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
  • [31] Successful rescue therapy with darunabir (TMC114) in HIV-infected patients who have failed several ritonavir-boosted protease inhibitors
    Poveda, Eva
    Blanco, Francisco
    Garcia-Gasco, Pilar
    Alcolea, Antonio
    Briz, Veronica
    Soriano, Vincent
    AIDS, 2006, 20 (11) : 1558 - 1560
  • [32] Effects of rosuvastatin versus pravastatin on low-density lipoprotein diameter in HIV-1-infected patients receiving ritonavir-boosted protease inhibitor
    Bittar, Randa
    Giral, Philippe
    Aslangul, Elisabeth
    Assoumou, Lambert
    Valantin, Marc A.
    Kalmykova, Olga
    Federspiel, Marie C.
    Cherfils, Corinne
    Costagliola, Dominique
    Bonnefont-Rousselot, Dominique
    AIDS, 2012, 26 (14) : 1801 - 1805
  • [33] Immunovirological Efficacy of Once-Daily Maraviroc Plus Ritonavir-Boosted Atazanavir After 48 Weeks in Naive HIV-Infected Patients
    Pulido, Ildefonso
    Genebat, Miguel
    Alvarez-Rios, Ana I.
    De Pablo-Bernal, Rebeca S.
    Rafii-El-Idrissi Benhnia, Mohammed
    Pacheco, Yolanda M.
    Ruiz-Mateos, Ezequiel
    Leal, Manuel
    VIRAL IMMUNOLOGY, 2016, 29 (08) : 471 - 477
  • [34] Improvement in liver steatosis after the switch from a ritonavir-boosted protease inhibitor to raltegravir in HIV-infected patients with non-alcoholic fatty liver disease
    Calza, Leonardo
    Colangeli, Vincenzo
    Borderi, Marco
    Coladonato, Simona
    Tazza, Beatrice
    Fornaro, Giacomo
    Badia, Lorenzo
    Guardigni, Viola
    Verucchi, Gabriella
    Viale, Pierluigi
    INFECTIOUS DISEASES, 2019, 51 (08) : 593 - 601
  • [35] Dual treatment with lopinavir-ritonavir plus lamivudine versus triple treatment with lopinavir-ritonavir plus lamivudine or emtricitabine and a second nucleos(t)ide reverse transcriptase inhibitor for maintenance of HIV-1 viral suppression (OLE): a randomised, open-label, non-inferiority trial (vol 15, pg 785, 2015)
    Arribas, Jose R.
    Girard, Pierre-Marie
    Landman, Roland
    LANCET INFECTIOUS DISEASES, 2015, 15 (08): : 875 - 875
  • [36] Lamivudine plus a boosted-protease inhibitor as simplification strategy in HIV-infected patients with toxicity to nucleoside analogues
    Casado, J.
    De la Calle, C.
    Del Palacio, M.
    Banon, S.
    Perez Elias, M.
    Moreno, A.
    Moreno, S.
    JOURNAL OF THE INTERNATIONAL AIDS SOCIETY, 2012, 15 : 168 - 168
  • [37] Efficacy and safety of once-daily maraviroc plus ritonavir-boosted darunavir in pretreated HIV-infected patients in a real-life setting
    Macias, J.
    Recio, E.
    Marquez, M.
    Garcia, C.
    Jimenez, P.
    Merino, D.
    Munoz, L.
    Pasquau, J.
    Ojeda, G.
    Bancalero, P.
    Chueca, N.
    Pineda, J. A.
    HIV MEDICINE, 2014, 15 (07) : 417 - 424
  • [38] High-sensitivity C-reactive protein levels fall during statin therapy in HIV-infected patients receiving ritonavir-boosted protease inhibitors
    Aslangul, Elisabeth
    Fellahi, Soraya
    Assoumou, Lambert K.
    Bastard, Jean-Philippe
    Capeau, Jacqueline
    Costagliola, Dominique
    AIDS, 2011, 25 (08) : 1128 - 1131
  • [39] Immunovirological Response to Triple Nucleotide Reverse-Transcriptase Inhibitors and Ritonavir-Boosted Protease Inhibitors in Treatment-Naive HIV-2-Infected Patients: The ACHIEV2E Collaboration Study Group
    Benard, Antoine
    van Sighem, Ard
    Taieb, Audrey
    Valadas, Emilia
    Ruelle, Jean
    Soriano, Vicente
    Calmy, Alexandra
    Balotta, Claudia
    Damond, Florence
    Brun-Vezinet, Francoise
    Chene, Genevieve
    Matheron, Sophie
    CLINICAL INFECTIOUS DISEASES, 2011, 52 (10) : 1257 - 1266
  • [40] Dual therapy (ritonavir boosted atazanavir plus raltegravir) versus standard triple therapy (ritonavir boosted atazanavir plus tenofovir/emtricitabine) in patients failing first line therapy: 48 week results from a randomized pilot study
    Sued, O.
    Figueroa, M. I.
    Cesar, C.
    Patterson, P.
    Yamamoto, C.
    Fink, V.
    Luna, N.
    Gun, A.
    Cahn, P.
    INTERNATIONAL JOURNAL OF INFECTIOUS DISEASES, 2018, 73 : 23 - 23