Division of AIDS NIAID, NIH, Bethesda, MD.
Harvard T.H. Chan School of Public Health, Boston, MA.
J Acquir Immune Defic Syndr. 2020 Jun 1;84(2):203-207. doi: 10.1097/QAI.0000000000002324.
Sex differences in studies of antiretroviral (ART) drug exposure and treatment outcomes support the hypothesis that some ART combinations may not be well tolerated in women. We evaluated disparities in outcomes between men and women participating in ACTG A5288, an interventional strategy trial for individuals failing a protease inhibitor-based second-line ART regimen in low- and middle-income countries.
Participants were assigned to one of 4 cohorts (A-D) based on resistance profiles and ART history. Cohort A had no lopinavir/ritonavir (LPV/r) resistance and stayed on their second-line regimen, and cohorts B, C, and D had increasing resistance and accessed novel ART regimens. In this secondary analysis, we evaluated sex differences in the primary endpoint, HIV-1 RNA ≤200 copies/mL at week 48; confirmed virologic failure ≥1000 copies/mL (VF); and clinical outcomes and adverse events (intent-to-treat).
Women made up 258/545 (47%) of the study population. More women than men were assigned to cohort A. Median follow-up was 72 weeks. Fewer women than men had HIV-1 RNA ≤200 copies/mL at week 48: 39% vs. 49% in cohort A and 83% vs. 89% in cohorts B, C, and D combined. More women experienced VF, grade ≥3 signs and symptoms, but similar grade ≥3 diagnoses or laboratory abnormalities.
More women than men entered the study with a resistance profile suggesting that their second-line regimen could have been effective in maintaining virologic suppression. The more frequent occurrence of grade ≥3 signs and symptoms in women suggests that tolerability issues were under recognized in women on protease inhibitor-based therapy.
抗逆转录病毒(ART)药物暴露和治疗结果的性别差异研究支持这样一种假设,即某些 ART 组合在女性中可能不能很好地耐受。我们评估了在中低收入国家参与 ACTG A5288 的个体中,基于蛋白酶抑制剂的二线 ART 方案失败的个体的干预策略试验中,男性和女性之间结局的差异。
根据耐药谱和 ART 史,将参与者分为 4 个队列(A-D)。队列 A 没有洛匹那韦/利托那韦(LPV/r)耐药,继续使用二线方案,而队列 B、C 和 D 的耐药性逐渐增加,并使用新型 ART 方案。在这项二次分析中,我们评估了主要终点(第 48 周时 HIV-1 RNA≤200 拷贝/ml)、确证病毒学失败(≥1000 拷贝/ml,VF)以及临床结局和不良事件(意向治疗)的性别差异。
女性占研究人群的 258/545(47%)。与男性相比,更多的女性被分配到队列 A。中位随访时间为 72 周。第 48 周时,HIV-1 RNA≤200 拷贝/ml 的女性少于男性:队列 A 中分别为 39%和 49%,队列 B、C 和 D 中分别为 83%和 89%。更多的女性经历了 VF、≥3 级体征和症状,但相似的≥3 级诊断或实验室异常。
与男性相比,更多的女性进入研究时的耐药谱表明,她们的二线方案可能有效地维持病毒学抑制。女性更频繁地出现≥3 级体征和症状表明,在基于蛋白酶抑制剂治疗的女性中,耐受性问题认识不足。