Department of Epidemiology of Microbial Diseases, Yale School of Public Health, Connecticut.
Department of Epidemiology.
AIDS. 2022 Feb 1;36(2):277-286. doi: 10.1097/QAD.0000000000003069.
BACKGROUND: Integrase strand transfer inhibitor (InSTI)-based regimens have been recommended as first-line antiretroviral therapy (ART) for adults with HIV. But data on long-term effects of InSTI-based regimens on virologic outcomes remain limited. Here we examined whether InSTI improved long-term virologic outcomes compared with efavirenz (EFV). METHODS: We included adults from the North American AIDS Cohort Collaboration on Research and Design who initiated their first ART regimen containing either InSTI or EFV between 2009 and 2016. We estimated differences in the proportion virologically suppressed up to 7 years of follow-up in observational intention-to-treat and per-protocol analyses. RESULTS: Of 15 318 participants, 5519 (36%) initiated an InSTI-based regimen and 9799 (64%) initiated the EFV-based regimen. In observational intention-to-treat analysis, 81.3% of patients in the InSTI group and 67.3% in the EFV group experienced virologic suppression at 3 months after ART initiation, corresponding to a difference of 14.0% (95% CI 12.4-15.6). At 1 year after ART initiation, the proportion virologically suppressed was 89.5% in the InSTI group and 90.2% in the EFV group, corresponding to a difference of -0.7% (95% CI -2.1 to 0.8). At 7 years, the proportion virologically suppressed was 94.5% in the InSTI group and 92.5% in the EFV group, corresponding to a difference of 2.0% (95% CI -7.3 to 11.3). The observational per-protocol results were similar to intention-to-treat analyses. CONCLUSIONS: Although InSTI-based initial ART regimens had more rapid virologic response than EFV-based regimens, the long-term virologic effect was similar. Our findings may inform guidelines regarding preferred initial regimens for HIV treatment.
背景:整合酶 strand 转移抑制剂(INSTI)为基础的方案已被推荐为成人 HIV 感染者的一线抗逆转录病毒治疗(ART)。但 INSTI 为基础的方案对病毒学结果的长期影响的数据仍然有限。在这里,我们研究了 INSTI 是否比依非韦伦(EFV)改善了长期病毒学结果。
方法:我们纳入了 2009 年至 2016 年间首次接受包含 INSTI 或 EFV 的 ART 方案的北美艾滋病队列合作研究与设计的成年人。我们在观察性意向治疗和按方案分析中估计了长达 7 年随访时病毒学抑制比例的差异。
结果:在 15318 名参与者中,5519 名(36%)开始使用 INSTI 为基础的方案,9799 名(64%)开始使用 EFV 为基础的方案。在观察性意向治疗分析中,INSTI 组有 81.3%的患者和 EFV 组有 67.3%的患者在 ART 起始后 3 个月时病毒学抑制,差异为 14.0%(95%CI 12.4-15.6)。在 ART 起始后 1 年时,INSTI 组有 89.5%的患者和 EFV 组有 90.2%的患者病毒学抑制,差异为 -0.7%(95%CI -2.1 至 0.8)。在 7 年时,INSTI 组有 94.5%的患者和 EFV 组有 92.5%的患者病毒学抑制,差异为 2.0%(95%CI -7.3 至 11.3)。按方案的观察结果与意向治疗分析相似。
结论:尽管 INSTI 为基础的初始 ART 方案比 EFV 为基础的方案有更快的病毒学反应,但长期病毒学效果相似。我们的研究结果可能为 HIV 治疗的首选初始方案的指南提供信息。
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