| Autor: |
Raguin, Gilles, Chêne, Geneviève, Morand-Joubert, Laurence, Taburet, Anne-Marie, Droz, Cécile, Le Tiec, Clotilde, Clavel, François, Girard, Pierre-Marie, Rozenbaum, W, Naït-Ighil, L, Nguyen, TH, Slama, L, Girard, PM, Molina, JM, Sereni, D, Colin de Verdière, N, Lascoux-Combes, C, Pintado, C, Ponscarme, D, Prevoteau de Clary, F, Tourneur, M, Bentata, M, Guillevin, L, Launay, O, Mansouri, R, Rouges, F, Kazatchkine, M, Aouba, A, Azizi, M, Fiessinger, JN, Le Houssine, P, Sicard, D, Bernasconi, C, Salmon, D, Silbermann, B, Cassuto, JP, Ceppi, C, Poiree, Dr, Raguin, G, Merad, M, Delfraissy, JF, Goujard, C, Quertainmont, Y, Perronne, C, de Truchis, P, Dupont, B, Bresson, JL, Calatroni, I, Raffi, F, Esnault, JL, Leautez, S |
| Zdroj: |
Antiviral Therapy; May 2004, Vol. 9 Issue: 4 p615-625, 11p |
| Abstrakt: |
Objectives To compare the antiviral efficacy of a salvage therapy combining lopinavir and amprenavir with 200 mg/d or 400 mg/d ritonavir, together with nucleoside reverse transcriptase inhibitors, over a 26-week period in HIV-infected patients in whom multiple anti-retroviral regimens had failed.Design Phase IIb, randomized, open-label, multicentre trial. Patients were eligible if they had <500 CD4+ cells/mm3and >4 log10copies/ml HIV-RNA after treatment with at least two protease inhibitors (PIs) and one non-nucleoside reverse transcriptase inhibitor.Results At baseline (n=37), the median CD4+ cell count was 207/mm3and the median plasma HIV-1 RNA level was 4.7 log10copies/ml; the median number of PI mutations was seven and the median decrease in phenotypic susceptibility to lopinavir and amprenavir was 9.7 and 2.6, respectively. The mean number of antiretrovirals received prior to randomization was 7.7. The fall in the median HIV-1 RNA level at week 26 was -1.4 log10copies/ml in the 200 mg/d ritonavir group and -2.5 log10copies/ml in the 400 mg/d group (P=0.02). Viral load fell below 50 copies/ml in 32% and 61% of patients, respectively (P=0.07). After adjustment for the ritonavir dose, a smaller number of PI mutations was the only baseline characteristic associated with a better virological response at week 26. Amprenavir concentrations were significantly lower in presence of lopinavir. The lopinavir inhibitory quotient at week 6 correlated weakly with the change in the HIV-RNA level at week 26.Conclusion Combination of amprenavir, lopinavir and 400 mg/d ritonavir shows significant virological efficacy without increased toxicity in HIV-infected patients in whom multiple antiretroviral regimens have failed. |
| Databáze: |
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