Barda Beatrice, Barilaro Giuseppe, Bellini Paola, Turicchi Giulia, Bernasconi Enos, Bongiovanni Marco
Division of Infectious Diseases, Ente Ospedaliero Cantonale, Lugano, Switzerland.
Department of Internal Medicine, Sant'Eugenio Hospital, Rome, Italy.
HIV Med. 2025 Apr 9. doi: 10.1111/hiv.70025.
Long-acting cabotegravir/rilpivirine (LA-CAB/RPV) is currently approved as a switch strategy in people living with HIV virally suppressed on oral antiretroviral therapy. Although small reports on specific, difficult-to-treat populations demonstrated the efficacy of LA-CAB/RPV in people living with HIV and unsuppressed viraemia, cumulative data on this issue are still lacking.
We conducted a systematic review and meta-analysis based on PRISMA guidelines using PubMed, Scopus, Google Scholar and Medline, including papers or abstracts that evaluated the use of LA-CAB/RPV in viraemic people living with HIV. Two papers were excluded as they reported only single clinical cases; one study was excluded for including only three perinatally infected subjects. Two papers were reviews and two papers and one abstract reported result from Ward 86, which were later included in a final paper. One paper presenting preliminary results from the OPERA cohort was excluded, as these data were subsequently updated. The ACTG LATITUDE (A5359) study was not included, as it did not specifically report outcomes for people living with HIV who initiated LA-CAB/RPV while viraemic. After applying these selection criteria, five papers and three abstracts were included in the meta-analysis. The main outcome was virologic success, as defined by each individual study, in people living with HIV with at least one HIV-RNA evaluation after initiating LA-CAB/RPV. We did not perform a meta-analysis on other variables due to inconsistent assessment across studies.
Overall, 244 people living with HIV started LA-CAB/RPV when viraemic. Most of them reported adherence, psychological or social issues that limited compliance to standard oral treatment. The cumulative probability of achieving virologic success was 87% (79%-95%). Most patients maintained adherence rates above 90% to their scheduled injection visits. Eleven patients living with HIV developed RPV-associated mutations and five CAB-associated mutations at virologic failure. No interruption of LA-CAB/RPV for adverse events was reported.
This is the first meta-analysis that assessed the efficacy of LA-CAB/RPV in viraemic people living with HIV; oral treatment efficacy was jeopardized by low compliance due to adherence or psychological issues. Our results can justify the use of LA-CAB/RPV also in viraemic patients without alternative oral options.
长效卡博特韦/利匹韦林(LA-CAB/RPV)目前被批准作为一种转换策略,用于接受口服抗逆转录病毒疗法且病毒得到抑制的HIV感染者。尽管有关于特定难治人群的小样本报告显示LA-CAB/RPV在HIV感染者且病毒血症未得到抑制的人群中具有疗效,但关于这一问题的累积数据仍然缺乏。
我们根据PRISMA指南,使用PubMed、Scopus、谷歌学术和Medline进行了系统评价和荟萃分析,纳入了评估LA-CAB/RPV在病毒血症HIV感染者中应用的论文或摘要。两篇论文因仅报告单个临床病例而被排除;一项研究因仅纳入三名围产期感染受试者而被排除。两篇论文为综述,两篇论文和一篇摘要报告了86病房的结果,这些结果后来被纳入一篇最终论文中。一篇展示OPERA队列初步结果的论文被排除,因为这些数据随后得到了更新。ACTG LATITUDE(A5359)研究未被纳入,因为它没有专门报告病毒血症时开始使用LA-CAB/RPV的HIV感染者的结局。应用这些选择标准后,五篇论文和三篇摘要被纳入荟萃分析。主要结局是病毒学成功,定义为每个个体研究中,在开始LA-CAB/RPV后至少进行一次HIV-RNA评估的HIV感染者的病毒学成功。由于各研究的评估不一致,我们未对其他变量进行荟萃分析。
总体而言,244名病毒血症的HIV感染者开始使用LA-CAB/RPV。他们中的大多数人报告了依从性、心理或社会问题,这些问题限制了对标准口服治疗的依从性。实现病毒学成功的累积概率为87%(79%-95%)。大多数患者对预定注射访视的依从率保持在90%以上。11名HIV感染者在病毒学失败时出现了与RPV相关的突变,5名出现了与CAB相关的突变。未报告因不良事件而中断LA-CAB/RPV治疗的情况。
这是第一项评估LA-CAB/RPV在病毒血症HIV感染者中疗效的荟萃分析;由于依从性或心理问题导致的低依从性危及口服治疗效果。我们的结果证明,在没有其他口服选择的病毒血症患者中也可以使用LA-CAB/RPV。