HIV-1 pretreatment drug resistance negatively impacts outcomes of first-line antiretroviral treatment

抗逆转录病毒药物 艾滋病毒耐药性 医学 人类免疫缺陷病毒(HIV) 抗药性 药品 西达 毒品假日 内科学 抗逆转录病毒治疗 慢病毒 药理学 病毒学
作者
Lucas E. Hermans,Laura M. Hofstra,Rob Schuurman,Rob Ter Heine,David M. Burger,Stijn A.J. Talboom,Dorien De Jong,Hugo A. Tempelman,Willem D.F. Venter,Monique Nijhuis,Annemarie M.J. Wensing
出处
期刊:AIDS [Lippincott Williams & Wilkins]
卷期号:36 (7): 923-931 被引量:4
标识
DOI:10.1097/qad.0000000000003182
摘要

Introduction: Pretreatment drug resistance (PDR) prevalence in sub-Saharan Africa is rising, but evidence of its impact on efavirenz (EFV)-based antiretroviral treatment (ART) is inconclusive. We determined the impact of PDR on outcomes of EFV-based ART in a subanalysis of a randomized clinical trial comparing different ART monitoring strategies implemented at a rural treatment facility in Limpopo, South Africa. Methods: Participants initiating EFV-based first-line ART (2015–2017) were enrolled and received 96 weeks follow-up. Resistance to nucleos(t)ide reverse transcriptase inhibitors (NRTIs) and non-NRTI's (NNRTIs) was retrospectively assessed by population-based sequencing. Virological failure was defined as a viral load of at least 1000 copies/ml after at least 24 weeks of ART. Results: A total of 207 participants were included, 60.4% (125/207) of whom were female. Median age was 38.8 (interquartile range: 31.4–46.7) years. Median CD4 + cell count was 191 (interquartile range: 70–355) cells/μl. PDR was detected in 12.9% (25/194) of participants with available sequencing results; 19 had NNRTI-resistance, and six had NRTI- and NNRTI-resistance. 26.0% of participants (40/154) with sequencing results and virological follow-up developed virological failure. PDR was independently associated with failure (adjusted hazard ratio: 3.7 [95% confidence interval: 1.68.5], P = 0.002). At failure, 87.5% (7/8) of participants with PDR harboured dual-class resistant virus, versus 16.7% (4/24) of participants without PDR ( P = 0.0007). Virological resuppression after failure on first-line ART occurred in 57.7% (15/26) of participants without PDR versus 14.3% (1/7) of participants with PDR ( P = 0.09). Conclusion: PDR was detected in 13% of study participants. PDR significantly increased the risk of virological failure of EFV-based ART. Accumulation of resistance at failure and inability to achieve virological resuppression illustrates the profound impact of PDR on treatment outcomes.
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