Quercia Romina, Di Perri Giovanni, Pein Carolina, Bodie Jennifer, Singh Ravi Shankar P, Hendrick Victoria, Boffito Marta
Chief Medical Affairs Office, Pfizer Inc, New York City, NY, USA.
Amedeo di Savoia Hospital, Turin, Italy.
Infect Dis Ther. 2024 May;13(5):1005-1017. doi: 10.1007/s40121-024-00959-6. Epub 2024 Apr 12.
Ritonavir is a potent inhibitor of the cytochrome P450 3A4 enzyme and is commonly used as a pharmacokinetic (PK) enhancer in antiviral therapies because it increases bioavailability of concomitantly administered antivirals. Decades of experience with ritonavir-enhanced HIV therapies and, more recently, COVID-19 therapies demonstrate that boosting doses of ritonavir are well tolerated, with an established safety profile. The mechanisms of PK enhancement by ritonavir result in the potential for drug-drug interactions (DDIs) with several classes of drugs, thus making co-medication management an important consideration with enhanced antiviral therapies. However, rates of DDIs with contraindicated medications are low, suggesting these risks are manageable by infectious disease specialists who have experience with the use of PK enhancers. In this review, we provide an overview of ritonavir's mechanisms of action and describe approaches and resources available to mitigate adverse events and manage concomitant medication in both chronic and short-term settings.
利托那韦是细胞色素P450 3A4酶的强效抑制剂,在抗病毒治疗中常用作药代动力学(PK)增强剂,因为它可提高同时给药的抗病毒药物的生物利用度。数十年使用利托那韦增强的HIV治疗经验,以及最近在COVID-19治疗中的经验表明,增加剂量的利托那韦耐受性良好,安全性已得到确立。利托那韦增强PK的机制导致其与几类药物存在药物相互作用(DDIs)的可能性,因此在增强抗病毒治疗中,联合用药管理是一个重要的考虑因素。然而,与禁忌药物发生DDIs的发生率较低,这表明有使用PK增强剂经验的传染病专家可以控制这些风险。在本综述中,我们概述了利托那韦的作用机制,并描述了在慢性和短期治疗环境中减轻不良事件以及管理联合用药的方法和可用资源。