Lopinavir-Ritonavir Monotherapy Versus Lopinavir-Ritonavir and 2 Nucleosides for Maintenance Therapy of HIV: 96-Week Analysis

被引:104
作者
Arribas, Jose R. [1 ]
Delgado, Rafael [2 ]
Arranz, Alberto [3 ]
Munoz, Rosa [1 ]
Portilla, Joaquin [4 ]
Pasquau, Juan [5 ]
Perez-Elias, Maria J. [6 ]
Iribarren, Jose A. [7 ]
Rubio, Rafael [8 ]
Ocampo, Antonio [9 ]
Sanchez-Conde, Matilde [10 ]
Knobel, Hernando [11 ]
Arazo, Piedad [12 ]
Sanz, Jesus [3 ,13 ]
Lopez-Aldeguer, Jose [14 ]
Montes, Maria L. [1 ]
Pulido, Federico
机构
[1] Univ Autonoma Madrid, Hosp La Paz, Med Interna Serv, Madrid 28046, Spain
[2] Univ Complutense Madrid, Mol Microbiol Lab, Hosp 12 Octubre, Madrid, Spain
[3] Hosp Principe Asturias, Alcala De Henares, Spain
[4] Hosp Gen Alicante, Alicante, Spain
[5] Hosp Virgen Nieves, Granada, Spain
[6] Hosp Ramon & Cajal, E-28034 Madrid, Spain
[7] Hosp Donostia, San Sebastian, Spain
[8] Univ Complutense Madrid, Hosp 12 Octubre, Unidad VIH, Madrid, Spain
[9] Univ Vigo, Complexo Hosp, Pontevedra, Spain
[10] Hosp Gen Gregorio Maranon, Madrid, Spain
[11] Hosp del Mar, Internal Med & Infect Dis Dept, Barcelona, Spain
[12] Hosp Miguel Servet, Zaragoza, Spain
[13] Hosp La Princesa, Madrid, Spain
[14] Hosp La Fe, E-46009 Valencia, Spain
关键词
HIV; lopinavir/ritonavir; monotherapy; LOPINAVIR/RITONAVIR MONOTHERAPY; INFECTED PATIENTS; SUPPRESSION;
D O I
10.1097/QAI.0b013e3181a56de5
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: The OK04 trial has shown that 48 weeks of lopinavir-ritonavir monotherapy with reintroduction of nucleosides as needed was noninferior to continuation of triple therapy with 2 nucleosides and lopinavir-ritonavir in patients with prior stable suppression. However, it is still uncertain if this experimental strategy can maintain suppression in the long term. Methods: Patients entered this noninferiority trial (upper limit 95% confidence interval: +12%) with no history of virological failure while receiving a protease inhibitor and receiving 2 nucleosides plus lopinavir/ritonavir, with HIV RNA <50 copies per milliliter for more than 6 months. Primary end point was percent of patients without therapeutic failure, defined as confirmed HIV RNA >500 copies per milliliter with exclusion of monotherapy patients who resuppressed to <50 copies per milliliter after resuming baseline nucleosides, or loss to follow-up, or change of randomized therapy other than reinduction. Results: Through 96 weeks, percentage of patient without therapeutic failure was 87% (monotherapy, n = 100) vs. 78% (triple therapy, n = 98; 95% confidence interval: -20% to +1.2%). Percentage with HIV RNA <50 copies per milliliter (intention to treat, missing = failure, reinduction = failure): 77% (monotherapy) vs. 78% (triple therapy). Low-level viral rebound was more frequent in the monotherapy group. Twelve patients in the monotherapy group (12%) needed reinduction with nucleosides. Discontinuations due to adverse events were significantly more frequent in the triple therapy group (8%) than in the monotherapy group (0%); P = 0.003. Conclusions: At 96-week lopinavir/ritonavir monotherapy with reintroduction of nucleosides as needed was noninferior to continuation of triple therapy. Incidence of adverse events leading to treatment discontinuation was significantly lower with monotherapy. (ClinicalTrials.gov number, NCT00114933).
引用
收藏
页码:147 / 152
页数:6
相关论文
共 14 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]   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
[3]  
CAMPO R, 2007, PROGR ABSTR 14 C RET
[4]   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
[5]   Pharmacoeconomic analysis of a maintenance strategy with lopinavir/ritonavir monotherapy in HIV-infected patients [J].
Escobar, Ismael ;
Pulido, Federico ;
Perez, Esther ;
Arribas, Jose Ramon ;
Garcia, Maria del Pilar ;
Hernando, Asuncion .
ENFERMEDADES INFECCIOSAS Y MICROBIOLOGIA CLINICA, 2006, 24 (08) :490-494
[6]  
GATHE JC, 2004, PROGR ABSTR 15 INT A
[7]   Validation of a simplified medication adherence questionnaire in a large cohort of HIV-infected patients:: the GEEMA Study [J].
Knobel, H ;
Alonso, J ;
Casado, JL ;
Collazos, J ;
González, J ;
Ruiz, I ;
Kindelan, JM ;
Carmona, A ;
Juega, J ;
Ocampo, A .
AIDS, 2002, 16 (04) :605-613
[8]   The level of persistent HIV viremia does not increase after successful simplification of maintenance therapy to lopinavir/ritonavir alone [J].
McKinnon, John E. ;
Arribas, Jose R. ;
Pulido, Federico ;
Delgado, Rafael ;
Mellors, John W. .
AIDS, 2006, 20 (18) :2331-2335
[9]  
*NAT I ALL INF DIS, 2004, DIV AIDS TABL GRAD S
[10]  
*PAN ANT GUID AD A, 2008, GUID US ANT AG HIV 1