Massachusetts General Hospital, Boston.
Miriam Hospital, Alpert Medical School of Brown University, Providence, Rhode Island.
J Infect Dis. 2020 Apr 7;221(9):1407-1415. doi: 10.1093/infdis/jiz281.
Short-term (48-week) results of the OPTIONS trial showed that nucleoside reverse transcriptase inhibitors (NRTIs) can be safely omitted from salvage therapy as long as the regimen has a cumulative activity of >2 active antiretroviral medications. The long-term durability of this approach and outcomes in persons who have more-extensive HIV-1 drug resistance are uncertain.
Participants with virologic failure and anticipated antiretroviral susceptibility received an optimized regimen and were randomized to omit or add NRTIs. A separate group with more resistance (cumulative activity ≤2 active agents) received an optimized regimen including NRTIs.
At week 96, among 360 participants randomized to omit or add NRTIs, 70% and 65% had HIV-1 RNA <200 copies/mL, respectively. Virologic failure was uncommon after week 48. Younger age and starting fewer new antiretroviral medications were associated with higher odds of virologic failure. In the highly resistant group, 53% had HIV-1 RNA <200 copies/mL at week 96.
HIV-1 salvage therapy can safely omit NRTIs without compromising efficacy or durability of response as long as the new regimen has a cumulative activity of >2 active drugs. Younger people and those receiving fewer new antiretrovirals require careful monitoring. Even among individuals with more-extensive resistance, most achieve virologic suppression.
NCT00537394.
OPTIONS 试验的短期(48 周)结果表明,只要方案具有>2 种活性抗逆转录病毒药物的累积活性,就可以安全地将核苷逆转录酶抑制剂(NRTIs)从挽救性治疗中省略。这种方法的长期耐久性以及具有更广泛 HIV-1 药物耐药性的人的结局尚不确定。
病毒学失败且预期抗逆转录病毒敏感性的参与者接受了优化的方案,并随机分为省略或添加 NRTIs 组。另一组具有更多耐药性(累积活性≤2 种活性药物)的患者接受了包含 NRTIs 的优化方案。
在 360 名随机分配省略或添加 NRTIs 的参与者中,分别有 70%和 65%的人在第 96 周时 HIV-1 RNA<200 拷贝/ml。第 48 周后病毒学失败并不常见。年龄较小和开始使用较少的新抗逆转录病毒药物与病毒学失败的几率较高相关。在高度耐药组中,53%的人在第 96 周时 HIV-1 RNA<200 拷贝/ml。
只要新方案具有>2 种活性药物的累积活性,HIV-1 挽救性治疗就可以安全地省略 NRTIs,而不会影响疗效或反应的持久性。年轻人和接受较少新抗逆转录病毒药物的人需要密切监测。即使在具有更广泛耐药性的个体中,大多数人也能实现病毒学抑制。
NCT00537394。