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
相关论文
共 50 条
  • [1] Pharmacological and therapeutic properties of ritonavir-boosted protease inhibitor therapy in HIV-infected patients
    Zeldin, RK
    Petruschke, RA
    JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2004, 53 (01) : 4 - 9
  • [2] Simplification from tenofovir disoproxil fumarate plus lamivudine or emtricitabine plus ritonavir-boosted protease inhibitor to ritonavir-boosted atazanavir plus lamivudine in virologically suppressed HIV-infected adults with osteopenia: a pilot study
    Blanco, Jose L.
    Rojas, Jhon
    de Lazzari, Elisa
    Inciarte, Alexy
    Subirana, Mar
    Callau, Pilar
    Martinez-Rebollar, Maria
    Laguno, Montserrat
    Mallolas, Josep
    de la Mora, Lorena
    Torres, Berta
    Gonzalez-Cordon, Ana
    Martinez, Esteban
    JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2022, 77 (07) : 1974 - 1979
  • [3] Confirmed efficacy and safety of dual therapy based in lamivudine plus a ritonavir-boosted protease inhibitor in the clinical setting
    Fontecha-Ortega, Maria
    Munoz-Mendoza, Vanessa
    Gomez, Cristina
    Sanchez-Conde, Matilde
    Angel Rodriguez, Miguel
    Jesus Vivancos, Maria
    Luis Casado, Jose
    JOURNAL OF THE INTERNATIONAL AIDS SOCIETY, 2016, 19
  • [4] Prevalence and predictors of protease inhibitor (PI) mutations in HIV-infected UK adults treated with ritonavir-boosted lopinavir as their first PI
    Barber, T.
    Harrison, L.
    Asboe, D.
    Williams, I.
    Bansi, L.
    Pillay, D.
    Dunn, D.
    HIV MEDICINE, 2011, 12 : 73 - 74
  • [5] Dual Raltegravir-Darunavir/Ritonavir Combination in Virologically Suppressed HIV-1-Infected Patients on Antiretroviral Therapy Including a Ritonavir-Boosted Protease Inhibitor Plus Two Nucleoside/Nucleotide Reverse Transcriptase Inhibitors
    Calza, Leonardo
    Danese, Ilaria
    Magistrelli, Eleonora
    Colangeli, Vincenzo
    Manfredi, Roberto
    Bon, Isabella
    Re, Maria Carla
    Conti, Matteo
    Viale, Pierluigi
    HIV CLINICAL TRIALS, 2016, 17 (01): : 38 - 47
  • [6] Dual therapy with dolutegravir plus ritonavir-boosted or unboosted atazanavir as a maintenance treatment in highly experienced HIV-infected patients
    Faycal, A.
    Abdi, B.
    Peytavin, G.
    Tebano, G.
    Schneider, L.
    Seang, S.
    Simon, A.
    Tubiana, R.
    Valantin, M.
    Marcelin, A.
    Katlama, C.
    Palich, R.
    JOURNAL OF THE INTERNATIONAL AIDS SOCIETY, 2018, 21
  • [7] Comparing albuvirtide plus ritonavir-boosted lopinavir regimen to two nucleotide reverse transcriptase inhibitors plus ritonavir-boosted lopinavir in HIV-infected individuals who failed initial treatment: a retrospective comparative cohort study
    Chen, Liyu
    Dai, Hua
    Wang, Jiayi
    Wang, Ming
    Ma, Yuanji
    Ma, Fanghua
    Li, Changmin
    Bai, Lang
    Du, Lingyao
    Tang, Hong
    ANNALS OF TRANSLATIONAL MEDICINE, 2022, 10 (20)
  • [8] Simplification to dual antiretroviral therapy including a ritonavir-boosted protease inhibitor in treatment-experienced HIV-1-infected patients
    Burgos, Joaquin
    Crespo, Manuel
    Falco, Vicenc
    Curran, Adria
    Navarro, Jordi
    Imaz, Arkaitz
    Domingo, Pere
    Podzamczer, Daniel
    Gracia Mateo, Ma
    Villar, Sara
    Van den Eynde, Eva
    Ribera, Esteve
    Pahissa, Albert
    JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2012, 67 (10) : 2479 - 2486
  • [9] Similar efficacy and tolerability of atazanavir compared with atazanavir/ritonavir, each with abacavir/lamivudine after initial suppression with abacavir/lamivudine plus ritonavir-boosted atazanavir in HIV-infected patients
    Squires, Kathleen E.
    Young, Benjamin
    DeJesus, Edwin
    Bellos, Nicholaos
    Murphy, Daniel
    Zhao, Henry H.
    Patel, Lisa G.
    Ross, Lisa L.
    Wannamaker, Paul G.
    Shaefer, Mark S.
    AIDS, 2010, 24 (13) : 2019 - 2027
  • [10] Lamivudine plus darunavir boosted with ritonavir as simplification dual regimen in HIV-infected patients
    Luis Casado, Jose
    Banon, Sara
    Moreno, Ana
    Diaz de Santiago, Alberto
    Gomez, Cristina
    Perez-Elias, Maria J.
    Moreno, Santiago
    JOURNAL OF THE INTERNATIONAL AIDS SOCIETY, 2014, 17 : 188 - 188