Virologic suppression in patients with a documented M184V/I mutation based on the number of active agents in the antiretroviral regimen

被引:2
作者
Mouradjian, Mallory T. [1 ,2 ]
Heil, Emily L. [3 ]
Sueng, Hyunuk [3 ]
Pandit, Neha Sheth [3 ]
机构
[1] Univ Maryland, Med Ctr, Dept Pharm Serv, Baltimore, MD 21201 USA
[2] MedStar Union Mem Hosp, Dept Pharm Serv, 201 E Univ Pkwy, Baltimore, MD 21218 USA
[3] Univ Maryland, Sch Pharm, Dept Pharm Practice & Sci, Baltimore, MD 21201 USA
来源
SAGE OPEN MEDICINE | 2020年 / 8卷
关键词
HIV; reverse transcriptase inhibitors; mutation; resistance; M184V/I; antiretroviral therapy; HIV-1-INFECTED PATIENTS; REVERSE-TRANSCRIPTASE; OPEN-LABEL; VIRUS; LAMIVUDINE; MAINTENANCE; MONOTHERAPY; THERAPY;
D O I
10.1177/2050312120960570
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives: The optimal antiretroviral therapy for patients with the M184V/I mutation is not known. The primary objective of this study was to determine the efficacy of various antiretroviral therapies in patients with HIV and the M184V/I mutation based on the number of active antiretroviral agents. Methods: A retrospective chart review was conducted of 100 treatment-experienced patients harboring the M184V/I mutation seen at an urban HIV clinic. Efficacy was classified as percentage of patients with viral suppression defined as HIV RNA viral load <200 copies/mL at last measurement on current antiretroviral therapy, stratified by the number of active antiretroviral agents. Results: The primary outcome of viral suppression occurred in 70.6% (12/17) of patients on <2 active agents, 77.2% (44/57) on 2-2.5 active agents, and 69.2% (18/26) on 3 active agents. No significant difference was found between viral suppression and patients on <2 and 2-2.5 antiretroviral agents (odds ratio = 0.71, 95% confidence interval = (0.21, 2.39), p = 0.8) or between patients on 3 and 2-2.5 active agents (odds ratio = 0.66, 95% confidence interval = (0.23, 1.88), p = 0.7). The most commonly prescribed regimen consisted of a boosted protease inhibitor with an integrase strand transfer inhibitor and two nucleoside reverse transcriptase inhibitors, one of which being lamivudine or emtricitabine. Conclusion: Similar rates of viral suppression were observed in patients regardless of the number of active antiretroviral agents prescribed. Regimens containing less than 3 active agents may maintain virologic suppression in patients with the M184V/I mutation. Further studies are needed to determine optimal antiretroviral therapy for patients with the M184V/I mutation.
引用
收藏
页数:7
相关论文
共 18 条
  • [1] [Anonymous], 2019, GUID US ANT AG AD AD
  • [2] Dolutegravir plus lamivudine versus dolutegravir plus tenofovir disoproxil fumarate and emtricitabine in antiretroviral-naive adults with HIV-1 infection (GEMINI-1 and GEMINI-2): week 48 results from two multicentre, double-blind, randomised, non-inferiority, phase 3 trials
    Cahn, Pedro
    Sierra Madero, Juan
    Ramon Arribas, Jose
    Antinori, Andrea
    Ortiz, Roberto
    Clarke, Amanda E.
    Hung, Chien-Ching
    Rockstroh, Jurgen K.
    Girard, Pierre-Marie
    Sievers, Jorg
    Man, Choy
    Currie, Alexander
    Underwood, Mark
    Tenorio, Allan R.
    Pappa, Keith
    Wynne, Brian
    Fettiplace, Anna
    Gartland, Martin
    Aboud, Michael
    Smith, Kimberly
    [J]. LANCET, 2019, 393 (10167) : 143 - 155
  • [3] Antiviral activity of lamivudine in salvage therapy for multidrug-resistant HIV-1 infection
    Campbell, TB
    Shulman, NS
    Johnson, SC
    Zolopa, AR
    Young, RK
    Bushman, L
    Fletcher, CV
    Lanier, ER
    Merigan, TC
    Kuritzkes, DR
    [J]. CLINICAL INFECTIOUS DISEASES, 2005, 41 (02) : 236 - 242
  • [4] Lamivudine monotherapy in HIV-1-infected patients harbouring a lamivudine-resistant virus: a randomized pilot study (E-184V study)
    Castagna, A
    Danise, A
    Menzo, S
    Galli, L
    Gianotti, N
    Carini, E
    Boeri, E
    Galli, A
    [J]. AIDS, 2006, 20 (06) : 795 - 803
  • [5] Boosted protease inhibitor monotherapy versus boosted protease inhibitor plus lamivudine dual therapy as second-line maintenance treatment for HIV-1-infected patients in sub-Saharan Africa (ANRS12 286/MOBIDIP): a multicentre, randomised, parallel, open-label, superiority trial
    Ciaffi, Laura
    Koulla-Shiro, Sinata
    Sawadogo, Adrien Bruno
    Ndour, Cheik Tidiane
    Eymard-Duvernay, Sabrina
    Mbouyap, Pretty Rosereine
    Ayangma, Liliane
    Zoungrana, Jacques
    Gueye, Ndeye Fatou Ngom
    Diallo, Mohamadou
    Izard, Suzanne
    Bado, Guillaume
    Kane, Coumba Toure
    Aghokeng, Avelin Fobang
    Peeters, Martine
    Girard, Pierre Marie
    Le Moing, Vincent
    Reynes, Jacques
    Delaporte, Eric
    [J]. LANCET HIV, 2017, 4 (09): : E384 - E392
  • [6] Molecular impact of the M184V mutation in human immunodeficiency virus type 1 reverse transcriptase
    Diallo, K
    Götte, M
    Wainberg, MA
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2003, 47 (11) : 3377 - 3383
  • [7] Impact of the M184V Resistance Mutation on Virological Efficacy and Durability of Lamivudine-Based Dual Antiretroviral Regimens as Maintenance Therapy in Individuals With Suppressed HIV-1 RNA: A Cohort Study
    Gagliardini, Roberta
    Ciccullo, Arturo
    Borghetti, Alberto
    Maggiolo, Franco
    Bartolozzi, Dario
    Borghi, Vanni
    Pecorari, Monica
    Di Biagio, Antonio
    Callegaro, Anna Paola
    Bruzzone, Bianca
    Saladini, Francesco
    Paolucci, Stefania
    Maserati, Renato
    Zazzi, Maurizio
    Di Giambenedetto, Simona
    De Luca, Andrea
    [J]. OPEN FORUM INFECTIOUS DISEASES, 2018, 5 (06):
  • [8] Genotypic susceptibility score (GSS) and CD4+T cell recovery in HIV-1 patients with suppressed viral load
    Gonzalez-Serna, Alejandro
    Glas, Arie C.
    Brumme, C. J.
    Poon, Art F. Y.
    De la Rosa, Adriana Nohpal
    Mudrikova, Tania
    Lima, Viviane Dias
    Wensing, Annemarie M. J.
    Harrigan, Richard
    [J]. JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2017, 72 (02) : 496 - 503
  • [9] The M184V mutation in the reverse transcriptase of human immunodeficiency virus type 1 impairs rescue of chain-terminated DNA synthesis
    Götte, M
    Arion, D
    Parniak, MA
    Wainberg, MA
    [J]. JOURNAL OF VIROLOGY, 2000, 74 (08) : 3579 - 3585
  • [10] A Randomized, Open-Label Trial to Evaluate Switching to Elvitegravir/Cobicistat/Emtricitabine/Tenofovir Alafenamide Plus Darunavir in Treatment-Experienced HIV-1-Infected Adults
    Huhn, Gregory D.
    Tebas, Pablo
    Gallant, Joel
    Wilkin, Timothy
    Cheng, Andrew
    Yan, Mingjin
    Zhong, Lijie
    Callebaut, Christian
    Custodio, Joseph M.
    Fordyce, Marshall W.
    Das, Moupali
    McCallister, Scott
    [J]. JAIDS-JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES, 2017, 74 (02) : 193 - 200