Long-term efficacy of dolutegravir in treatment-experienced subjects failing therapy with HIV-1 integrase strand inhibitor-resistant virus

被引:27
作者
Castagna, Antonella [1 ]
Ferrara, Micol [2 ]
Galli, Laura [3 ]
Comi, Laura [4 ]
Sterrantino, Gaetana [5 ]
Cenderello, Giovanni [6 ]
Zaccarelli, Mauro [7 ]
Foca, Emanuele [8 ]
Roncadori, Andrea [9 ]
Lazzarin, Adriano [3 ]
机构
[1] Univ Vita Salute San Raffaele, Clin Infect Dis, Milan, Italy
[2] Univ Turin, Dept Med Sci, Unit Infect Dis, Turin, Italy
[3] Ist Sci San Raffaele, Clin Infect Dis, Milan, Italy
[4] Azienda Osped Papa Giovanni XXIII, Bergamo, Italy
[5] Azienda Osped Univ Careggi, Florence, Italy
[6] Galliera Hosp, Infect Dis Dept, Genoa, Italy
[7] Lazzaro Spallanzani IRCCS, Ist Nazl Malattie Infett, Rome, Italy
[8] Univ Brescia, Spedali Civili Brescia, Brescia, Italy
[9] CINECA, Healthcare Syst Dept, Bologna, Italy
关键词
DRUG-RESISTANCE; VIRAL LOAD;
D O I
10.1093/jac/dkx371
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Objectives: This study evaluated the virological efficacy of dolutegravir 50 mg twice daily in 190 HIV-1 failing antiretroviral-experienced patients with previous exposure to first-generation integrase strand transfer inhibitor (INSTI) over a 5 year follow-up using data from clinical practice. Patients and methods: This analysis included HIV-1-infected patients who were >= 18 years of age, treatment experienced, had HIV-1 RNA > 50 copies/mL, with INSTI-resistant virus, who started dolutegravir 50 mg twice daily plus optimized background therapy (OBT), recorded in the national prospective database PRESTIGIO (www.proget toprestigio.it). Follow-up accrued from the start of dolutegravir 50 mg twice daily + OBT until virological failure (VF) or dolutegravir discontinuation for any reason or the last treatment visit on dolutegravir 50mg twice daily treatment. VF was defined by the lack of achievement of HIV-1 RNA <50 copies/mL by 6 months and thereafter, or the occurrence of two consecutive HIV-1 RNA >= 50 copies/mL after achievement of undetectable viral load. Results: The estimated VF probabilities were 17% (95% CI = 12%-24%), 28% (95% CI = 21%-37%), 33% (95% CI = 25%-43%), 39% (95% CI = 29%-51%) and 52% (95% CI = 39%-67%) at 12, 24, 36, 48 and 60 months since baseline, respectively. A higher risk of VF was independently associated with baseline viral load >100000 copies/mL (adjusted HR = 4.73, 95% CI = 1.33-16.78, P = 0.016) and with >= 1 INSTI mutations plus Q148H/K/R/N and the G140S/A/C as compared with other subjects (adjusted HR = 4.18, 95% CI = 1.32-13.23, P = 0.015). Conclusions: Our data showed a favourable long-term efficacy of dolutegravir 50 mg twice daily in association with OBT in treatment-experienced failing subjects, with INSTI-resistant virus, in the real world. A close monitoring of adherence is crucial for maintenance of virological response in this fragile subgroup of subjects.
引用
收藏
页码:177 / 182
页数:6
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