Long-term (96-week) follow-up of antiretroviral-naive HIV-infected patients treated with first-line lopinavir/ritonavir monotherapy in the MONARK trial

被引:38
作者
Ghosn, J. [1 ,2 ]
Flandre, P. [3 ]
Cohen-Codar, I. [4 ]
Girard, P-M [5 ]
Chaix, M-L [2 ]
Raffi, F. [6 ]
Dellamonica, P. [7 ]
NgoVan, P. [4 ]
Norton, M. [8 ]
Delfraissy, J-F [1 ]
机构
[1] Bicetre Univ Hosp, AP HP, Dept Internal Med & Infect Dis, Le Kremlin Bicetre, France
[2] Paris Descartes Univ, Dept Virol, Necker Univ Hosp, AP HP,EA MRT 3620, Paris, France
[3] Univ Paris 06, INSERM, U720, Paris, France
[4] Abbott Labs, Rungis, France
[5] St Antoine Univ Hosp, AP HP, Dept Infect Dis, Paris, France
[6] Hop Hotel Dieu, Dept Infect Dis, Nantes, France
[7] Archet Hosp, Dept Infect Dis, Nice, France
[8] Abbott Pk, Chicago, IL USA
关键词
antiretroviral monotherapy; clinical study; HIV infection; HIV protease inhibitors; lopinavir; LOPINAVIR-RITONAVIR MONOTHERAPY; PROTEASE INHIBITOR; CEREBROSPINAL-FLUID; PLUS ZIDOVUDINE; CLINICAL-TRIAL; REGIMEN; THERAPY; RESISTANCE; SIMPLIFICATION; MAINTENANCE;
D O I
10.1111/j.1468-1293.2009.00752.x
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background The toxicities, cost and complexity of triple combinations warrant the search for other treatment options, such as boosted protease inhibitor (PI) monotherapy. MONotherapy AntiRetroviral Kaletra (MONARK) is the first randomized trial comparing lopinavir/ritonavir monotherapy to triple combination therapy with zidovudine/lamivudine and lopinavir/ritonavir in antiretroviral-naive patients. Methods A total of 136 antiretroviral-naive patients, with a CD4 cell count above 100 cells/mu L and a plasma HIV RNA below 100 000 HIV-1 RNA copies/mL, were randomized and dosed with either lopinavir/ritonavir monotherapy (n=83) or lopinavir/ritonavir+zidovudine/lamivudine (n=53). We focus here on patients in the lopinavir/ritonavir monotherapy arm followed to week 96. The intent-to-treat (ITT) analysis initially involved all patients randomized to lopinavir/ritonavir monotherapy (n=83), and then focused on patients who had an HIV RNA < 50 copies/mL at week 48 (n=56). Results At week 96, 39 of 83 patients (47%) had HIV RNA < 50 copies/mL, five of 83 had HIV RNA between 50 and 400 copies/mL, and three of 83 had HIV RNA > 400 copies/mL. Focusing on the 56 patients with an HIV RNA < 50 copies/mL at week 48, 38 of 56 patients (68%) had a sustained HIV RNA < 50 copies/mL to week 96. To week 96, a total of 28 patients (34%) had discontinued the study treatment. In addition, the allocated treatment was changed for seven patients. PI-associated resistance mutations were evident in five of 83 patients in the monotherapy arm from baseline to week 96. Conclusion By ITT analysis, 39 of the 83 patients initially randomized to lopinavir/ritonavir monotherapy had HIV RNA < 50 copies/mL at week 96. The occurrence in some patients of low-level viraemia (50-500 copies/mL) may increase the risk of drug resistance. First-line lopinavir/ritonavir monotherapy cannot be systematically recommended.
引用
收藏
页码:137 / 142
页数:6
相关论文
共 24 条
[1]   Lopinavir/ritonavir as single-drug therapy for maintenance of HlV-1 viral suppression -: 48-week results of a randomized, controlled, open-label, proof-of-concept pilot clinical trial (OK study) [J].
Arribas, JR ;
Pulido, F ;
Delgado, R ;
Lorenzo, A ;
Miralles, P ;
Arranz, A ;
González-García, JJ ;
Cepeda, C ;
Hervás, R ;
Paño, JR ;
Gaya, F ;
Carcas, A ;
Montes, ML ;
Costa, JR ;
Peña, JM .
JAIDS-JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES, 2005, 40 (03) :280-287
[2]  
Bongiovanni M, 2003, ANTIVIR THER, V8, P209
[3]   A 96-week comparison of lopinavir-ritonavir combination therapy followed by lopinavir-ritonavir monotherapy versus efavirenz combination therapy [J].
Cameron, D. William ;
da Silva, Barbara A. ;
Arribas, Jose R. ;
Myers, Robert A. ;
Bellos, Nicholaos C. ;
Gilmore, Norbert ;
King, Martin S. ;
Bernstein, Barry M. ;
Brun, Scott C. ;
Hanna, George J. .
JOURNAL OF INFECTIOUS DISEASES, 2008, 198 (02) :234-240
[4]   Lopinavir concentrations in cerebrospinal fluid exceed the 50% inhibitory concentration for HIV [J].
Capparelli, EV ;
Holland, D ;
Okamoto, C ;
Gragg, B ;
Durelle, J ;
Marquie-Beck, J ;
van den Brande, G ;
Ellis, R ;
Letendre, S .
AIDS, 2005, 19 (09) :949-952
[5]   Failure of lopinavir-ritonavir (Kaletra)-containing regimen in an aintiretroviral-naive patient [J].
Conradie, F ;
Sanne, I ;
Venter, W ;
Eron, J .
AIDS, 2004, 18 (07) :1084-1085
[6]   Protease Inhibitor Resistance Analysis in the MONARK Trial Comparing First-Line Lopinavir-Ritonavir Monotherapy to Lopinavir-Ritonavir plus Zidovudine and Lamivudine Triple Therapy [J].
Delaugerre, Constance ;
Flandre, Philippe ;
Chaix, Marie Laure ;
Ghosn, Jade ;
Raffi, Francois ;
Dellamonica, Pierre ;
Jaeger, H. ;
Shuermann, D. ;
Cohen-Codar, Isabelle ;
Van, Philippe Ngo ;
Norton, Michael ;
Taburet, Anne-Marie ;
Delfraissy, Jean-Francois ;
Rouzioux, Christine .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2009, 53 (07) :2934-2939
[7]   Lopinavir/ritonavir monotherapy or plus zidovudine and lamivudine in antiretroviral-naive HIV-infected patients [J].
Delfraissy, Jean-Fran Ois ;
Flandre, Philippe ;
Delaugerre, Constance ;
Ghosn, Jade ;
Horban, Andrzej ;
Girard, Pierre-Marie ;
Norton, Michael ;
Rouzioux, Christine ;
Taburet, Anne-Marie ;
Cohen-Codar, Isabelle ;
Van, Philippe Ngo ;
Chauvin, Jean-Pierre .
AIDS, 2008, 22 (03) :385-393
[8]   Isolated lopinavir resistance after virological rebound of a ritonavir/lopinavir-based regimen [J].
Friend, J ;
Parkin, N ;
Liegler, T ;
Martin, JN ;
Deeks, SG .
AIDS, 2004, 18 (14) :1965-1966
[9]  
GATHE JC, 2006, 8 ANN INT C DRUG THE
[10]  
GATHE JC, 2007, 4 IAS C SYDN AUSTR J