Cabotegravir:一种新型HIV整合酶抑制剂与利匹韦林联合作为治疗HIV感染的第一个长效注射方案。

IF 1.8 4区 医学 Q2 Medicine Drugs of today Pub Date : 2022-12-01 DOI:10.1358/dot.2022.58.12.3448340
John D Zeuli, Christina G Rivera, Bradley L Smith, Ashley Otto, Zelalem Temesgen
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引用次数: 0

摘要

Cabotegravir是一种新型HIV整合酶抑制剂,与dolutegravir和bictegravir具有结构相似性。其口服半衰期为32小时,但肌肉注射用卡博特重力韦纳米混悬液的半衰期为25至54天,可延长给药间隔。药物相互作用最小,尽管口服剂量需要与多价阳离子间隔,并且由于预期的亚治疗性卡波特韦暴露时间延长,需要避免有效的尿嘧啶葡萄糖醛酸糖基转移酶诱导(如利福平、卡马西平)。随机临床试验将卡博特韦与利匹韦林联合治疗,以证明对获得病毒学抑制、缺乏已知/可疑突变的HIV患者的治疗效果,并且之前没有经历过HIV治疗失败。在LATTE研究中,口服卡博特重力韦和利匹韦林共同维持了病毒抑制,而在LATTE-2中,肌肉注射联合用药的效果与常规口服治疗相当。FLAIR和ATLAS分别显示,在未接受治疗的参与者和有治疗经验的患者中,每月注射一次可维持HIV抑制,ATLAS- 2m支持每2个月注射一次的疗效。迄今为止的调查显示其具有良好的安全性。注射用卡博特韦引起短暂的、轻微的注射部位反应(主要是给药部位疼痛/酸痛),随着时间的推移,这种反应发生的频率会降低,可归因的停药率至少为2%,并且产生的满意度评分表明注射治疗优于口服治疗。伴随耐药发展的病毒学失败是罕见的,主要发生在治疗的第一年,并且与共同给药利匹韦林的基线前病毒DNA突变有关。作为美国食品和药物管理局(FDA)批准的第一个可注射的艾滋病毒维持治疗项目的关键组成部分,可注射卡波特韦预示着艾滋病毒治疗创新的新时代。本文详细回顾了新型HIV整合酶抑制剂cabotegravir的临床药理学、给药和可用配方,并深入分析了临床试验数据、安全性、满意度和病毒耐药性的发展,并将其与利匹韦林(rilpivirine)联合作为治疗HIV感染的第一个长效注射方案。
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Cabotegravir: a novel HIV integrase inhibitor combined with rilpivirine as the first long-acting injectable program for the treatment of HIV infection.

Cabotegravir, a novel HIV integrase inhibitor, shares structural similarity with dolutegravir and bictegravir. Its oral half-life is 32 hours, but cabotegravir nanosuspension for intramuscular injection yields half-lives ranging from 25 to 54 days, enabling extended interval dosing. Drug interactions are minimal, although oral doses require spacing from polyvalent cations, and potent uridine glucuronosyltransferase induction (e.g., rifampin, carbamazepine) requires avoidance due to anticipated subtherapeutic cabotegravir exposure through extended intervals. Randomized clinical trials combined cabotegravir treatment with rilpivirine to demonstrate treatment efficacy in patients living with HIV who had attained virologic suppression, lacked known/suspected mutations to either component, and had not experienced prior HIV treatment failure. Together, oral cabotegravir and rilpivirine maintained viral suppression in the LATTE study while the combination, given intramuscularly, performed comparably to conventional oral therapy in LATTE-2. FLAIR and ATLAS, respectively, demonstrated HIV suppression maintenance for monthly injections in treatment-naive participants and treatment-experienced patients, with ATLAS-2M supporting the efficacy of injections given every 2 months. Investigations to date show an excellent safety profile. Injectable cabotegravir causes short-lived, mild injection site reactions (primarily administration site pain/soreness) that decrease in frequency over time, produce attributable discontinuation rates of at least 2%, and generate satisfaction scores that favor injectable therapy over oral therapy. Virologic failure with resistance development is rare, primarily occurs in the first year of therapy, and is associated with baseline proviral DNA mutations to coadministered rilpivirine. A key component of the first U.S. Food and Drug Administration (FDA)-approved injectable maintenance treatment program for HIV, injectable cabotegravir heralds a new era in HIV treatment innovation. Here we provide a detailed review of the clinical pharmacology, administration and available formulations of the novel HIV integrase inhibitor cabotegravir with in-depth analysis of the clinical trial data, safety, satisfaction and viral resistance development when combined with rilpivirine as the first long-acting injectable program for the treatment of HIV infection.

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来源期刊
Drugs of today
Drugs of today 医学-药学
CiteScore
3.90
自引率
0.00%
发文量
48
审稿时长
6-12 weeks
期刊介绍: An international, peer-reviewed journal publishing monographs on new products entering the market and review articles. Since its inception in 1965, Drugs of Today has established a reputation for excellence in providing physicians and other key healthcare professionals with practical, up-to-date monographs on recently approved and launched drugs.
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