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Dual therapy with dolutegravir plus boosted protease inhibitor as maintenance or salvage therapy in highly experienced people living with HIV.

Authors :
Lee, Yu-Lin
Lin, Kuan-Yin
Cheng, Shu-Hsing
Lu, Po-Liang
Wang, Ning-Chi
Ho, Mao-Wang
Yang, Chia-Jui
Liou, Bo-Huang
Tang, Hung-Jen
Huang, Shie-Shian
Huang, Sung-Hsi
Chen, Tun-Chieh
Lin, Chi-Ying
Lin, Shih-Ping
Lee, Yuan-Ti
Hung, Chien-Ching
Source :
International Journal of Antimicrobial Agents. Sep2021, Vol. 58 Issue 3, pN.PAG-N.PAG. 1p.
Publication Year :
2021

Abstract

• Dolutegravir + boosted protease inhibitor is recommended as salvage therapy for highly experienced HIV-positive patients. • Evidence for the two-drug regimen of DTG + bPI is limited. • DTG + bPI demonstrated high efficacy and genetic barrier to resistance for patients with multiple resistance. • The two-drug regimen had metabolic impact on increased level of total cholesterol and low-density lipoprotein cholesterol. • Weight gain of 1.3 kg and 2.8 kg was noted after switching to the two-drug regimen at Weeks 24 and 48, respectively. Real-world experience with dolutegravir (DTG) plus boosted protease inhibitor (bPI) as a two-drug regimen is limited for highly experienced HIV-positive patients with virological failure or intolerance to antiretroviral therapy. Patients receiving DTG plus bPI between September 2016 and June 2019 at 15 designated hospitals for HIV care in Taiwan were retrospectively included in this study. A standardised case record form was used to collect clinical data. The primary endpoint was virological response, defined as achieving or maintaining plasma HIV-RNA <50 copies/mL at Week 48. A total of 77 patients were included; 58 (75.3%) had documented genotypic resistance to 1–4 antiretroviral classes. The most commonly used PI was darunavir (87.0%; 67/77). Seven patients (9.1%) had no virological data at Week 48, including three with loss to follow-up, one severe hyperlipidaemia, one renal failure and cardiovascular disease, one superimposed HBV infection and one death from anal cancer. The virological response rate increased from 59.7% at baseline to 90.9% at Week 24 and 85.7% at Week 48. The only patient (1.3%) with virological failure at Week 48 had poor adherence and baseline low-level resistance to darunavir with resistance-associated mutations at M46L, I50V and V82A. Compared with baseline, mean total cholesterol increased by 20.1 mg/dL and weight by 2.8 kg at Week 48, while the estimated glomerular filtration rate decreased by 14.4 mL/min/1.73m2 (both P < 0.05). We conclude that a two-drug regimen containing DTG plus bPI was effective in highly-experienced HIV-positive patients, but metabolic impact and weight gain should be closely monitored. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09248579
Volume :
58
Issue :
3
Database :
Academic Search Index
Journal :
International Journal of Antimicrobial Agents
Publication Type :
Academic Journal
Accession number :
151883846
Full Text :
https://doi.org/10.1016/j.ijantimicag.2021.106403