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

被引:4
作者
Hermans, Lucas E. [1 ,2 ,3 ]
Hofstra, Laura M. [1 ]
Schuurman, Rob [1 ]
Ter Heine, Rob [4 ]
Burger, David M. [4 ]
Talboom, Stijn A. J. [5 ]
De Jong, Dorien [1 ]
Tempelman, Hugo A. [2 ,3 ]
Venter, Willem D. F. [2 ,3 ]
Nijhuis, Monique [1 ,3 ,6 ]
Wensing, Annemarie M. J. [1 ,2 ,3 ]
机构
[1] Univ Med Ctr Utrecht UMCU, Dept Med Microbiol, Virol, Utrecht, Netherlands
[2] Univ Witwatersrand, Ezintsha, Johannesburg, South Africa
[3] Ndlovu Res Consortium, Elandsdoorn, South Africa
[4] Radboud Univ Nijmegen, Med Ctr, Radboud Inst Hlth Sci, Dept Pharm, Nijmegen, Netherlands
[5] Radboud Univ Nijmegen, Med Ctr, Nijmegen, Netherlands
[6] Univ Witwatersrand, Fac Hlth Sci, HIV Pathogenesis Res Unit, Johannesburg, South Africa
关键词
antiretroviral treatment; HIV; pretreatment drug resistance; VIROLOGICAL FAILURE; THERAPY; DOLUTEGRAVIR; EFAVIRENZ;
D O I
10.1097/QAD.0000000000003182
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
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/mu l. 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.
引用
收藏
页码:923 / 931
页数:9
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