Effect of dolutegravir in combination with Nucleoside Reverse Transcriptase Inhibitors (NRTIs) on people living with HIV who have pre-existing NRTI mutations

被引:20
|
作者
Sorstedt, Erik [1 ]
Carlander, Christina [2 ]
Flamholc, Leo [3 ]
Hejdeman, Bo [4 ,5 ]
Svedhem, Veronica [6 ]
Sonnerborg, Anders [6 ,7 ]
Gisslen, Magnus [1 ]
Yilmaz, Aylin [1 ]
机构
[1] Univ Gothenburg, Sahlgrenska Acad, Inst Biomed, Dept Infect Dis, S-41390 Gothenburg, Sweden
[2] Hosp Vastmanland Vasteras, Dept Infect Dis, S-72189 Vasteras, Sweden
[3] Malmo Univ Hosp, Dept Infect Dis, S-20502 Malmo, Sweden
[4] Karolinska Inst, Sodersjukhuset, Dept Clin Sci & Educ, S-14186 Stockholm, Sweden
[5] Soder Sjukhuset, Unit Infect Dis Venhalsan, SE-11883 Stockholm, Sweden
[6] Karolinska Inst, Karolinska Univ Hosp, Dept Infect Dis, S-14186 Stockholm, Sweden
[7] Karolinska Inst, Karolinska Univ Hosp, Dept Clin Microbiol, S-14186 Stockholm, Sweden
关键词
HIV-1; Antiretroviral therapy; Nucleoside reverse transcriptase inhibitor; NRTI; Resistance; Dolutegravir; TREATMENT-EXPERIENCED SUBJECTS; ANTIRETROVIRAL-NAIVE ADULTS; TWICE-DAILY RALTEGRAVIR; ONCE-DAILY DOLUTEGRAVIR; DRUG-RESISTANCE; NON-INFERIORITY; DOUBLE-BLIND; TYPE-1; INFECTION; ELVITEGRAVIR; MONOTHERAPY;
D O I
10.1016/j.ijantimicag.2018.01.009
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Until the introduction of dolutegravir (DTG), people living with HIV (PLWH) who have developed nucleoside reverse transcriptase inhibitor (NRTI) mutations have had few other treatment options outside of regimens based on ritonavir-boosted protease inhibitors (PI/r). Here we report treatment results among PLWH in Sweden with pre-existing NRTI mutations on antiretroviral treatment (ART) with DTG and one to two NRTIs. All PLWH on ART with DTG and one to two NRTIs with pre-existing NRTI mutations were retrospectively identified from the National InfCare HIV database. As controls, PLWH on PI/r and one to two NRTIs, matched according to Genotypic Susceptibility Score and observation time, were included. Data were collected as long as the study population was on treatment with DTG; controls were monitored for the same interval. Outcome was classified as either treatment success or failure. In total, 244 participants (122 individuals treated with DTG and 122 individuals treated with PI/r) were included. Median observation time was 78 weeks (interquartile range 50-98 weeks) for participants on DTG and 75 weeks (50-101 weeks) for individuals on PI/r. Viral failure was detected in four individuals treated with DTG and three individuals treated with PI/r, resulting in similar success rates of 96.7% and 97.5%, respectively. No new mutations were found among participants with treatment failure. DTG in combination with one to two NRTIs was as efficient as PI/r in individuals with pre-existing NRTI mutations in this setting. It may be considered an alternative to PI/r-based ART even in the presence of NRTI resistance. (c) 2018 Elsevier B.V. and International Society of Chemotherapy. All rights reserved.
引用
收藏
页码:733 / 738
页数:6
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