Department of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, TN.
Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD.
J Acquir Immune Defic Syndr. 2018 Apr 1;77(4):383-392. doi: 10.1097/QAI.0000000000001612.
No randomized trial has directly compared the efficacy of prolonged infant antiretroviral prophylaxis versus maternal antiretroviral therapy (mART) for prevention of mother-to-child transmission throughout the breastfeeding period.
Fourteen sites in Sub-Saharan Africa and India.
A randomized, open-label strategy trial was conducted in HIV-1-infected women with CD4 counts ≥350 cells/mm (or ≥country-specific ART threshold if higher) and their breastfeeding HIV-1-uninfected newborns. Randomization at 6-14 days postpartum was to mART or infant nevirapine (iNVP) prophylaxis continued until 18 months after delivery or breastfeeding cessation, infant HIV-1 infection, or toxicity, whichever occurred first. The primary efficacy outcome was confirmed infant HIV-1 infection. Efficacy analyses included all randomized mother-infant pairs except those with infant HIV-1 infection at entry.
Between June 2011 and October 2014, 2431 mother-infant pairs were enrolled; 97% of women were World Health Organization Clinical Stage I, median screening CD4 count 686 cells/mm. Median infant gestational age/birth weight was 39 weeks/2.9 kilograms. Seven of 1219 (0.57%) and 7 of 1211 (0.58%) analyzed infants in the mART and iNVP arms, respectively, were HIV-infected (hazard ratio 1.0, 96% repeated confidence interval 0.3-3.1); infant HIV-free survival was high (97.1%, mART and 97.7%, iNVP, at 24 months). There were no significant differences between arms in median time to breastfeeding cessation (16 months) or incidence of severe, life-threatening, or fatal adverse events for mothers or infants (14 and 42 per 100 person-years, respectively).
Both mART and iNVP prophylaxis strategies were safe and associated with very low breastfeeding HIV-1 transmission and high infant HIV-1-free survival at 24 months.
没有随机试验直接比较过在整个哺乳期内延长婴儿抗逆转录病毒预防与母婴抗逆转录病毒治疗(mART)对预防母婴传播的疗效。
撒哈拉以南非洲和印度的 14 个地点。
在 CD4 计数≥350 个细胞/mm(或更高的国家特定 ART 阈值)的 HIV-1 感染妇女及其未感染 HIV-1 的母乳喂养新生儿中进行了一项随机、开放性标签策略试验。产后 6-14 天随机分配到 mART 或婴儿奈韦拉平(iNVP)预防,直至分娩后 18 个月或母乳喂养停止、婴儿 HIV-1 感染或毒性发生,以先发生者为准。主要疗效结局是确认婴儿 HIV-1 感染。疗效分析包括所有随机分配的母婴对,除非婴儿在入组时已感染 HIV-1。
2011 年 6 月至 2014 年 10 月,共纳入 2431 对母婴;97%的妇女为世界卫生组织临床分期 I 期,中位筛查 CD4 计数为 686 个细胞/mm。婴儿的中位妊娠周数/出生体重为 39 周/2.9 公斤。mART 组和 iNVP 组分别有 7/1219(0.57%)和 7/1211(0.58%)分析的婴儿感染 HIV(危险比 1.0,96%重复置信区间 0.3-3.1);婴儿无 HIV 生存很高(24 个月时 mART 组为 97.1%,iNVP 组为 97.7%)。两组中位母乳喂养停止时间(16 个月)或母婴严重、危及生命或致命不良事件发生率(分别为每 100 人年 14 例和 42 例)无显著差异。
mART 和 iNVP 预防策略均安全,与 24 个月时婴儿 HIV-1 传播率低和婴儿 HIV-1 无生存高相关。