Department of Pediatrics, University of Nairobi, Nairobi, Kenya.
J Acquir Immune Defic Syndr. 2013 Mar 1;62(3):267-74. doi: 10.1097/QAI.0b013e31827b4ac8.
HIV-infected children may require the use of combination antiretroviral treatment (cART) into adulthood. However, regimens are limited to first line and second line in many African settings. Therefore, understanding the long-term rate of virologic failure and drug resistance during prolonged antiretroviral treatment is important for establishing treatment strategies in African pediatric cohorts.
Children aged 18 months to 12 years initiated first-line cART and were followed every 1-3 months, for up to 5.5 years. Treatment was switched to second-line cART based on clinical and immunologic criteria according to national guidelines. Virologic failure was determined retrospectively as defined by ≥2 viral loads >5000 copies per milliliter. Drug resistance was assessed during viral failure by population-based sequencing.
Among 100 children on first-line cART followed for a median of 49 months, 34% children experienced virologic failure. Twenty-three (68%) of the 34 children with viral failure had detectable resistance mutations, of whom 14 (61%) had multiclass resistance. Fourteen (14%) children were switched to second-line regimens and followed for a median of 28 months. Retrospective analysis revealed that virologic failure had occurred at a median of 12 months before switching to second line. During prolonged first-line treatment in the presence of viral failure, additional resistance mutations accumulated; however, only 1 (7%) of 14 children had persistent viremia during second-line treatment.
Virologic suppression was maintained on first-line cART in two-thirds of HIV-infected children for up to 5 years. Switch to second line based on clinical/immunologic criteria occurred ∼1 year after viral failure, but the delay did not consistently compromise second-line treatment.
HIV 感染儿童在成年后可能需要使用联合抗逆转录病毒治疗(cART)。然而,在许多非洲国家,方案仅限于一线和二线。因此,了解长期抗病毒治疗期间病毒学失败和耐药性的发生率对于在非洲儿科队列中制定治疗策略非常重要。
18 个月至 12 岁的儿童开始一线 cART,并每 1-3 个月随访一次,最长随访 5.5 年。根据国家指南的临床和免疫标准,根据治疗失败转为二线 cART。病毒学失败是根据≥2 次病毒载量>5000 拷贝/毫升定义的。在病毒学失败期间,通过基于人群的测序评估耐药性。
在 100 名接受一线 cART 治疗、中位随访 49 个月的儿童中,34%的儿童出现病毒学失败。34 名病毒学失败的儿童中有 23 名(68%)检测到耐药突变,其中 14 名(61%)有多种耐药性。14 名儿童(14%)转为二线方案,并随访中位时间为 28 个月。回顾性分析显示,在转为二线方案之前,病毒学失败中位数发生在 12 个月。在存在病毒学失败的情况下,一线治疗期间额外的耐药突变积累;然而,在二线治疗期间,只有 1 名(7%)儿童持续出现病毒血症。
在多达三分之二的 HIV 感染儿童中,一线 cART 治疗可维持病毒学抑制长达 5 年。根据临床/免疫标准转为二线方案发生在病毒学失败后约 1 年,但这种延迟并未始终影响二线治疗。