Simplification to dual antiretroviral therapy including a ritonavir-boosted protease inhibitor in treatment-experienced HIV-1-infected patients


Por: Burgos, J, Crespo, M, Falco, V, Curran, A, Navarro, J, Imaz, A, Domingo, P, Podzamczer, D, Mateo, MG, Villar, S, Van den Eynde, E, Ribera, E, Pahissa, A

Publicada: 1 oct 2012
Resumen:
To assess the effectiveness of simplification to a dual antiretroviral regimen containing a ritonavir-boosted protease inhibitor (PI/r) in treatment-experienced HIV-1-infected patients. Retrospective analysis of 131 HIV-1-infected patients on suppressive antiretroviral treatment (HIV-RNA 50 copies/mL) who switched to a maintenance dual antiretroviral regimen, containing a PI/r, in three hospitals in Spain. Virological failure was defined as confirmed HIV-RNA 50 copies/mL. The percentage of patients remaining free of therapeutic failure was estimated using the time-to-loss-of-therapeutic-response algorithm, by intent-to-treat analysis. Median baseline characteristics of the patients were 14 years on antiretroviral therapy, five prior HAART regimens and 10 different drugs, 24 months on a suppressive regimen and 522 CD4 cells/mL. Reasons for simplification to dual therapy were nucleoside reverse transcriptase inhibitor-related toxicity (46.6), removal of lamivudine/emtricitabine due to resistance (16.8), simplification from regimens containing a dual PI, enfuvirtide or tipranavir (20.6) and simplification from other complex regimens (16.0). Darunavir (58.0), lopinavir (16.8) or atazanavir (13.0) were the preferred PIs, used in combination with tenofovir (50.4), raltegravir (22.1) or etravirine (12.2). At the end of follow-up (median 14 months), 90.1 of patients remained free of therapeutic failure; corresponding data at treatment weeks 24, 48 and 96 were 93.6 (95 CI, 89.397.9), 90.9 (95 CI, 84.995.9) and 87.4 (95 CI, 80.794.1), respectively. Two (1.5) patients had virological failure and 11 (8.4) discontinued treatment due to side effects or were lost to follow-up. Simplification to a dual-therapy regimen including a PI/r might be useful to enhance convenience and/or diminish toxicity in selected treatment-experienced patients.

Filiaciones:
Burgos, J:
 Univ Autonoma Barcelona, Hosp Univ Vall dHebron, Dept Infect Dis, E-08193 Barcelona, Spain

Crespo, M:
 Univ Autonoma Barcelona, Hosp Univ Vall dHebron, Dept Infect Dis, E-08193 Barcelona, Spain

Falco, V:
 Univ Autonoma Barcelona, Hosp Univ Vall dHebron, Dept Infect Dis, E-08193 Barcelona, Spain

Curran, A:
 Univ Autonoma Barcelona, Hosp Univ Vall dHebron, Dept Infect Dis, E-08193 Barcelona, Spain

Navarro, J:
 Univ Autonoma Barcelona, Hosp Univ Vall dHebron, Dept Infect Dis, E-08193 Barcelona, Spain

Imaz, A:
 Univ Barcelona, Hosp Univ Bellvitge, Dept Infect Dis, Barcelona, Spain

Domingo, P:
 Univ Autonoma Barcelona, Infect Dis Unit, Hosp Santa Creu & St Pau, E-08193 Barcelona, Spain

Podzamczer, D:
 Univ Barcelona, Hosp Univ Bellvitge, Dept Infect Dis, Barcelona, Spain

Mateo, MG:
 Univ Autonoma Barcelona, Infect Dis Unit, Hosp Santa Creu & St Pau, E-08193 Barcelona, Spain

Villar, S:
 Univ Autonoma Barcelona, Hosp Univ Vall dHebron, Dept Infect Dis, E-08193 Barcelona, Spain

Van den Eynde, E:
 Univ Autonoma Barcelona, Hosp Univ Vall dHebron, Dept Infect Dis, E-08193 Barcelona, Spain

Ribera, E:
 Univ Autonoma Barcelona, Hosp Univ Vall dHebron, Dept Infect Dis, E-08193 Barcelona, Spain

Pahissa, A:
 Univ Autonoma Barcelona, Hosp Univ Vall dHebron, Dept Infect Dis, E-08193 Barcelona, Spain
ISSN: 03057453





JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY
Editorial
OXFORD UNIV PRESS, GREAT CLARENDON ST, OXFORD OX2 6DP, ENGLAND, Reino Unido
Tipo de documento: Article
Volumen: 67 Número: 10
Páginas: 2479-2486
WOS Id: 000309140900030
ID de PubMed: 22729925
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