared to females. Overall, 172 PWH (92%) remained suppressed and three experienced virologic failures (1·6%), of those, two had sub-optimal drug exposure. No association was found between low trough levels and detectable viral load.
Real-world cabotegravir concentrations are substantially lower than previously reported. However, these concentrations appear sufficient to ensure sustained virological suppression in almost every PWH. These reassuring data challenge the rather conservative thresholds adopted to date, which may raise unnecessary concerns. Yet, our study reveals that some PWH have repeatedly very low drug levels, for reasons that remain to be elucidated.
This work was funded by the Swiss National Science Foundation, grant number N <sup>◦</sup> 324730_192449. This study received no support from pharmaceutical industries. This study was performed within the framework of the Swiss HIV Cohort Study, supported by the Swiss National Science Foundation (grant #201369), by SHCS project #879, and by the SHCS research foundation. The SHCS data were gathered by the Five Swiss University Hospitals, two Cantonal Hospitals, 15 affiliated hospitals and 36 private physicians (listed in http://www.shcs.ch/180-health-care-providers).
Mots-clé
Health Policy, Oncology, Internal Medicine, Drug concentration monitoring, Long-acting cabotegravir and rilpivirine, Real-world
Pubmed
Open Access
Oui
Financement(s)
Fonds national suisse
Création de la notice
13/12/2023 11:32
Dernière modification de la notice
26/03/2024 8:10
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