Perez Navarro Andrea, Nutt Cameron T, Siedner Mark J, McCluskey Suzanne M, Hill Andrew
Imperial College London School of Medicine, London, UK.
Harvard Medical School, Boston, MA, USA.
Clin Infect Dis. 2024 Dec 26. doi: 10.1093/cid/ciae631.
The long-acting injectable regimen of cabotegravir plus rilpivirine (CAB/RPV) emerged as an alternative to oral standard of care integrase strand transfer inhibitor (INSTI)-based regimens for individuals with adherence challenges or preference for reduced dosing schedules. Although oral INSTI regimens have a high barrier to emergent resistance, less is known about the potency and durability of CAB/RPV.
We reviewed clinical trial registries, PubMed, EMBASE, and conference abstract databases to identify published reports of CAB/RPV for HIV therapy. We abstracted data on virologic failure (VF) and treatment-emergent INSTI resistance at 48 weeks (range 24-52 weeks). We used single-proportion meta-analysis to summarize outcomes in three populations: 1) antiretroviral (ART)-naïve individuals initiating CAB/RPV following suppression on oral ART, 2) ART-experienced individuals switched to CAB/RPV with virologic suppression, and 3) ART-experienced individuals switched to CAB/RPV with detectable viremia. Cochrane's RoB2.0 and ROBINS-1 tools assessed risk of bias. PROSPERO registration CRD42024543919.
Thirty-three studies (N=9224) reported VF prevalence. Nineteen studies (N=5662) reported resistance data. VF prevalence was 1% (95% confidence intervals [CI] 1-3%) in induction-maintenance studies, 1% (CI 1-2%) in switch-suppressed studies, and 5% (CI 3-10%) in switch-viraemic studies. INSTI resistance prevalence among successfully genotyped participants at failure was 71% (CI 25-95%), 61% (CI 44-75%), and 41% (CI 20-65%) respectively. Dolutegravir cross-resistance was common (64% of those with emergent resistance).
Although VF rates with CAB/RPV were low, INSTI resistance emerged in approximately 40-70% of individuals experiencing VF. These rates are significantly higher than those for oral INSTI-based regimens. Both individual-level and broader resistance surveillance may be warranted in individuals and populations with expanding CAB/RPV use.
对于存在依从性挑战或倾向于减少给药方案的个体,长效注射用卡博特韦加rilpivirine(CAB/RPV)方案成为基于整合酶链转移抑制剂(INSTI)的口服标准治疗方案的替代方案。尽管口服INSTI方案对新出现的耐药性有很高的屏障,但关于CAB/RPV的效力和持久性知之甚少。
我们检索了临床试验注册库、PubMed、EMBASE和会议摘要数据库,以确定已发表的关于CAB/RPV用于HIV治疗的报告。我们提取了48周(范围24 - 52周)时病毒学失败(VF)和治疗中出现的INSTI耐药性的数据。我们使用单比例荟萃分析来总结三组人群的结果:1)在口服抗逆转录病毒治疗(ART)抑制后开始使用CAB/RPV的初治抗逆转录病毒(ART)个体,2)病毒学抑制的情况下转换为CAB/RPV的有ART经验的个体,以及3)病毒血症可检测的情况下转换为CAB/RPV的有ART经验的个体。Cochrane的RoB2.0和ROBINS-1工具评估了偏倚风险。PROSPERO注册号CRD42024543919。
33项研究(N = 9224)报告了VF患病率。19项研究(N = 5662)报告了耐药性数据。在诱导 - 维持研究中VF患病率为1%(95%置信区间[CI] 1 - 3%),在转换 - 抑制研究中为1%(CI 1 - 2%),在转换 - 病毒血症研究中为5%(CI 3 - 10%)。失败时成功进行基因分型的参与者中INSTI耐药率分别为71%(CI 25 - 95%)、61%(CI 44 - 75%)和41%(CI 20 - 65%)。多替拉韦交叉耐药很常见(出现耐药的个体中有64%)。
尽管CAB/RPV的VF率较低,但在约40 - 70%经历VF的个体中出现了INSTI耐药。这些比率显著高于基于口服INSTI的方案。在使用CAB/RPV不断增加的个体和人群中,可能需要进行个体水平和更广泛的耐药监测。