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开始使用含非核苷类逆转录酶抑制剂的抗逆转录病毒治疗的患者的预处理人类免疫缺陷病毒耐药性的临床影响:系统评价和荟萃分析。

Clinical Impact of Pretreatment Human Immunodeficiency Virus Drug Resistance in People Initiating Nonnucleoside Reverse Transcriptase Inhibitor-Containing Antiretroviral Therapy: A Systematic Review and Meta-analysis.

机构信息

Global HIV, Hepatitis and STI Programmes, World Health Organization, Geneva, Switzerland.

Virology, Department of Medical Microbiology, University Medical Center Utrecht, Utrecht, The Netherlands.

出版信息

J Infect Dis. 2021 Aug 2;224(3):377-388. doi: 10.1093/infdis/jiaa683.

Abstract

BACKGROUND

Increased access to antiretroviral therapy (ART) has resulted in rising levels of pretreatment human immunodeficiency virus drug resistance (PDR). This is the first systematic review and meta-analysis to assess the impact of PDR on treatment outcomes among people initiating nonnucleoside reverse transcriptase inhibitor (NNRTI)-based ART, including the combination of efavirenz (EFV), tenofovir (TDF), and lamivudine or emtricitabine (XTC).

METHODS

We systematically reviewed studies and conference proceedings comparing treatment outcomes in populations initiating NNRTI-based ART with and without PDR. We conducted subgroup analyses by regimen: (1) NNRTIs + 2 nucleoside reverse transcriptase inhibitors (NRTIs), (2) EFV + 2 NRTIs, or (3) EFV/TDF/XTC; by population (children vs adults); and by definition of resistance (PDR vs NNRTI PDR).

RESULTS

Among 6197 studies screened, 32 were analyzed (31 441 patients). We found that individuals with PDR initiating NNRTIs across all the subgroups had increased risk of virological failure compared to those without PDR. Risk of acquisition of new resistance mutations and ART switch was also higher in people with PDR.

CONCLUSIONS

This review shows poorer treatment outcomes in the presence of PDR, supporting the World Health Organization's recommendation to avoid using NNRTIs in countries where levels of PDR are high.

摘要

背景

抗逆转录病毒疗法(ART)的可及性增加导致了预处理人类免疫缺陷病毒耐药性(PDR)水平的上升。这是第一项评估 PDR 对开始使用非核苷类逆转录酶抑制剂(NNRTI)为基础的 ART 人群治疗结果影响的系统评价和荟萃分析,包括使用依非韦伦(EFV)、替诺福韦(TDF)和拉米夫定或恩曲他滨(XTC)的组合。

方法

我们系统地回顾了比较开始 NNRTI 为基础的 ART 时有无 PDR 的人群治疗结果的研究和会议论文。我们按方案进行了亚组分析:(1)NNRTIs + 2 种核苷逆转录酶抑制剂(NRTIs),(2)EFV + 2 NRTIs,或(3)EFV/TDF/XTC;按人群(儿童与成人);以及按耐药性定义(PDR 与 NNRTI PDR)。

结果

在筛选的 6197 项研究中,有 32 项进行了分析(31441 名患者)。我们发现,与无 PDR 者相比,所有亚组中开始使用 NNRTIs 的 PDR 个体发生病毒学失败的风险增加。PDR 患者发生新耐药突变和 ART 转换的风险也更高。

结论

本综述表明 PDR 存在时治疗结果较差,支持世界卫生组织建议在 PDR 水平较高的国家避免使用 NNRTI。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eff7/8328216/84cdc6a2c1c2/jiaa683f0001.jpg

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