长效卡博特韦治疗HIV的病毒学失败和紧急整合酶链转移抑制剂耐药性:一项荟萃分析

IF 8.2 1区 医学 Q1 IMMUNOLOGY Clinical Infectious Diseases Pub Date : 2024-12-26 DOI:10.1093/cid/ciae631
Andrea Perez Navarro, Cameron T Nutt, Mark J Siedner, Suzanne M McCluskey, Andrew Hill
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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. Results 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). 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引用次数: 0

摘要

cabotegravir + rilpivirine (CAB/RPV)的长效注射方案作为口服标准护理整合酶链转移抑制剂(INSTI)方案的替代方案出现,用于具有依从性挑战或偏好减少给药计划的个体。尽管口服INSTI方案对出现的耐药性具有很高的屏障,但对CAB/RPV的效力和持久性知之甚少。方法我们回顾了临床试验注册、PubMed、EMBASE和会议摘要数据库,以确定CAB/RPV用于HIV治疗的已发表报告。我们提取了48周(24-52周)病毒学失败(VF)和治疗后出现的INSTI耐药的数据。我们使用单比例荟萃分析来总结三个人群的结果:1)抗逆转录病毒(ART)-naïve患者在口服ART抑制后开始使用CAB/RPV, 2)抗逆转录病毒治疗的患者在病毒抑制后改用CAB/RPV, 3)抗逆转录病毒治疗的患者在病毒血症可检测的情况下改用CAB/RPV。Cochrane的RoB2.0和ROBINS-1工具评估偏倚风险。普洛斯彼罗注册号CRD42024543919。结果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%可信区间[CI] 1-3%),在开关抑制研究中为1% (CI 1-2%),在开关病毒研究中为5% (CI 3-10%)。在基因分型成功的参与者中,失败时INSTI耐药率分别为71% (CI 25-95%)、61% (CI 44-75%)和41% (CI 20-65%)。多替格拉韦交叉耐药很常见(64%的患者出现紧急耐药)。尽管CAB/RPV的VF发生率较低,但大约40-70%的VF患者出现了INSTI耐药性。这些比率明显高于口服以胰岛素为基础的方案。在CAB/RPV使用扩大的个人和人群中,可能需要进行个体水平和更广泛的耐药性监测。
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Virologic failure and emergent integrase strand transfer inhibitor drug resistance with long acting cabotegravir for HIV treatment: A meta-analysis
Background 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. Methods 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. Results 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). Discussion 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.
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来源期刊
Clinical Infectious Diseases
Clinical Infectious Diseases 医学-传染病学
CiteScore
25.00
自引率
2.50%
发文量
900
审稿时长
3 months
期刊介绍: Clinical Infectious Diseases (CID) is dedicated to publishing original research, reviews, guidelines, and perspectives with the potential to reshape clinical practice, providing clinicians with valuable insights for patient care. CID comprehensively addresses the clinical presentation, diagnosis, treatment, and prevention of a wide spectrum of infectious diseases. The journal places a high priority on the assessment of current and innovative treatments, microbiology, immunology, and policies, ensuring relevance to patient care in its commitment to advancing the field of infectious diseases.
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