Médecins Sans Frontières, Cape Town, South Africa.
Institute for Global Health, UCL, London, UK.
AIDS. 2019 Aug 1;33(10):1635-1644. doi: 10.1097/QAD.0000000000002234.
Many individuals failing first-line antiretroviral therapy (ART) in sub-Saharan Africa never initiate second-line ART or do so after significant delay. For people on ART with a viral load more than 1000 copies/ml, the WHO recommends a second viral load measurement 3 months after the first viral load and enhanced adherence support. Switch to a second-line regimen is contingent upon a persistently elevated viral load more than 1000 copies/ml. Delayed second-line switch places patients at increased risk for opportunistic infections and mortality.
To assess the potential benefits of a simplified second-line ART switch strategy, we use an individual-based model of HIV transmission, progression and the effect of ART which incorporates consideration of adherence and drug resistance, to compare predicted outcomes of two policies, defining first-line regimen failure for patients on efavirenz-based ART as either two consecutive viral load values more than 1000 copies/ml, with the second after an enhanced adherence intervention (implemented as per current WHO guidelines) or a single viral load value more than 1000 copies/ml. We simulated a range of setting-scenarios reflecting the breadth of the sub-Saharan African HIV epidemic, taking into account potential delays in defining failure and switch to second-line ART.
The use of a single viral load more than 1000 copies/ml to define ART failure would lead to a higher proportion of persons with nonnucleoside reverse-transcriptase inhibitor resistance switched to second-line ART [65 vs. 48%; difference 17% (90% range 14-20%)], resulting in a median 18% reduction in the rate of AIDS-related death over setting scenarios (90% range 6-30%; from a median of 3.1 to 2.5 per 100 person-years) over 3 years. The simplified strategy also is predicted to reduce the rate of AIDS conditions by a median of 31% (90% range 8-49%) among people on first-line ART with a viral load more than 1000 copies/ml in the past 6 months. For a country of 10 million adults (and a median of 880 000 people with HIV), we estimate that this approach would lead to a median of 1322 (90% range 67-3513) AIDS deaths averted per year over 3 years. For South Africa this would represent around 10 215 deaths averted annually.
As a step towards reducing unnecessary mortality associated with delayed second-line ART switch, defining failure of first-line efavirenz-based regimens as a single viral load more than 1000 copies/ml should be considered.
在撒哈拉以南非洲,许多未能首次接受抗逆转录病毒疗法(ART)的人从未启动二线 ART 治疗,或在出现明显延迟后才开始二线 ART 治疗。对于 HIV 载量超过 1000 拷贝/ml 的接受 ART 治疗的患者,世卫组织建议在首次病毒载量测量后 3 个月进行第二次病毒载量测量,并加强依从性支持。如果病毒载量持续高于 1000 拷贝/ml,则可转换为二线方案。二线方案转换延迟会使患者面临更高的机会性感染和死亡风险。
为了评估简化二线 ART 转换策略的潜在益处,我们使用基于个体的 HIV 传播、进展和 ART 效果模型,该模型考虑了依从性和耐药性,比较了两种政策的预测结果,将基于依非韦伦的 ART 患者的一线方案失败定义为两种连续的病毒载量值超过 1000 拷贝/ml,第二次发生在增强依从性干预后(按照世卫组织现行指南实施)或单次病毒载量值超过 1000 拷贝/ml。我们模拟了一系列反映撒哈拉以南非洲 HIV 流行范围的设定情景,考虑到在确定一线方案失败和转换为二线 ART 方面可能存在的延迟。
使用单次病毒载量超过 1000 拷贝/ml 来定义 ART 失败,将导致更多具有非核苷类逆转录酶抑制剂耐药性的患者转换为二线 ART [65%比 48%;差异 17%(90%范围 14-20%)],这将导致设定情景下(90%范围 6-30%),3 年内艾滋病相关死亡的中位数降低 18%(从每 100 人年 3.1 降至 2.5)。在过去 6 个月内 HIV 载量超过 1000 拷贝/ml 的一线治疗患者中,简化策略还预计将使 AIDS 发生率中位数降低 31%(90%范围 8-49%)。
对于一个拥有 1000 万成年人(中位数为 88 万 HIV 感染者)的国家,我们估计,这种方法将使 3 年内每年平均减少 1322 例(90%范围 67-3513)艾滋病死亡。对于南非,这将代表每年约可避免 10215 例死亡。
作为减少与二线 ART 转换延迟相关的不必要死亡的一种措施,将基于依非韦伦的一线方案失败定义为单次病毒载量超过 1000 拷贝/ml 应该被考虑。