Drug-drug interaction between itraconazole capsule and efavirenz in adults with HIV for talaromycosis treatment.


Journal

The Journal of antimicrobial chemotherapy
ISSN: 1460-2091
Titre abrégé: J Antimicrob Chemother
Pays: England
ID NLM: 7513617

Informations de publication

Date de publication:
12 03 2021
Historique:
received: 01 09 2020
accepted: 18 11 2020
pubmed: 23 12 2020
medline: 6 7 2021
entrez: 22 12 2020
Statut: ppublish

Résumé

To assess the pharmacokinetic of itraconazole capsule formulation and its active metabolite, hydroxyitraconazole, in adults with HIV diagnosed with talaromycosis in an endemic area, and to evaluate the drug-drug interaction between itraconazole/hydroxyitraconazole (ITC/OH-ITC) and efavirenz. Open-label, single arm, sequential pharmacokinetic study. Eligible subjects were adults with HIV, ≥18 years old, with confirmed talaromycosis, initiating itraconazole capsule as part of standard talaromycosis treatment, in whom efavirenz-based ART was anticipated. Steady-state pharmacokinetic assessments (pre-dose and at 1, 3, 4, 5, 6, 8 and 12 h post dose) were performed for itraconazole/hydroxyitraconazole without and with efavirenz use. Mid-dose efavirenz concentrations were also assessed. Pharmacokinetics parameters were calculated using non-compartmental analysis. Ten subjects (70% male) were enrolled. At entry, median (range) age was 29.5 years (22-64), and CD4 cell count was 18.0 (1-39) cells/mm3. Geometric mean (95% CI) of itraconazole and hydroxyitraconazole AUC0-12 without efavirenz were 9097 (6761-12 239) and 11 705 (8586-15 959) ng·h/mL, respectively, with a median metabolic ratio of OH-ITC : ITC of 1.3 (95% CI 0.9-1.9). Intra-subject comparison revealed that both itraconazole and hydroxyitraconazole exposures were significantly reduced with concomitant efavirenz use, with the mean AUC0-12 of itraconazole and hydroxyitraconazole being 86% (71%-94%) and 84% (64%-97%) lower, respectively. With efavirenz, itraconazole trough concentrations were also below the recommended therapeutic level (0.5 μg/mL). All subjects had mid-dose efavirenz concentrations >1000 ng/mL. Concomitant administration of itraconazole capsule with efavirenz significantly reduced itraconazole and hydroxyitraconazole exposures. The clinical impact of this drug-drug interaction on talaromycosis treatment or prophylaxis in the era of potent ART needs further evaluation.

Identifiants

pubmed: 33349869
pii: 6043735
doi: 10.1093/jac/dkaa521
doi:

Substances chimiques

Alkynes 0
Antifungal Agents 0
Benzoxazines 0
Cyclopropanes 0
Pharmaceutical Preparations 0
Itraconazole 304NUG5GF4
efavirenz JE6H2O27P8

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1041-1045

Informations de copyright

© The Author(s) 2020. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Auteurs

Quanhathai Kaewpoowat (Q)

Department of Medicine, Faculty of Medicine, Chiang Mai University, Thailand.
Research Institute for Health Sciences, Chiang Mai University, Thailand.
Department of Medicine, University of Iowa Hospitals and Clinics, Iowa City, Iowa, USA.

Romanee Chaiwarith (R)

Department of Medicine, Faculty of Medicine, Chiang Mai University, Thailand.

Saowaluck Yasri (S)

Department of Medicine, Faculty of Medicine, Chiang Mai University, Thailand.

Navaporn Worasilchai (N)

Department of Microbiology, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.

Ariya Chindamporn (A)

Department of Microbiology, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.

Thira Sirisanthana (T)

Department of Medicine, Faculty of Medicine, Chiang Mai University, Thailand.

Tim R Cressey (TR)

PHPT/IRD UMI 174, Faculty of Associated Medical Sciences, Chiang Mai University, Chiang Mai, Thailand.
Department of Molecular & Clinical Pharmacology, University of Liverpool, UK.

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Classifications MeSH