Dual therapy with ritonavir-boosted protease inhibitor (PI) plus lamivudine versus triple therapy with ritonavir-boosted PI plus two nucleos(t)ide reverse-transcriptase inhibitor in HIV-infected patients with viral suppression

被引:3
作者
Hung, Tung-Che [1 ,5 ]
Chen, Guan-Jhou [2 ,3 ,4 ]
Cheng, Shu-Hsing [1 ]
Chen, Jhen-Hong [6 ]
Wei, Jheng-Lun [6 ]
Cheng, Chien-Yu [1 ,7 ]
Hung, Chien-Ching [3 ,4 ,8 ]
机构
[1] Taoyuan Gen Hosp, Minist Hlth & Welf, Dept Internal Med, Taoyuan, Taiwan
[2] Natl Taiwan Univ Hosp, Yun Lin Branch, Dept Internal Med, Touliu, Yunlin, Taiwan
[3] Natl Taiwan Univ Hosp, Dept Internal Med, Taipei, Taiwan
[4] Natl Taiwan Univ, Coll Med, Taipei, Taiwan
[5] Taipei Med Univ, Sch Publ Hlth, Taipei, Taiwan
[6] Taoyuan Gen Hosp, Dept Pharm, Minist Hlth & Welf, Taoyuan, Taiwan
[7] Natl Yang Ming Univ, Sch Publ Hlth, Taipei, Taiwan
[8] Natl Taiwan Univ, Coll Med, Dept Trop Med & Parasitol, Taipei, Taiwan
关键词
Combination antiretroviral therapy; Stable switch; Simplification; Adverse effect; Mitochondrial toxicity; VIROLOGICALLY STABLE PATIENTS; NON-INFERIORITY; OPEN-LABEL; RANDOMIZED-TRIAL; ANTIRETROVIRAL THERAPY; NAIVE ADULTS; MAINTENANCE; EMTRICITABINE; SIMPLIFICATION; RALTEGRAVIR;
D O I
10.1016/j.jmii.2019.07.002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: Dual antiretroviral regimens are attractive options to optimize the combination antiretroviral therapy in light of potential toxicities with long-term cumulative exposure to nucleos(t)ide reverse-transcriptase inhibitors (NRTIs). Methods: In this retrospective observational study, we included HIV-infected patients on suppressive antiretroviral therapy with plasma viral load (PVL) < 200 copies/mL for at least 6 months who were switched to dual regimens containing lamivudine (3TC) (150 mg twice daily or 300 mg once daily) plus lopinavir/ritonavir (LPV/r) 250/50 mg twice daily or darunavir/ritonavir (DRV/r) 800/100 mg once daily. Patients maintaining on suppressive triple therapy with DRV/r or LPV/r plus two NRTIs were included for comparisons. The primary endpoint was the proportion of patients with PVL <50 copies/mL after 48 weeks of follow-up. Results: In total, 364 patients were included with 93 (25.5%) switched to dual therapy After 48 weeks of observation, PVL <50 copies/mL was observed in 96.8% and 94.1% of dual-therapy and triple-therapy group, respectively, in per-protocol analysis (difference 2.7%; 95% CI -2.5%-7.9%). Nineteen patients (3 [3.2%] in dual-therapy and 16 [7.6%] in triple-therapy group) developed virologic failure, with none having emergent M184V resistance-associated mutation. A statistically significant increase of cholesterol level (13 mg/dL versus 2 mg/dL, p = 0.003) and high-density lipoprotein (3 mg/dL versus -2 mg/dL, p = 0.019) were observed in dual-therapy than in triple-therapy group. Changes of triglyceride, low-density lipoprotein and glycated hemoglobin levels were similar between the two groups. Conclusion: Dual therapy with DRV/r or LPV/r plus lamivudine demonstrated similar effectiveness in maintaining viral suppression to triple therapy. Copyright (C) 2019, Taiwan Society of Microbiology. Published by Elsevier Taiwan LLC.
引用
收藏
页码:865 / 871
页数:7
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