Zeuli John D, Rivera Christina G, Smith Bradley L, Otto Ashley, Temesgen Zelalem
HIV Program, Division of Infectious Diseases, Mayo Clinic, Rochester, Minnesota, USA.
Department of Pharmacy, Mayo Clinic, Rochester, Minnesota, USA.
Drugs Today (Barc). 2022 Dec;58(12):555-576. doi: 10.1358/dot.2022.58.12.3448340.
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.
卡博特韦是一种新型的HIV整合酶抑制剂,与多替拉韦和比克替拉韦结构相似。其口服半衰期为32小时,但用于肌肉注射的卡博特韦纳米混悬液的半衰期为25至54天,可延长给药间隔。药物相互作用极小,不过口服剂量需与多价阳离子间隔服用,且由于预期通过延长间隔会导致卡博特韦暴露不足而达不到治疗效果,所以需要避免与强效尿苷葡萄糖醛酸转移酶诱导剂(如利福平、卡马西平)联用。随机临床试验将卡博特韦治疗与利匹韦林联合使用,以证明其对已实现病毒学抑制、对两种药物均无已知/疑似突变且既往未出现HIV治疗失败的HIV感染者的治疗效果。在LATTE研究中,口服卡博特韦和利匹韦林联合使用可维持病毒抑制,而在LATTE - 2研究中,肌肉注射这两种药物的联合疗法与传统口服疗法效果相当。FLAIR和ATLAS研究分别证明了每月注射一次对初治参与者和经治患者的HIV抑制维持效果,ATLAS - 2M研究则支持每两个月注射一次的疗效。迄今为止的研究表明其安全性良好。注射用卡博特韦会引起短暂、轻微的注射部位反应(主要是给药部位疼痛/酸痛),且随着时间推移频率会降低,导致停药率至少为2%,患者满意度评分显示注射疗法优于口服疗法。出现耐药性的病毒学失败情况罕见,主要发生在治疗的第一年,且与同时使用的利匹韦林的基线前病毒DNA突变有关。注射用卡博特韦是美国食品药品监督管理局(FDA)批准的首个用于HIV的注射用维持治疗方案的关键组成部分,开创了HIV治疗创新的新时代。在此,我们详细综述新型HIV整合酶抑制剂卡博特韦的临床药理学、给药方法和可用剂型,并深入分析其与利匹韦林联合作为首个长效注射用HIV感染治疗方案时的临床试验数据、安全性、满意度和病毒耐药性发展情况。