Wamalwa Dalton, Benki-Nugent Sarah, Langat Agnes, Tapia Kenneth, Ngugi Evelyn, Moraa Helen, Maleche-Obimbo Elizabeth, Otieno Vincent, Inwani Irene, Richardson Barbra A, Chohan Bhavna, Overbaugh Julie, John-Stewart Grace C
aDepartment of Paediatrics, University of Nairobi, Nairobi, Kenya bDepartment of Global Health cBiostatistics, University of Washington, Seattle, Washington, USA dDepartment of Medical Microbiology, University of Nairobi, Nairobi, Kenya eDepartment of Human Biology, Fred Hutchinson Cancer Research Center fMedicine gPediatrics hEpidemiology, University of Washington, Seattle, Washington, USA.
AIDS. 2016 Sep 24;30(15):2303-13. doi: 10.1097/QAD.0000000000001158.
Treatment interruption has been well tolerated and durable in some pediatric studies but none have compared treatment interruption with continued antiretroviral treatment (ART) following ART initiation in early HIV. The objective of this study was to compare outcomes in treatment interruption versus continued ART among early-treated infants.
Randomized trial (OPH-03; NCT00428116).
The trial included HIV-infected infants who initiated ART at less than 13 months of age, received ART for 24 months, and, if eligible (CD4% >25%, normal growth), were randomized to treatment interruption versus continued ART. Children in the treatment interruption group restarted ART if they met WHO ART-eligibility criteria. During 18-months postrandomization, primary outcomes were incidence of serious adverse events and growth. CD4%, viral load, morbidity, and growth were compared.
Of 140 infants enrolled, 121 started ART, of whom 75 completed at least 24 months ART and 42 were randomized (21 per arm). ART was initiated at median age 5 months and randomization at 30 months. Among 21 treatment interruption children, 14 met ART restart criteria within 3 months. Randomization was discontinued by Data and Safety Monitoring Board due to low treatment interruption durability. At 18 months postrandomization, growth and serious adverse events were comparable between arms; hypercholesteremia incidence was higher in the continued arm (P = 0.03). CD4% and viral load did not differ between arms [CD4% 35% and median viral load undetectable (<150 copies/ml) in both arms, P = 0.9 for each comparison]. No infants had post-treatment viral control.
Short treatment interruption did not compromise 18-month CD4%, viral control, growth, or morbidity compared with continued ART among infants who started ART in early HIV infection.
在一些儿科研究中,治疗中断耐受性良好且效果持久,但尚无研究比较早期感染艾滋病毒后开始抗逆转录病毒治疗(ART)时治疗中断与继续ART的情况。本研究的目的是比较早期接受治疗的婴儿中治疗中断与继续ART的结果。
随机试验(OPH-03;NCT00428116)。
该试验纳入了在13个月龄前开始ART、接受ART治疗24个月且符合条件(CD4%>25%,生长正常)的艾滋病毒感染婴儿,将其随机分为治疗中断组和继续ART组。治疗中断组的儿童若符合世界卫生组织ART资格标准则重新开始ART。在随机分组后的18个月内,主要结局为严重不良事件的发生率和生长情况。比较了CD4%、病毒载量、发病率和生长情况。
在140名登记的婴儿中,121名开始ART,其中75名完成了至少24个月的ART治疗,42名被随机分组(每组21名)。ART开始的中位年龄为5个月,随机分组时为3个月。在21名治疗中断的儿童中,14名在3个月内符合ART重新开始标准。由于治疗中断的持久性较低,数据与安全监测委员会停止了随机分组。在随机分组后的18个月,两组间生长情况和严重不良事件相当;继续治疗组的高胆固醇血症发生率更高(P = 0.03)。两组间CD4%和病毒载量无差异[两组的CD4%均为35%,病毒载量中位数均未检测到(<150拷贝/ml),每次比较P = 0.9]。没有婴儿实现治疗后病毒控制。
与早期感染艾滋病毒后开始ART的婴儿继续接受ART相比,短期治疗中断并未损害18个月时的CD4%、病毒控制、生长或发病率。