Jansen Klaus, Sönnerborg Anders, Brockmeyer Norbert, Thalme Anders, Svedhem Veronica, Dupke Stephan, Eychenne Jean-Luc, Nakonz Tina, Jimenez-Exposito Maria Jesus, Pugliese Pascal
Competence Network for HIV/AIDS, Ruhr-Universität, Bochum, Germany.
AIDS Res Hum Retroviruses. 2013 Mar;29(3):564-73. doi: 10.1089/aid.2012.0092. Epub 2012 Nov 27.
Atazanavir-based regimens have established efficacy and safety in both antiretroviral (ARV)-naive and -experienced patients. However, data evaluating effectiveness beyond 2 years is sparse. Therefore, we assessed the long-term outcomes of ritonavir-boosted atazanavir (ATV/r)-containing regimens in ARV-experienced patients in a clinical setting in a noncomparative, retrospective, observational study collecting data from three European HIV databases on ARV-experienced adults with HIV-1 infection starting an ATV/r-based regimen. Data were extracted every 6 months (maximum follow-up 5 years). Primary outcome was the proportion of patients remaining on ATV/r by baseline HIV-1 RNA (<500 or ≥500 copies/ml). Secondary outcomes included time to virologic failure, reasons for discontinuation, and long-term safety profile. The duration of treatment and time to virologic failure were analyzed using the Kaplan-Meier method. Data were analyzed for 1,294 ARV-experienced patients (male 74%; mean ART exposure 5.7 years). After 3 years, 56% (95% CI: 52%, 60%) of patients with baseline HIV-1 RNA <500 copies/ml and 53% (95% CI: 49%, 58%) of those with HIV-1 RNA ≥500 copies/ml remained on ATV/r. After 3 years, 75% (95% CI: 69%, 80%) of patients with baseline HIV-1 RNA <50 copies/ml remained suppressed and 51% (95% CI: 47%, 55%) of those with baseline HIV-1 RNA ≥50 copies/ml achieved and maintained virologic suppression. Although adverse events (AEs) were the main known reason for discontinuation, no unexpected AEs were observed. In a real-life setting ATV/r-based regimens demonstrated sustained virologic suppression in ARV-experienced patients. After long-term therapy the majority of patients remained on treatment and no unexpected AEs were observed.
基于阿扎那韦的治疗方案在初治和经治抗逆转录病毒(ARV)患者中均已确立了疗效和安全性。然而,评估超过2年有效性的数据较少。因此,我们在一项非对照、回顾性、观察性研究中,评估了含利托那韦增强阿扎那韦(ATV/r)方案在经治患者中的长期结局,该研究从三个欧洲HIV数据库收集了开始基于ATV/r方案的HIV-1感染成年经治患者的数据。每6个月提取一次数据(最长随访5年)。主要结局是按基线HIV-1 RNA水平(<500或≥500拷贝/毫升)计算仍接受ATV/r治疗的患者比例。次要结局包括病毒学失败时间、停药原因和长期安全性。使用Kaplan-Meier方法分析治疗持续时间和病毒学失败时间。对1294例经治患者(男性占74%;平均抗逆转录病毒治疗暴露时间5.7年)的数据进行了分析。3年后,基线HIV-1 RNA<500拷贝/毫升的患者中有56%(95%CI:52%,60%)、HIV-1 RNA≥500拷贝/毫升的患者中有53%(95%CI:49%,58%)仍接受ATV/r治疗。3年后,基线HIV-1 RNA<50拷贝/毫升的患者中有75%(95%CI:69%,80%)病毒载量仍被抑制,基线HIV-1 RNA≥50拷贝/毫升的患者中有51%(95%CI:47%,55%)实现并维持了病毒学抑制。虽然不良事件(AE)是已知的停药主要原因,但未观察到意外不良事件。在现实生活环境中,基于ATV/r的方案在经治患者中显示出持续的病毒学抑制。长期治疗后,大多数患者仍在接受治疗,且未观察到意外不良事件。