Fundación Huésped, Buenos Aires, Argentina.
Vanderbilt University, Nashville, TN, USA.
Lancet HIV. 2015 Nov;2(11):e492-500. doi: 10.1016/S2352-3018(15)00183-6. Epub 2015 Oct 22.
Access to combination antiretroviral therapy (ART) is expanding in Latin America (Mexico, Central America, and South America) and the Caribbean. We assessed the incidence of and factors associated with regimen failure and regimen change of initial ART in this region.
This observational cohort study included antiretroviral-naive adults starting ART from 2000 to 2014 at sites in seven countries throughout Latin America and the Caribbean. Primary outcomes were time from ART initiation until virological failure, major regimen modification, and a composite endpoint of the first of virological failure or major regimen modification. Cumulative incidence of the primary outcomes was estimated with death considered a competing event.
14,027 patients starting ART were followed up for a median of 3.9 years (2.0-6.5): 8374 (60%) men, median age 37 years (IQR 30-44), median CD4 count 156 cells per μL (61-253), median plasma HIV RNA 5.0 log10 copies per mL (4.4-5.4), and 3567 (28%) had clinical AIDS. 1719 (12%) patients had virological failure and 1955 (14%) had a major regimen change. Excluding the site in Haiti, which did not regularly measure HIV RNA, cumulative incidence of virological failure was 7.8% (95% CI 7.2-8.5) 1 year after ART initiation, 19.2% (18.2-20.2) at 3 years, and 25.8% (24.6-27.0) at 5 years; cumulative incidence of major regimen change was 5.9% (5.3-6.4) at 1 year, 12.7% (11.9-13.5) at 3 years, and 18.2% (17.2-19.2) at 5 years. Incidence of major regimen change at the site in Haiti was 10.7% (95% CI 9.7-11.6) at 5 years. Virological failure was associated with younger age (adjusted hazard ratio [HR] 2.03, 95% CI 1.68-2.44, for 20 years vs 40 years), infection through injection drug use (vs infection through heterosexual sex; 1.60, 1.02-2.52), and initiation in earlier calendar years (1.28, 1.13-1.46, for 2002 vs 2006), but was not significantly associated with boosted protease inhibitor-based regimens (vs non-nucleoside reverse transcriptase inhibitor; 1.17, 1.00-1.36).
Incidence of virological failure in Latin America and the Caribbean was generally lower than that reported in North America or Europe. Our results suggest the need to design strategies to reduce failure and major regimen change in young patients and those with a history of injection drug use.
US National Institutes of Health.
在拉丁美洲(墨西哥、中美洲和南美洲)和加勒比地区,获得联合抗逆转录病毒疗法(ART)的机会正在增加。我们评估了该地区初始 ART 治疗方案失败和改变的发生率及相关因素。
这项观察性队列研究纳入了 2000 年至 2014 年在拉丁美洲和加勒比地区 7 个国家的多个地点开始接受 ART 的抗逆转录病毒初治成人患者。主要结局是从 ART 开始到病毒学失败、主要治疗方案改变和病毒学失败或主要治疗方案改变的复合终点的时间。采用死亡作为竞争事件来估计主要结局的累积发生率。
共有 14027 例开始 ART 的患者接受了中位时间为 3.9 年(2.0-6.5 年)的随访:8374 例(60%)为男性,中位年龄 37 岁(IQR 30-44),中位 CD4 计数为每 μL 156 个细胞(61-253),中位血浆 HIV RNA 为每毫升 5.0 log10 拷贝(4.4-5.4),3567 例(28%)有临床艾滋病。1719 例(12%)患者出现病毒学失败,1955 例(14%)出现主要治疗方案改变。排除未定期测量 HIV RNA 的海地地点后,ART 开始后 1 年病毒学失败的累积发生率为 7.8%(95%CI 7.2-8.5),3 年时为 19.2%(18.2-20.2),5 年时为 25.8%(24.6-27.0);1 年时主要治疗方案改变的累积发生率为 5.9%(5.3-6.4),3 年时为 12.7%(11.9-13.5),5 年时为 18.2%(17.2-19.2)。海地地点的主要治疗方案改变发生率为 5 年时的 10.7%(95%CI 9.7-11.6)。病毒学失败与年龄较小(调整后的危险比[HR]2.03,95%CI 1.68-2.44,与 40 岁相比为 20 岁)、通过注射吸毒感染(与异性性传播感染相比;1.60,1.02-2.52)和更早的日历年份开始治疗(1.28,1.13-1.46,与 2002 年相比为 2006 年)相关,但与基于增效蛋白酶抑制剂的治疗方案无显著相关性(与非核苷类逆转录酶抑制剂相比;1.17,1.00-1.36)。
拉丁美洲和加勒比地区病毒学失败的发生率通常低于北美或欧洲报道的发生率。我们的研究结果表明,需要制定策略来减少年轻患者和有注射吸毒史患者的失败和主要治疗方案改变。
美国国立卫生研究院。