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二线基于蛋白酶抑制剂的抗逆转录病毒治疗中 HIV 感染儿童的治疗失败。

Treatment Failure in HIV-Infected Children on Second-line Protease Inhibitor-Based Antiretroviral Therapy.

机构信息

Institut de Recherche pour le Développement, UMI 174-PHPT Bioinformatics Research Laboratory, Faculty of Science.

Institut de Recherche pour le Développement, UMI 174-PHPT Department of Medical Technology, Faculty of Associated Medical Sciences, Chiang Mai University, Thailand Harvard T.H. Chan School of Public Health, Boston, Massachusetts.

出版信息

Clin Infect Dis. 2015 Jul 1;61(1):95-101. doi: 10.1093/cid/civ271. Epub 2015 Apr 1.

Abstract

BACKGROUND

Human immunodeficiency virus (HIV)-infected children failing second-line antiretroviral therapy (ART) have no access to third-line antiretroviral drugs in many resource-limited settings. It is important to identify risk factors for second-line regimen failure.

METHODS

HIV-infected children initiating protease inhibitor (PI)-containing second-line ART within the Program for HIV Prevention and Treatment observational cohort study in Thailand between 2002 and 2010 were included. Treatment failure was defined as confirmed HIV type 1 RNA load >400 copies/mL after at least 6 months on second-line regimen or death. Adherence was assessed by drug plasma levels and patient self-report. Cox proportional hazards regression analyses were used to identify risk factors for failure.

RESULTS

A total of 111 children started a PI-based second-line regimen, including 59 girls (53%). Median first-line ART duration was 1.9 years (interquartile range [IQR], 1.4-3.3 years), and median age at second-line initiation was 10.7 years (IQR, 6.3-13.4 years). Fifty-four children (49%) experienced virologic failure, and 2 (2%) died. The risk of treatment failure 24 months after second-line initiation was 41%. In multivariate analyses, failure was independently associated with exposure to first-line ART for >2 years (adjusted hazard ratio [aHR], 1.8; P = .03), age >13 years (aHR, 2.9; P < .001), body mass index-for-age z score < -2 standard deviations at second-line initiation (aHR, 2.8; P = .03), and undetectable drug levels within 6 months following second-line initiation (aHR, 4.5; P < .001).

CONCLUSIONS

Children with longer exposure to first-line ART, entry to adolescence, underweight, and/or undetectable drug levels were at higher risk of failing second-line ART and thus should be closely monitored.

摘要

背景

在许多资源有限的环境中,感染人类免疫缺陷病毒(HIV)的儿童在二线抗逆转录病毒治疗(ART)失败后无法获得三线抗逆转录病毒药物。因此,确定二线方案失败的风险因素非常重要。

方法

本研究纳入了 2002 年至 2010 年期间在泰国的 HIV 预防和治疗观察队列研究项目中接受包含蛋白酶抑制剂(PI)的二线 ART 的 HIV 感染儿童。治疗失败定义为二线方案至少 6 个月后确认 HIV-1 RNA 载量>400 拷贝/mL 或死亡。通过药物血浆水平和患者自我报告评估依从性。采用 Cox 比例风险回归分析识别失败的风险因素。

结果

共有 111 名儿童开始了基于 PI 的二线方案,其中 59 名女孩(53%)。一线 ART 治疗的中位时间为 1.9 年(四分位距[IQR],1.4-3.3 年),二线开始时的中位年龄为 10.7 岁(IQR,6.3-13.4 岁)。54 名儿童(49%)出现病毒学失败,2 名儿童(2%)死亡。二线开始后 24 个月时治疗失败的风险为 41%。多变量分析显示,失败与一线 ART 暴露时间>2 年(调整后的危险比[aHR],1.8;P=0.03)、年龄>13 岁(aHR,2.9;P<0.001)、二线起始时体重指数-年龄 z 评分<-2 个标准差(aHR,2.8;P=0.03)和二线起始后 6 个月内药物水平未检测到(aHR,4.5;P<0.001)独立相关。

结论

暴露于一线 ART 时间更长、进入青春期、体重不足和/或药物水平未检测到的儿童二线 ART 失败的风险更高,因此应密切监测。

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